Senior OEM Partnerships Manager, Scientific Instruments & QC (REMOTE)
USP
Remote job
Who is USP? The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world's leading health and science experts to develop rigorous quality standards for medicines, dietary supplements, and food ingredients. At USP, we believe that scientific excellence is driven by a commitment to fairness, integrity, and global collaboration. This belief is embedded in our core value of Passion for Quality and is demonstrated through the contributions of more than 1,300 professionals across twenty global locations, working to strengthen the supply of safe, high-quality medicines worldwide. At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health. USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds-regardless of background-to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment. Remote employees must reside in one of the following states: MD, VA, DC, PA, WV, CA, MI, IL, KS, FL, NC, or MN. Brief Job Overview The Senior OEM Partnerships Manager, Scientific Instruments & QC is a key individual contributor position in USP's Digital and Innovation division. The incumbent is responsible for B2B sales of USP's digital products and for establishing collaborations with vendor/distributors. This role will be 100% remote. The position reports to the Senior Business Development Manager, in the Digital and Innovation division. USP's Digital and Innovation division is developing next-generation digital tools for the future of analytical chemistry, pharmaceutical manufacturing, supply chain management, and more. In this position, you will help organizations to realize that digital future by leading external engagements that increase the adoption and sustainability of the digital products. The applicant's current portfolio includes USP method digitalization, NMR analysis, and digital standards related software products and services, but more may be added in the future. How will YOU create impact here at USP? As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards. Additionally, USP's People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments. The Senior OEM Partnerships Manager, Scientific Instruments & QC has the following responsibilities: OEM & Strategic Partner Development Identify, engage, and cultivate relationships with instrument and analytical technology OEM partners to jointly position digital USP reference standards within their product ecosystems. Develop joint go-to-market strategies with OEMs and distributors to drive adoption among pharmaceutical manufacturers, CDMOs, CROs, and QC laboratories. Serve as the primary liaison for partner enablement, including training, co-marketing, and pipeline development. New Business Development Prospect and identify mutual opportunities with OEMs and end users to integrate USP's digital products within existing instrument and informatics workflows. Build and maintain a qualified pipeline of partner-led opportunities, ensuring consistent alignment with joint business objectives. Sales Execution Lead consultative sales discussions with end users in collaboration with OEM partners, highlighting the value of digital USP reference standards in improving data integrity, compliance, and lab efficiency. Deliver co-branded product demos and presentations that showcase the integration of USP digital solutions with OEM instruments or QC workflows. Collaborate with USP Product, Science, and Legal teams to structure proof-of-concept engagements, negotiate agreements, and accelerate deal closure. Account & Partner Management Develop long-term, trust-based relationships with OEM partners and key customer accounts, ensuring sustained collaboration and market growth. Partner with Customer Success and Product teams to ensure seamless onboarding, integration, and customer satisfaction for OEM-linked deployments. Market Feedback & Strategy Capture and communicate market insights from OEMs and end users to inform product roadmap and partnership strategy. Stay current on scientific instrument trends, lab digitalization initiatives, and regulatory standards (e.g., 21 CFR Part 11, USP-NF) to position USP as a forward-thinking collaborator in the digital QC space. Who is USP Looking For? The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience: Bachelor degree in Life Sciences (chemistry, chemical engineering, cheminformatics, etc) or a related field. 5 years of B2B SaaS or laboratory technology, or scientific instrument sales experience, preferably in pharma, life sciences, or lab informatics. Demonstrated success in partner selling and go-to-market collaboration with instrument or analytical technology OEMs to drive end-user adoption. Strong understanding of QC laboratory workflows and the digitalization of analytical methods or reference standards. Experience engaging technical, commercial, and regulatory stakeholders to position joint solutions that deliver measurable value. Excellent consultative selling, negotiation, and account development skills, with a track record of building long-term partnerships. Familiarity with laboratory systems (Chromatography Data Systems, LIMS, ELNs) and analytical instruments (HPLC, NMR, FTIR, Raman, etc.). Working knowledge of pharmaceutical quality and regulatory standards (e.g., USP-NF, 21 CFR Part 11, data integrity). Exceptional communication, presentation, and OEM relationship management skills, including the ability to co-present joint digital solutions to end users. Proficiency with CRM platforms (Salesforce, HubSpot) and partner pipeline reporting for joint business planning and forecast management. Additional Desired Preferences Advanced scientific degree preferred. MBA preferred. Knowledge and experience with pharmaceutical process development, technology transfer, manufacturing, and QC. Experience with OEM or channel partnerships in pharma, life sciences, or QC environments. Experience with bio/pharma analytics products. Experience leading multiple, complex, cross-functional projects; and doing so in a highly matrixed organization. Experience with consultative sales and business development in bio/pharma. Excellent relationship-building, partnering, facilitating, negotiating and influencing skills. Supervisory Responsibilities None, this is an individual contributor role. Benefits USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected. Compensation Base Salary Range: USD $123,400.00 - $156,550.00 annually. Target Annual Bonus: % Varies based on level of role. Individual compensation packages are based on various factors unique to each candidate's skill set, experience, qualifications, equity, and other job-related reasons. Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP$123.4k-156.6k yearly 53d agoTechnical Marketing Specialist
Wuxi Apptec
Remote job
Technical Marketing Specialist-CMC (San Diego, CA) - Analyze pharmaceutical project and technical requirements for CMC projects for business development; Help maintain relationships with external vendors and identify the right opportunities to enhance our technical visibility; Support business growth objectives of contract pharmaceutical research, development, and manufacturing (CRDMO) business through industry and engineering engagement and conferences, applying knowledge of chemical engineering, biochemistry, pharmaceutical project management, Chemistry, Manufacturing, and Controls (CMC) management, applying HPLC, LCMS, UV, IR; Develop scientific messaging, drive branding, and engage in communications with technical staff on the side of pharmaceutical companies; Lead technical project marketing alignment activities by applying technical expertise in chemical engineering, chemistry, and biochemistry in communication with scientific and technical subject matter experts and business development teams; Contribute to customer engagement strategy, maximizing ROI through conferences and events. Qualifications Must have a Bachelor's Degree in Pharmaceutical Science, Chemistry, or Chemical Engineering plus 2 years of experience in business development in pharmaceutical industry or in CRDMO. Require skills and knowledge in CRDMO and CMC management. $124,090.00~$127k/year. Allow telecommuting. Require 10% travel for events in the US. Job location: San Diego, CA. Submit résumé referencing job code LIL011 to HR, STA Pharmaceuticals US LLC, 6114 Nancy Ridge Drive, Building D, San Diego, CA 92121. An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status, and will not be discriminated against on the basis of disability. This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. Employees holding this position will be required to perform any other job-related duties as requested by Management. We can recommend jobs specifically for you! An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability Click here to get started.$124.1k-127k yearly Auto-Apply 5d agoURGENTLY HIRING: R&D Scientist I
Actalent
Columbus, OH
As an R&D Scientist I, you will conduct chemical and physical analyses to support the development of manufacturable multisource pharmaceutical products. You will provide analytical support for the release of registration materials in support of regulatory submissions and assist in analytical method validation and transfer activities. Responsibilities * Prepare samples and conduct standard weighing and dilutions. * Perform wet chemistry, titrations, HPLC, NGI, and admitted dose analyses. * Support product development, registration lot release, and regulatory submission activities. * Execute analytical tasks within assigned timelines, ensuring compliance with cGXP's and company procedures. * Follow work instructions, SOPs, and company practices, documenting analytical activities accurately and maintaining data integrity. * Identify challenges in analytical methods and support troubleshooting activities. Essential Skills * Proficiency in sample preparation, chemistry, and biochemistry. * Experience with wet chemistry, titration, and pH and viscosity measurement. * Ability to conduct research and development for new product development. * Strong analytical skills and the ability to work with data acquisition software. * Good written and verbal communication skills. * Ability to work on multiple tasks in a fast-paced environment with supervision using scientific judgment. Additional Skills & Qualifications * Bachelor's degree in Chemistry or a related field. * Entry-level graduates with lab experience from school are encouraged to apply. * Prefer candidates with lab experience outside of academia. * Experience in physical and chemical testing of organic materials. * Ability to work effectively in a team environment. Work Environment You will be part of a team consisting of Scientist I's, II's, and III's, collaborating to complete tasks while also working independently. The lab is state-of-the-art and maintains a very clean GMP environment. The dress code is business casual. The work schedule is Monday to Friday from 8:00 AM to 4:30 PM. This role offers significant opportunities for growth in one of the largest pharmaceutical manufacturing companies in Columbus, Ohio. Job Type & Location This is a Contract to Hire position based out of Columbus, OH. Pay and Benefits The pay range for this position is $24.00 - $24.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Columbus,OH. Application Deadline This position is anticipated to close on Dec 16, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.$24-24 hourly 10d agoREMOTE Healthcare Data Analyst
Insight Global
Remote job
Insight Global is seeking a fully remote Healthcare Data Analyst to join the team of one of their largest healthcare clients. This individual will join the team as a contract employee and will be working alongside the Health Partner Lifecycle (HPLC) team on exisiting provider data as well as new market implementations. This person will help with the decision-making process for proposed initiatives as well as operational objectives. They will be expected to manage the scope across the HPLC's strategic initiatives and will be assuming a leading role in operational readiness. There will be cross- functional communication and mentorship where ideas will be challenged and new approaches will be found. This opportunity will impact the HPLC team greatly. We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to ********************.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: **************************************************** Skills and Requirements 5+ years of experience as a Data Analyst within healthcare Facets experience Provider Data Experience Strong independent worker$57k-80k yearly est. 25d agoManager, Analytical Development
Axsome Therapeutics, Inc.
