QC laboratory Analyst at Pride Global
Vacaville, CA 95688, USA -
Full Time


Start Date

Immediate

Expiry Date

04 Dec, 25

Salary

32.03

Posted On

04 Sep, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Communication Skills, Laboratory Techniques, Computerized Systems, Physical Sciences

Industry

Hospital/Health Care

Description

The Science Team at Russell Tobin & Associates supporting the Biologics Industry that has an opening for QC Analyst in Vacaville, CA!

POSITION SUMMARY:

We are seeking a motivated and detail-oriented QC Analyst / Laboratory Associate to support GMP laboratory operations. This role will focus on sampling of utility systems and manufacturing process spaces, along with performing a broad range of chemical and microbiological analyses. The position also contributes to continuous improvement efforts to ensure compliance, maintain operational efficiency, and support supply to patients.

Qualifications:

  • BS/BA in Biological Sciences, Physical Sciences, Engineering, or related field preferred.
  • Experience in GMP-regulated laboratory or equivalent environment.
  • Strong knowledge of scientific theories, assay principles, and laboratory techniques.
  • Excellent verbal and written communication skills; ability to present information clearly.
  • Organized, detail-oriented, and able to manage short-term priorities under moderate supervision.
  • Familiarity with computerized systems, Microsoft Office Suite, and cGMP guidelines a plus
Responsibilities
  • Perform routine and non-routine testing of samples with complete and accurate GMP documentation.
  • Conduct sampling of utilities and manufacturing environments.
  • Prepare reagents, including both basic and complex formulations.
  • Troubleshoot and support resolution of technical issues.
  • Mentor colleagues on assays and laboratory functions.
  • Maintain laboratory operations, including supply inventory and routine equipment upkeep.
  • Coordinate with internal stakeholders to support testing and operational activities.
  • Contribute to group projects, process improvements, and continuous improvement initiatives.Ensure testing and assignments meet scheduled deadlines with
  • 95% on-time performance.
  • Support Quality by completing tasks assigned by leadership.
  • Follow all GMP rules and maintain accurate records.

Qualifications:

  • BS/BA in Biological Sciences, Physical Sciences, Engineering, or related field preferred.
  • Experience in GMP-regulated laboratory or equivalent environment.
  • Strong knowledge of scientific theories, assay principles, and laboratory techniques.
  • Excellent verbal and written communication skills; ability to present information clearly.
  • Organized, detail-oriented, and able to manage short-term priorities under moderate supervision.
  • Familiarity with computerized systems, Microsoft Office Suite, and cGMP guidelines a plus.

Must be authorized to work in the United States.
Russell Tobin offers eligible employee’s comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance and hospital indemnity), a 401(k)-retirement savings, life & disability insurance, an employee assistance program, identity theft protection, legal support, auto and home insurance, pet insurance, and employee discounts with some preferred vendors.

Loading...