English
French
Spanish
Quality Assurance Associate, Batch Record Review
South San Francisco, CA, US
Scientific
Bachelors Degree
Part Time, Temporary
$40-45 per hour
Experienced (Non-Manager)
On-site
Biotechnology/Pharmaceuticals
First Shift (Day)
South San Francisco, CA, US
$40-45 per hour
Experienced (Non-Manager)
Part Time, Temporary
Biotechnology/Pharmaceuticals
On-site
Scientific
Bachelors Degree
First Shift (Day)
Job details
Kelly® Science & Clinical is seeking a Quality Assurance Associate for a 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!
#P1
10180129
I want more jobs like this in my inbox.
Similar Jobs
Why Kelly® Science & Clinical?
Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals—it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.About Kelly
Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life—just ask the 300,000 people we employ each year.Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.