Remote job
Axsome Therapeutics is a biopharmaceutical company leading a new era in the treatment of central nervous system (CNS) conditions. We deliver scientific breakthroughs by identifying critical gaps in care and develop differentiated products with a focus on novel mechanisms of action that enable meaningful advancements in patient outcomes. Our industry-leading neuroscience portfolio includes FDA-approved treatments for major depressive disorder, excessive daytime sleepiness associated with narcolepsy and obstructive sleep apnea, and migraine, and multiple late-stage development programs addressing a broad range of serious neurological and psychiatric conditions that impact over 150 million people in the United States. Together, we are on a mission to solve some of the brain's biggest problems so patients and their loved ones can flourish. For more information, please visit us at ************** and follow us on LinkedIn and X. About This Role Axsome Therapeutics is seeking a Manager, Analytical Development to manage and coordinate analytical activities on multiple early and/or late phase clinical development programs. The ideal candidate will be a team player comfortable working on a small team in a fast-paced environment and with contract manufacturing and development organizations. Excellent time management skills and communication will be key in succeeding in this role. This position requires an extensive hands-on laboratory experience using a broad array of analytical instrumentation. This role is based at Axsome's HQ in New York City with an on-site requirement of at least three days per week. We are unable to consider candidates who are looking for fully remote roles. Job Responsibilities and Duties include, but are not limited to, the following: * Work closely with the CMC team (and specifically the head of analytical development) to manage and coordinate analytical activities on multiple early phase drug substance (40%) and drug product (60%) small molecule solid oral formulation programs * Manage early and/or late phase drug substance and drug product analytical activities at contract development laboratories (method development, method qualifications/validations, method transfers, analytical investigations support) * Review and/or author analytical technical/development and method qualification/validation reports and raw data as well as release and stability data packages * Assist in authoring CMC sections for regulatory submissions * Manage drug substance and drug product stability programs (QC and technical review of stability data packages that includes raw data, and stability data trend analysis) * Assist in the development of standard operating procedures * Manage reference materials and reference standards inventory and (re)qualification testing Requirements / Qualifications * Bachelor's degree in Analytical Chemistry or Chemistry or related field with 5+ years' experience or MS/PhD with 3+ years of GMP and GLP-related pharmaceutical industry experience in small molecule solid oral formulation analytical development * Knowledge of drug product solid oral dose formulations * Hands-on experience with drug substance and drug product analytical techniques such as HPLC, GC, KF, MS, dissolution, spectroscopy, and particle size * Functional understanding of small molecule analytical development and associated regulatory and quality requirements * Hands on experience with LC-MS/MS and GC-MS is a plus * Ability to work on site Monday, Tuesday & Thursday. We are unable to consider candidates who are looking for fully remote roles Experience, Knowledge and Skills * Demonstrated experience in managing outsourced analytical activities * Demonstrated experience in QC data review of release and stability data packages for both drug substance and drug product * Experience working on commercial stage products highly valued * Excellent verbal and written communication skills * Excellent problem solving and interpersonal skills * Exceptional organizational skills with the ability to multi-task and prioritize workload based upon changing priorities. * Ability to work in a cross-functional team environment and to be a team player as well as the ability to work independently * Flexibility to accommodate multiple time zones as needed * Preference to energetic candidates with a desire to think "outside the box" * Willingness to travel periodically as needed Salary & Benefits The anticipated salary range for this role is $120,000 - $135,000. We encourage candidates of all levels to apply as there may be flexibility on final job title and responsibilities. The salary offer will be based on a variety of factors, including experience, qualifications, internal equity and location. Axsome offers a competitive employment package that includes an annual bonus, significant equity and a generous benefits package. Axsome is committed to equal employment opportunity and providing reasonable accommodations to applicants with physical and/or mental disabilities. We value and encourage diversity and solicit applications from all qualified applicants without regard to race, color, gender, sex, age, religion, creed, national origin, sexual orientation, gender identity, ancestry, citizenship, marital status, physical or mental disability, medical condition, veteran status, genetic information, or any other characteristic protected by federal, state, or local law. Axsome Therapeutics does not accept unsolicited resumes from recruiters or third-party recruitment agencies and will not pay placement fees for unsolicited candidates that are sent to hiring managers, the HR team or other Axsome team members. Only approved vendors who have been explicitly asked to support a specific search will receive access to our Applicant Tracking System to submit candidates for consideration.$120k-135k yearly 12d agoSenior Technician, Repair Center
Danaher
Remote job
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At SCIEX, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. As part of SCIEX, you will help to influence life changing research and outcomes, while accelerating your potential. For more than 50 years, we have been empowering our customers to solve the most impactful analytical challenges in quantitation and characterization through ground-breaking innovation and outstanding reliability and support. You will be part of a winning team, enabled by DBS, that is passionate about helping life science experts around the world get to answers they can trust. Learn about the Danaher Business System which makes everything possible. Are you looking to further develop your career in the scientific instrumentation maintenance & repair industry? The Repair Center Technician is responsible for unpacking, setup, troubleshooting/repair, calibrations and performance testing of instrumentation in support of the SCIEX service certification process. This position works independently to resolve all assigned technical issues in a WO (work order) driven high-transaction repair depot environment. Willing and able to mentor and develop less experienced staff members. This position reports to the Manager, Repair Center and is part of the Field Service organization working onsite at the Dallas Repair Center facility located in Coppell, TX. In this role, you will have the opportunity to: Perform advanced troubleshooting and maintenance on mass spectrometers, HPLC and/or capillary electrophoresis instrumentation with a solid understanding of Sciex instrumentation. Maintain a high-quality focus and efficiency with Repair Center activities. Assists with researching root cause and implementing corrective actions for reported quality issues using available DBS tools and methodology. Completes administrative duties (logging repair center activities, expense reporting, inventory management, etc.) The essential requirements of the job include Associate's degree (A.S./A.A.S) or Bachelor's degree (B.S./B.A.) in Life Sciences, Chemistry, Engineering or equivalent experience (i.e. Military Certificates in electronics or avionics). Liquid chromatography and/or capillary electrophoresis experience, prior experience operating and/or servicing mass spectrometry or scientific instrumentation. Travel, Motor Vehicle Record & Physical/Environment Requirements: Ability to travel - Limited travel, primarily for job training Ability and willingness to lift up to 50 lbs. along with ability to walk, climb, stand, carry materials, stoop, kneel, and bend at the waist for extended periods of time. It would be a plus if you also possess previous experience in: Strong mechanical, electro-mechanical, and/or electronics troubleshooting skills Salesforce administrative workflows, e.g. debriefing Inventory tracking and reporting SCIEX, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info. At SCIEX we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for SCIEX can provide. #LI-JP1 Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit **************** Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The U.S. EEO posters are available here. We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:************** or applyassistance@danaher.com.$39k-45k yearly est. Auto-Apply 60d+ agoSenior Flavourist Beverages (m/f/d)
Givaudan Ltd.
