Associate scientist jobs in Durham, NC

Reality Labs at Meta is seeking Research Scientists with experience in product-focused machine learning and signal processing research to advance our pioneering work in neuromotor interfaces, which has grown out of the acquisition of CTRL-labs. We're building a practical interface drawing on the rich neuromotor signals that can be measured non-invasively via surface electromyography (EMG) with single motor neuron resolution. This technology could become one of the main pillars for interaction with virtual and augmented worlds.We are a multi-disciplinary team of researchers investigating the nature of human neuromotor signals, developing novel signal processing and machine learning methods to infer a user's intent, and creating novel interaction techniques and user experiences. Help us unleash human potential by removing the bottlenecks between user intent and action. **Required Skills:** Research Scientist - CTRL Labs Responsibilities: 1. Research and develop Deep Learning or other computational models 2. Design methods, tools and infrastructure to analyze and leverage rich multimodal data sets 3. Set technical direction for a project of 2-3 researchers and engineers 4. Help transition and deliver our work from research into product 5. Adapt standard machine learning methods to best leverage modern parallel environments (e.g. distributed clusters, multicore SMP, and GPU) **Minimum Qualifications:** Minimum Qualifications: 6. Bachelor's degree in Computer Science, Computer Engineering, relevant technical field, or equivalent practical experience 7. Ph.D. degree in Computer Science and Engineering, Electrical Engineering, Statistics/Mathematics 8. Experience with developing machine learning models at scale from inception to business impact 9. Programming experience in Python and hands-on experience with frameworks such as PyTorch 10. Exposure to architectural patterns of large scale software applications 11. Must obtain work authorization in the country of employment at the time of hire, and maintain ongoing work authorization during employment **Preferred Qualifications:** Preferred Qualifications: 12. Proven track record of achieving significant results as demonstrated by grants, fellowships, patents, as well as first-authored publications at peer-reviewed AI conferences (e.g. NeurIPS, CVPR, ICML, ICLR, ICCV, ACL, and ICASSP) 13. Demonstrated software engineer experience via an internship, work experience, coding competitions, or widely used contributions in open source repositories (e.g. GitHub) 14. Experience bringing machine learning-based products from research to production **Public Compensation:** $213,000/year to $251,000/year + benefits **Industry:** Internet **Equal Opportunity:** Meta is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender, gender identity, gender expression, transgender status, sexual stereotypes, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. We also consider qualified applicants with criminal histories, consistent with applicable federal, state and local law. Meta participates in the E-Verify program in certain locations, as required by law. Please note that Meta may leverage artificial intelligence and machine learning technologies in connection with applications for employment. Meta is committed to providing reasonable accommodations for candidates with disabilities in our recruiting process. If you need any assistance or accommodations due to a disability, please let us know at accommodations-ext@fb.com.

ABOUT GREENLIGHT GreenLight Biosciences is using RNA to create a world where plants, people, and the planet can thrive together. The company is developing highly effective agricultural solutions for farmers and beekeepers that are targeted to specific pests and degrade quickly in the environment. Our pipeline includes products to protect honeybees and a range of fruits and vegetables. The GreenLight platform allows us to research, design, and manufacture across multiple product categories including insecticides, fungicides, and herbicides. For more information, visit ********************** The Associate Scientist, Process Development at GreenLight BioSciences in Durham, NC will serve as a key member and technical leader of the process development team and support their overall mission of delivering high performance RNA production processes and products to the market. Specific responsibilities include: Support early-stage product development by performing laboratory scale fermentation, RNA production and downstream processing; Run 10 L fermentation experiment to produce plasmid DNA using strains developed by strain engineering team; Collect samples from fermentation experiment and assess process metrics such as plasmid DNA titer, plasmid DNA yield and quality; Perform downstream unit operations to recover plasmid DNA; Run 10 L RNA synthesis experiment using the plasmid DNA and assess process metrics such as RNA titer, yield and purity; Troubleshoot and identify opportunities for improvements in RNA production process by doing DoE based optimization experiments; Do statistically designed multifactorial optimization experiment i.e., Design of Experiment (DoE); Design, plan, execute the experiment, collect samples and run analytical methods for RNA titer, yield, analyze the data, fit curves, make model, do model predictions using statistical data analysis tool; Validate the model prediction, test reproducibility and robustness of the optimized RNA synthesis process conditions; Lead development of next generation processes to improve RNA production metrics; Using DoE and rationally designed experiments, identify the parameters limiting performance of RNA synthesis process; Formulate strategies to address the limitations such as developing new processes, identifying better raw materials, etc., to improve RNA production metrics; Create tasks, delegate and supervise team members towards completion of project goals; Develop, author and implement Standard Operating Procedures (SOPs) for process development activities; Write protocols and development reports for the new processes; Document in Quality Management System; train team members on the new protocols; Scale-up and tech transfer bench-scale processes to pilot production scale; Demonstrate scale-up by evaluating the new process in 10 L scale; Train production team members; Perform and report on procedures to quantitatively measure analytes (DNA, RNA, proteins, ions, etc.,) in a variety of matrices for analytical testing support; Run RNA analysis methods such as RNA concentration, RNA purity; Run DNA analysis methods such as restriction digestion and agarose gel electrophoresis; Run HPLC for small molecules, DNA, RNA; Make data driven decisions and identifies root causes to help solve problems and achieve opportunities; Test assays on different lots of DNA, enzyme samples to evaluate batch-to-batch variability; Identify causes for variability using the assay data; Work collaboratively with operations and quality management team members and communicate effectively to accomplish project goals and milestones; Work with cross-functional teams such as Strain Engineering, Manufacturing, QA/QC; and Plan data review meetings, present results and conclusions, suggest directions and next steps REQUIREMENTS: B.S. in Chemical Engineering, Biochemistry or related field, plus 24 months of experience or similar role in strain engineering field for aseptic techniques, bacterial culture, extraction and characterization of DNA, UV/VIS absorbance, gel electrophoresis, sequencing data analysis is required. Such experience must include: 12 months of experience as a research associate or similar role in process development handling lab-scale bioreactors for running fermentation, downstream processing equipment such as cell harvest by centrifugation, TFF, DNA column chromatography purification; 12 months of experience as a research associate or similar role handling analytical equipment such as HPLC to quantify DNA, RNA, organic acids; and 12 months of experience working with electronic lab notebook, laboratory information management system and statistical software such as GMP. Greenlight Biosciences Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

