Freshers Quality Control Jobs in Biopharma | Life Science Graduates Apply
Looking for Quality Control jobs in biopharma? Miltenyi Biotec is hiring a QC Analyst I โ Swing Shift in San Jose, CA. This exciting full-time role offers hands-on experience in GMP testing, assay development, and client-focused QC projects while building a rewarding career in one of the most innovative biotech environments. Ideal for candidates exploring life science jobs, this position combines technical expertise with real-world impact in cell and gene therapy.
- Job Position: QC Analyst I โ Swing Shift
- Job Category: Manufacturing
- Requisition Number: QCANA003385
- Location: San Jose, CA 95134, USA
- Pay Range: $31.58 โ $37.11/hour, based on qualifications and experience.
About the Company:
Miltenyi Biotec, Inc. is a global leader in biomedical research and biopharma manufacturing. Through its Miltenyi Bioindustry (CDMO) division, the company provides end-to-end solutions for the development and manufacturing of cell and gene therapy products, including lentiviral vectors. With complete control over the supply chain, Miltenyi ensures innovation, quality, and reliability โ making it an employer of choice for professionals seeking life science jobs that have a global impact.
Qualifications:
Bachelorโs degree in Life Sciences or related field.
- 0โ2 years of laboratory or cGMP/cGTP experience.
- Hands-on experience with flow cytometry, qPCR, ELISA, and cell-based assays.
- Familiarity with deviations, CAPA, and GxP quality systems.
- Proficiency with MS Office tools.
- Availability to work Swing Shift: SundayโThursday, 1:00 PM โ 9:30 PM.
Job Description:
This role is ideal for graduates seeking Freshers Quality Control jobs in biopharma. As a QC Analyst I, you will gain valuable experience in life science jobs while performing day-to-day Quality Control operations. From assay development to GMP release testing, this position offers an excellent opportunity to develop core lab skills and advance in the biopharma industry.
Key Responsibilities:
- Perform flow cytometry, qPCR, ELISA, and other QC assays.
- Support GMP release testing and method development.
- Collaborate with Quality, Manufacturing, and client teams.
- Maintain lab inventory and QC materials.
- Participate in continuous improvement and compliance activities.
- Assist in equipment qualification and troubleshooting.
Benefits: Health, vision, dental insurance, 401(k) plan, and eligibility for bonuses.
