About the Company
Genentech, a member of the Roche Group, is a leading biotechnology company that discovers, develops, manufactures, and commercializes medicines to treat patients with serious and life-threatening medical conditions. We are pioneers in biotechnology and are committed to pursuing groundbreaking science to develop innovative medicines for people with unmet medical needs. Our culture fosters innovation, collaboration, and a deep commitment to making a difference in patients’ lives.
Job Description
We are seeking a highly motivated and detail-oriented QC Chemist to join our Quality Control team. The successful candidate will be responsible for performing analytical testing of raw materials, in-process samples, and finished pharmaceutical products according to cGMP guidelines and established procedures. This role is critical in ensuring the quality, safety, and efficacy of our pharmaceutical products. You will utilize a variety of analytical techniques and contribute to maintaining our high-quality standards.
Key Responsibilities
- Perform routine and non-routine analytical testing on raw materials, in-process samples, and finished products using techniques such as HPLC, GC, UV/Vis, FTIR, Karl Fischer, and dissolution testing.
- Document all analytical data and results accurately and in compliance with cGMP regulations and internal SOPs.
- Calibrate, maintain, and troubleshoot laboratory equipment and instrumentation.
- Review and interpret analytical data, identifying and investigating out-of-specification (OOS) results or deviations.
- Participate in method transfer, validation, and qualification activities as required.
- Contribute to the development and revision of QC Standard Operating Procedures (SOPs) and test methods.
- Collaborate with manufacturing, R&D, and Quality Assurance teams to resolve quality-related issues.
- Adhere to all safety regulations and maintain a clean and organized laboratory environment.
Required Skills
- Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific field.
- 2-4 years of experience in a Quality Control laboratory within the pharmaceutical or biotechnology industry.
- Proficiency in common analytical techniques, including HPLC, GC, and spectroscopy.
- Strong understanding of cGMP regulations, USP methodologies, and quality systems.
- Excellent written and verbal communication skills.
- Ability to work independently and as part of a team in a fast-paced environment.
- Strong problem-solving and critical thinking abilities.
Preferred Qualifications
- Master's degree in a scientific discipline.
- Experience with LIMS (Laboratory Information Management System) and other electronic data management systems.
- Familiarity with method development and validation principles.
- Experience in deviation investigations and CAPA implementation.
Perks & Benefits
- Comprehensive Medical, Dental, and Vision insurance plans.
- Robust 401(k) retirement plan with company match.
- Generous Paid Time Off (PTO) and paid holidays.
- On-site fitness centers and wellness programs.
- Employee stock purchase plan.
- Tuition reimbursement and professional development opportunities.
- Exclusive pharmaceutical benefits program for employees and dependents.
- Life and disability insurance.
How to Apply
If you are interested in this position, please click the "Apply Now" button below. To ensure your application is properly considered, please prepare the following:
- An up-to-date Resume or CV
- A brief cover letter summarizing your experience and motivation
Applications are reviewed on a rolling basis. Only shortlisted candidates will be contacted for an interview.
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