Job Description To perform experiments, ensuring that projects are completed to plan, while complying with all quality and safety regulations. Assist with study plan writing, data analysis and interpretation, and report writing. Essential Functions: Assist or act as the lead scientist on assigned studies. Draft study plans and contribute to the preparation of reports for sponsors. Review literature and appropriate guidances (FDA and/or EMA) in preparation for studies and to regularly update knowledge by reviewing appropriate literature. Perform experiments (with supervision as needed) in line with in vitro testing such as in vitro permeation and penetration studies, in vitro release testing studies, extractions, stability studies, etc. Assist with data analysis for studies related to in vitro testing. Confer with scientists, study managers, and management to conduct analyses of research projects, interpret test results, or develop nonstandard tests. Crosstrain and assist with research biology activities (e.g. PCR, PK/PD, etc.) as needed. Report any amendments or deviations from Study Plans/SOPs to Lead Scientist and/or Study Director, as appropriate. Maintain laboratory instruments to ensure proper working order and troubleshoot malfunctions with scientists when needed. Adhere to MedPharm Standard Operating Procedures (SOPs) and guidance documents, where applicable. Contribute to the preparation and review of SOPs and Forms where applicable. Where applicable, promptly record all data according to Good Documentation Practices. Adhere to MedPharm Health & Safety Policy and OSHA regulations at all times and to ensure the safety of others in any procedures or tasks performed. Ensure that all documentation, computer data, and records are stored appropriately. Any other duties and/or tasks that may be assigned Powered by JazzHR CgdzTtjodV

Job DescriptionDescriptionThis position is ideal for an early-career machine learning scientist to join the AI & Machine Learning team as a Machine Learning Scientist, supporting photo-based diagnostics and remote treatment monitoring. Partnering with other machine learning specialists and product marketing, you'll provide technical solutions to complex problems in computer vision and 3D data analysis to support Align's product portfolio. This role is key to building out Align's core technology capabilities. Role expectations Use data science and machine learning to solve complex, multidisciplinary challenges in applied research and turn technology know-how into execution in a dynamic business environment Develop algorithms and models in collaboration with business partners, product managers, and software engineers to solve key business initiatives Design and implement machine learning techniques to improve treatment planning, customer engagement, and device manufacturing based on historical data Collaborate effectively with other data science teams globally to ensure technology re-use and transfer of new capabilities to drive innovation Quickly learn and assimilate new business processes, ideas and concepts to formulate conclusions and deliver results. Identify features and data needed for machine learning solutions. Help to deliver a vision for our product evolution using machine learning Stay current on the emerging directions in AI-technologies and support the development of the AI/ML roadmap Stay current on specific AI-technologies and apply them in an appropriate manner to applicable projects What we're looking for What we're looking for 5+ years of relevant experience 2+ years of machine learning research practice (including graduate work) Masters degree or higher in Computer Science, Statistics, Machine Learning, Statistical Data Modeling or related field. Knowledge of machine learning theory and practice. 2+ years in a data-science-oriented programming language such as Python or R Strong interpersonal, oral, written, and visual communication skills, with ability to present findings concisely and effectively. Ability to collaborate effectively with developers, program management, and internal customers on objectives, requirements and design constraints in a distributed development environment. Able to solve complex, multidisciplinary challenges in applied research and turn technology know-how into execution in a dynamic business environment Experience in developing software in an Agile SDLC Experience in collaborative work with users and other technical teams Strong background in Computer Vision, Pattern Matching, or Medical Applications. Pay TransparencyIf provided, base salary or wage rate ranges are the range in which Align reasonably expects to set a candidate's pay for the posted position. Actual placement depends on the individual skills and experience level of a candidate plus the total compensation and equity across team members. For other locations outside of the primary location, the base salary range will be adjusted geographically. For Field Sales roles, the salary listed is the base pay only and does not include the applicable incentive compensation plan. A cost of living adjustment may be added to base pay for higher cost areas in the U.S. Our internship hourly rates are a standard pay determined based on the position and your location, year in school, degree, and experience. General Description of All BenefitsWe are pleased to provide a general description of the benefits Align offers to full-time employees in this position. Family Benefits. Align offers employees and their eligible dependents medical (with a Health Savings Account option for some plan offerings), dental, and vision in accordance with those plans. Align also offers to employees: Discounts on Invisalign and Vivera to employees and their eligible dependents after 90 days of employment Back-up Child/Elder Care and access to a caregiving concierge Family Forming Benefits - Available to Employees, and their spouse or domestic partner, covered under one of Align's health plans Breast Milk Delivery and Lactation Support Services Employee Assistance Program Hinge Health Virtual Physical Therapy - Available to all employees and eligible dependents (age 18+) enrolled in an Align medical Plan Employee benefits. Align offers its employees: Short-term and long-term disability insurance in accordance with those plans. Basic Life Insurance and Accidental Death and Dismemberment. Voluntary Supplemental Life Insurance for Employee, Spouse/Domestic Partner, and Child(ren) are available for purchase in accordance with those plans. Flexible Spending Accounts - Employees may be eligible to participate in a health care account (including a limited health FSA if enrolled in a HDHP), dependent care account, and a pre-tax commuter benefit plan. 401k plan (with a discretionary Company match of 50% up to 6% of eligible earnings up to a maximum match of 3%.). Employer match vests after two years - 25% year one and 100% at year two. Align offers traditional, Roth, and after-tax options. Employee Stock Purchase Program (Employees must work 20 hours or more and be employed on purchase date to be eligible). Paid vacation of up to 17 days during the first full year of employment (currently accrued at the rate of 5.24 hours each pay-period), which carries over to a maximum cap of 30 days. Annual paid vacation time accrual increases based on tenure. Both exempt and non-exempt employees who work 32 hours or more per week receive prorated vacation accrual based on their regularly scheduled work hours and tenure. Sick time is accrued throughout the year at the rate of one hour for every thirty worked. Employees can carry over unused sick leave each year, up to a maximum balance of 80 hours. 11 Company-designated paid holidays throughout the year. If employed for at least 12 consecutive months, Align will grant up to 6 weeks of paid Parental Leave. If employed for less than 12 consecutive months, Align will grant up to 4 weeks of paid Parental Leave. All parental leave must be completed within one year of the birth or placement of the child. Parental leave is in addition to any state and/or local parental leave benefits. Three days of paid bereavement leave. In some cases, due to travel the amount of paid leave may be extended to 5 paid days off. To the extent applicable state or local law offers more generous benefits, Align complies with any such law. Non-exempt employees will receive full pay for up to 10 days of jury duty. Exempt employees will receive their full salary during any week they serve and perform any work. Other insurance such as legal, critical illness, voluntary accident, long-term care, auto, home and pet insurance are available for purchase. To the extent applicable state or local law offers more generous benefits, Align complies with any such law.

