Scientist - Quality Control Analytics (Sunday to Thursday)
Job Description
Celltrion is a leading biopharmaceutical company that specializes in research, development and manufacturing of innovative therapeutics. We are committed to delivering innovative and affordable medications to promote patients’ access to advanced therapies. We have been at the forefront of biotherapeutic development uncovering new ways of targeting the drivers of disease by creating next-generation biologics and small molecule products.Celltrion Branchburg, LLC is a subsidiary of Celltrion USA, established in 2025 following Celltrion USA’s acquisition of Eli Lilly’s drug substance (DS) manufacturing facility located in Branchburg. By linking robust local manufacturing capabilities with an existing direct sales network, we aim to generate greater synergies across our operations. Looking ahead, we also anticipate expanding into the global contract manufacturing organization (CMO) sector.
Position Brand Description:
This position will conduct routine and non-routine analyses of in-process materials, raw materials, environmental/water samples, finished goods and stability samples by appropriate biochemical methods as assigned by supervisor. Perform routine QC responsibilities as needed. This role will apply acceptable cGMP practices during execution of all work tasks. Work independently with moderate supervisory guidance.
Key Objectives/Deliverables:
Manage for Results /Strategic Planning:
- Perform routine QC responsibilities as assigned by supervisor such as (as applicable):
- Conduct routine and non-routine analyses of test articles as assigned by supervisor by appropriate biochemical methods.
- Demonstrate initiative to perform routine QC responsibilities such as sample coordination, lab equipment maintenance, QC document management, QC inventory control and reconciliation of sample requests/documents as needed.
- Monitor laboratory equipment for temperature and conformance to specifications.
- Apply acceptable cGMP practices during execution of all work tasks.
- Work independently with minimal supervisory guidance. Exhibit strong teamwork skills.
- Update supervisor of progress at scheduled intervals. Seek additional guidance as needed.
- Use scientific expertise to provide assistance for troubleshooting, laboratory investigations and problem resolution. Suggest process improvements to QC management.
- Perform assay data review.
- Perform independent assignments such as:
- Compile data and prepare graphs for documentation of test procedures and preparation of reports.
- Conduct document reviews, author standard operating procedures (SOPs), and assay review.
- Lead special projects such as method validation, troubleshooting, optimization, and investigations.
Education Requirements:
1. A.S with 2+ years industry experience in a related science such as Biology, Biochemistry or other science discipline
2. B.S or M.S with 0 + years industry experience in a related science such as Biology, Biochemistry or other science discipline.
Basic Requirements:
- Good working knowledge of cGMP regulations is required.
- Ability to work independently with moderate supervisory guidance.
- Excellent teamwork and communication skills. Attentive to detail. Good computer skills
Additional Preferences:
- MS in a related science such as a Biology or Biochemistry is required
This role is exempt and the anticipated compensation for this role is $71,250 - $116,000.
This is a banded role, and candidates will be placed within the range based on experience, skills, internal equity, and market considerations.
Celltrion Branchburg, LLC offers a comprehensive benefits package that includes paid time off (holidays, vacation, and additional leave), medical, dental, and vision insurance, life insurance, a company-matched retirement savings plan, wellness programs, and short- and long-term disability benefits. Relocation assistance is not provided.
Celltrion Branchburg, LLC is proud to be Equal Opportunity Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity or expression, national origin, protected veteran status, disability, or any other legally protected status.
Sunday to Thursday