Remote job
Join us and celebrate the beauty of human experience. Create for happier, healthier lives, with love for nature. Together, with passion and creativity, we deliver food innovations, craft inspired fragrances and develop beauty and wellbeing solutions. There's much to learn and many to learn from, with more than 16,000 employees around the world to explore ideas and ambitions with. Every day, your talent, your innovative spirit, and your determination will shape our future, making a positive difference on billions of people. Every essence of you enriches our world. We are Givaudan. Human by nature. As Sr Flavourist in Givaudan, you will work for a company that touches billions of consumers more than a hundred times a day. Our passion for our customers - the big food and beverage companies - and their brands brings a new dimension to our Business to Business industry. You will work for the market leader that is at the forefront of innovation in an industry of emotions. We have a culture that works to inspire, challenge and capture the heart and soul of consumers and customers. Our customers have national and international profiles, which brings diversity and curiosity to our daily job. In your role, you will contribute to our business growth by developing flavours for our customers in Germany. You will work on reactive customer briefs, but also come with proactive ideas to help our customers bring consumer preferred and differentiating products on the market. You will be part of the Commercial team Germany based on Dortmund and you will report to the Technical Manager Germany. Sounds interesting? It could well be your perfect opportunity if, like us, you always aim to exceed customer needs, deliver value and are skilled at fostering strong customer relationships. In this exciting job you will: * Formulate new flavour creations or modify existing flavours to meet customer requirements, internal test-ing needs, or new technology development at an expert level for selected flavour types * Execute daily brief-related tasks and manage assigned projects and provide flavours which meet all defined customer needs and which meet good manufacturing practices, sample scale-up, production re-quirements, regulatory compliance, etc. as well as leading customer visits for flavor creation and product presentations at the customer when required * Establish and maintain relationships with a broad number of complex customers; able to gain their trust and respect * Be a technical expert and advisor to marketing, sales, and customers for ingredient and flavour performance at an expert level for selected flavour types to resolve flavour production issues and customer complaints and complete ownership of created flavours * Coordinate the evaluation of materials developed internally or from external sources and assess potential for flavour creation * Prepare flavour samples as requested for customer briefs, applications needs, technology performance assessment, QC standards and physical testing * Be a local champion for new technologies * Coach, train, mentor and manage flavour assistants and flavourists * Maintain a safe, clean and organized lab environment in accordance with EH&S policies and hold others accountable for following these guidelines, and participate in designing the rules which are required About You: * 7+ years experience as a Flavourist after completion of Givaudan Flavourist Training programme or accepted industry equivalent * Flavour Creation experience in the Beverages segment * Demonstrates expert level tasting skills with an expert level ability to understand how to adjust a flavour formulation in the direction needed for flavour modifications * Expert level knowledge of raw materials and flavour ingredients with an expert level ability to formulate many flavour types to deliver flavour performance for customer briefs, problem solving processes, re-search and development needs, etc. * Expert level ability to interface with customers and effectively discuss flavour creation needs for multiple flavour types and provide direction to help solve flavour performance issues in their applications * Ability to prepare and present flavour creation related technical presentations with some basic elements of other functions such as applications, sensory, consumer understanding, analytical science, marketing, etc. * Expert level knowledge of formulating suitable delivery systems for various application bases * Expert level knowledge of analytical methodologies (GC-MS, HPLC) * Expert level of knowledge of the technology used for improved performance, specific technical aspects affecting flavour stability in base, etc. for a few flavour types * Ability to supervise and manage flavour assistant(s) * Fluent knowledge of English (spoken and written) Our Benefits: * Company pension scheme * Flaxible working hours * Bicycle leasing * 30 days holiday * Access to the fitness center * Massage at work * Fresh bio-fruit, water/coffee/tea for free of charge * And so much more In accordance with the General Equal Treatment Act (AGG), all applications are treated fairly and without discrimination, regardless of any disability. We strive to create an inclusive working environment in which all employees can develop their full potential. At Givaudan, you contribute to delightful taste and scent experiences that touch people's lives. You work within an inspiring teamwork culture - where you can thrive, collaborate and learn from other talented and passionate people across disciplines, regions and divisions. Every essence of you enriches our world. Diversity drives innovation and creates closer connections with our employees, customers and partners. Givaudan embraces diversity and is committed to building an inclusive environment where everyone impacts our world. Remote working: On-site At Givaudan, you contribute to delightful taste and scent experiences that touch people's lives. You work within an inspiring teamwork culture - where you can thrive, collaborate and learn from other talented and passionate people across disciplines, regions and divisions. Join us and Impact Your World Diversity drives innovation and creates closer connections with our employees, customers and partners. Givaudan embraces diversity and is committed to building an inclusive environment where everyone impacts our world.$96k-122k yearly est. 58d agoQC Scientist I
Actalent
Columbus, OH
We are seeking a dedicated QC Scientist I to join our team, where you will play a vital role in bench testing. This includes sample preparation, wet chemistry, standard weighs, and dilutions. Over time, you will receive training in High-Performance Liquid Chromatography (HPLC) and Gas Chromatography (GC). You will gain experience in both Oral Dose Solids and Nasals departments, conducting chemical and physical analyses to support the development of manufacturable multisource pharmaceutical products. Your work will provide analytical support for the release of registration materials and assist in analytical method validation and transfer activities. Responsibilities * Conduct chemical and physical analyses in support of product development and registration lot release. * Provide analytical support for regulatory submissions. * Perform assigned analytical tasks within timelines and in compliance with cGXP's and company procedures. * Follow work instructions, SOPs, and company practices to document analytical activities and results accurately. * Maintain data integrity and follow written analytical procedures. * Identify execution challenges of analytical methods and support troubleshooting activities. Essential Skills * Proficiency in dilutions, sample preparation, and chemistry. * Experience in quality control and chemical testing. * Bachelor's degree in a science field, preferably in Chemistry or Biochemistry. * Prior lab experience, preferably outside of academia. * Ability to work in a team environment and handle multiple tasks in a fast-paced environment. * Strong written and verbal communication skills. * Capability to work with supervision using scientific judgment and professional competency. Additional Skills & Qualifications * Candidates with degrees in Biology, Microbiology, or Pharmaceutical Science may be considered if they have strong chemistry lab experience. Work Environment This position is in a fast-paced environment, with work conducted in both the quality group and occasionally the manufacturing area. The role operates on the 2nd shift, Monday through Friday, from 3:00 PM to 11:30 PM. Flexibility is available, starting with a 5-day, 8-hour schedule, which can transition to a 4-day, 10-hour schedule after training. This is a great opportunity for growth, as the company promotes from within and offers ample upward mobility. Job Type & Location This is a Contract to Hire position based out of Columbus, OH. Pay and Benefits The pay range for this position is $24.00 - $24.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Columbus,OH. Application Deadline This position is anticipated to close on Dec 16, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.$24-24 hourly 10d agoAssociate Director/Director, Analytical Development
Bridgebio
Remote job
Mavericks Wanted When was the last time you achieved the impossible? If that thought feels overwhelming, you might want to pause here, but if it sparks excitement...read on In 2015, we pioneered a “moneyball for biotech” approach, pooling projects and promising early-stage research from academia together under one financial umbrella to reduce risk and unleash innovation. This model allows science and small teams of experts to lead the way. We build bridges to groundbreaking advancements in rare disease, and develop life-changing medicines for patients with unmet needs as fast as humanly possible. Together we define white space, push boundaries and empower people to solve problems. If you're someone who defies convention, join us and work alongside some of the most respected minds in the industry. Together, we'll ask "why not?" and help reengineer the future of biopharma. What You'll Do We are looking for an experienced Analytical Associate Director/Director to join our expanding CMC team. This position works directly with the Senior Director of Analytical Development, CMC and manages an analytical team that oversees multiple CDMOs analytical development and quality control activities. If you have a complete understanding of GMP requirements and experience working on various drug development phases, we would love to hear from you! Responsibilities Oversee both international and US based contract development and manufacturing organizations (CDMOs) to manage analytical development and quality control (QC) activities for our drug substance (DS) and drug product (DP) suppliers Lead, coach and develop a team of direct reports, fostering a high-performance growth-oriented culture Manage DS and DP stability programs and corresponding shelf-life determinations Regularly and clearly communicate Analytical Development and QC topics both verbally and in visual presentation form, efficiently and contextually Support and author analytical content for CMC Regulatory for US and Rest of World dossiers Support Quality Assurance audits, as a QC subject matter expert, as needed Provide on-site technical support on an as-needed basis to oversee various manufacturing/scale-up/validation activities Proactively interface effectively with other CMC team members (e.g. Process Chemistry, Formulation Development, Quality Assurance, Supply Chain, etc.) Where You'll Work This is a U.S.