Purpose of your Job As part of our dynamic Formulation Development & Analytics unit, you will directly contribute to enabling the next generation of biopharmaceutical therapies. Our team drives innovative formulation and analytical strategies under BSL‑1/2 and S1/S2 safety levels, as well as GMP quality standards. By joining us, you will help ensure that advanced scientific work is carried out with excellence, precision, and curiosity. This role plays a key part in shaping Coriolis Pharma's global growth - including our build‑up of new U.S. facilities in North Carolina's Research Triangle Park (RTP), one of the world's most vibrant biotech innovation hubs. You will be involved in transferring expertise, establishing scientific capabilities, and supporting the seamless integration of processes across locations. In this position, you will transform scientific questions into meaningful analytical insights. You'll develop and implement state‑of‑the‑art methods, interpret complex data, and influence the scientific direction of client projects in an international, highly collaborative environment. Throughout your journey, you'll be supported in growing your technical strengths (e.g., analytical method development, instrumentation, troubleshooting) as well as your personal skills (e.g., project ownership, communication, organization). This opportunity is ideal for someone who enjoys hands‑on laboratory work, thrives in a project‑driven setting, and is excited about contributing to both scientific excellence and the establishment of a new, forward‑looking site in the U.S! Your Responsibility Be part of project teams for client projects (e.g., liquid/lyophilization formulation development, comparability and stress testing, storage stability study) as assigned by the superior with special focus on in‑use stability studies and primary packaging material (PPM) testing: Work as (i) 1st, 2nd project leader and/or (ii) team member for projects. Contribution/responsible for the development of work plans, testing procedures and/or amendments for customer projects. Correctly, timely and independently plan and execute formulation preparation / analytical testing / experiments. Independently perform analytical method transfer/implementation. Demonstrate solid understanding of performed analytical methods and be able to apply the knowledge to interpret the data. Perform data analysis and subsequently put data into context for data presentation and/or report. Support scientific discussion in client meeting. Appropriately act on unforeseen events. Be specialist / expert on several instruments / analytical methods / application areas (e.g., able to perform method development, interpretation of data, troubleshooting and training of new users). Implementation of new analytical equipment / technologies and application of the methods within client projects. Support on-boarding of new team members. Liaise with superior on training needs. Act as mentor. System Owner for laboratory equipment: responsible for operator training, equipment maintenance, calibration and qualification. Ensures that GRP rules are followed and documented. Ensures general laboratory cleanliness. Other duties as assigned by superior. What you need to succeed University degree in pharmaceutical sciences, (bio)chemistry, biology, or a related field Minimum 3 years of relevant experiences, e.g. employment in pharmaceutical industry / analytical laboratory (e.g. CDMO) or PhD studies Experience with equipment commissioning, maintenance, and LIMS Proven track record and hands- on experience in planning and executing in-use stability studies and PPM comparability testing is strongly preferred Proficiency in HPLC/UPLC-analysis (SEC, IEX, RP, LC-CAD), CE-analysis and subvisible particle analysis (MFI, LO) highly beneficial Additional expertise in biophysical characterization (AUC, CD, µDSC, FTIR, fluorescence), osmolality and turbidity is a plus Knowhow in biopharmaceutical formulation development beneficial Strong verbal and written communication skills Good knowledge of English (both written and spoken) Good time management and prioritization skills Eagerness to learn and develop new skills Open-minded and able to adapt strategies to changes Strong intercultural and interdisciplinary team player Strong problem-solving skills Hands-on mentality: practical, solution-oriented approach with a willingness to take initiative Candidates must be based in North Carolina (NC) or willing to relocate to NC Invest in yourself Let's formulate innovation together… Our success & development is created by the people working ********************** put People first! That's why we have a growth mindset, and value personality, collaboration and community to create an empowering and inspiring working space with focus on quality and customers. We would like to grow together with you! Let's continue building and creating the future now! Join our Team of currently around 200 employees. In a highly motivated and interdisciplinary team, we provide you with a great chance to increase your experience. We offer an attractive work space at the Martinsried site. Let's make a difference together! Coriolis Pharma is an equal opportunity employer and welcomes applications from all qualified individuals regardless of ethnicity, sex, citizenship or gender identity, color, disability, religion/belief, sexual orientation, marital status, age or individual preferences. Different backgrounds, experiences and ideas push us further and raise the bar. Thank you for your interest! We look forward to receiving your application documents. Please use our career portal exclusively for this purpose. We would like to support you from the very beginning to shape your development possibilities here at Coriolis. For questions or further information, please visit our website or contact us directly. We are looking forward to your application! Your Contact Dominik Schwemmer Senior Business Partner - Talent & Development People, Organization & Culture Unit Coriolis Pharma Research GmbH Phone: +49 (0) 89 - 417760 - 0 Fraunhoferstraße 18 b, 82152 Martinsried *********************** About us Coriolis Pharma is a global contract research and development organization (CRDO) and a premier partner for the development of liquid and lyophilized drug products, analytical services, and manufacturing services across a vast array of therapeutic modalities, including biologics, gene and cell therapies and vaccines. Our scientists design and execute platform and custom services to accelerate and derisk our clients' programs right from the start and throughout the entire product lifecycle. Our company culture is based on diversity, teamwork and open and appreciative communication. That's why wonderful people from over 36 nations around the world work together successfully at Coriolis. Our headquarters are located in Martinsried near Munich, Germany. An additional project management and business development team in the United States enables our US clients to work seamlessly with our German offices. What motivates us? Our motivation is to improve the quality of life for humankind by enabling the development of innovative drugs through outstanding biopharmaceutical services from preclinical to commercialization

