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Qc Stability Jobs in California (NOW HIRING)

Unicon Pharma Inc.

QC Analyst I - Vacaville, CA

Vacaville, CA · On-site

$27.25 - $36.50/hr

Title: QC Stability Study Coordinator I Summary * With limited supervision, QC Stability Study Coordinator, is responsible for the oversight of stability program management in accordance with cGMP ...

Avid Bioservices

Specialist, Quality Control

Tustin, CA · On-site

$32.30 - $40.38/hr

Your Role: The Quality Control Specialist is an individual contributor who works within the QC ... Prepare/aliquot R&D stability samples * Assist in Reference Standard Generation activities

TekWissen LLC

QC Analyst I

Vacaville, CA · On-site

$20 - $25/hr

Onsite Summary The QC Stability Study Coordinator I is responsible for overseeing stability program management in compliance with cGMP regulations, with limited supervision. This role includes ...

Vaxcyte

Stability Manager

San Carlos, CA · On-site

$147K - $171K/yr

This individual will collaborate with QC members in a highly collaborative and cross-functional environment. The ideal candidate will apply strong stability experience, ensure compliant operations ...

Vaxcyte

Stability Manager

San Carlos, CA · On-site

$134K - $162K/yr

This individual will collaborate with QC members in a highly collaborative and cross-functional environment. The ideal candidate will apply strong stability experience, ensure compliant operations ...

NCSL International

QC DIRECTOR

Rocklin, CA · On-site

$180 - $240/hr

Manage reference standards, retention sample library and full stability study programs, ensure ... Serve primary QC liaison for global CDMO clients, address analytical requests, technical ...

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Qc Stability information

What are the typical day-to-day responsibilities of a QC Stability professional?

A QC Stability professional is responsible for managing stability studies on pharmaceutical products, which includes preparing stability samples, testing products at specified intervals, analyzing and documenting results, and ensuring data integrity. This role often involves working closely with cross-functional teams such as quality assurance, production, and research and development to address any findings or deviations. You can expect to spend time in the laboratory conducting tests, as well as at your desk compiling reports and supporting regulatory submissions. The position requires meticulous organization and the ability to handle multiple studies simultaneously, making time management a valuable asset.

What are the key skills and qualifications needed to thrive in the QC Stability position, and why are they important?

To thrive as a QC Stability professional, you need a solid background in chemistry, analytical testing, and good documentation practices, typically supported by a degree in life sciences or related field. Familiarity with laboratory information management systems (LIMS), chromatography software (such as HPLC or GC), and regulatory guidelines like GMP and ICH is essential. Strong attention to detail, problem-solving abilities, and effective communication skills are key soft skills in this role. These competencies ensure accurate data analysis, regulatory compliance, and efficient teamwork in maintaining product quality over time.

What is a QC Stability?

A QC Stability job focuses on monitoring and evaluating the stability of pharmaceutical products over time to ensure they maintain their quality, safety, and efficacy. Responsibilities typically include designing stability studies, analyzing samples at different time points, and documenting results in compliance with regulatory guidelines (e.g., ICH, FDA). QC Stability professionals work closely with quality control and regulatory teams to ensure data integrity and provide critical information for product shelf-life determination.

What are popular job titles related to Qc Stability jobs in California? For Qc Stability jobs in California, the most frequently searched job titles are:
What job categories do people searching Qc Stability jobs in California look for? The top searched job categories for Qc Stability jobs in California are:
What cities in California are hiring for Qc Stability jobs? Cities in California with the most Qc Stability job openings:
Qc Stability jobs near you
Infographic showing various Qc Stability job openings in California as of August 2026, with employment types broken down into 85% Full Time, 13% Contract, and 2% Nights. Highlights an 100% In-person job distribution.

QC Analyst I - Vacaville, CA

Unicon Pharma Inc.

Vacaville, CA • On-site

$27.25 - $36.50/hr

Contractor

Re-posted 6 days ago

Job description

Description:

  • Title: QC Stability Study Coordinator I

Summary

  • With limited supervision, QC Stability Study Coordinator, is responsible for the oversight of stability program management in accordance with cGMP regulations.
  • These duties include execution of trend analysis, documentation review, support of deviations (OOS, OOT, OOE) and other laboratory support activities. In conjunction with Quality Control leadership, the QC Stability Study Coordinator works to meet departmental and organizational goals.

Job Responsibilities

  • Review data and assess against established acceptance criteria
  • Perform technical review of peer-generated data
  • Evaluate data to identify trends and/or establish limits
  • Identify discrepancies; provide input to design of quality investigations and CAPA (corrective actions preventive actions) initiatives as needed
  • Identify and troubleshoot technical problems
  • Identify gaps in systems and procedures
  • Receive training
  • Support the maintenance and compliance of operational areas
  • Assure and apply GMP throughout operations
  • Coordinate with customers to support multi-site operational activities
  • Support internal and external audits and regulatory inspections
  • Works to meet schedules, timelines, deadlines
  • Participate in and/or lead group and project teamwork; project and process improvements
  • Stability Protocol Creation
    Stability deviation assessments
  • Routine Master Data Testing Creation
  • Routine Master Data Testing Review
  • Routine and non-routine Out Of Trend linear regression assessments.
  • Annual Product Quality Reviews (APQRs) - Author assistance develop to authoring
  • Time Point Approval assistance
    Change control of various documents
  • Data / Data Table requests / annual report requests (non-routine requests) (e.g.,
    Client monitor requests)
  • Actively participate in various stability related projects
  • Data entry and review
  • Assist with training coordination
  • Assist with Perform other duties as requested by managers to support Quality activities

Job Requirements

  • B.S. /B.A. degree and 1-3 years of experience or an equivalent combination of education and experience. Degrees are preferably in relevant scientific disciplines and experience is in the pharmaceutical or biopharmaceutical industry.
    Strong verbal and written communication skills, ability to organize and present information both formally and informally.
  • Demonstrated ability to apply knowledge of scientific theories, principles, and techniques used in analytical or biological test procedures.
  • Routinely exercises sound judgment, reasoning and problem solving.
  • Capable of working under limited supervision and determining own short term priorities.