Research Scientist Jobs in Piney Green, NC

Z-Alpha Therapeutics is a pharmaceutical company dedicated to the discovery and development of radiotherapeutics targeting key biological pathways for solid tumors.The company has a revolutionary technology platform in the next generation of alpha particle therapy with potential to be a more targeted therapy, increasing efficacy and limiting toxicity compared to competitors in the radiotherapeutics space. The company has a world-class team of scientists with decades of experience and foundational intellectual property that enables the potential to bring multiple drug candidates into the clinic. Job Summary As a Principal Scientist in Biology with project management responsibilities, you will lead scientific initiatives and oversee project execution for Z-Alpha's radiopharmaceutical programs. This role requires the ability to design experiments that support drug discovery and development. In addition to scientific leadership, you will manage cross-functional projects, ensuring alignment of research activities with overall program objectives and timelines. Key Responsibilities: Scientific Leadership: Conceptualize, design, and execute innovative functional assays for target validation and drug lead selection for radiopharmaceutical candidates. Project Management: Lead and manage project workflows, coordinating activities across biology and chemistry teams. Ensure projects are completed on time and within scope. Experimentation: Independently design and conduct cell-based and biochemical assays to generate high-quality, actionable data. Analytical Development: Optimize and troubleshoot analytical assays, ensuring technical robustness and consistency with program needs. Data Analysis & Reporting: Analyze complex datasets, interpret experimental outcomes, and present findings at project team and company-wide meetings. Collaboration & Communication: Act as a liaison between cross-functional teams, external collaborators, and vendors to ensure smooth project execution. Documentation: Maintain meticulous records of experiments, ensuring data integrity, reproducibility, and adherence to regulatory standards. Mentorship: Provide scientific guidance and mentorship to junior team members, fostering a collaborative and innovative research environment. Leadership: Establish and manage laboratory infrastructure and standard operation process. Radiation Safety: Conduct radioligand assays in strict adherence to radiation safety protocols, ensuring a safe laboratory environment. Required Qualifications: Ph.D. in Biology, Oncology, or a related discipline with a strong focus on drug discovery. 5+ years of experience in oncology or drug discovery within biotech or pharmaceutical research. Demonstrated success in leading cross-functional projects in a biotech or pharmaceutical setting. Extensive expertise in molecular and cell biology techniques including cell culture, flow cytometry, ELISA, western blotting, qPCR, and single-cell cloning. Strong proficiency in project management tools, along with software like GraphPad Prism, FlowJo, Excel, and PowerPoint. Highly organized, with strong time-management skills and the ability to adapt to rapidly changing project landscapes. Collaborative team player with the ability to work independently and manage competing priorities effectively. Excellent communication and leadership skills Preferred Skills: Experience in targeted radiotherapies, radiopharmaceutical development, or nuclear medicine.

Serving the community since 1961, WakeMed Health & Hospitals is the leading provider of health services in Wake County. With a mission to improve the health and well-being of our community, we are committed to providing outstanding and compassionate care. For more information, visit **************** EOE Position Information: The CV Testing Scholar is a pre-graduate ultrasonography student under the supervision of Registered staff Sonographers performs Cardiac and/or Peripheral Vascular ultrasound imaging and a variety of supportive tasks related to these procedures. Experience Requirements: 6 Months Related Position Experience Preferred Education Required: High School Diploma or Equivalent Required - And College Courses Radiologic Technology Required Licensure/Certification Requirements: Cardiopulmonary Resuscitation Certification Or Basic Life Support Required Hours of Work: Days Weekend Requirements: As Needed Call Requirements: No

Piper Companies is seeking an Associate Scientist (Environmental Monitoring) to fill an opportunity with an innovative Pharmaceutical company in Durham, NC. Responsibilities for the Associate Scientist (Environmental Monitoring) •Provide environmental monitoring support to manufacturing and laboratory groups •Support water sampling, and pH water testing •Clean steam and compressed gas sample collection •Maintain laboratory material and reagent inventory•Analyze environmental monitoring data and complete routine trend reports•Assist in laboratory and product failure investigations•Document testing in accordance with cGMP requirements Qualifications for the Associate Scientist (Environmental Monitoring) •1+ years of experience working in a cGMP microbiology laboratory•Experience collecting samples from manufacturing and laboratory •pH and water testing experience is preferred •Bachelor of Science in related field is a plus Compensation for the Associate Scientist (Environmental Monitoring) Salary Range: $28 - $40/hr Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and HolidaysThis job opens for applications on 1/17/2025. Applications for this job will be accepted for at least 30 days from the posting date. Keywords: Microbiology, Microbiologist, QC, Endotoxin, Environmental Monitoring, cGMP, Microbial Tests, cGMP, Aseptic Technique, Pharmaceutical #LI-JM1 #LI-ONSITE

****LOCAL CANDIDATES ONLY**** Responsibilities Conducting routine and complex data analysis to obtain and report results, as well as monitoring analytical procedures to ensure performance is within expectations and results are within acceptable tolerances. Partnering with Assay Development to operationalize and deploy cell-mediated immune assays, including flow cytometry and ELISpot/Fluorospots, as well as other assays as needed. Performing and documenting hands-on training of laboratory staff in areas of demonstrated competency as assigned. Leading quality investigations, assigning and completing CAPAs, and conducting effectiveness checks. Maintaining laboratory notebooks and other documentation using good documentation practices to ensure traceability. Working proactively across functions to ensure effective delivery and maintain and enhance operational standards of the lab. Qualifications PhD in Immunology or related discipline preferred, or Bachelor's/Master's degree with an equivalent combination of education and experience. At least 3-5 years of relevant laboratory experience. Superior knowledge of laboratory testing and documentation best practices, flow cytometry, ELISpot/Fluorospot, and data analysis.

Senior / Principal Analytical Development Scientist We are partnered with a niche CDMO that has developed an outstanding reputation in supporting start-ups and small to medium sized businesses work through analytical development, process optimization and scale up challenges. Having increased in headcount over the past 12 months, we are now looking to support the expansion of key groups. For this hire, we are looking for experienced Analytical Development Scientists. This could be at Scientist, Senior Scientist or Principal Scientist level due to the flexibility of how this business is structured. This role will focus on the method development and method validation of for both organic pharmaceuticals and biopharmaceuticals. Working in a broad role that will involve not just hands on work in the laboratory but also the opportunity and need to work closely with the end client through project and study management. With the expansion plans in this CDMO, there is a real opportunity to develop and build experience in position where you will have an immediate impact. For further information, please contact Mark Bux-Ryan. Key experience: Experienced in analytical method development using a range of key techniques including ELISA and Spectroscopy. Experienced in project and/or people leadership Management experience is advantageous but not essential The ability and desire to work both hands on in the laboratory as well as work commercially in-front of a client Analytical, development, method, validation, spectroscopy, mass, MS, ELISA, organic, pharmaceutical, biopharmaceutical, biologic, process