-based remote role that will require quarterly, or as needed visits to our San Francisco Office. Who You Are Degree (BS or MS) with 7+ years of relevant analytical chemistry experience. PhD preferred Oversite of external QC laboratories (e.g., method development, method validation & troubleshooting analytical procedures) Experience with stability and shelf-life management Practical working knowledge of ICH guidance Knowledge of small molecule chemical characterization techniques Broad understanding of analytical techniques, with a focus on (U) HPLC Hands-on GMP experience with all phases of drug development including experiencing authoring IND/IMPD and marketing applications, as well as in-depth knowledge and complete understanding of GMP requirements Ability to critically evaluate and troubleshoot complex problems while offering timely and informed options for resolution Strong verbal & written communication skills, with the ability to effectively interact with and influence different functional groups across all levels of management Position requires up to 20% travel Strong focus on quality and attention to detail Rewarding Those Who Make the Mission Possible We have high expectations for our team members. We make sure those working hard for patients are rewarded and cared for in return. Financial Benefits: Market leading compensation 401K with 100% employer match on first 3% & 50% on the next 2% Employee stock purchase program Pre-tax commuter benefits Referral program with $2,500 award for hired referrals Health & Wellbeing: Comprehensive health care with 100% premiums covered - no cost to you and dependents Mental health support via Spring Health (6 therapy sessions & 6 coaching sessions) Hybrid work model - employees have the autonomy in where and how they do their work Unlimited flexible paid time off - take the time that you need Paid parental leave - 4 months for birthing parents & 2 months for non-birthing parents Flex spending accounts & company-provided group term life & disability Subsidized lunch via Forkable on days worked from our office Skill Development & Career Paths: People are part of our growth and success story - from discovery to active drug trials and FDA pipelines, there are endless opportunities for skill development and internal mobility We provide career pathing through regular feedback, continuous education and professional development programs via LinkedIn Learning, LifeLabs, Spring Health & BetterUp Coaching We celebrate strong performance with financial rewards, peer-to-peer recognition, and growth opportunities At BridgeBio, we strive to provide a market-competitive total rewards package, including base pay, an annual performance bonus, company equity, and generous health benefits. Below is the anticipated salary range for candidates for this role who will work in California. The final salary offered to a successful candidate will depend on several factors that may include but are not limited to the type and length of experience within the job, type, and length of experience within the industry, educational background, location of residence and performance during the interview process. BridgeBio is a multi-state employer, and this salary range may not reflect positions based in other states. Salary$208,200-$239,720 USD$208.2k-239.7k yearly Auto-Apply 4d agoSenior Scientist, Radiochemistry
Telix Pharmaceuticals
Remote job
Telix Pharmaceuticals is a dynamic, fast-growing radiopharmaceutical company with offices in Australia (HQ), Belgium, Japan, Switzerland, and the United States. Our mission is to deliver on the promise of precision medicine through targeted radiation. At our core, we exist to create products that seek to improve the quality of life for people living with cancer and rare diseases. You will be supporting the international roll-out of our approved prostate cancer imaging agent and helping us to advance our portfolio of late clinical-stage products that address significant unmet need in oncology and rare diseases. See Yourself at Telix The Sr Scientist, Radiochemisty position will support the development of clinical-stage radiopharmaceutical assets. This role is responsible for managing the development required to ensure manufacturing and QC procedures meet the corporate requirements to support clinical trials, regulatory submissions, and transition to commercial-stage manufacturing. Key Accountabilities Interface with key stakeholders, including external CMOs, to manage the development of manufacturing and QC procedures for clinical-stage radiopharmaceutical assets in compliance with all applicable GMP regulations. Demonstrate the ability to manage multiple CMOs with little oversight from management. Manage the development and validation of manual or automated manufacturing procedures as required. Manage the development and validation of non-compendial QC procedures as required. Generate development, validation, method transfer, and various other types of protocols and reports. Author CMC sections for INDs, NDAs, BLAs, and foreign equivalents. Generate SOPs for manufacturing and QC procedures. Support method transfers to external manufacturers. Participate in the streamlining, optimization, and scale-up of manufacturing procedures in preparation for commercial supply. Provide technical support for manufacturing and QC procedures for all Telix products as required. Ensure all documentation generated is consistent with Telix QMS and general principles of GMP manufacturing. Education and Experience Bachelor's degree plus 8+ years experience, or Masters degree plus 6+ years experience, or doctorate plus 5+ years experience required. Practical radiochemistry experience is required. Experience developing HPLC, TLC, or GC QC methods for radiopharmaceuticals is required. Experience working in GMP-compliant manufacturing is required. Strong written and verbal communication skills. Experience with conjugation and radiolabeling of biologics is preferred. Experience of method development to support regulatory filings is preferred. At Telix, we believe everyone counts, we strive to be extraordinary, and we pursue our goals with determination and integrity. You will be part of an engaged and supportive group of colleagues who all have a shared purpose: to help people with cancer and rare diseases live longer, better quality lives. Being a Telix employee means being a part of a unique, global, interdisciplinary team working to deliver what's next in precision medicine. We have hybrid and remote employees located all around the world. We offer competitive salaries, annual performance-based bonuses, an equity-based incentive program, generous vacation, paid wellness days and support for learning and development. Telix Pharmaceuticals is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics. VIEW OUR PRIVACY POLICY HERE$88k-129k yearly est. Auto-Apply 1d agoPUBLIC HEALTH SCIENTIST SUPERVISOR
State of Arizona
Remote job
DEPT OF HEALTH SERVICES The Arizona Department of Health Services promotes and protects the health of Arizona's children and adults. Our mission is to promote, protect, and improve the health and wellness of individuals and communities in Arizona. We strive to set the standard for personal and community health through direct care, science, public policy, and leadership. ADHS promotes alternative work schedules, flexible hours. We have positions that can fit any stage in your career, from entry to senior level. We offer a robust benefit package, including the ADHS Student Loan Assistance Program, where eligible employees can receive up to $437.50 per month for their outstanding student loans. Come check us out and see how you can make a difference in the lives of all Arizonans. PUBLIC HEALTH SCIENTIST SUPERVISOR Job Location: Address: 250 N 17th Ave Phoenix, AZ 85007 Posting Details: Salary: $84,700 Grade: 23 Job Summary: This position provides oversight for the performance of all statutorily-required testing and quality assurance activities done in the Newborn Screening laboratory, including the release and reporting of results and coordinating related activities. The purpose of this position is to ensure the accurate, appropriate and timely receipt, preparation, analysis, interpretation and reporting of results on a large volume of clinical specimens for twenty-eight inherited disorders in newborns. This position will also serve as the technical specialist and primary supervisor for the Tandem Mass Spectrometry and Cystic Fibrosis testing sections. Job Duties: Plan and direct all daily activities and manage and direct subordinate staff (work assignments, setting priorities, hiring, discipline, provide training, approving leave requests, and preparing evaluations). Monitor test analyses and specimen examinations to ensure acceptable levels of analytic performance. Conduct laboratory testing analyses in accordance with laboratory standard operating procedures. Oversee training and orientation to all laboratory personnel within the section. Evaluate and document the performance of all testing personnel. Monitor the section's budget and forecast section needs. Manage reagent and supply inventory and monitor equipment performance. Provide oversight of the section's quality assurance program. Draft monthly Quality Assurance Reviews for regulatory compliance. Other duties as assigned as related to the position (typically 5% - 10%). Knowledge, Skills & Abilities (KSAs): Knowledge of: * Causes of inherited disorders, their effects and their laboratory evaluation. * Specialized microbiological and chemical laboratory techniques and specialized equipment. * Theory of colorimetric assays, fluorometric immunoassays, isoelectric focusing, HPLC, MS/MS, and PCR. * High volume clinical laboratory setting. * Department, Division, and Bureau policies. * Contract procedures. * Budget tracking. * Familiarity with statistical analyses. * Performance Management (PM), and Continuous Quality Improvement (CQI) and Lean methodologies. Skill in: * Proper Microbiological/Clinical Chemistry techniques. * Operation of specialized equipment. * Leadership, supervision, and establishing and maintaining effective work relationships. Ability to: * Teach and coach. * Dilution, pipetting, and centrifugation. * Interpersonal skills in dealing with wide variety of persons and organizations. * Manual dexterity. * Support a diverse multi-cultural workforce that reflects the community, promotes equal opportunity at all levels of public employment, and creates an inclusive work environment that enables all individuals to perform to their fullest potential free from discrimination. Selective Preference(s): Bachelor's degree in laboratory science or a related field and at least 4 years of professional level work experience in a laboratory as a Chemist or Microbiologist. Master's degree in a related field may substitute for 1 year of experience. PhD degree in a related field may substitute for two years of experience. Pre-Employment Requirements: Driver's License. If this position requires driving or the use of a vehicle as an essential function of the job to conduct State business, then the following requirements apply: Driver's License Requirements. All newly hired State employees are subject to and must successfully complete the Electronic Employment Eligibility Verification Program (E-Verify). Benefits: The State of Arizona provides an excellent comprehensive benefits package including: − Affordable medical and dental insurance plans − Paid