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description • The incumbent will join the Manufacturing Science and Technology (MSAT) organization supporting biological therapeutics and vaccines. Within MSAT, the candidate will work in the Purification Group, which develops processes for isolation and purification of recombinant proteins, polysaccharides, bioconjugates, and other biologics. • Execution of lab or pilot-scale purifications using column chromatography, Tangential Flow Filtration (TFF), and/or Normal Flow Filtration (NFF), as needed. • Preparation of equipment, solutions, consumable materials, etc. as needed to support experiment execution. • Preparation of technical reports and presentations to communicate results to scientists and management, as required. Qualifications Able to execute experimental protocols, interpret data, and communicate results from experimental studies conducted at lab, pilot, or commercial scales. Additional Information Best Regards, Anuj Mehta ************

Requirements Advanced degree (e.g., M.D., Ph.D., J.D.) or equivalent experience Five years of professional experience Peer-reviewed publications Demonstrated experience securing and managing funded grants or contracts

Summary of Key Responsibilities: • Conducts experiments under limited supervision and maintains excellent notebook documentation in a GMP/GLP laboratory following Good Documentation Practices and ALCOA principles. • Performs In Vitro Release Testing (IVRT) for topical formulations such as Gels, Creams, Ointments, Films and Ophthalmic Solutions as per customer needs. • Prepares solutions for IVRT and High Performance Liquid Chromatography (HPLC) analysis such as Mobile Phase and Buffer. • Calibrates and operates micro and analytical balances for reference standard and reagent weighing. • Calibrates and operates pH meter for Buffer solution adjustments. • Operates data acquisitions system Empower 3. • Compiles data for quantitative analyses using Empower 3 and Microsoft Excel. • Manages daily activities in the laboratory, including chemical inventory and equipment maintenance and troubleshooting • Safely handles and disposes of hazardous materials including Category 3 and 4 potent compounds. • Has capacity to don half face respirator and disposable PPE for hazardous materials. • Provides support to team members as needed. • Works with limited supervision and interact with colleagues efficiently. • Drafts reports, protocols, and methods • Performs logbook and notebook review Required Qualifications and Skills: • B.S. in Pharmaceutical Sciences, Chemistry, Pharmacology, Biochemistry, Biology, or equivalent. • 1-2 years of relevant laboratory experience, university setting or other (GMP experience is preferred). • Possesses technical skills including handling of reference standards and topical products. • Previous experience in dissolution and USP general chapter is preferred. • Experience with general laboratory instruments. • Proficiency in Microsoft Office, use of data acquisitions systems, and document management systems. • Follows instructions meticulously, reads and executes protocols and methods as written. • Methodical, well-organized, conscientious, and thorough • Demonstrates logical thinking and attention to detail. • Has the ability to work with limited supervision and interact with colleagues efficiently.

THIS POSTING IS FOR TWO IDENTICAL POSITIONS ( POSITION NUMBERS 20071670 & 20071671). BY APPLYING TO THIS POSTING , YOU WILL BE CONSIDERED FOR BOTH AVAILABLE POSITIONS . The University of North Carolina at Chapel Hill is seeking a Research Scientist to direct, perform and attract funding for research in its Institute for Risk Management and Insurance Innovation ( IRMII ). This research involves a unique set of skills and expertise to be used in developing computational models that characterize and manage financial risk across a wide range of contexts, from flooding to pandemics to cyberattacks. This includes knowledge of engineering, data science and domain specific expertise in at least one additional area related to financial risk (e.g., environment, public health). Outcomes from this research involve (1) quantification of financial risk through the linking of models that characterize natural, engineered/managed and economic systems, and (2) the subsequent development of novel tools and strategies for managing financial risk. The successful candidate will engage in the development of interdisciplinary computational models that link natural, engineered/managed and economic systems for the purpose of quantifying financial risk, and then develop tools and strategies for managing that risk. Model development will include detailed computational renderings of these coupled systems in a stochastic simulation environment. These projects will span a range of regions (e.g., California, U.S. Pacific Northwest, U.S. Southeast, Africa) and a number of different economic sectors (e.g., power utilities, water utilities, agriculture, real estate, health care facilities), requiring an understanding of the financial linkages in these sectors, as well as the modeling skills to represent them accurately. In addition to model development, this individual will undertake to train graduate students and post-doctoral researchers in the conduct of this research and oversee their modeling efforts, then assist in the drafting of manuscripts, reports and oral presentations detailing the research. The successful candidate will be responsible for managing research personnel, including graduate students and post-doctoral associates to ensure that project milestones are met, project reports are completed and all requirements of the funders are fulfilled on time and in a satisfactory manner. The individual may also play a central role in coordinating activities with industry partners and/or multiple PIs in large interdisciplinary studies, ensuring that each member of a research team remains connected and coordinated. Other duties will include overseeing the collection, organization and storage of project data in appropriate repositories; monitoring of data sharing/data use agreements with partner organizations, and; coordinating multi-institutional modeling efforts by facilitating intra-team communication and the use of appropriate model sharing platforms (e.g. Github). The successful candidate will be responsible for assisting with, and in some cases leading, the conception, writing and preparation of new proposals to state and federal funding agencies, as well as other groups for the purpose of securing research funds. This will include not only the development of the research hypotheses and proposal framing, but budget development, inter-institutional partnership arrangements and coordination with both the Institute's operations manager and the University's Office of Sponsored Research. This individual will also be involved in communications with the funders, including response to reviewers, budget revisions and the preparation of annual reports. Required Qualifications, Competencies, And Experience The successful candidate must have experience in computational modeling that includes elements of engineering, natural science, economics and finance. Experience must also extend to developing interdisciplinary models that incorporate principles from each of these areas into a cohesive whole that enables the characterization of financial risk and subsequent strategies for managing this risk. Computational modeling skills are critical, as is fluency in one or more programming languages (e.g., Python, R, C++). The individual should have the ability to foster partnerships across diverse areas of research expertise and the ability to facilitate collaboration with other institutions, industry partners, and funding agencies. The individual should also have experience in manuscript writing. Preferred Qualifications, Competencies, And Experience At least 3 years of relevant experience is preferred. Research experience that would support the case for an eventual appointment as a research or adjunct faculty member at some future point would be a plus.