Nemours Children's Health - Delaware Swank Autism Center Wilmington, DE The Swank Autism Center at Nemours Children's Health is seeking a Research Scientist (open rank) to join our team. The Swank Autism Center provides comprehensive clinical services for children up to age 21 years and conducts research and community-based outreach and training. We are seeking applicants with demonstrable training and experience working in clinical and/or research settings with autistic/neurodivergent children, adolescents, and/or young adults, and their families. The Research Scientist will develop a targeted research program in autism. Current research studies or immediate potential opportunities are available in examining inequities and disparities in healthcare delivery, progressive assessment models, hospital-wide autism initiatives, adolescence/postsecondary transition, and other areas. The Research Scientist will also provide some clinical services as a part of this role, which might include autism diagnostic services, individual/group therapy, and supervising trainees in working with patients and families from the larger Delaware Valley community. This position will have joint appointments in the Swank Autism Center and the Center for Healthcare Delivery Science - Delaware Valley (********************** The CHDS is a research center across the Nemours enterprise. Anne E. Kazak, Ph.D., ABPP is the enterprise director, Melissa A. Alderfer, PhD is the Center Director in Delaware and Susana Patton, PhD is the Center Director in Florida. The CHDS includes 20+ investigators that study ways to improve health care, health equity, and health and wellness beyond medicine for youth and their families. Research projects span a variety of medical conditions (e.g., diabetes, cancer, cardiac conditions, obesity, sickle cell disease, cystic fibrosis, pain) and other health-related challenges (COVID-19 vaccine hesitancy, homelessness, maternal post-partum depression, racism). The research scientist will join a multidisciplinary team including providers in psychology, developmental medicine, psychiatry, neurology, social work, nursing, and applied behavior analysis, as well as colleagues who are autistic and/or caregivers. The Swank Autism Center has a dedicated Clinical Research Coordinator and CHDS has additional research coordination and data analysis resources. Equity, diversity, and inclusion guide our growth and strategy. We are looking for individuals who are passionate about, and committed to, leading efforts to provide culturally relevant, neuro-affirming care, promoting anti-ableist mental health care, reducing health disparities, and helping build a diverse and inclusive team environment. Autistic/neurodivergent applicants are welcomed. The Research Scientist would have opportunities to precept trainees including externs, residents, and/or fellows who rotate through the center. Teaching, training, and mentoring are core values in our division and these efforts are supported and encouraged. We are committed to expanding pathways that promote a diverse workforce and as such, are intentional in our hiring and retention practices. We practice continuous learning through awareness-enhancing and bias-reduction educational opportunities that guide our overarching lens of health equity. Faculty are encouraged to participate in the Division of Behavioral Health's active and energetic Diversity Committee. Minimum Qualifications Education Candidates must hold a PhD, MD, MD/PhD, or other doctoral degree in a health-related discipline and demonstrate evidence of collaborative academic productivity and either success in obtaining funding for research or a strong potential to obtain funding for research. APPLICATION: Please send a letter of interest and CV to ******************************* and please state “Autism Research Scientist” in the subject line. Applications currently are being reviewed and will be accepted until the position is filled. About Nemours: As one of the nation's leading pediatric health care systems, Nemours is committed to providing all children with their best chance to grow up healthy. We offer integrated, family-centered care to more than 300,000 children each year in our pediatric hospitals, specialty clinics, primary care practices, and school-based health centers in Delaware, Florida, Maryland, New Jersey and Pennsylvania. Nemours strives to ensure a healthier tomorrow for all children - even those who may never enter our doors - through our world-changing research, education, and advocacy efforts. At Nemours, our Associates help us deliver on the promise we make to every family we have the privilege of serving: to treat their child as if they were our own. Psychologists are members of the medical staff at Nemours Children's Hospital, Delaware and are supported with applying for an academic appointment through the Sidney Kimmel Medical College at Thomas Jefferson University. Nemours (Nemours.org) is an open and welcoming place to work, and values diversity in all its forms. Additionally, Nemours aspires to have its workforce and providers reflect the rich diversity of the communities we serve. Candidates of diverse backgrounds, Spanish-speaking applicants, and those committed to working with diverse populations and conversant in multicultural values are strongly encouraged to apply. Associates are encouraged to join Associate Resource Groups as members or allies to support colleagues of diverse identities and lived experiences.

**Job Details** **Associate Research Scientist - (2024-16)** Share this job as a link in your status update to LinkedIn. **** Job Title Associate Research Scientist Shift Type Education Master's Degree Location Chapel Hill Center - Chapel Hill, NC 27514 US (Primary) Career Level Experienced (Non-Manager) Category Research Job Type Full-time and Part-time Travel PIRE has a significant national presence in the area of applied science, with funded research projects at its centers on prevention, treatment, and policy research. PIRE scientists and practitioners continually focus on the design and implementation of complex program evaluation strategies and the conduct of research related to health and social issues, and criminal justice. PIRE practitioners and scientists provide training and technical assistance in many health-related areas to states and communities that are attempting to improve public health. For more information about PIRE go to ************ . Position Summary Pacific Institute for Research and Evaluation's (PIRE) Chapel Hill, NC Center is seeking **early career investigators and evaluators** to join our team. This opportunity is open to early career investigators and evaluators who wish to grow their research program while enhancing PIRE's growing portfolio, including research in areas such as: health, mental health, and substance use; child welfare; education; criminal justice; public policy; state, county, and community partnerships and, program evaluation. PIRE is an independent, nonprofit organization merging scientific knowledge and proven practice to create solutions that improve the health, safety and well-being of individuals, communities, tribes, and nations around the world. For full-time researchers and evaluators, we have excellent health coverage, a retirement plan and flexible work arrangements available to support our nationally recognized institution of independent scientists. **Benefits Overview:** * 3.5-7 weeks of accrued PTO during the first year * Company provided Retirement Plan * Company provided Life and Accidental Death and Dismemberment of $100k * Company provided Short- and Long-Term Disability * Medical, Dental and Vision coverage We invite a CV and letter of introduction from early career investigators who have: * Strong skills in project management, working as part of a research team and with various partners/audiences, quantitative data analysis, and writing reports or manuscripts. **PIRE is a soft-money and self-funded research organization. This independence and freedom come with the responsibility of seeking and securing one's own funding. As part of your CV and introduction, please share a brief description of your research interests and potential funders.** **Successful applicants will be expected to pursue their own research while collaborating with other PIRE scientists in areas of mutual interest. Current or recent funding from NIH, SAMHSA, and/or other federal or state agencies is desired but not required. PIRE is prepared to assist researchers who submit applications with startup funding, mentorship, administrative assistance, and collaborative scientific support. Employment is contingent upon successful awards.** PIRE has a strong commitment to research dissemination and moving science to practice and practice to science. The implementation of our work is demonstrated in peer-reviewed journal articles, reports for government and lay audiences and professional presentations. Documentation of PIRE's capabilities and work in these areas can be found on PIRE's website (************). We look forward to talking with you about your interests and how your research can grow with PIRE. Job Requirements * M ast er's D egr ee, an a dvanced degree (e.g., M.D., Ph.D., J.D.) or equivalent experience * Proof of COVID-19 vaccination is required prior to beginning work at PIRE except in limited circumstances where an employee is legally entitled to an accommodation. Some Primary Duties and Responsibilities ** Exemption Type Exempt PIRE is a diverse community devoted to the promotion and acceptance of all people regardless of race, color, national origin, religion, sexual orientation, gender identity, age, gender or physical ability or veteran status. PIRE is committed to employ, and advance in employment, individuals with disabilities and protected veterans, and to treat qualified individuals without discrimination on the basis of their physical or mental disability or veteran status. PIRE will provide reasonable accommodations with the application process upon your request as required to comply with applicable laws. If you have a disability and require assistance in this application process, please contact Human Resources by email at ***********