vacation and sick time − Paid Parental Leave-Up to 12 weeks per year paid leave for newborn or newly-placed foster/adopted child (pilot program). − 10 paid holidays per year − Wellness program and plans − Life insurance − Short/long-term disability insurance − Defined retirement plan − Award winning Infant at Work program − Credit union membership − Transit subsidy − ADHS Student Assistance Pilot Program By providing the option of a full-time or part-time remote work schedule, employees enjoy improved work/life balance, report higher job satisfaction, and are more productive. Remote work is a management option and not an employee entitlement or right. An agency may terminate a remote work agreement at its discretion. Learn more about the Paid Parental Leave pilot program here. For a complete list of benefits provided by The State of Arizona, please visit our benefits page Retirement: To help you build a financially secure future, the State makes monthly contributions to finance your retirement benefit. The State will make a contribution to the ASRS in an amount equal to your contribution. In other words, you and the State will each pay 50% of the total cost of the benefit. New State employees have a 27 week wait period for contributions to begin. Contact Us: The State of Arizona is an Equal Opportunity/Reasonable Accommodation Employer. Persons with a disability may request a reasonable accommodation such as a sign language interpreter or an alternative format by emailing **************************. Requests should be made as early as possible to allow sufficient time to arrange the accommodation. DHS is an Equal Employment Opportunity Employer. All newly hired employees will be subject to E-Verify Employment Eligibility Verification.$84.7k yearly 60d+ agoResearch Specialist - School of Medicine Ophthalmic Biochemistry Lab
Emory Healthcare/Emory University
Remote job
**Discover Your Career at Emory University** Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate today and prepare leaders for the future. We welcome candidates who can contribute to the excellence of our academic community. **Description** The Hass lab at Emory is looking to hire a research specialist. The lab (**************************************************************************************** is focused on understanding and quantifying metabolic flux in tissues of the eye, and how they are altered in degenerative conditions that affect vision. We use a combination of biochemical approaches, including isotopic tracing, mass spectrometry, and enzymatic assays in the majority of our experiments. If you join our team, you'll learn these approaches, carry out projects under the direction of more senior personnel, document experimental details, and report results. We're also committed to your success - our goal is to provide an environment in which you can learn and grow as a scientist. We prefer candidates who are interested in using this opportunity as a stepping stone in their career as a scientist. KEY RESPONSIBILITIES: + Under general supervision, performs a variety of defined research and laboratory tests and experiments according to prescribed protocols and assigned schedules. + Sets up experiments as prescribed by a principal investigator. + May be required to participate in laboratory maintenance activities such as sterilization and cleaning of equipment, ordering of supplies, inventory and media preparation. + Maintains records, files and logs of work performed in laboratory notebooks and computer databases. + Compiles data and records results of studies for publications, grants and seminar presentations. + Employees in this classification may be required to work with, take specific precautions against and/or be immunized against potentially hazardous agents. + Performs related responsibilities as required by principal investigator. MINIMUM QUALIFICATIONS: + Bachelor's degree in a scientific field OR equivalent combination of experience, education, and training. Preferred Qualifications: - Prior experience with HPLC and/or mass spectrometry (strongly preferred) - Strong communication skills (strongly preferred) - Comfort interacting with mice in a scientific setting NOTE: Position tasks are required to be performed in-person at an Emory University location; working remote is not an option. Emory reserves the right to change this status with notice to employee. **Additional Details** Emory is an equal opportunity employer, and qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status or other characteristics protected by state or federal law. Emory University does not discriminate in admissions, educational programs, or employment, including recruitment, hiring, promotions, transfers, discipline, terminations, wage and salary administration, benefits, and training. Students, faculty, and staff are assured of participation in university programs and in the use of facilities without such discrimination. Emory University complies with Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veteran's Readjustment Assistance Act, and applicable executive orders, federal and state regulations regarding nondiscrimination, equal opportunity, and affirmative action (for protected veterans and individuals with disabilities). Inquiries regarding this policy should be directed to the Emory University Department of Equity and Civil Rights Compliance, 201 Dowman Drive, Administration Building, Atlanta, GA 30322. Telephone: ************ (V) | ************ (TDD). Emory University is committed to ensuring equal access and providing reasonable accommodations to qualified individuals with disabilities upon request. To request this document in an alternate format or to seek a reasonable accommodation, please contact the Department of Accessibility Services at accessibility@emory.edu or call ************ (Voice) | ************ (TDD). We kindly ask that requests be made at least seven business days in advance to allow adequate time for coordination. **Connect With Us!** Connect with us for general consideration! **Job Number** _157262_ **Job Type** _Regular Full-Time_ **Division** _School Of Medicine_ **Department** _SOM: Ophthal: Admin_ **Job Category** _Laboratory Research_ **Campus Location (For Posting) : Location** _US-GA-Atlanta_ **_Location : Name_** _Emory Clinic Bldg B_ **Remote Work Classification** _No Remote_ **Health and Safety Information** _Working in a laboratory, Working with animals_$42k-58k yearly est. 13d agoSenior Research Associate, Analytical Development
Moderna Theraputics
Remote job
The Role Moderna is seeking a Senior Research Associate (SRA) to join the Analytical Development team in Norwood, MA. This individual will play a critical role in developing, optimizing, and implementing advanced analytical methods that support Moderna's expanding therapeutic and vaccine portfolio. The successful candidate will generate high-quality data to drive method development, process understanding, and analytical readiness across new programs and manufacturing platforms. The ideal candidate is hands-on, detail-oriented, and thrives in a collaborative, fast-paced environment. This role requires strong technical skills in chromatography, spectroscopy, and separation sciences, along with the ability to manage multiple projects and communicate effectively with cross-functional partners in Analytical Development, Process Development, and Quality. Here's What You'll Do * Develop and execute analytical methods (e.g., HPLC, CE, UV/Vis spectroscopy, dd PCR..) to characterize and assess Moderna's mRNA and LNP-based products. * Support analytical roadmap implementation, including next-generation methods such as MAM, high-throughput spectroscopy, and advanced separation tools. * Generate feasibility data and contribute to method development and optimization for novel platforms (e.g., T-cell LNP, me DNA, plasmid manufacturing, oncology programs). * Conduct bridging studies between legacy and optimized methods, supporting comparability and qualification activities for analytical deep-dive remediation. * Prepare and analyze samples for method development, qualification support, and technology transfer to Quality Control (QC) and Analytical Technical Operation (ATO). * Document experimental work in electronic lab notebooks and author technical reports, summaries, and method implementation documents. * Collaborate cross-functionally with PD and MS&T to ensure analytical readiness for process innovation and scale-up. * Maintain a strong focus on quality and data integrity, ensuring compliance with internal standards and regulatory expectations. Here's What You'll Bring to the Table * BS degree with ≥5 years of relevant industry experience in Analytical Chemistry, Biochemistry, Chemistry, or related discipline. * Hands-on experience with analytical techniques such as HPLC, CE, UV/Vis, spectroscopy, dd PCR, and/or MAM workflows. * Proven ability to perform method development, troubleshooting, and data analysis in support of biologics, RNA, or complex formulations. * Familiarity with LNP characterization or nucleic acid-based analytical methods is a plus. * Strong technical writing and documentation skills. * Excellent organizational and multitasking ability in a fast-paced environment. * Demonstrated collaboration and communication skills to work effectively with cross-functional teams. * Highly motivated, scientifically curious, and capable of working independently with minimal supervision. * At Moderna, we are focused on delivering on our mission by enabling talent to thrive. For this role, we are currently unable to offer immigration sponsorship. Candidates must already hold work authorization in US and be able to maintain that status without the need for future sponsorship. Pay & Benefits At Moderna, we believe that when you feel your best, you can do your best work. That's why our US benefits and global well-being resources are designed to support you-at work, at home, and everywhere in between. * Best-in-class healthcare coverage, plus voluntary benefit programs to support your unique needs * A holistic approach to well-being, with access to fitness, mindfulness, and mental health support * Family planning benefits, including fertility, adoption, and surrogacy support * Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown * Savings and investment opportunities to help you plan for the future * Location-specific perks and extras The salary range for this role is $74,000.00 - $118,400.00. This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An individual's position within the salary range will be based on several factors including, but not limited to, specific competencies, relevant education, qualifications, certifications, experience, skills, performance, and business or organizational needs. The successful candidate may be eligible for an annual discretionary bonus, other incentive compensation, or equity award, subject to company plan eligibility criteria and individual performance. About Moderna Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world. By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities. We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities. Our Working Model As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact. Moderna is a smoke-free, alcohol-free, and drug-free work environment. Equal Opportunities Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply! Moderna is an E-Verify Employer in the United States. We consider qualified applicants regardless of criminal histories, consistent with legal requirements. Accommodations We're focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best. Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations team at leavesandaccommodations@modernatx.com. Export Control Notice This position may involve access to technology or data that is subject to U.S. export control laws, including the Export Administration Regulations (EAR). As such, employment is contingent upon the applicant's ability to access export-controlled information in accordance with U.S. law. Due to the nature of the work and regulatory requirements, only individuals who qualify as U.S. persons (citizens, permanent residents, asylees, or refugees) are eligible for this position. For this role Moderna is unable to sponsor non-U.S. persons to apply for an export control license. #LI-TR2 *$74k-118.4k yearly Auto-Apply 54d agoDirector, Quality Control
