Loading, Please wait..!!
Quality Assurance Associate
-
Posted on: Oct 14, 2026
-
San Diego, Texas
-
Onsite
-
Full-time
Curious about compensation?
Explore the historical salary trends, average pay, and estimated compensation for Quality Assurance Associate roles in Texas.
View Salary Guide →Find your match !
Job Title :
Quality Assurance Associate
Job Type :
Full-Time
Job Location :
San Diego Texas United States
Remote :
No
Job Description :
Job Description
QC Associate I / II (Contract)
\nQuality Control | Biologics | GMP Environment
\nAre you a detail-oriented laboratory professional with experience in biologics testing and GMP-regulated environments? We are seeking a QC Associate I or II to join a growing Quality Control team, supporting analytical testing, method transfers, validation activities, and release testing for biologic products.
\nThis is an excellent opportunity to contribute to the development and manufacture of innovative biologics while working within a highly collaborative, quality-focused environment.
\nThe Opportunity
\nAs a QC Associate I / II, you will perform analytical testing and laboratory activities supporting stability programs, method qualifications, validations, and product release testing. You will play a key role in maintaining compliance with cGMP, GDP, ALCOA+ data integrity principles, and global regulatory standards while ensuring laboratory inspection readiness.
\nWorking closely with Quality Assurance, Analytical Development, Manufacturing, MSAT, and other cross-functional teams, you will help drive quality, compliance, and operational excellence across QC operations.
\nRole overview
\nEmployment type: Contract
\nLength: 6-months with a view to extend or go permanent
\nHours: Full-time
\nWorking model: On-site in San Diego
\nPayment options: W2 or 1099
\nKey Responsibilities
\nAnalytical Testing & Laboratory Operations
\n- \n
- Perform routine and non-routine testing of: \n
- In-process samples \n
- Release samples \n
- Stability samples \n
- Raw materials \n
- Reference standards \n
- Investigational materials \n
- Execute analytical methods for biologics and large molecule products using: \n
- HPLC/UHPLC \n
- CE-SDS \n
- cIEF/icIEF \n
- ELISA \n
- UV-Vis Spectroscopy \n
- Compendial methods \n
- Additional biochemical and physicochemical techniques \n
- Complete testing accurately and within established timelines. \n
- Maintain laboratory notebooks, worksheets, logbooks, and electronic records in accordance with GDP and data integrity requirements. \n
- Support method transfer, method qualification, verification, and validation activities. \n
Data Review & Documentation
\n- \n
- Perform first-person review of analytical data. \n
- Prepare and review: \n
- Certificates of Analysis (CoA) \n
- Stability Summary Sheets (SSS) \n
- Analytical reports \n
- Method qualification reports \n
- Validation reports \n
- Technical documentation \n
- Ensure all documentation remains complete, attributable, contemporaneous, and inspection-ready. \n
Compliance & Continuous Improvement
\n- \n
- Participate in laboratory investigations including: \n
- OOS (Out of Specification) \n
- OOT (Out of Trend) \n
- Invalid result investigations \n
- Support internal audits, client audits, and regulatory inspections. \n
- Assist with equipment maintenance and qualification activities. \n
- Contribute to process improvement initiatives and implementation of new technologies. \n
- Identify and escalate compliance or data integrity concerns. \n
What We're Looking For
\nEducation
\n- \n
- Bachelor's degree in: \n
- Biology \n
- Biochemistry \n
- Chemistry \n
- Biotechnology \n
- Pharmaceutical Sciences \n
- Or a related scientific discipline \n
Experience
\nQC Associate I
\n- \n
- 0-3 years of laboratory experience within biotechnology, pharmaceutical, or related industries. \n
QC Associate II
\n- \n
- 3-6+ years of experience in a GMP-regulated Quality Control laboratory environment. \n
Technical Skills
\nExperience with one or more of the following is highly desirable:
\n- \n
- HPLC/UHPLC \n
- CE-SDS \n
- ELISA \n
- cIEF/icIEF \n
- UV-Vis \n
- Stability testing \n
- GMP documentation \n
- Method transfer and validation \n
- Data integrity and ALCOA+ principles \n
- LIMS systems (preferred) \n
Ideal Candidate
\nYou are:
\n- \n
- Highly organized and detail-oriented \n
- Passionate about quality and compliance \n
- Comfortable working in a fast-paced GMP environment \n
- Experienced in biologics or large-molecule analytical testing \n
- A collaborative team player with strong communication skills \n
- Committed to maintaining inspection readiness and data integrity \n
Physical Requirements
\n- \n
- Ability to stand and walk for extended periods. \n
- Frequently lift and/or move objects up to 20 lbs. \n
- Ability to use hands and arms for laboratory activities. \n
- Ability to bend, kneel, crouch, balance, and reach as required. \n
- Strong visual acuity, including color vision and depth perception. \n
Position Details
Posted:
Oct 14, 2026
Reference Number:
7cdb7b3b0a61a645
Employment:
Full-time
City:
San Diego
Job Origin:
ziprecruiter
Share this job:
Please wait..!!