Share If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process. **Associate Scientist, Oncology Research** 30+ days ago Requisition ID: 1022 Aktis Oncology is a biotechnology company pioneering the discovery and development of a new class of targeted radiopharmaceuticals to treat a broad range of solid tumor cancers. Founded and incubated by MPM Capital with its seasoned team of entrepreneurs and drug developers, Aktis has developed proprietary platforms to generate tumor-targeting agents with ideal properties for radiotherapy. Designed for high tumor penetration and long residence time, Aktis Oncology's molecules can quickly clear other areas of the body, thereby maximizing tumor elimination while minimizing the side effects of treatment. These are therapies that would also enable clinicians to visualize and verify target engagement prior to exposure to therapeutic radioisotopes. The role within Oncology Research will work in cross-functional teams to identify and develop novel therapies to treat targeted patient populations within multiple oncology indications. Under minimal supervision, the candidate will conduct laboratory experiments, interpret data and contribute to project goals as part of the Oncology Research Team. **BACKGROUND/TRAINING** * BS/MS/MA in biological sciences or related field, preferably related to cancer biology, pharmacology or related field * 2-8 years of biopharmaceutical research experience in drug discovery and/or translational research **EXPERIENCE/ACCOMPLISHMENTS** * Strong technical background in planning, designing, and executing pre-clinical in vitro (required) and in vivo (preferred) experiments in order to evaluate target biology and characterize the efficacy and safety of development candidates + Desired expertise includes: - Mammalian cell culture / cell line engineering - Common molecular and biochemical techniques (DNA/RNA isolation, qPCR, Western, ELISA, antibody characterization and QC, Flow cytometry, etc.) - Imaging, microscopy, or pathology experience that can be leveraged to examine target expression across cell lines and/or tissue sections - FFPE tissue embedding, sectioning, and immunohistochemistry staining experience + Demonstrated experience in the adoption of new technologies and dissemination of information to colleagues for deployment across programs / initiatives * Experience with evaluation of target biology including but not limited to + Biophysical characterization of targets - Subcellular / tissue localization - Target:ligand interactions - Target density evaluation + Ex vivo examination of tumor samples + Evaluation of target engagement and proof-of-biology marks in vivo * Demonstrated success in the area of target discovery, target evaluation or drug discovery, translational research, and integration with matrixed project teams * Demonstrated ability to gather relevant information systematically, break down problems into simple components, and make sound decisions * Willingness to take on new challenges and build a culture of rigor and data-driven decision-making to bring novel therapies to the clinic * Effectively communicates and collaborates with other R&D team members and collaborators to progress the development candidate compounds * Demonstrated high standards for scientific rigor, team behaviors, excellence, and building a culture of innovation that is fully aligned with company objectives * Demonstrated tenacity and drive for enterprise benefit * Position title to be finalized commensurate with experience and accomplishments Aktis Oncology is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.

**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) **Job Description** As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. **Discover Impactful Work** This opening is for a highly qualified and self-motivated individual to support our latest generation Ion Chromatography (IC) instrumentation as a field-based Application Scientist. As a member of the Thermo Fisher Scientific North Americas application support team, the candidate will work within a multi-disciplinary matrix team that includes regional sales representatives, marketing and service professionals, product development scientists, and engineers. **A day in the life** + Provide training on how to use Thermo Scientific's Ion Chromatography instruments and software for a wide range of applications, both in person and remotely. + Provide pre- and post-sales technical support as well as applications assistance in response to customer inquiries, including education, training and on-site visits. + Connect with customers in a professional manner. + Build well-organized information-rich tools (documents and seminars) and effectively deliver them in an engaging manner. + Combine conceptual and analytical knowledge to independently address difficult problems. + Prioritize projects to most effectively accomplish core job functions. **Keys to Success** **Education** + A bachelor's degree in chemistry, biochemistry, or a related scientific field and/or equivalent work experience. + Research experience, such as a Masters or a Ph.D. or equivalent experience, is an asset. **Experience** + 3+ years of hands-on IC experience. + Automated Photometric Analysis (DIA) experience a plus. **Knowledge, Skills and Abilities** + This position involves frequent interaction with customers, so excellent verbal and written communication skills are a must. + A consistent track record of working independently and a strong work ethic are essential. + Ability to travel up to 75% mainly within Central and South United States with occasional international travel, primarily to the Canada. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued. **Apply today!** **************************** **Benefits:** We offer competitive remuneration, annual incentive plan bonus scheme, healthcare, company pension/retirement, and a range of employee benefits! Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation. Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status. We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform critical job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation. **Compensation and Benefits** The salary range estimated for this position based in Florida is $75,800.00-$113,675.00. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes: + A choice of national medical and dental plans, and a national vision plan, including health incentive programs + Employee assistance and family support programs, including commuter benefits and tuition reimbursement + At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy + Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan + Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount For more information on our benefits, please visit: ***************************************************** Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Ashland Specialty Ingredients, GP Are you the kind of person that is always thinking, sketching, seeking, and adjusting? Who needs to understand how things work and then figure out how they can work better? Are you a passionate, tenacious, solver who loves to work with others who share your drive? Are you positive, constructive, and ingenious? Are you always solving? Then we'd like to meet you and bet you'd like to meet us. Ashland has an exciting opportunity for a Coatings Scientist to join our Specialty Additives business unit at our Wilmington DE research center. This is a very visible, significant role within the Company and the specialty additives innovation function. This position will report to the North America Innovation Lead. The responsibilities of the position include, but are not limited to, the following: Responsible to provide technical support for customers to assist their implementation of Ashland products; form strong relationships with senior technical staff at key customers Identify new product opportunities or new applications of existing products through customer contact and market knowledge - and work with the team to turn these into new product projects Evaluate new technologies in customer specific formulations and provide input on technical and market development to promote the growth of Ashland technology platforms Work with marketing and sales professionals to understand industry needs; lead or participate in multiple research projects with members of multi-disciplinary teams to achieve targets Maintain a strong awareness of new technologies, competitive threats and opportunities and regulatory developments in the coatings and allied fields In order to be qualified for this role, you must possess the following: B.S. degree in polymer science or chemistry 5 years experience with BS (or MS with >3 years and PhD with >1 year) of coating formulation and additives 5 years of tech service experience in coatings related industries Have experience working with multidisciplinary project teams; and be able to lead such teams Effective oral and written communications skills Travel up to 30% of time The following skill sets are preferred by the business unit: Advanced degree in polymer or chemistry 10+ years of experience in coating application and additive development In more than 100 countries, the people of Ashland LLC. (NYSE: ASH) provide the specialty chemicals, technologies and insights to help customers create new and improved products for today and sustainable solutions for tomorrow. Our chemistry is at work every day in a wide variety of markets and applications, including architectural coatings, automotive, construction, energy, personal care and pharmaceutical. Visit *************** to see the innovations we offer. At Ashland our vision is to be a leading, global specialty chemicals company whose inspired and engaged employees add value to all we touch. In fact our people, employees, customers and vendors define who we are. They are the driving force behind everything we do. Not only do we value our customers but we value our employees, and we work to offer them a dynamic and challenging environment. We hold ourselves to high standards at Ashland, and we value integrity and honesty. Ashland has a history of attracting the best people and keeping them. The reasons are simple: industry competitive salary and benefits, pay-for-performance incentive plans and a diverse work environment where employees feel challenged and valued. People come to Ashland and stay. As a growing Fortune 500 specialty chemicals company, we offer opportunities for development and advancement throughout our global organization. Our values define who we are and what we care about as a company. If you are looking for a relationship with a company instead of simply a job, this may be a great fit. Ashland is proud to be an Equal Opportunity Employer Minorities/Women/Veterans/Disabled/Gender Identity/Sexual Orientation. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, or protected veteran status and will not be discriminated against on the basis of disability. NOTE: We do not accept resumes from external staffing agencies or independent recruiters for any of our openings unless we have a signed recruiting agreement in place to fill a specific position.