Real Staffing Group is a global staffing and recruitment specialist providing contract and permanent talent to a wide range of companies and industries. We take time to understand your career ambitions, working with you and for you at every stage of your job search. By applying our industry knowledge to your specific requirements we aim to supply you with the most effective route to your new career opportunity. To find out more about Real Staffing Group please visit http://www.RealStaffingGroup.com Job Description • Will assist with cell bank production operations and associated ongoing projects. • Individual will support cell bank operations by executing activities ranging from cell bank production, execution of protocol studies in a lab setting, as well as general daily support including document preparation and review. • Good lab safety awareness and a good foundation in biology or microbiology. • Experience working within a GMP framework with particular regard to manufacturing environments Qualifications Preference would be for an individual with a BS in Biology/Microbiology (or similar). • Lab experience (or small scale fermentation experience) is a very strong preference. • Need someone that wouldn't need to necessarily be taught the basics of GMP and GLP (i.e., good documentation practices, basic Micro lab skills, etc.). • So, a minimum of at least 2-5 years of experience would probably be ideal. If the person has sound lab experience, but not necessarily within the industry, I would not necessarily discount them. Additional Information All your information will be kept confidential according to EEO guidelines. IF THIS IS THE JOB OPPORTUNITY FOR YOU GIVE ME A CALL AT 646-357-1104 ASAP! I want to know more about your preferences. If in case you know someone who might be interested for this, feel free to pass it along. I look forward to hearing from you!

The Duke Center for In Vivo Microscopy, Dept of Radiology has a strong history in high-field magnetic resonance microscopy. One of our research teams develops hyperpolarized 129Xenon (Xe) MR for preclinical imaging of pulmonary disease in small animal models, and for clinical imaging in patients. The person in this position will oversee the operations and continued development of our 129Xe hyperpolarization infrastructure. Job Description The person in this position will oversee the operations and continued development of our 129Xe hyperpolarization infrastructure. • Operate, maintain, and perform quality assurance of hyperpolarization systems (preclinical and clinical polarizers) and small animal ventilators • Oversee equipment upgrades and performance enhancements • Order and maintain all gases and consumables required for their use • Develop and maintain standard operating procedures, and train operators • Maintain batch record documentation • Assist with preclinical and clinical studies, image archiving, and transfer of images • Develop other technical capabilities - coils, pulse sequences, analysis code • Initiate, develop, and perform tasks for new projects Qualifications EDUCATION: PhD preferred, but will consider BS (or higher) in biomedical engineering or physical sciences EXPERIENCE: Strong hands-on capabilities. Proficiency with vacuum systems, optics, electronics, and computer software/hardware, machining, and data acquisition techniques. ADDITIONAL BENEFICIAL SKILLS: Hyperpolarized gas physics, vacuum technology, MATLAB, LabVIEW, C, electromechanical assembly and testing. Additional Information All your information will be kept confidential according to EEO guidelines.

**Join Amgen's Mission of Serving Patients** At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do. Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. **Process Development Associate (Attribute Sciences)** **What you will do** Let's do this. Let's change the world. This role is part of Amgen's Attribute Sciences (AS) department within the Process Development (PD) organization that defines the favorable quality characteristics of the therapies it produces and optimizes innovative analytical tools to guide that development. In this vital role, you will work to provide scientific and technical contributions within Process Development Attribute Sciences at Amgen's FleX Batch facility. This laboratory-based role will evaluate attributes of materials based upon multiple analytical techniques, focusing on analytical testing, support, and troubleshooting. + Responsibilities include effectively delivering to the site, process development team, and quality control through rapid and robust analytical testing. + Ensure analysis support for small-scale model transfer, method transfers, investigation support, and continuous improvements + Work closely with functions including but not limited to Drug Substance, Quality, and Manufacturing + Understand analytical methodologies to detect product quality attributes and process-related impurities' testing using a variety of techniques including but not limited to UV-Vis spectroscopy, chromatography, capillary electrophoresis, and PCR. + Execute methods, author reports and ensure safety and compliance for all activities. **What we expect of you** We are all different, yet we all use our unique contributions to serve patients. The [vital attribute] professional we seek is a [type of person] with these qualifications. **Basic Qualifications:** + High school diploma / GED and 4 years of Process Development / Chemistry or related experience OR + Associate's degree and 2 years of Process Development / Chemistry or related experience OR + Bachelor's degree **Preferred Qualifications:** + Degree in Chemistry or related area. + Experience in pharmaceutical process development with related experience in analytical support, execution of methods, and investigational testing. + Experience in single or multiple analytical techniques (i.e., CE (Capillary Electrophoresis), ELISA, DNA, Chromatography (SE and RP), PCR). + Experience in method transfers, method validation, and method troubleshooting. + Familiarity with United States Pharmacopeia (USP) monographs and chapters, and International Conference on Harmonization (ICH) / Food & Drug Administration (FDA) mentorship documents related to analytical method transfer and validation. + Effective oral and verbal communication skills. + Technical writing skills and attention to details in documents. + A self-starter and valuable teammate. **What you can expect of us** As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. **Apply now and make a lasting impact with the Amgen team.** **careers.amgen.com** As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

