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Director Quality Control Biotech Pharmaceutical Jobs

... pharmaceutical products. Good things are happening at Omeros ... Who is Omeros? Omeros is an innovative biotechnology company that discovers, develops, and ...

POSITION SUMMARY The Director, Quality Control provides strategic and operational leadership for ... Minimum 12 years of experience in pharmaceutical or biotechnology QC, with. 8 years in leadership ...

POSITION SUMMARY The Director, Quality Control provides strategic and operational leadership for ... Minimum 12 years of experience in pharmaceutical or biotechnology QC, with. 8 years in leadership ...

Summary The Director, QC & Microbiology provides strategic and operational leadership for the site ... Typically 12 or more years of progressive pharmaceutical, biotechnology, or CDMO laboratory ...

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Director Quality Control Biotech Pharmaceutical information

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$31K

$125.6K

$213.5K

How much do director quality control biotech pharmaceutical jobs pay per year?

As of Sep 12, 2026, the average yearly pay for director quality control biotech pharmaceutical in the United States is $125,600.00, according to ZipRecruiter salary data. Most workers in this role earn between $91,000.00 and $151,000.00 per year, depending on experience, location, and employer.

What does a director of quality control do in biotech pharmaceutical?

A Director of Quality Control in the biotech and pharmaceutical industry oversees all quality control activities to ensure products meet regulatory standards and company specifications. They manage teams responsible for testing raw materials, in-process samples, and finished products for safety, efficacy, and compliance. This role involves developing and implementing quality control policies, collaborating with other departments, and staying up to date with industry regulations. Directors also handle audits, resolve quality issues, and drive continuous improvement initiatives within the organization.

What are the key skills and qualifications needed to thrive as a director of quality control in biotech pharmaceutical?

To thrive as a Director of Quality Control in Biotech or Pharmaceutical industries, you need extensive knowledge of quality assurance principles, regulatory compliance (such as FDA, EMA, or ICH guidelines), and a relevant science degree, often complemented by advanced degrees or industry certifications. Familiarity with laboratory information management systems (LIMS), quality management systems (QMS), and analytical instrumentation is typically required. Leadership, strategic thinking, and strong interpersonal skills are crucial for managing cross-functional teams and driving a culture of quality. These skills and qualities are vital to ensure product safety, regulatory compliance, and organizational reputation in a highly regulated environment.

What are the primary challenges faced by a director of quality control in biotech pharmaceutical, and how can they be addressed?

A Director of Quality Control in biotech pharmaceuticals often faces challenges such as keeping up with rapidly evolving regulatory requirements, managing complex testing protocols for biologics, and leading cross-functional teams to ensure product quality. Addressing these challenges requires staying informed about global compliance standards, fostering strong communication between QC, R&D, and manufacturing teams, and implementing robust quality management systems. Effective leadership and proactive risk management are also essential to ensure timely product release and maintain high-quality standards.

What are popular job titles related to Director Quality Control Biotech Pharmaceutical jobs?

For Director Quality Control Biotech Pharmaceutical jobs, the most frequently searched job titles are:

Infographic showing various Director Quality Control Biotech Pharmaceutical job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $125,600 per year, or $60.4 per hour.

QA Specialist (Biotech / Pharmaceutical manufacturing)

Oceanside, CA • On-site

Dawar Consulting
IT Services • 11 - 50 employees

$45/hr

Other

Medical, Dental, Vision, Retirement

Posted 11 days ago


Job description

QA Specialist (Biotech / Pharmaceutical manufacturing)

Oceanside, United States | Posted on 06/09/2026

Our client, a world leader in biotechnology and life sciences, is seeking a "QA Specialist (Biotech / Pharmaceutical manufacturing)".

Location: Oceanside, CA

Duration: Long-Term Contract (Possibility Of Further Extension)

Pay Rate: $45/hr on W2

Company Benefits: Medical, Dental, Vision, Paid Sick Leave, 401K

Job Summary:

This role provides on‑the‑floor QA oversight, batch record review, QC support, and ensures compliance with regulatory and site quality standards.

Key Responsibilities
  • Review batch records, perform line clearance, and provide floor QA support
  • QA oversight of QC activities (method transfer, COAs, stability)
  • Approve shipments and support packaging operations
  • Manage deviations, CAPAs, change controls, investigations, and hold events
  • Support regulatory inspections and GMP compliance
  • Perform walkthroughs, document control tasks, and update procedures/forms
Preferred Skills
  • QA
  • Batch Records
  • QC
  • GMP Manufacturing
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