Scientist I page is loaded **Scientist I** **Scientist I** locations USA - NC - Durham - Hamlin Rd time type Full time posted on Posted 8 Days Ago job requisition id R00006802 At KBI Biopharma, we are advancing science and accelerating breakthroughs. As a global leader in biopharmaceutical development and manufacturing, we empower life science companies to bring new medicines and vaccines to the world faster. Explore your potential at KBI, where innovation meets impact. **Position Summary:** Join a highly technical analytical team in a dynamic work environment. Participate in contracted client analytical programs as a member of Analytical, Formulation and Stability (AFS). With a focus on plate-based assays (ELISA and qPCR), abilities in other analytical techniques applicable to the business needs are desirable (HPLC, UPLC, western blot, SDS-PAGE, CE-SDS, etc). **Responsibilities:** * Analytical scientist for late phase clinical development and scale up for Biopharmaceutical commercialization. * Participates in product development and/or QC efforts in the formulations and/or analytical areas. Includes testing to support method transfer, development, qualification, product characterization, routine GMP and non-GMP analysis, etc. **Requirements:** * Ph.D. and 0 years directly related experience or Master's and seven years related experience or Bachelor's and nine years related experience in biotechnology or pharmaceutical industries. * Experience in plate-based analytical techniques are preferred. * Good oral presentation and technical writing skills are required. * Records (accurately, clearly, and consistently) information, facts, and measurements that are required by cGMP, GLP, GCP, and/or by co-workers to understand situations and to perform their assignments. * Understanding of biotherapeutic regulatory requirements and expectations. * Strong communication skills. **Salary Range: $90,000 - $110,000** Salary range provided per current averages and expectations. The salary and job title for this opening will be based on the selected candidate's qualifications and experience and may be outside this range. KBI has a robust total rewards strategy which includes an annual bonus structure for all employees, medical, dental, and vision coverage, paid PTO and holidays, Sabbatical program, 401K matching with 100% vesting in 60 days and employee recognition programs. **About KBI:** KBI Biopharma, Inc., a JSR Life Sciences company, is a global contract development and manufacturing organization (CDMO) providing fully integrated and accelerated drug development and biologics manufacturing services to life science companies. KBI supports its 500+ customers in advancing more than 160 drug candidates from preclinical and clinical stages to market, including the manufacture of ten commercial products. Recognized for quality manufacturing, KBI delivers robust process development and cGMP manufacturing services across its six global locations in the USA and Europe. For more information, visit . *KBI is a proud EEO/AA employer dedicated to building a diverse and inclusive workforce. We believe that innovation thrives in an environment where all voices are heard and valued. That's why we actively seek individuals from all backgrounds - regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability, or veteran status - and strongly encourage all qualified candidates to apply and bring their unique perspectives to our team.* *KBI Biopharma is committed to providing a safe and healthy workplace. Any employee entering a KBI site located in the US must inform KBI Biopharma of their vaccination status and must submit their vaccination status. All vaccinated employees are required to provide proof of their COVID-19 vaccination, with a COVID-19 vaccination which has been granted FDA approval or Emergency Use Authorization.* *KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply.* *I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.* *I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.* At KBI, we are constantly seeking to improve our team with accomplished individuals who share in our commitment to serve our clients as they seek to advance important medicines to the patients who need them. We offer our employees a challenging, rewarding and fast-paced environment along with the opportunity for career advancement through the development of one's technical skills. At KBI, employees work in a collaborative, team environment, where sharing knowledge and expertise with one another is strongly encouraged. If you do not see a position that matches your background, we invite you to return to our site often as positions are updated frequently. Please Note: To 3rd Party Search Firms/Employment Agencies: All inquiries must be directed to ******************************** . Please do not call or email any KBI Biopharma employee about current or future job openings. All resumes submitted by search firms or employment agencies to any employee at KBI Biopharma via-email, telephone, social media or other means will be deemed to be the sole property of KBI Biopharma, unless the firm submitting the resume has previously entered into a written agreement with KBI Biopharma regarding recruitment services and has been approved by Human Resources to work on an open position . KBI Biopharma will not pay any fee or remuneration with respect to candidates without complying with this requirement.