We are seeking a highly motivated and scientifically rigorous Scientist to join our Bioscience Process and Validation team. This role operates at the critical intersection of engineering innovation and animal welfare, supporting the development and validation of novel biodevice technologies through hands-on, field-based bioscience. Unlike traditional bench or assay-focused roles, this position involves comprehensive ownership of the testing lifecycle-from drafting protocols and conducting field studies to collecting and analyzing large-scale data sets, and synthesizing results into actionable insights for cross-functional teams. The successful candidate will be expected to pressure-test device concepts and refinements, ensuring both product safety and animal welfare are held to the highest standards. This role requires resilience, scientific integrity, and a high degree of ownership. It offers a unique opportunity to engage deeply in meaningful work, contributing directly to the safety, performance, and successful deployment of animal-focused biodevices. Position Responsibilities: * Lead product development initiatives for innovative biodevice offerings, ensuring a thorough understanding of biological impacts and device safety. * Collaborate with engineering, Technical Service, and Field Service teams to refine design requirements, specifications, and product testing. * Design, develop, execute, and analyze experiments and testing protocols for product characterization and validation, applying bioscience development and statistical analysis methodologies. * Conduct evaluations both in-house and at customer test sites, including field-testing and assay execution, while overseeing trial-related activities such as onsite visits, data collection, and reporting, ensuring meticulous and compliant records of experimental data. * Communicate effectively with internal teams, trial sites, sponsors, and external collaborators to foster collaboration and ensure project success. * Adapt to both fast-paced and slower-paced environments, demonstrating enthusiasm, initiative, and self-motivation as needed. * Work efficiently in both independent and team settings, fostering collaboration and shared success. * Train and mentor junior staff on research activities and protocols, fostering professional growth within the team. * Collaborate with study team members to support project execution and ensure alignment with objectives. * Uphold the team values of respect, integrity, and open communication, creating an environment where all members feel valued and empowered to contribute. Education and Experience: * BS or MS in a relevant scientific field, or equivalent training/experience. * Minimum of 5 years in animal research or relevant laboratory science. * Practical and relevant laboratory experience. * Demonstrated hands-on interactions integrating mechanical devices and biological processes. * Medical device development exposure is a plus. Technical Skills Requirements: * Strong leadership skills with the ability to take initiative while ensuring team collaboration. * Experience working in a matrix environment and managing multiple projects simultaneously. * Willingness to travel for field work, with hands-on experience in animal handling and specialized laboratory equipment. * Experience in animal handling and/or with animal models. * Experience and success with multiple veterinary procedures in a research environment. * Excellent problem-solving and critical thinking skills in a complex, multiple variables, applied science environment. * High attention to detail. * Good communication skills to work in an interdisciplinary environment. * Ability to lift up to 50 pounds. * Endure long periods of sitting, standing, walking, and/or repetitive motions. * Ability to travel. * Ability to work non-standard working hours (e.g., early morning or late-night work) with a potential for overnight work. * Excellent written and oral communication skills, with the ability to develop and implement testing protocols. * Experience with GLP/GCP compliance is a plus. * Commitment to team values such as collaboration, continuous learning, and mutual respect. Full time Regular Colleague Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume. Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search. Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at ********************************** to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at ********************** site, or (2) via email to/from addresses using only the Zoetis domain of "@zoetis.com". In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.

Essential Responsibilities * Perform dose formulation analysis in support of GLP Toxicology assays * Perform method validations for HPLC and correlating stability studies for analysis of test articles or other chemicals. * Setup, maintenance and daily operation of HPLC system and related equipment. * Aid in the writing and editing of analytical and formulation sections within protocols and reports. * Prepare reagents, vehicles, solutions and suspensions following applicable SOPs, Protocols, and GLPs. * Receipt of controlled and non-controlled chemicals * Assures proper labeling, handling, and storage of all chemicals. * Maintain up-to-date chemical inventory * Perform solubility testing * Perform dose formulation calculations and preparations * Ensure chemical disposal is handled per local, state, and federal regulations * Communicate with Study Directors, Program Managers, and analytical labs to ensure adherence to study protocols Additional Responsibilities * Prepare dose formulations for in vitro and in vivo experiments as needed * Training of junior staff as needed. * Work in a team environment with a professional and positive attitude * Other duties as needed Minimum Acceptable Qualifications * Education: o B.S. in chemistry or related field * Experience: o Two years' experience in a GLP scientific environment * Skills: o Ability to perform basic unit conversion calculations o Experience working under GLP or regulatory requirements o Ability to use, troubleshoot, and maintain standard chromatography laboratory equipment. o Excellent written and oral communication skills o Excellent computer skills working with MS Word/Excel/Powerpoint o Attention to detail o Excellent organizational skills o Ability to exercise independent judgment * This position could be offered at different levels for candidates who qualify with a combination of advanced levels of education and/or years of experience. The salary range will adjust along with the level of the role to match the person's relevant experience and/or education level. Inotiv is a growing contemporary drug discovery and development company where we "Play to Win" in an industry rich with opportunity. Together, we face challenges and together we win in the delivery of world-class drug discovery and development solutions that impact the health and well-being of people all over the world. There's an opportunity for everyone at all phases of a career, each individual's unique skill set has an impact on the work we conduct. If you have the talent and desire to impact the quality of people's lives, we have the career opportunities to make it happen. Join us in embracing research and science to impact the health and well-being of people all over the world. Salary will be commensurate with experience and responsibilities. Benefits include health and dental coverage, short- and long-term disability, paid time off, paid parental leave, 401K, and more! Inotiv is an Equal Opportunity Employer. It is our policy to provide a fair and equal employment opportunity to all persons, regardless of age, race, color, religion, sex, gender, gender identity, gender expression, sexual orientation, genetic information, disability, national origin, veteran status, or any other basis prohibited by law. This policy governs all aspects of employment, including selection, job assignment, compensation, discipline, termination and access to benefits and training.

