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Pharmaceutical Quality Control Manager Jobs (NOW HIRING)

Antheia

Senior Quality Control Manager

Menlo Park, CA · On-site

$160K - $195K/yr

Antheia is the advanced biosynthesis company transforming pharmaceutical manufacturing and ... We're looking for a Senior QC Manager to own quality control across our GMP and non-GMP ...

Antheia

Senior Quality Control Manager

Menlo Park, CA

$160K - $195K/yr

Advanced degree preferred. * 10+ years of progressive experience in pharmaceutical QC under GMP regulations, with 5+ years in a leadership or managerial role. * Demonstrated experience managing QC ...

Kelly Services

Quality Control Manager

Rosenberg, TX

$95K - $105K/yr

Quality Control Manager Kelly ® Science & Clinical is seeking a Quality Control Manager for a Direct Hire position at a premier pharmaceutical manufacturing company in Rosenberg, TX . If you're ...

Semiserve

Quality Control Manager

Lemoore, CA · On-site

Job: QC Manager Location: Lemoore, CA (93245) Schedule: Monday-Friday Pay: $130,000 - $135,000 Duration: Direct Hire Overview I'm working with a well-established, family-owned national Design-Build ...

ECC

Quality Control Manager

Tamuning, GU

$110K - $135K/yr

Must have been the QC Manager on a vertical construction project of at least $75 million. The Quality Control Manager must manage the Contractor Quality Control program and organization for the ...

Raya Workforce

Quality Control Manager

Fort Belvoir, VA · On-site

Quality Control Manager Location: Fort Belvoir, VA Employment Type: Full-Time | On-site The candidate will be performing all facets of safety and quality control management, submittal tracking, daily ...

PL Developments

Quality Control Manager

Miami, FL

... OTC) pharmaceutical products and consumer healthcare goods SUMMARY: The Quality Control (QC) ... Manage the development, implementation, and continuous improvement of QC goals, objectives ...

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Pharmaceutical Quality Control Manager information

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$30.5K

$81.3K

$129.5K

How much do pharmaceutical quality control manager jobs pay per year?

As of Jun 14, 2026, the average yearly pay for pharmaceutical quality control manager in the United States is $81,324.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,500.00 and $100,000.00 per year, depending on experience, location, and employer.

What does a Pharmaceutical Quality Control Manager do?

A Pharmaceutical Quality Control Manager oversees the testing and quality assurance processes involved in manufacturing pharmaceutical products. They ensure that all products meet regulatory standards and company specifications for safety, efficacy, and quality. This role includes supervising laboratory staff, developing and implementing quality control procedures, and maintaining compliance with government regulations such as Good Manufacturing Practices (GMP). They also analyze data, investigate quality issues, and work closely with other departments to resolve any problems. The ultimate goal is to ensure that patients receive safe and effective medications.

What is the difference between Pharmaceutical Quality Control Manager vs Pharmaceutical Quality Assurance Specialist?

AspectPharmaceutical Quality Control ManagerPharmaceutical Quality Assurance Specialist
CredentialsTypically requires a degree in pharmacy, chemistry, or related field; certifications like CQE or GMP training are commonSimilar credentials; often holds degrees in life sciences and certifications in GMP and QA practices
Work EnvironmentOversees laboratory testing, quality control labs, and production environmentsFocuses on developing, implementing, and auditing quality assurance systems across production
Employer & Industry UsageUsed in pharmaceutical manufacturing, biotech, and related industriesCommonly employed in pharmaceutical companies, ensuring compliance and process quality

While both roles require similar educational backgrounds and certifications, the Pharmaceutical Quality Control Manager primarily manages laboratory testing and quality control processes, whereas the Pharmaceutical Quality Assurance Specialist focuses on establishing and maintaining quality systems and compliance. Both are essential for ensuring product safety and efficacy in the pharmaceutical industry.

What are some common challenges faced by Pharmaceutical Quality Control Managers in ensuring compliance with regulatory standards?

Pharmaceutical Quality Control Managers often face the challenge of staying current with evolving regulatory requirements from agencies such as the FDA or EMA. They must ensure all laboratory processes, documentation, and product testing meet strict guidelines, which can be complicated by new technologies or changing manufacturing practices. Another challenge is managing cross-functional communication between production, R&D, and regulatory affairs to promptly address quality issues. Successfully navigating these challenges requires a keen eye for detail, strong leadership, and ongoing professional development.

What are the key skills and qualifications needed to thrive as a Pharmaceutical Quality Control Manager, and why are they important?

To thrive as a Pharmaceutical Quality Control Manager, you need a strong background in pharmaceutical sciences, chemistry, or a related field, often supported by a relevant degree and experience in quality assurance. Familiarity with analytical instruments (e.g., HPLC, GC), quality management systems, and regulatory standards like GMP or FDA guidelines is typically required. Leadership, attention to detail, and effective communication are crucial soft skills for managing teams and ensuring compliance. These skills ensure product safety, regulatory adherence, and efficient team operations in a highly regulated industry.

What is the highest paying job in pharmaceuticals?

In pharmaceutical quality control, senior roles such as Director of Quality Assurance or Vice President of Quality typically have the highest salaries, often exceeding six figures. These positions require extensive experience, leadership skills, and knowledge of regulatory standards like GMP and ISO.