Staff Scientist page is loaded **Staff Scientist** **Staff Scientist** locations USA-NC-Wilmington-Market St. time type Full time posted on Posted 24 Days Ago job requisition id R6024 **ABOUT YOU** We have over 90 offices across the United States, Canada, Europe and Australia and are approaching 3500 employees - all ready to provide solutions for environmental needs. The Environmental Engineering and Consulting team delivers solutions for complex environmental challenges using our regulatory expertise and implementing practical and cost-effective compliance management processes and programs. We address our clients' biggest concerns around permitting, ecoservices, assessment, and remediation. Our highly trained and experienced engineers and scientists, environmental and remediation specialists, geologists, hydrogeologists, biologists, and environmental compliance specialists work with both public- and private-sector clients, delivering turnkey solutions. **A DAY IN THE LIFE** Our **Staff Scientist** position is located in **Wilmington, NC**. As a key member of the MES team, this role will be responsible for a full range of activities including: * Provide assistance on a variety of environmental compliance projects including but not limited to: Emergency Planning and Community Right-to-Know Act Reports; Solid Waste and Hazardous Waste Management Plans; Spill Prevention, Control, and Countermeasure Plans; Stormwater Pollution Prevention Plans; Hazardous Waste Stream Determinations. * Prepare environmental compliance documents, permits, plans, and procedures * Work effectively, both independently and in a team setting * Conduct field work at client sites to collect data * Lead data collection efforts and research projects as requested by the project managers * Knowledgeable of regulatory standards in an environmental technical area * Maintain confidentiality at all times * Exercise safe work practices by following all Company safety rules and OSHA regulations, including attendance at all required safety training programs * Participate in the company's continuous improvement programs and provide support to team efforts * Keep up-to-date and current on industry trends by completing formal training, reviewing professional publications, and attending professional workshops * Perform other duties as assigned **YOUR EXPERTISE AND SKILLS** To perform this job successfully, individuals must be able to perform each duty and responsibility satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. * Bachelor's Degree in Environmental Science, Biology, Chemistry, Geology, Engineering or Environmental Studies * 2+ years of related experience, including internships and/or related scientific/field of study experience * Prior consulting experience is a plus * Basic understanding of EPCRA, CAA, CWA, OSHA, RCRA, TSCA, NPDES, and DOT preferred * Organizational skills and attention to detail * Strong written and verbal communication skills * Strong time management skills with the ability to work well under pressure with multiple deadlines * Ability to define problems, collect data, establish facts, and draw valid conclusions to present to supervisors * Knowledge of computer aided software (Microsoft Suite, Google Suite, AutoCAD, ArcGIS etc.) * OSHA 40-hour HAZWOPER preferred * Team player with strong problem-solving skills and the ability to manage multiple tasks and priorities * Ability to work well in a team-driven environment * Ability to establish and maintain effective working relationships with employees and leaders. * Ability to travel ( **WHAT WE CAN OFFER TO YOU** As a key member of our Montrose team, you can expect: * Mentorship and professional development resources to advance your career * Direct exposure to our industry's leading experts who are solving the world's toughest environmental challenges * An entrepreneurial environment where you can learn, thrive and collaborate with talented colleagues * Opportunities to engage and contribute to our Diversity, Fairness and Inclusion and Women Empowering Leadership employee resource groups * Competitive compensation package: annual salary ranging from $60,000 to $65,000, commensurate with accomplishments, performance, credentials and geography * Competitive medical, dental, and vision insurance coverage * 401k with a competitive 4% employer match * Progressive vacation policies, company holidays and paid parental leave benefits to ensure work/life balance * A financial assistance program that supports peers in need, known as the Montrose Foundation * Access to attractive student loan rates to optimize your student loan payoff plans The above statements are intended to describe the general nature of work being performed by people assigned to this classification. They are not to be construed as an exhaustive list of all responsibilities, duties and skills required of employees so classified. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact ************ or ************************ for assistance. **MAKE THE MOVE TO ACCELERATE YOUR CAREER** We are going to be blunt - the way we work may not suit everyone. We are a fast-paced, dynamic and high-growth company. You are your own boss, but you will get tons of guidance and plenty of support from talented, super-smart colleagues and its service providers. and have fun! Montrose is an Equal Opportunity Employer. Montrose is committed to recruiting and hiring qualified candidates without regard to race, religion, sex, sexual orientation, gender identity, age, national origin, ancestry, citizenship, disability, or veteran status. Montrose is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. #INDMEG **We're blazing new trails.** Forget everything you think you know about how environmental companies work. Montrose Environmental Group was designed from the ground up to deliver a better experience and better outcomes for both our clients and our employees. We're growing rapidly-with a purpose. We're bringing the best minds on board, and giving them the freedom to focus on what matters most: coming up with ingenious, effective ways to measure, assess, and address real-world situations. The kind that face industries of all kinds right now, and the kind that we want to be the first to see on the horizon. When we do that, we add value. We create opportunities for our clients and ourselves. We grow. We learn. We make a real difference in the world around us. **You can help lead the way.** **Montrose is committed to being an inclusive workplace.** Montrose is an Affirmative Action and 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. You can read more about EEO or view the . If you'd like to view a copy of the company's affirmative action plan or policy statement, please email *********************** . If you have a disability and you believe you need a reasonable accommodation in order to search for a job opening or to submit an online application, please e-mail ************************ or call ************. This email and phone number are created exclusively to assist disabled job seekers whose disability prevents them from being able to apply online. Only messages left for this purpose will be returned. Messages left for other purposes, such as following up on an application or technical issues not related to a disability, will not receive a re

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. Organization Overview: At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism. Lilly is designing and building a new state of the art Parenteral, Device Assembly, and Packaging Facility located at the Research Triangle Park (RTP) in North Carolina. This is an exciting opportunity to help build and operate a state-of-the-art manufacturing site and Quality System from the ground up. Responsibilities: The Visual Inspection Scientist/Engineer - Technical Services / Manufacturing Science (TS/MS) role provides technical guidance for visual inspection operations and projects involving existing and new inspection processes. The role is responsible for teaching, mentoring, and coaching peronnel in all aspects relating to visual inspection processes within the Lilly RTP site. This role will span the design and delivery of prefilled syringe visual inspection operations as well as support of routine manufacturing operations. The Visual Inspection Scientist/Engineer will be responsible for the training and qualification program associated with visual inspection, classification of defects and maintenance of defect kits, and maintaining the visual inspection strategy for parenteral operations. This role will also participate in troubleshooting and driving continuous improvement as it relates to the visual inspection program. The role will regularly interact with peers within the parenteral network and in Global TS/MS to share learnings and ensure strategies are in line with technical, quality, and regulatory guidance, while supporting business expectations. A key part of this role is ensuring that there is consistency in approach / processes throughout the product lifecycle, from tech transfer to regulatory submission and beyond to routine manufacturing. Key Objectives / Deliverables: Understand the scientific principles required for manufacturing parenteral drug products, including the interaction of the chemistry, equipment, aseptic processes, and container closure systems. Provide technical oversight regarding defect classification, visual inspection technique, and visual inspection qualification program to support production operations. Perform root cause analysis and apply scientific principles and understanding in response to manufacturing deviations. Provide technical support for all start-up activities (e.g., tech transfer, process validation), including support of equipment qualification and validation. Author, review, approve and provide technical support for the preparation of technical documents, including personnel qualification strategies, control strategies, investigations, change controls, expert opinions, procedures, processing records, protocols and summary reports, defect classifications, technical studies, and regulatory submissions. Provide technical support for non-routine investigations (e.g., deviations, complaints), including consultation on quality. Ensure that an accurate instruction set (tickets & procedures) describes the process as performed and the control strategy for the discrete manufacturing steps. Develop, monitor, and appropriately react to established statistically based metrics in real-time to assess process variability and capability. Apply process knowledge and data analysis skills to support the management of daily manufacturing operations. Support and/or lead TS/MS technical projects to ensure a successful start-up, improve process control, yield, product quality and/or productivity. Implement process changes and improvements through the technical agenda. Serve as technical interface external to the RTP site. Provide audit support, as needed. Work within or lead cross-functional teams in a positive fashion to implement TS/MS objectives and deliver on business plan and quality objectives. Collaborate with and influence partners across the Parenteral Network and teams along a specific product supply chain. Ensure a safe working environment through compliance with safety rules and improve safety culture by actively participating in safety-related activities. Basic Requirements: BS or MS in Chemical Engineering, Biochemical Engineering, Mechanical Engineering, Chemistry, Biochemistry, or other related scientific discipline Minimum 5 years of experience supporting cGMP manufacturing (specifically within Operations, Validation, Engineering, Technical Services/MSAT, Quality Assurance, etc.) Additional Preferences: Strong interpersonal and teamwork skills Strong self-management and organizational skills Oral and written communication skills that demonstrate an ability to effectively communicate with all levels of the organization Experience in TS/MS, MSAT, Quality, Engineering, or Operations, particularly with visual inspection of parenteral drug products Experience with qualification or/and support of automated and semi-automated visual inspection equipment for parenteral operations Technical Transfer experience, including equipment qualification and process validation Experience with data trending and analysis Ability to analyze complex data and solve problems Demonstrated successful leadership of cross-functional teams Previous experience with deviation and change management systems, including Trackwise Additional Information: Role is Monday through Friday based but must be flexible in providing support to accommodate other inputs (production schedules, shutdowns, etc.). Occasional extended hour and / or off-hour work may be required. Position will be based out of RTP site with ability to travel to Indianapolis and other global Lilly sites as required Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women's Network, Working and Living with Disabilities. Learn more about all of our groups. #WeAreLilly