Purpose of your Job As part of our dynamic Formulation Development & Analytics unit, you will directly contribute to enabling the next generation of biopharmaceutical therapies. Our team drives innovative formulation and analytical strategies under BSL‑1/2 and S1/S2 safety levels, as well as GMP quality standards. By joining us, you will help ensure that advanced scientific work is carried out with excellence, precision, and curiosity. This role plays a key part in shaping Coriolis Pharma's global growth - including our build‑up of new U.S. facilities in North Carolina's Research Triangle Park (RTP), one of the world's most vibrant biotech innovation hubs. You will be involved in transferring expertise, establishing scientific capabilities, and supporting the seamless integration of processes across locations. In this position, you will transform scientific questions into meaningful analytical insights. You'll develop and implement state‑of‑the‑art methods, interpret complex data, and influence the scientific direction of client projects in an international, highly collaborative environment. Throughout your journey, you'll be supported in growing your technical strengths (e.g., analytical method development, instrumentation, troubleshooting) as well as your personal skills (e.g., project ownership, communication, organization). This opportunity is ideal for someone who enjoys hands‑on laboratory work, thrives in a project‑driven setting, and is excited about contributing to both scientific excellence and the establishment of a new, forward‑looking site in the U.S! Your Responsibility Be part of project teams for client projects (e.g., liquid/lyophilization formulation development, comparability and stress testing, storage stability study) as assigned by the superior with special focus on particle identification: Work as (i) 1st, 2nd project leader and/or (ii) team member for projects. Contribution/responsible for the development of work plans, testing procedures and/or amendments for customer projects. Correctly, timely and independently plan and execute formulation preparation / analytical testing / experiments. Independently perform analytical method transfer/implementation. Demonstrate solid understanding of performed analytical methods and be able to apply the knowledge to interpret the data. Perform data analysis and subsequently put data into context for data presentation and/or report. Support scientific discussion in client meeting. Appropriately act on unforeseen events. Be specialist / expert on several instruments / analytical methods / application areas (e.g., able to perform method development, interpretation of data, troubleshooting and training of new users). Implementation of new analytical equipment / technologies and application of the methods within client projects. Support on-boarding of new team members. Liaise with superior on training needs. Act as mentor. System Owner for laboratory equipment: responsible for operator training, equipment maintenance, calibration and qualification. Ensures that GRP rules are followed and documented. Ensures general laboratory cleanliness. Other duties as assigned by superior. What you need to succeed University degree in pharmaceutical sciences, (bio)chemistry, biology, or a related field Minimum 3 years of relevant experiences, e.g. employment in pharmaceutical industry / analytical laboratory (e.g. CDMO) or PhD studies Experience with equipment commissioning, maintenance, and LIMS Proven track record and hands-on experience in particle identification methodologies (e.g., visual inspection, particle isolation, FTIR-microscopy, SEM-EDX) is strongly preferred Proficiency in subvisible particle analysis (e.g., micro-flow imaging, light obscuration) highly beneficial Additional expertise in HPLC/UPLC-analysis, CE, UV-Vis, osmolality, turbidity, biophysical characterization is a plus Knowhow in biopharmaceutical formulation development beneficial Strong verbal and written communication skills Good knowledge of English (both written and spoken) Good time management and prioritization skills Eagerness to learn and develop new skills Open-minded and able to adapt strategies to changes Strong intercultural and interdisciplinary team player Strong problem-solving skills Hands-on mentality: practical, solution-oriented approach with a willingness to take initiative Candidates must be based in North Carolina (NC) or willing to relocate to NC Invest in yourself Let's formulate innovation together… Our success & development is created by the people working ********************** put People first! That's why we have a growth mindset, and value personality, collaboration and community to create an empowering and inspiring working space with focus on quality and customers. We would like to grow together with you! Let's continue building and creating the future now! Join our Team of currently around 200 employees. In a highly motivated and interdisciplinary team, we provide you with a great chance to increase your experience. We offer an attractive work space at the Martinsried site. Let's make a difference together! Coriolis Pharma is an equal opportunity employer and welcomes applications from all qualified individuals regardless of ethnicity, sex, citizenship or gender identity, color, disability, religion/belief, sexual orientation, marital status, age or individual preferences. Different backgrounds, experiences and ideas push us further and raise the bar. Thank you for your interest! We look forward to receiving your application documents. Please use our career portal exclusively for this purpose. We would like to support you from the very beginning to shape your development possibilities here at Coriolis. For questions or further information, please visit our website or contact us directly. We are looking forward to your application! Your Contact Dominik Schwemmer Senior Business Partner - Talent & Development People, Organization & Culture Unit Coriolis Pharma Research GmbH Phone: +49 (0) 89 - 417760 - 0 Fraunhoferstraße 18 b, 82152 Martinsried *********************** About us Coriolis Pharma is a global contract research and development organization (CRDO) and a premier partner for the development of liquid and lyophilized drug products, analytical services, and manufacturing services across a vast array of therapeutic modalities, including biologics, gene and cell therapies and vaccines. Our scientists design and execute platform and custom services to accelerate and derisk our clients' programs right from the start and throughout the entire product lifecycle. Our company culture is based on diversity, teamwork and open and appreciative communication. That's why wonderful people from over 36 nations around the world work together successfully at Coriolis. Our headquarters are located in Martinsried near Munich, Germany. An additional project management and business development team in the United States enables our US clients to work seamlessly with our German offices. What motivates us? Our motivation is to improve the quality of life for humankind by enabling the development of innovative drugs through outstanding biopharmaceutical services from preclinical to commercialization

Summary of Key Responsibilities: Develop and validate skin permeation and/or LC-MS/MS analytical test methods with minimal guidance from senior laboratory personnel Carry out laboratory work as directed by senior laboratory personnel Conduct routine analytical experiments using established analytical methods and procedures Assist with assembling and review of data packs Prepare detailed protocols and technical reports for development, validation, and post-validation activities Conduct experiments by developing new analytical methods or using established analytical methods including in vitro permeation testing techniques and LC-MS/MS Data entry into spreadsheets, as directed by senior laboratory personnel For LC-MS/MS experiments independently perform full data review of chromatography, transcription checking of spreadsheets, and calculation review of spreadsheets For Skin permeation/IVPT experiments transcription checking and calculation review of spreadsheets Review and maintain laboratory notebooks Assist in training of entry-level employees Manage essential laboratory activities including equipment maintenance schedules, chemical and laboratory supply inventory Required Qualifications and Skills: B.S with 3-8 years of experience, or M.S with 2-6 years of experience: focus in chemistry, biology, pharmaceutical sciences or related scientific discipline 2-5 years of experience in a GxP laboratory setting in the pharmaceutical industry Experience in either LC-MS/MS or IVPT/Skin permeation testing, troubleshooting and validation Demonstrated experience in developing and implementing new technologies, ways of working, and/or tools to improve capability Technical report writing proficiency Experience with other general laboratory instruments and wet chemistry techniques Proficiency in Analyst and/or MassLynx and MS Excel Speaks, writes, listens and presents information in a logical and articulate manner appropriate for the audience Thorough when performing work, conscientious about attending to detail, and uses logical thinking that is well-organized and methodical

