Job Description
Kelly® Science & Clinical is seeking a Quality Assurance Associate for an 8-month contract opportunity with a leading biopharmaceutical company in South San Francisco, CA. If you are driven by the prospect of translating cutting-edge scientific discoveries into tangible advancements and are poised to advance your career, join us as we pioneer progress in the biotechnology and medical device industries.
Workplace: Hybrid, onsite in South San Francisco, CA, 3 days/week
Position Title: Quality Assurance Associate
Position Type: 8-month contract
Pay rate: $40-45 per hour
Are you ready to put your quality assurance expertise into action at a cutting-edge biotechnology company? We are seeking a dedicated and detail-oriented Quality Assurance Specialist to join our team on a part-time basis. This role offers the unique opportunity to gain hands-on experience supporting core Quality and Compliance functions within the dynamic biotech sector.
Key Highlights:
- Schedule: 3 days/week (Tuesday–Thursday), on-site, 24 hours/week
- Contract Term: April through December
Key Responsibilities
- Review batch records and handle product complaints.
- Organize and track documents from CDMOs (contract manufacturers) and vendors.
- Create and maintain standardized templates for procedures and forms.
- Support audits by sending templates to auditors, collecting necessary documents, and tracking audit progress and outcomes.
- Track and manage other contracts and agreements, ensuring timely review, approval, and proper filing.
- Provide other support as needed to the Quality, CMC, and Clinical Operations teams.
Qualifications
- 2–5+ years of experience in Quality Assurance within the pharma/biopharma industry
- Knowledge of pharmaceutical GMP (Good Manufacturing Practice) requirements.
- Experience with Executed Batch Record review
- Strong organizational skills and attention to detail.
- Ability to prioritize and multitask in a fast-paced environment.
- Excellent written and verbal communication skills.
Preferred Qualifications
- Experience with MasterControl, SharePoint, Box, and Visio
- Experience supporting small molecule drug development
Additional Information
- This is an on-site position requiring weekly in-office attendance (Tuesday–Thursday) with some flexibility.
Why Join Us?
This is a fantastic opportunity for individuals passionate about quality and compliance in the life sciences field. You’ll work with cross-functional teams, support critical QA operations, and contribute directly to delivering high-impact products to patients.
Apply now and help shape the future of biotechnology quality assurance!