Jade Biosciences
Remote job
Jade Biosciences is focused on developing innovative, best-in-class therapies to address critical unmet needs in autoimmune diseases. Our lead candidate, JADE101, is designed to inhibit the cytokine APRIL (A Proliferation-Inducing Ligand) and is being developed for the treatment of immunoglobulin A nephropathy (IgAN), a chronic kidney disease that can impair kidney function over time. JADE101 aims to reduce harmful IgA antibodies, lower proteinuria (a key marker of kidney damage), and preserve long-term kidney function. A Phase 1 healthy-volunteer study of JADE101 is ongoing, with interim, biomarker-rich data expected in the first half of 2026. Jade's pipeline also includes a second development candidate, JADE201, and an undisclosed antibody discovery program, JADE-003, both currently in preclinical development. For more information, visit JadeBiosciences.com and follow us on LinkedIn. Role Overview The Director, Quality Control will lead critical Quality Control activities to support Jade's product pipeline across various stages of development. The Director will manage analytical method life cycle including method development, qualification, testing, transfer and validation as phase appropriate. This individual will work very closely with internal stakeholders and external CDMO partners and will be responsible for developing and executing product release testing, stability study and product shelf-life strategy while ensuring full quality compliance with regulatory requirements and internal quality systems. Key Responsibilities Work with both internal (other CMC functions, Quality Assurance, Regulatory and other key stakeholders) and external CDMO partners to develop and implement QC strategies appropriate for different phases of development programs Oversee batch release and stability testing, method development, qualification, transfer and validation activities at and cross CDMOs Develop product specifications and oversee product in-process, release, and stability testing strategy and execution in compliance with both cGMP and ICH guidance and internal quality standard Work with Quality Assurance to create and manage QC documentation including SOPs, protocols, and technical reports Collaborate cross-functionally with other CMC functions, QA and Regulatory to support tech transfers and lifecycle management, regulatory filing and interactions etc. Manage CDMO relationships to ensure compliance with quality standards, timely deliverables, and effective communication Review and approve CDMO generated data, investigations, and documentation Ensure timely investigation and resolution of OOS results, deviations, and CAPAs Serve as QC subject matter expert during regulatory inspections and audits Qualifications MS or PhD degree in Chemistry, Biology, Biochemistry, or related field with 10+ years of related experience 7+ years in Quality Control management for director level within the biotech or pharmaceutical industry A strong quality compliance and collaborative mindset, and ability to thrive in a fast paced working environment Strong knowledge of cGMP, FDA, EMA, and ICH regulations Strong experience in analytical method development including phase appropriate method qualification, transfer and validations from early to late phase development including BLA filing Experience with common analytical techniques such as common compendial methods, HPLC/UPLC, CE-SDS, ELISA, and cell-based assays for biologics development Proven leadership in managing internal QC operations or external CDMOs Excellent communication, organizational, and problem-solving skills Position Location This is a fully remote role with up to 15% domestic and/or international travel. The anticipated salary range for director level in this role is $210,000 - $235,000. The final salary offered will depend on several factors, which may include, but not limited to, relevant years of experience, educational background, and geography. As part of the I-9 verification of authorization to work in the United States, Jade Bioscience participates in E-Verify. To learn more about E-Verify please review this poster. Jade Biosciences is proud to be an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.$210k-235k yearly Auto-Apply 37d agoAccount Manager-New Jersey Outside Sales
Danaher
Remote job
Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Phenomenex, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. Phenomenex isn't your typical scientific company. Founded nearly 40 years ago, Phenomenex is a global technology leader committed to developing novel analytical chemistry solutions that solve the separation and purification challenges of researchers, advancing the future of scientific analysis and investigation, ensuring the quality of essentials like your food, water, shampoo, and even cold medication. Be part of our global success and together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health. Learn about the Danaher Business System which makes everything possible. The Account Manager - Outside Sales is responsible for managing the New Jersey territory by meeting and exceeding sales, gross profit, and unit goals. They will maintain customer accounts to ensure advanced service and technical support to customers through regular on-site consultative visits. This position reports to the District Manager and is part of the Sales team working remotely to cover the New Jersey region. In this role, you will have the opportunity to: Conduct on-site customer visits to provide technical information and seminars regarding chromatography-related products and services. Ensure that the assigned territory meets sales, gross profit, and unit goals Attend local vendor shows and company-sponsored trade shows. Develop business plans, market analysis, and sales strategies for the assigned territory. Have a positive attitude, be a team player, and strive to learn and contribute to the company culture. The essential requirements of the job include: Bachelor's Degree or greater in a Life Sciences field. At least 2 years of experience in Sales and/or post-bachelor experience as a Research Scientist, Product Specialist, Field Application/Technical Specialist, or related experience. Experience in LCMS/HPLC. Requires analytical thinking and the ability to present clearly to large groups as well as individuals Strong organizational skills, plans, and assigns resources in a detailed fashion. Travel, Motor Vehicle Record & Physical/Environment Requirements: Ability to travel up to 75% within territory with overnight travel on occasion for sales conferences, trainings and sales meetings Must have a valid driver's license with an acceptable driving record It would be a plus if you also possess: Good working knowledge of the chromatography consumables market and various industry customers Strong Biopharma background Phenomenex, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info. At Phenomenex we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Phenomenex can provide. The annual salary for this role is $110,000-$115,000 . This role is also eligible for Sales Incentive Compensation (SIC). The total target compensation at plan (base + SIC) is $180,000 - $185,000 annually. Actual SIC earnings may exceed or fall below the target based on individual sales performance. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future. We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law. #LI-DC1 #LI-Remote Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit **************** Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The U.S. EEO posters are available here. We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:************** or applyassistance@danaher.com.$56k-63k yearly est. Auto-Apply 60d+ agoPost Doctoral Fellow - Pathology
Emory Healthcare/Emory University
Remote job
**Discover Your Career at Emory University** Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate today and prepare leaders for the future. We welcome candidates who can contribute to the excellence of our academic community. **Description** **Ovarian Cancer Metabolomics and Proteomics** **Postdoctoral Fellow** **Gordon Lab - Emory University, Atlanta USA** Position Description: The Gordon Laboratory seeks a motivated **Postdoctoral Fellow** to spearhead cutting-edge **metabolomics studies** focused on developing **ovarian cancer diagnostics and** **therapeutics** . Ovarian cancer is among the most fatal cancers for women. Since it is often detected at a latestage (Stage 3 / 4), these patients suffer from very poor survival rates, therefore early detection of ovarian cancer is essential for improving clinical outcomes. Ovarian cancer is also characterized by drug resistance, therefore new treatments for ovarian cancer are crucial for improved outcomes. This project will utilize cutting edge metabolomics, proteomics, and cellbased functional assays. **Minimum qualifications include:** + Metabolomics mass spectrometry and metabolomics data analysis **Preferred qualifications include:** + Cancer model systems (e.g. animal models, organoids, cell culture models, relevantfunctional assays). + Proteomics mass spectrometry and/or proteomics data analysis + Biochemistry expertise (e.g. protein interaction studies, HPLC operation, etc.) + Molecular biology and experimental genetics (si RNA, CRISPR, PCR, DNA cloning, etc.) + DNA sequence analysis (Snapgene, Geneious or other DNA analysis tools) + Experience analyzing large datasets **The Gordon Lab pioneers advanced mass spectrometry, experimental genetics, and** **computational approaches to map biochemical networks and functional pathways,** **and leverages this information for improved therapeutics** . Based in the Emory University Department of Pathology and Laboratory Medicine we have ample access to primary tissue samples, and our affiliation with the Winship Cancer Center Discovery and Developmental Therapeutics Program supports translation of our research into therapeuticapproaches. Additionally, our affiliation with the Pathology Translational Research Unit provides extraordinary collaboration opportunities towards data-driven analyses and synergy with world-leading immunologists.Lastly, our work with Georgia Tech through the Center for the Study of Systems Biology (CSSB) and the Coulter Department of Biomedical Engineering enables transformative collaborations in technology development, including computational prediction of molecular interactions. Notably, our research program includes academic, nonprofit, and industry collaborations. Our Culture: We strongly believe that the best science emerges from an environment of generous