Job Title: Clinical Research Intern Job Contract Type: Full-time Job Seniority Level: Work Schedule Standard (Mon-Fri) Environmental Conditions Office When you're part of the team at Thermo Fisher Scientific, you'll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you'll be supported in achieving your career goals. Our staff members are committed to making a difference in our organization, for our client partners and the patients we serve. We seek individuals with proven competencies and strong character to help lead our organization now and into the future. Our interns receive professional mentorship and leadership development opportunities to support future career growth with us. Whether you're looking to come back as a repeat intern, transition into one of our Leadership Development Programs, or pursue a full-time position post-graduation, our team is here to support your next step! How will you make an impact? Our interns are matched to projects based on their abilities and current business needs. All projects will have significant strategic and/or operating importance to the business to which they are assigned. Summer projects may include the following responsibilities: Use your Clinical/Healthcare care degree skills and knowledge to understand our business and assist teams in real life projects. Gain exposure through networking, events, and shadowing opportunities. Participate in professional development opportunities focused on topics such as: networking, interviewing and resume building, career preparedness, and engaging in continuous coaching and development with the assistance of a team of mentors. Attending and participating in meetings and conference calls. Other ad-hoc tasks under the direction of the assigned supervisor. Start Date: This internship is set to begin in May 2024 for a 13-week duration ending in August 2024. Compensation & Relocation: Our undergraduate Clinical Research internships offer an hourly rate of $18. Additionally, please note that opportunity is designed to be conducted remotely and a relocation stipend is not provided. How will you get here? Undergraduate student completing a Clinical/Healthcare-related degree in one of the following Clinical Research, Biology, Health Care Administration, Pharma Sciences, Public/Global Health, Health Education, Pharma Product Development, Nursing, or related field of study between December 2025 and June 2026. 0 years of work experience required; previous related internships preferred. Consistent track record of results demonstrating integrity, innovation, involvement, and intensity. Energized through championing change, driven in getting results, and savvy in navigating ambiguity. Excellent interpersonal communication skills with a high degree of emotional intelligence. If this sounds like you, we'd love to hear from you! To qualify, applicants must be legally authorized to work in the United States and should not require sponsorship (current or future) for employment visa status. Thermo Fisher does not offer employment in this position to holders of F-1, J-1, H-1, OPT, and CPT Visas for the purpose of obtaining practical experience. Lifelancer ( ********************** ) is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains. For more details and to find similar roles, please check out the below Lifelancer link. **********************/jobs/view/8507d8976d10f0d68b11e848b0f4c00a

Essential Job Duties This position will assist with fieldwork, lab work, and data management for a study on how urbanization and climate change are impacting the Crystal skipper butterfly, a species only found along a 50 km strip of the barrier islands off of North Carolina's coast. Primary fieldwork duties will occur along the barrier islands between Hammocks Beach State Park and Cape Lookout National Seashore. Example field duties include surveying sites for Crystal skipper butterfly presence and abundance; measuring habitat and environmental variables; observing and handling Crystal skippers for demographic experiments and surveys; rearing Crystal skippers from egg to adulthood. Example lab duties include estimating floral nectar production. Example data management duties include data entry. The person in this position may also contribute to outreach and communication activities related to the Crystal skipper. Lodging at the coast is provided from March 17 - August 15, 2025. **Schedule:**Monday - Friday between the hours of 8 and 5 is the baseline schedule. However, flexibility will be required during fieldwork, when the work schedule is dictated by biology of the system under study and the weather. Work may begin as early as 6:30am and may occur on weekends. Working Title Temporary Research Technician Requirements and Preferences Work Schedule 20-40/hrs per week Other Work/Responsibilities * n/a Minimum Experience/Education * Demonstrated possession of the competencies necessary to perform the work. Department Required Skills * Experience in ecological field and lab research * Ability to follow established protocols * Ability to work independently and as part of a team * Ability to work outdoors in high heat and humidity * Experience collecting and accurately entering data * Attention to detail * Punctual * Ability to handle small, live insects Preferred Years Experience, Skills, Training, Education * Associate's or Bachelor's degree and experience in entomology, ecology, or a related field * Experience working with live insects * Experience identifying butterflies and/or caterpillars Required License or Certification * Valid driver's license Yes No AA/EEO NC State University is an equal opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, national origin, religion, sex, gender identity, age, sexual orientation, genetic information, status as an individual with a disability, or status as a protected veteran. Individuals with disabilities requiring disability-related accommodations in the application and interview process are welcome to contact ************ to speak with a representative at the Office of Institutional Equity and Diversity. If you have general questions about the application process, you may contact Human Resources at ************** or **************************. Final candidates are subject to criminal & sex offender background checks. Some vacancies also require credit or motor vehicle checks. Degree(s) must be obtained prior to start date in order to meet qualifications and receive credit. NC State University participates in E-Verify. Federal law requires all employers to verify the identity and employment eligibility of all persons hired to work in the United States. * NCSU Website * Job Alert (automated email from our system) * NCSU Executive Search Services * Monster.com * CareerBuilder.com * InsideHigherEd.com * HigherEdJobs.com * Other Online Job Board * Carolina Job Finder / Employment Guide * Job / Career Fair * The Chronicle of Higher Education * Professional Journal * Print Advertisement (Newspaper / Periodical) * Radio / Television Advertisement * Professional Organization * Higher Education Recruitment Consortium (HERC) * Direct Contact from NCSU HR Representative / Recruiter * NCSU Employee Referral * Social Media (LinkedIn, Twitter, Facebook, Other) * Other * Yes * No * * Yes * No * * Yes * No * * Yes * No * * Yes * No * * Yes * No * * Yes * No - - If you learned about this vacancy from "other source" or "other website", please provide the source. (Open Ended Question) - * * Yes * No - * * Yes * No * Yes * No - * * Yes * No