Is Pharma QA a good career?

A career as a Pharmaceutical Quality Control Manager offers stability and opportunities for advancement in the pharmaceutical industry. It requires strong attention to detail, knowledge of Good Manufacturing Practices (GMP), and often involves working with laboratory testing, documentation, and regulatory compliance. The role is essential for ensuring product safety and quality, making it a valuable and in-demand profession.

How much do QC managers make in the US?

Pharmaceutical Quality Control Managers typically earn between $80,000 and $130,000 annually in the US, depending on experience, location, and company size. Salaries can be higher with advanced certifications and specialized skills in laboratory testing and compliance standards.

What is the role of a quality control manager in pharmaceuticals?

A pharmaceutical quality control manager oversees testing and inspection of raw materials, in-process samples, and finished products to ensure they meet quality standards and regulatory requirements. They develop and implement quality control procedures, manage laboratory staff, and ensure compliance with Good Manufacturing Practices (GMP) and industry regulations.
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Pharmaceutical Quality Control Manager jobs near you
Infographic showing various Pharmaceutical Quality Control Manager job openings in the United States as of June 2026, with employment types broken down into 2% As Needed, 96% Full Time, 1% Part Time, and 1% Temporary. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $81,324 per year, or $39.1 per hour.
Pharmaceutical Quality Control Manager

Pharmaceutical Quality Control Manager

Yoh, A Day & Zimmermann Company

Rosenberg, TX

$105K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 9 days ago

Job description

Yoh Life Sciences is hiring for a Pharmaceutical Quality Control Manager in Houston, TX.  The QC Manager will serve as a scientific liaison in the lab by supporting method development validation and verification of protocols in a regulated pharmaceutical laboratory environment. General responsibilities include analytical testing of raw materials, in-process samples, finished products and  laboratory instrumentation calibration, such as HPLC, GC, CE, ICP, FTIR, TOC, dissolution apparatus within a cGMP environment. This role requires a minimum of 8 years within a quality control or analytical chemistry laboratory.
Title: QC Manager
Duration: Permanent
Pay: $80,000-105,000 DOE
Location: Houston, TX
Shift: M-F 8-5pm
PRIMARY DUTIES AND RESPONSIBILITIES:
  • Write method validation protocols/reports and perform method development/validation/ verification for API and finished drug products. 
  • Familiar with analytical testing of raw materials, in-process samples, finished products, and analytical laboratory instrumentation, such as HPLC, GC, CE, ICP, FTIR, TOC, dissolution apparatus, etc.
  • Supervise the daily activities of the pharmaceutical QC laboratory by establishing testing priorities and schedules, and assignments of staff based on company priorities and objectives. 
  • Serves as scientific liaison to other facilities and departments and scientific/quality control member of the Material Review Board.
  • Assists with appropriate review of analytical results of completed raw material, stability samples, and finished product testing. 
  • Reviews and approves laboratory investigations, corrective and preventive actions, change requests, and deviations as necessary.
  • Maintain equipment calibration schedule and ensure that all required calibrations and maintenance are completed in a timely fashion.
  • Author SOP's and assist with the revision process of current procedures.
  • Ensure pharmaceutical laboratory compliance with applicable regulations. 
  • Assist with procedural, cGMP, and safety training of laboratory staff.
  • Assist with preparations for internal and external (including FDA) laboratory audits and inspections.
  • Administers annual laboratory budget and other related duties as required.

REQUIRED SKILLS, ABILITIES, AND QUALIFICATIONS:
  • Bachelor's or higher degree in Chemistry or related discipline.
  • 10+ years of experience in a pharmaceutical QC or Analytical chemistry laboratory.
  • Experience with semi-solid and liquid pharmaceutical environment.  
  • 3+ years of experience in GLP or GMP (preferred) environment.
  • Strong leadership experience, team of 4 or more
  • Strong communication with the ability to build relationships at all levels of the organization.
  • Ability to organize, prioritize, and effectively perform concurrent tasks with minimal supervision.

Estimated Min Rate: $73500.00
Estimated Max Rate: $105000.00
What’s In It for You?
We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include:
  • Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week)
  • Health Savings Account (HSA) (for employees working 20+ hours per week)
  • Life & Disability Insurance (for employees working 20+ hours per week)
  • MetLife Voluntary Benefits
  • Employee Assistance Program (EAP)
  • 401K Retirement Savings Plan
  • Direct Deposit & weekly epayroll
  • Referral Bonus Programs
  • Certification and training opportunities

Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.
Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Visit https://www.yoh.com/applicants-with-disabilities to contact us if you are an individual with a disability and require accommodation in the application process.
For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh’s hiring clients’ preferences. To learn more about Yoh’s privacy practices, please see our Candidate Privacy Notice: https://www.yoh.com/privacy-notice

Company Description

Yoh delivers expertise, methodology, and momentum to keep work moving forward. From strategy to execution, we deliver bold ideas and big results through consulting, staffing, and enterprise solutions. Nearly a century after our founding, Yoh remains STEM-centered, collaborative, and committed to client success. Yoh is a proud member of the Day & Zimmermann family of companies. Visit us at https://www.yoh.com/