collaboration, reinforced by a culture of learning, curiosity, and the sharing of skills and advice. In considering new members of our group, we value a positive can-do attitude, evidence of previous success in laboratory environments, and attention to detail.This is a superb opportunity for a sharp scientist to rapidly develop new research skills and spearhead impactful projects in a supportive learning environment. **Additional Details** Emory is an equal opportunity employer, and qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status or other characteristics protected by state or federal law. Emory University does not discriminate in admissions, educational programs, or employment, including recruitment, hiring, promotions, transfers, discipline, terminations, wage and salary administration, benefits, and training. Students, faculty, and staff are assured of participation in university programs and in the use of facilities without such discrimination. Emory University complies with Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veteran's Readjustment Assistance Act, and applicable executive orders, federal and state regulations regarding nondiscrimination, equal opportunity, and affirmative action (for protected veterans and individuals with disabilities). Inquiries regarding this policy should be directed to the Emory University Department of Equity and Civil Rights Compliance, 201 Dowman Drive, Administration Building, Atlanta, GA 30322. Telephone: ************ (V) | ************ (TDD). Emory University is committed to ensuring equal access and providing reasonable accommodations to qualified individuals with disabilities upon request. To request this document in an alternate format or to seek a reasonable accommodation, please contact the Department of Accessibility Services at accessibility@emory.edu or call ************ (Voice) | ************ (TDD). We kindly ask that requests be made at least seven business days in advance to allow adequate time for coordination. **Connect With Us!** Connect with us for general consideration! **Job Number** _141893_ **Job Type** _Regular Full-Time_ **Division** _School Of Medicine_ **Department** _SOM: Pathology: Admin_ **Campus Location (For Posting) : Location** _US-GA-Atlanta_ **_Location : Name_** _HSRB II (Health Sciences Research Building II)_ **Remote Work Classification** _Primarily On Campus_ **Health and Safety Information** _Working in a laboratory_$36k-46k yearly est. 60d+ agoSr. R&D Procurement Specialist
Grns
Remote job
We're so happy you're here! Thank you for checking our job out and we hope to have the chance to meet you in our interview process! About the role We're looking for an Sr. R&D Procurement Specialist to fuel Grüns' innovation pipeline by finding, vetting, and delivering the very best ingredients - fast. This role sits at the intersection of science and sourcing, combining a curiosity for what's next in nutrition with the rigor to evaluate ingredient efficacy, quality, and feasibility. You'll uncover novel and proven actives, build supplier partnerships, and critically assess clinical evidence (especially for branded ingredients) to ensure our formulations are both effective and defensible. This role collaborates closely with R&D, Product Development, Quality, Regulatory, and Operations, and reports directly to our Sr. Manager, R&D within the Product organization. This is a remote HQ role - we operate in a fully remote, high-trust environment and meet bi-annually for energizing in-person offsites. Occasional travel to suppliers, audits, and industry events (e.g., SupplySide, NPEW) is expected. In this role, you will: Source & Scout Proactively identify ingredients (botanicals, minerals, vitamins, fibers, functional actives, flavors, excipients) with a focus on clinically supported, label-friendly, and gummy-compatible options. Build and maintain a competitive inventory of ingredients, capturing efficacy claims, standardization markers, and differentiation potential. Evaluate the Science Critically assess clinical and preclinical data for candidate ingredients, evaluating study design, endpoints, dosage, and reliability. Summarize findings in clear, decision-ready briefs for Product and Brand to support innovation and claims. Qualify & Negotiate with Suppliers Lead supplier due diligence, including quality questionnaires, certifications (GFSI), audit coordination, CoA review, and method validation (e.g., HPLC, ICP-MS). Review contaminant, micro, and allergen specs, and negotiate MOQ, lead times, and sample delivery for pilot and scale-up trials. Enable Fast Formulation Partner with R&D to maintain a living ingredient portfolio considering cost, stability, sensory impact, and manufacturability. Support formulation timelines through proactive communication and data organization. Operationalize & De-risk Build supply resiliency through multi-tier sourcing and vendor diversification. Collaborate with QA to ensure ingredient qualification, traceability, and acceptance criteria are met. Cross-Functional Collaboration Work with R&D on trials and V2 improvements, Ops on PO timing and inventory planning, and Brand on credible ingredient storytelling. Support CX with ingredient FAQs and claims accuracy. We're looking for someone who: 2-4 years of experience in ingredient sourcing, procurement, or ingredient science within CPG, nutraceuticals, or food-tech (gummy experience a plus). Hands-on experience with supplier qualification, audits, and sustainability questionnaires, and experience negotiating commercial terms. A Bachelor's degree in Food Science, Nutrition, Chemistry, Biology, or a related field. Strong understanding of clinical research methods (RCTs, meta-analyses, confidence intervals, power, bias, validity). Fluency in quality and analytical fundamentals - CoA review, potency/purity testing, stability, and shelf-life considerations. Excellent communication skills - able to translate scientific and technical detail into actionable insights for diverse teams. Approach to the role: Scientifically curious: constantly learning and scanning the market for new, validated ingredients. Operationally sharp: builds structure, documentation, and repeatable systems for scale. Cross-functional collaborator: aligns science, product, and operations seamlessly. Quality-driven: never compromises on data integrity or sourcing standards. Strategic communicator: translates complex data into clear, confident recommendations. At Grüns, we're committed to providing a competitive total compensation package - grounded in market data that considers our size, stage, and industry. For this role, the base salary range is $80,000-$100,000, depending on experience. Beyond base salary, we offer competitive equity packages and a comprehensive set of benefits designed to support your well-being, growth, and balance. A bit about us... At Grüns, we believe that foundational nutrition should be simple and convenient for everyone. We're dedicated to bringing comprehensive and real nutrition to you through our gummies, formulated from 60 nutrient-dense and whole-food ingredients. Simply enjoy a grab-and-go snack pack of gummies daily whenever fits best in your schedule and wherever life takes you. Like you, we were disappointed. There's an infinite number of “nutrition” companies, all focused on what's best for them - not what's best for you. Hundreds of products to sell you on, low-quality ingredients, and small nutrient doses. We've seen it all. So we decided it was time to fix it. No more choking on and popping pills like a pharmacy. No more clean-up and disgust from gross powders. And no more cobbling together handfuls to dozens of supplements. Grüns is comprehensive nutrition, made convenient and delicious. What we care about... Autonomy: Only the best work at Grüns. We're all confident, independent leaders. We are proactive. We find opportunities for improvement. Don't ask; just do. When our actions impact other areas of the organization, we communicate with those functional leaders to ensure connectivity. Growth: We love to take on new challenges, learn new things, and express interest in new functions. “I've never done this before” is not an excuse; it's an opportunity. Community: We care deeply about each other. We're good humans and provide support wherever we can. We care, not just professionally but personally as well. Compensation & Perks: For every role, we aim to have highly competitive compensation and opportunity for impact and career growth. Everyone at Grüns works hard, but we believe in wellness and balance too. We have super strong benefits coverage -- for you and your family, generous PTO, free Grüns subscriptions, and a few more perks centered around health and well-being that we can't wait to tell you about!$80k-100k yearly Auto-Apply 25d agoPharmaceutical QC Scientist I
Actalent
Columbus, OH
We are seeking a QC Scientist I to join our team, focusing on bench testing and analytical support for pharmaceutical product development. You will conduct chemical and physical analyses to aid in developing and manufacturing multisource pharmaceutical products, providing analytical support for registration materials and regulatory submissions. Over time, you will receive training in both the Oral Dose Solids and Nasals departments, as well as on HPLC and GC methods. Responsibilities * Prepare samples and perform wet chemistry, standard weighing, and dilutions. * Conduct chemical and physical analyses supporting product development and registration lot release. * Assist in analytical method validation and transfer activities. * Perform tasks within assigned timelines in compliance with cGXP's and company procedures. * Document analytical activities and results accurately and promptly, maintaining data integrity. * Follow work instructions, SOPs, and company practices. * Identify challenges in analytical methods and support troubleshooting activities. Essential Skills * Proficiency in dilutions, sample preparation, and wet chemistry. * Strong in chemistry or biochemistry. * Bachelor's degree in a Science field, preferably in Chemistry or Biochemistry. * Previous lab experience, which may include academic experience. * Ability to work in a team and manage multiple tasks in a fast-paced environment. * Good written and verbal communication skills. Additional Skills & Qualifications * Experience outside of academia in a lab setting is strongly preferred. * Ability to work with supervision using scientific judgment and professional competency. * Candidates with degrees in Biology, Microbiology, or Pharmaceutical Science with strong chemistry lab experience will be considered. Work Environment This position is set in a fast-paced environment, where you will work both in the quality group and occasionally in the manufacturing area. The work schedule is on the 2nd shift, Monday to Friday, from 3:00 PM to 11:30 PM, with some flexibility. Initially, the schedule is five 8-hour days, with the potential to transition to a four 10-hour day schedule after training. Job Type & Location This is a Contract to Hire position based out of Columbus, OH. Pay and Benefits The pay range for this position is $24.00 - $24.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Columbus,OH. Application Deadline This position is anticipated to close on Dec 16, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.$24-24 hourly 10d agoManager, Analytical Development
Axsome Therapeutics
Remote job