Company Information You Matter to Cambrex. Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance, drug product, and analytical services across the entire drug lifecycle. With more than 40 years of experience and a growing team of over 2,000 professionals servicing global clients. Cambrex is a trusted partner in branded and generic markets for API and dosage form development and manufacturing. Your Work Matters. At Cambrex, we strive to build a culture where all colleagues have the opportunity to: engage in work that matters to our customers and the patients they serve learn new skills and enjoy new experiences in an engaging and safe environment strengthen connections with coworkers and the community We're committed to attracting and nurturing a passionate team of valued professionals in our fast-paced and growing company. We offer a competitive benefits package that includes healthcare, life insurance, planning for retirement, and more! Your Future Matters. Known for our customer-focused scientific and manufacturing excellence, as well as our strong commitment to quality and safety, we offer a range of career and growth opportunities across our global network of locations. Together with our customers, we aim to improve the quality of life for patients around the world. Start a career where You Matter by applying today! Job Overview Execute analytical methods and provide general analytical support, such as release and stability testing of drug substances and drug products. Able to organize routine work with supervision and to evaluate and interpret generated data. Works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors. Exercises judgment within defined procedures and practices to determine appropriate action. Responsibilities Execute analytical methods for in-process control, release testing and stability monitoring of bulk drug substances and drug products under cGMP guidelines Participates in experimental design, including development of methods and testing requirements to demonstrate method suitability. Maintains compliant records with little or no supervision Able to write technical documents with assistance Strong understanding and proficiency in use and maintenance of instrumentation, equipment, and scientific methodologies necessary to perform assigned tasks Perform assigned tasks carefully, safely and on schedule according to SOPs and supervisor instructions Sets up various instrumentation for testing according to written test methods and with little to no supervision. As needed, troubleshoots laboratory instrumentation Leads a sample project with assistance May participate in client level meetings, with approval Responsible for ensuring compliance with cGMP and other regulatory guidelines. Analyze information for technical correctness and accuracy Compile, maintain, interpret and extrapolate data on results of analysis and communicate these results to supervisor Perform routine laboratory procedures in a timely and efficient manner Gain familiarization with analytical techniques Participate cGMP activities Maintain laboratory equipment and supplies as directed May support peer-led laboratory investigations process with assistance Maintain a clean and safe work-space Maintain laboratory notebook and/or computer files (i. e. LIMS) according to standard, accepted practices Participate in group and project meetings as required Enter project hours promptly and update project status on appropriate tracking and/or timekeeping systems Attend seminars as required Participate in and comply with all current safety, health and environmental programs Shows initiative and interest in learning new techniques and tests Participates in technical discussions and brainstorming sessions Communicates issues or challenges to senior staff and/or management May review test data acquired by others and witness others' notebooks Assists with writing technical documentation such as OOS, atypical investigations, deviations and CAPAs Assists with writings standard operating procedures (SOPs), methods, qualification protocols and other standard documents as directed With guidance, prepares well written and organized development reports Performs other related duties as assigned. Qualifications/Skills Working knowledge of experimental design, including chemistry supporting method development Working knowledge of analytical techniques and instrumentation such as NMR, IR, MS and HPLC. Working exposure to cross functional techniques including organic chemistry. Able to comply to SOPs and basic regulatory compliance Working knowledge of scientific concepts, principles and procedures Actively and positively engages with team and supports process improvements Ability to read and execute compendial methodologies Strong understanding of current FDA and cGMP regulations General knowledge of chemistry and scientific calculations Hands on experience in analytical techniques such as HPLC, GC, etc Good computer skills Ability to operate laboratory equipment and computers Ability to take direction from experienced scientists and contributes in a team environment Good problem-solving skills Good attention to details Can repeat and follow detailed scientific procedures with supervision Able to clearly present results verbally in group meetings and in written progress reports Good interpersonal skills and is willing to ask questions about procedures and concepts Aptitude and willingness to gain more skills and knowledge in support of GMP regulations Good written and verbal communication skills Familiarity with computer software such as Empower, ChemDraw, Microsoft Word, PowerPoint, and Excel. Aptitude and willingness to gain more skills & knowledge. Good attention to detail and good problem-solving skills. Education, Experience & Licensing Requirements B. S. /B. A. Chemistry with 4+ years of experience in related industry or MS with 0+ years related experience Supervision Received: Works under limited supervision. Physical Demands, Work Environment, and Travel Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this Job, the employee is regularly required to use hands to finger, handle, or feel; reach with hands and arms; talk or hear and smell. The employee is frequently required to sit. The employee is occasionally required to stand; walk and stoop, The employee must be able to regularly lift and/or move up to 10 pounds, and occasionally lift and/or move up to 25 pounds. Specific vision abilities required. Environment and Protective Equipment The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this Job, the employee is occasionally exposed to moving mechanical parts and vibration. The noise level in the work environment is usually very quiet. Travel: Little to no expected travel time. Cambrex is committed to providing a safe and productive work environment. All offers of employment are contingent on the successful completion of a comprehensive pre-employment screen. The pre-employment screen may consist of several components including but not limited to a drug test, criminal record check, identity verification, reference checks, education and employment verification, and may vary based on federal, state, and local laws. Refusal to submit to testing will result in disqualification of further employment consideration. All requirements are subject to possible modifications to reasonably accommodate individuals with disabilities. Cambrex Corporation is an Equal Opportunity / Affirmative Action employer and will consider all qualified applicants for employment without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), ancestry, national origin, place of birth, age, marital status, disability/handicap, genetic information, veteran status, or other characteristics protected by federal, state, and/or local law. B. S. /B. A. Chemistry with 4+ years of experience in related industry or MS with 0+ years related experience Execute analytical methods for in-process control, release testing and stability monitoring of bulk drug substances and drug products under cGMP guidelines Participates in experimental design, including development of methods and testing requirements to demonstrate method suitability. Maintains compliant records with little or no supervision Able to write technical documents with assistance Strong understanding and proficiency in use and maintenance of instrumentation, equipment, and scientific methodologies necessary to perform assigned tasks Perform assigned tasks carefully, safely and on schedule according to SOPs and supervisor instructions Sets up various instrumentation for testing according to written test methods and with little to no supervision. As needed, troubleshoots laboratory instrumentation Leads a sample project with assistance May participate in client level meetings, with approval Responsible for ensuring compliance with cGMP and other regulatory guidelines. Analyze information for technical correctness and accuracy Compile, maintain, interpret and extrapolate data on results of analysis and communicate these results to supervisor Perform routine laboratory procedures in a timely and efficient manner Gain familiarization with analytical techniques Participate cGMP activities Maintain laboratory equipment and supplies as directed May support peer-led laboratory investigations process with assistance Maintain a clean and safe work-space Maintain laboratory notebook and/or computer files (i. e. LIMS) according to standard, accepted practices Participate in group and project meetings as required Enter project hours promptly and update project status on appropriate tracking and/or timekeeping systems Attend seminars as required Participate in and comply with all current safety, health and environmental programs Shows initiative and interest in learning new techniques and tests Participates in technical discussions and brainstorming sessions Communicates issues or challenges to senior staff and/or management May review test data acquired by others and witness others' notebooks Assists with writing technical documentation such as OOS, atypical investigations, deviations and CAPAs Assists with writings standard operating procedures (SOPs), methods, qualification protocols and other standard documents as directed With guidance, prepares well written and organized development reports Performs other related duties as assigned.

