QC Compliance Specialist

Location: Vacaville, California (On-site)

Join our Quality Control Deviation Management Team in Vacaville and play a critical role in ensuring compliance with global and local standards. As a QC Compliance Specialist, you’ll lead deviation investigations, analyze and manage performance metrics and support continuous improvement initiatives that safeguard product quality and patient safety.

What you will get

The full-time base annual salary for this position is expected to range between $88,000 – $140,000. In addition, below you will find a comprehensive summary of the benefits package we offer:

• Performance-related bonus

• Medical, dental and vision insurance

• 401(k) matching plan

• Life insurance, as well as short-term and long-term disability insurance

• Employee assistance programs

• Paid Time Off

Compensation for this role will be determined by the candidate’s qualifications, skills, experience, and relevant knowledge.

What you will do

• Lead and manage Quality Control deviation investigations, ensuring timely completion and compliance with cGMP standards.

• Perform root cause analysis and recurring deviation assessments to identify and mitigate risks.

• Work closely with QC and other teams to ensure compliance.

• Contribute to process improvement initiatives and departmental performance metrics.

• Support internal and external audits and regulatory inspections.

• Mentor and train QC personnel on compliance best practices.

What we are looking for

• Bachelor’s degree in a scientific discipline or equivalent experience in a pharmaceutical or biopharmaceutical industry.

• Strong knowledge of cGMP regulations and quality systems.

• Experience managing deviations and change control processes.

• Excellent communication skills and ability to work cross-functionally.

• Familiarity with computer-based systems and Quality Management tools (e.g., VEEVA).

• Ability to lead investigations and make sound decisions under pressure.