Axsome Therapeutics is a biopharmaceutical company leading a new era in the treatment of central nervous system (CNS) conditions. We deliver scientific breakthroughs by identifying critical gaps in care and develop differentiated products with a focus on novel mechanisms of action that enable meaningful advancements in patient outcomes. Our industry-leading neuroscience portfolio includes FDA-approved treatments for major depressive disorder, excessive daytime sleepiness associated with narcolepsy and obstructive sleep apnea, and migraine, and multiple late-stage development programs addressing a broad range of serious neurological and psychiatric conditions that impact over 150 million people in the United States. Together, we are on a mission to solve some of the brain's biggest problems so patients and their loved ones can flourish. For more information, please visit us at ************** and follow us on LinkedIn and X. About This Role Axsome Therapeutics is seeking a Manager, Analytical Development to manage and coordinate analytical activities on multiple early and/or late phase clinical development programs. The ideal candidate will be a team player comfortable working on a small team in a fast-paced environment and with contract manufacturing and development organizations. Excellent time management skills and communication will be key in succeeding in this role. This position requires an extensive hands-on laboratory experience using a broad array of analytical instrumentation. This role is based at Axsome's HQ in New York City with an on-site requirement of at least three days per week. We are unable to consider candidates who are looking for fully remote roles. Job Responsibilities and Duties include, but are not limited to, the following: Work closely with the CMC team (and specifically the head of analytical development) to manage and coordinate analytical activities on multiple early phase drug substance (40%) and drug product (60%) small molecule solid oral formulation programs Manage early and/or late phase drug substance and drug product analytical activities at contract development laboratories (method development, method qualifications/validations, method transfers, analytical investigations support) Review and/or author analytical technical/development and method qualification/validation reports and raw data as well as release and stability data packages Assist in authoring CMC sections for regulatory submissions Manage drug substance and drug product stability programs (QC and technical review of stability data packages that includes raw data, and stability data trend analysis) Assist in the development of standard operating procedures Manage reference materials and reference standards inventory and (re)qualification testing Requirements / Qualifications Bachelor's degree in Analytical Chemistry or Chemistry or related field with 5+ years' experience or MS/PhD with 3+ years of GMP and GLP-related pharmaceutical industry experience in small molecule solid oral formulation analytical development Knowledge of drug product solid oral dose formulations Hands-on experience with drug substance and drug product analytical techniques such as HPLC, GC, KF, MS, dissolution, spectroscopy, and particle size Functional understanding of small molecule analytical development and associated regulatory and quality requirements Hands on experience with LC-MS/MS and GC-MS is a plus Ability to work on site Monday, Tuesday & Thursday. We are unable to consider candidates who are looking for fully remote roles Experience, Knowledge and Skills Demonstrated experience in managing outsourced analytical activities Demonstrated experience in QC data review of release and stability data packages for both drug substance and drug product Experience working on commercial stage products highly valued Excellent verbal and written communication skills Excellent problem solving and interpersonal skills Exceptional organizational skills with the ability to multi-task and prioritize workload based upon changing priorities. Ability to work in a cross-functional team environment and to be a team player as well as the ability to work independently Flexibility to accommodate multiple time zones as needed Preference to energetic candidates with a desire to think “outside the box” Willingness to travel periodically as needed Salary & Benefits The anticipated salary range for this role is $120,000 - $135,000. We encourage candidates of all levels to apply as there may be flexibility on final job title and responsibilities. The salary offer will be based on a variety of factors, including experience, qualifications, internal equity and location. Axsome offers a competitive employment package that includes an annual bonus, significant equity and a generous benefits package. Axsome is committed to equal employment opportunity and providing reasonable accommodations to applicants with physical and/or mental disabilities. We value and encourage diversity and solicit applications from all qualified applicants without regard to race, color, gender, sex, age, religion, creed, national origin, sexual orientation, gender identity, ancestry, citizenship, marital status, physical or mental disability, medical condition, veteran status, genetic information, or any other characteristic protected by federal, state, or local law. Axsome Therapeutics does not accept unsolicited resumes from recruiters or third-party recruitment agencies and will not pay placement fees for unsolicited candidates that are sent to hiring managers, the HR team or other Axsome team members. Only approved vendors who have been explicitly asked to support a specific search will receive access to our Applicant Tracking System to submit candidates for consideration.$120k-135k yearly Auto-Apply 11d agoResearch Specialist - School of Medicine, Pathology
Emory Healthcare/Emory University
Remote job
**Discover Your Career at Emory University** Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate today and prepare leaders for the future. We welcome candidates who can contribute to the excellence of our academic community. **Description** The Gordon Laboratory seeks a motivated Research Specialist to spearhead cutting-edge Proteomics and Experimental Genetics studies focused on virus-host interactions, immune regulation, and carcinogenesis. The Gordon Lab pioneers advanced mass spectrometry, experimental genetics, and computational approaches to map functional pathways. Based in the Emory University Department of Pathology and Laboratory Medicine, we have ample access to primary tissue samples, and our affiliation with the Pathology Translational Research Unit provides extraordinary collaboration opportunities towards data-driven analyses and synergy with world-leading immunologists. Our affiliation with Georgia Tech through the Coulter Department of Biomedical Engineering enables transformative collaborations in technology development, including computational prediction of molecular interactions. Lastly, our affiliation with therapeutic development programs such as the Winship Cancer Center Discovery and Developmental Therapeutics Program translates our research into therapeutic approaches. Our research program includes both academic and industry collaborations. We strongly believe that the best science emerges from an environment of generous collaboration, reinforced by a culture of learning, curiosity, and the sharing of skills and advice. In considering new members of our group, we value a positive can-do attitude, evidence of previous success in laboratory environments, attention to detail, and cultural add. This is a superb opportunity to rapidly develop new research skills and spearhead impactful projects in a supportive learning environment. KEY RESPONSIBILITIES: + Under general supervision, performs a variety of defined research and laboratory tests and experiments according to prescribed protocols and assigned schedules. + Sets up experiments as prescribed by a principal investigator. + May be required to participate in laboratory maintenance activities such as sterilization and cleaning of equipment, ordering of supplies, inventory and media preparation. + Maintains records, files and logs of work performed in laboratory notebooks and computer databases. + Compiles data and records results of studies for publications, grants and seminar presentations. + Employees in this classification may be required to work with, take specific precautions against and/or be immunized against potentially hazardous agents. + Performs related responsibilities as required by principal investigator. MINIMUM QUALIFICATIONS: + Bachelor's degree in a scientific field OR equivalent combination of experience, education, and training. PREFERRED QUALIFICATIONS: + Molecular biology experience (PCR, DNA cloning, agarose gel electrophoresis, etc.). + Cell culture experience. + Strong training in biochemistry and molecular biology-related coursework. + Mass spectrometry and/or proteomics data analysis. + Biochemistry expertise (e.g. protein interaction studies, HPLC operation, etc.). + Molecular biology and experimental genetics (si RNA, CRISPR, PCR, DNA cloning, etc.). + DNA sequence analysis (Snapgene, Geneious or other DNA analysis tools). + Experience analyzing large datasets. NOTE: Position tasks are required to be performed in-person at an Emory University location; working remote is not an option. Emory reserves the right to change this status with notice to employee. **Additional Details** Emory is an equal opportunity employer, and qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status or other characteristics protected by state or federal law. Emory University does not discriminate in admissions, educational programs, or employment, including recruitment, hiring, promotions, transfers, discipline, terminations, wage and salary administration, benefits, and training. Students, faculty, and staff are assured of participation in university programs and in the use of facilities without such discrimination. Emory University complies with Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veteran's Readjustment Assistance Act, and applicable executive orders, federal and state regulations regarding nondiscrimination, equal opportunity, and affirmative action (for protected veterans and individuals with disabilities). Inquiries regarding this policy should be directed to the Emory University Department of Equity and Civil Rights Compliance, 201 Dowman Drive, Administration Building, Atlanta, GA 30322. Telephone: ************ (V) | ************ (TDD). Emory University is committed to ensuring equal access and providing reasonable accommodations to qualified individuals with disabilities upon request. To request this document in an alternate format or to seek a reasonable accommodation, please contact the Department of Accessibility Services at accessibility@emory.edu or call ************ (Voice) | ************ (TDD). We kindly ask that requests be made at least seven business days in advance to allow adequate time for coordination. **Connect With Us!** Connect with us for general consideration! **Job Number** _141097_ **Job Type** _Regular Full-Time_ **Division** _School Of Medicine_ **Department** _SOM: Pathology: Admin_ **Job Category** _Laboratory Research_ **Campus Location (For Posting) : Location** _US-GA-Atlanta_ **_Location : Name_** _HSRB II (Health Sciences Research Building II)_ **Remote Work Classification** _Onsite_ **Health and Safety Information** _Working in a laboratory_$42k-58k yearly est. 60d+ ago
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