Piper Health & Sciences is seeking a motivated Research Associate (Cellular Production) to join a groundbreaking biopharmaceutical organization in the Durham, NC area. This is a unique opportunity to support the research & development of life-saving treatments for rare diseases. Responsibilities for the Research Associate include:·Performs routine laboratory testing on the bench and data analysis. ·Routinely and independently pipette samples accurately and efficiently. ·Utilize aseptic/sterile laboratory techniques, especially when working with primary cells. ·In-depth understanding and analysis of rt-PCR assays, data, and results. ·Assist with loading samples and running flow cytometry testing, utilizing flow software to conduct data analysis/interpretation. ·Follow all laboratory guidelines and SOPs (GLP, GXP, etc. ) Qualifications for the Research Associate include:·2+ years of scientific experience within a regulated industry or academic laboratory setting. ·Prior experience using pipettes and performing cell culture techniques is required. ·Prior experience with flow cytometry and/or rt-PCR is strongly preferred. ·Bachelor's degree in Biology, Biochemistry, Bioengineering, or similar scientific field is required. Compensation for the Research Associate includes:·Salary range: approximately $22. 00 - $28. 00 hourly, commensurate with experience·Comprehensive Benefits: Cigna Medical, Dental, Vision, ADP 401k, STD, LTD, Sick leave as required by law This job opens for applications on 1/10/2025. Applications will be accepted at least 30 days from the posting date. Research associate, r&d, research and development, life sciences, biotechnology, pharmaceutical, biopharma, tissue, lung, cell, primary cell, cell culture, pcr, rt-pcr, flow cytometry, flow cytometer, cell production, ipsc, aseptic, glp, gdp, gxp, pipette, micro pipette, pipetting, data analysis, flowjo, facs, diva, cell sorting, cell counting#LI-CP1 #LI-ONSITE

Durham, NC The Bioinformatics Scientist I will work closely with Genomics team members to improve and polish current in-house software and translate scripts into software for general scientific consumption. The individual will also leverage current literature to propose and implement new data analysis pipelines that complement and advance the current system of genomic analysis as well as run current analysis pipelines as needed. Responsibilities Leverage advanced computational approaches and collaborate with Genomics team members to create advanced assays for genome editing outcomes Analyze experimental data produced by next-generation sequencing (NGS) including indel and structural variant data Maintain current and develop new computational and bioinformatic tools Develop visualization tools for large scale genomic projects Work with the team to develop software to enable end-user use of custom bioinformatics tools Communicate cross-functionally and present data to internal teams Adhere to best practices in pipeline development and data integrity Perform additional duties and responsibilities, as assigned Qualifications Required : PhD in Computational Biology, Bioinformatics or related field or Master's degree and 2+ years of experience in Computational Biology, Bioinformatics or related fields, or equivalent combination of training and experience Proficiency using R and/or Python for data analysis Proficient in NGS data processing in a Linux computing environment Strong foundation in genomics concepts Familiarity with publicly available bioinformatics databases, tools, algorithms, and websites, such as NCBI, UCSC, ENSEMBL, ENCODE, 1000 Genomes or NHGRI Experience using visualization tools (ggplot2, seaborne, etc.) Basic understanding of statistics and algorithms associated with genomics analysis Experience working independently and within a team depending on project needs Strong communications skills Preferred : 1+ years of experience performing relevant tasks in Industry setting Software development experience - bioinformatics centric software to enable end-user interaction with industry standard and customized bioinformatics toolsets Versioning software (git, etc.) Experience using Nextflow Experience using Rmarkdown or Jupyter notebooks R Shiny app development experience Experience with RNAseq or sc RNAseq analysis

Job Title Associate Research Scientist Education Master's Degree Location Durham, NC - NC US (Primary) PIRE is an independent, nonprofit organization merging scientific knowledge and proven practice to create solutions that improve the health, safety and well-being of individuals, communities, and nations around the world. We have excellent health coverage, retirement opportunities and flexible work arrangements available to support our nationally recognized institution of independent scientists and research staff. PIRE is looking for an outgoing, personable, independent and highly organized individual who will help coordinate the implementation of research and evaluation activities for **TakeCare**, a national initiative, rooted in science, that invites people to take care of their Whole Health: Mind, Body, Spirit, and Community. **TakeCare** programming is currently being pilot tested in Durham County, NC with statewide rollout planned in 2025. The ideal candidate will be intellectually curious and passionate about making a difference in the world through public health research. Ideal candidates will also have experience conducting research and publishing in Whole Health / Integrative Health areas. Applicants must be able to synthesize large amounts of information coherently, as well as have excellent verbal/written communication, organization, and presentation skills. They will also be expected to co-author papers in peer-reviewed journals, participate in professional meetings, develop procedures and methods to advance project activities, and assist with grant writing. We are particularly seeking applicants that have extensive experience and excel in quantitative and qualitative data collection, data management and data analysis, as well as REDCap and Alchemer Programming. Applicants are required to submit a cover letter, resume/CV, and writing sample for consideration. There is no relocation assistance for this position. **SaLARY and Benefits Overview:** * 3.5-7 weeks of accrued PTO during the first year * Company provided Retirement Plan * Company provided Life and Accidental Death and Dismemberment plans * Company provided Short- and Long-Term Disability plans * Company supported Medical, Dental and Vision coverage The salary for this position is commiserate with experience and ranges between $86,580 - $96,600. Job Requirements **JOB EXPECTATIONS:** * Ability to manage multiple priorities/tasks simultaneously to ensure on time project deliverables of excellent quality. * Work closely with the Project Leadership Team, to develop and oversee the execution of research protocols and project activities. * Coordination of internal and external project communications and meetings, including scheduling meetings, development of meeting agendas, detailed-notetaking, and further follow up as necessary, as well as drafting progress reports and monitoring achievement of project milestones. * Analyze data, and assist in the preparation of text, statistical tables and graphics for project reports and related presentations. * Prepare scientific reports and manuscripts along with community facing reports and presentations. * Provide technical assistance/support for data collection and data management as well as quality assurance / quality control activities. * Assist with qualitative and quantitative data collection and monitoring from community events, community facilitators, and group program participants * Maintain project files on shared drives, SharePoint and MS Teams **QUALIFIED APPLICANTS MUST HAVE:** * Master's Degree required; Doctorate preferred. A minimum of three years highly relevant professional experience is highly desired * Excellent communication skills - phone skills, writing skills; clear and consistent communication * Excellent organizational skills * Ability to meet frequent, multiple and tight project deadlines and deliverables * Proficiency in Microsoft Office programs including Word, Excel, & PowerPoint * Proficiency in REDcap and SPSS * Experience with IRB applications * Experience with instrument and protocol development including the creation of online instruments through software such as Survey Monkey, Qualtrics, Alchemer, and REDCap * Previous experience providing supervision of research tasks, interviewers or field staff during the data collection process is highly desirable. * Their own transportation and valid driver's license and access to licensed, insured, and reliable personal transportation for required travel within Durham. Travel is estimated to be 5-10% of working time. **PREFERENCE** **GIVEN TO APPLICANTS WITH:** * Experience living in and/or working in Durham County, NC * Demonstrated proficiency with REDCap * Demonstrated ability/experience to work independently and implement several simultaneous project activities with minimal supervision Some Primary Duties and Responsibilities * PIRE is a diverse community devoted to the promotion and acceptance of all people regardless of race, color, national origin, religion, sexual orientation, gender identity, age, gender or physical ability or veteran status. PIRE is committed to employ, and advance in employment, individuals with disabilities and protected veterans, and to treat qualified individuals without discrimination on the basis of their physical or mental disability or veteran status. PIRE will provide reasonable accommodations with the application process upon your request as required to comply with applicable laws. If you have a disability and require assistance in this application process, please contact Human Resources by email at ***********