The Tiley Lab is seeking to fill a temporary Research Scientist/Scholar position with expertise conducting research on quantitative targeted proteomics using LC-MS/MS in tissues and cells from humans. This project will be funded by the NIH - NICHD InTEC UC2 Grant. Active dates: July 1-September 1 2025. The Integrated Transporter Elucidation Center (InTEC) is a consortium of multiple universities that aims to advance our understanding of how placental transporters impact the disposition of endobiotics, xenobiotics, and overall pregnancy health. Funded by NICHD , InTEC utilizes novel technologies to profile the SLC and ABC transporter proteome, predict and validate novel substrates and regulators of placental transport, and simulate maternal-fetal disposition using a vascularized placenta-on-a-chip. The University of North Carolina ( UNC ) at Chapel Hill, Eshelman School of Pharmacy, Division of Pharmacotherapy and Experimental Therapeutics ( DPET ) is part of InTEC and is seeking to identify placental transport proteins measurable by targeted proteomics and to create new methods to improve detectability of transport proteins. The division works closely with all InTEC institutions (Rutgers University, Tulane University and the University of Pennsylvania) and with other divisions within the UNC Eshelman School of Pharmacy. Required Qualifications, Competencies, And Experience Relevant post-Baccalaureate degree required (or foreign degree equivalent); for candidates demonstrating comparable independent research productivity, will accept a relevant Bachelor's degree (or foreign degree equivalent) and 3 or more years of relevant experience in substitution. May require terminal degree and licensure. Preferred Qualifications, Competencies, And Experience - Ph.D. in Pharmacology and Toxicology, or related field. - Previous experience in LC-MS/MS targeted proteomics and tissue and cell sample preparation.

Real Staffing Group is a global staffing and recruitment specialist providing contract and permanent talent to a wide range of companies and industries. We take time to understand your career ambitions, working with you and for you at every stage of your job search. By applying our industry knowledge to your specific requirements we aim to supply you with the most effective route to your new career opportunity. To find out more about Real Staffing Group please visit http://www.RealStaffingGroup.com Job Description: • The incumbent will join the Manufacturing Science and Technology (MSAT) organization supporting biological therapeutics and vaccines. • Within MSAT, the candidate will work in the Purification Group, which develops processes for isolation and purification of recombinant proteins, polysaccharides, bioconjugates, and other biologics The incumbent responsibilities will include the following: • Execution of lab or pilot-scale purifications using column chromatography, Tangential Flow Filtration (TFF), and/or Normal Flow Filtration (NFF), as needed. • Preparation of equipment, solutions, consumable materials, etc. as needed to support experiment execution • Preparation of technical reports and presentations to communicate results to scientists and management, as required. Qualifications Requirement: • Bachelor's degree or graduate degree in Chemistry, Chemical Engineering or related biotechnology field. Industrial experience is preferred. • Experience with operating and monitoring of Tangential Flow Filtration (TFF), Normal Flow Filtration (NFF), and chromatography systems is desired • Experience with conjugation chemistry is highly desired. Additional Information All your information will be kept confidential according to EEO guidelines. IF THIS IS THE JOB OPPORTUNITY FOR YOU GIVE ME A CALL AT 646-357-1104 ASAP! I look forward to hearing from you!

Career CategoryProcess DevelopmentJob DescriptionJoin Amgen's Mission of Serving Patients At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do. Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Process Development Associate (Attribute Sciences) What you will do Let's do this. Let's change the world. This role is part of Amgen's Attribute Sciences (AS) department within the Process Development (PD) organization that defines the favorable quality characteristics of the therapies it produces and optimizes innovative analytical tools to guide that development. In this vital role, you will work to provide scientific and technical contributions within Process Development Attribute Sciences at Amgen's FleX Batch facility. This laboratory-based role will evaluate attributes of materials based upon multiple analytical techniques, focusing on analytical testing, support, and troubleshooting. Responsibilities include effectively delivering to the site, process development team, and quality control through rapid and robust analytical testing. Ensure analysis support for small-scale model transfer, method transfers, investigation support, and continuous improvements Work closely with functions including but not limited to Drug Substance, Quality, and Manufacturing Understand analytical methodologies to detect product quality attributes and process-related impurities' testing using a variety of techniques including but not limited to UV-Vis spectroscopy, chromatography, capillary electrophoresis, and PCR. Execute methods, author reports and ensure safety and compliance for all activities. What we expect of you We are all different, yet we all use our unique contributions to serve patients. The [vital attribute] professional we seek is a [type of person] with these qualifications. Basic Qualifications: High school diploma / GED and 4 years of Process Development / Chemistry or related experience OR Associate's degree and 2 years of Process Development / Chemistry or related experience OR Bachelor's degree Preferred Qualifications: Degree in Chemistry or related area. Experience in pharmaceutical process development with related experience in analytical support, execution of methods, and investigational testing. Experience in single or multiple analytical techniques (i.e., CE (Capillary Electrophoresis), ELISA, DNA, Chromatography (SE and RP), PCR). Experience in method transfers, method validation, and method troubleshooting. Familiarity with United States Pharmacopeia (USP) monographs and chapters, and International Conference on Harmonization (ICH) / Food & Drug Administration (FDA) mentorship documents related to analytical method transfer and validation. Effective oral and verbal communication skills. Technical writing skills and attention to details in documents. A self-starter and valuable teammate. What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now and make a lasting impact with the Amgen team.careers.amgen.com As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. . Salary Range 79,971.00 USD - 89,221.00 USD