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Pharmaceutical Quality Manager Jobs (NOW HIRING)

synergy

Pharmaceutical GMP QA Specialist

Dallas, TX · On-site

Pharmaceutical GMP QA Specialist Synergy is seeking a detail-oriented and experienced ... The QA Specialist will be responsible for implementing and maintaining quality management systems ...

synergy

Pharmaceutical GMP QA Specialist

Dallas, TX · On-site

Pharmaceutical GMP QA Specialist Synergy is seeking a detail-oriented and experienced ... The QA Specialist will be responsible for implementing and maintaining quality management systems ...

Medix

Quality Manager

Deerfield, IL · On-site

$50 - $65/hr

The role involves managing regulatory intelligence activities, supporting document control ... Prior experience in pharmaceutical quality systems and proficiency with Veeva are essential.

Jones Lang LaSalle IP, Inc.

Quality Manager

Juncos, PR · On-site

Job Summary Quality Manager responsible for leading Quality Assurance, Compliance, Vendor Quality Management, and Quality Engineering activities supporting GMP-regulated pharmaceutical manufacturing ...

JLL

Quality Manager

Juncos, PR · On-site

Job Summary Quality Manager responsible for leading Quality Assurance, Compliance, Vendor Quality Management, and Quality Engineering activities supporting GMP-regulated pharmaceutical manufacturing ...

Shionogi Inc.

QA Product Manager

Florham Park, NJ · On-site

The QA Product Manager is responsible for ensuring the quality and compliance of pharmaceutical products (active pharmaceutical ingredients and/or drug products) manufactured by third-party ...

Shionogi Inc.

QA Product Manager

Florham Park, NJ · On-site

Overview The QA Product Manager is responsible for ensuring the quality and compliance of pharmaceutical products (active pharmaceutical ingredients and/or drug products) manufactured by third-party ...

Shionogi Inc.

QA Product Manager

Florham Park, NJ · On-site

Overview The QA Product Manager is responsible for ensuring the quality and compliance of pharmaceutical products (active pharmaceutical ingredients and/or drug products) manufactured by third-party ...

ORGANIC POAG LLC

Quality Manager

Little Rock, AR · On-site

Join My Medical Supply, a leading pharmaceutical warehouse distribution facility committed to ... We are seeking a dedicated and detail-oriented Quality Manager to oversee our quality assurance ...

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Pharmaceutical Quality Manager information

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$24K

$86.2K

$158K

How much do pharmaceutical quality manager jobs pay per year?

As of Jun 16, 2026, the average yearly pay for pharmaceutical quality manager in the United States is $86,159.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,000.00 and $136,000.00 per year, depending on experience, location, and employer.

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

AspectPharmaceutical Quality ManagerQuality Assurance Specialist
CredentialsTypically requires a Bachelor's degree in Pharmacy, Chemistry, or related field; often holds certifications like ASQ CQE or ISO auditorUsually holds a Bachelor's degree in Life Sciences or related; may also have certifications like ASQ CQPA or ISO auditor
Work EnvironmentManages quality teams, oversees quality systems, and ensures compliance across manufacturing facilitiesPerforms audits, reviews documentation, and supports quality processes within labs or production lines
Employer & Industry UsageCommonly employed in pharmaceutical manufacturing, biotech, and healthcare companiesFound in pharmaceutical, biotech, and medical device industries, often within quality departments

The Pharmaceutical Quality Manager focuses on leading quality management systems and strategic oversight, while the Quality Assurance Specialist handles day-to-day quality checks and documentation. Both roles are essential for ensuring product compliance and safety in the pharmaceutical industry.

What is the salary of a QA manager?

The salary of a Pharmaceutical Quality Manager typically ranges from $80,000 to $130,000 annually, depending on experience, location, and company size. They often hold certifications such as ASQ CQE or ISO auditor and work in regulated environments requiring strong knowledge of GMP and quality systems.

What are some common challenges faced by Pharmaceutical Quality Managers, and how can they be addressed?

Pharmaceutical Quality Managers often face challenges such as keeping up with evolving regulatory requirements, managing cross-functional teams, and ensuring continuous compliance throughout manufacturing processes. Staying current with global regulations and fostering open communication between departments are crucial for success. Implementing robust quality management systems and investing in ongoing staff training can help address these challenges, ensuring product safety and regulatory adherence.

Which pays more, QA or QC?

For a Pharmaceutical Quality Manager, salaries for Quality Assurance (QA) roles tend to be higher than those for Quality Control (QC) roles due to broader responsibilities, strategic planning, and compliance oversight. QA positions often require more experience, certifications, and leadership skills, which can lead to higher compensation. However, actual pay varies based on company, location, and individual qualifications.

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

To thrive as a Pharmaceutical Quality Manager, you need a solid background in pharmaceutical sciences, regulatory compliance, and quality management systems, often supported by a relevant degree and experience in GMP environments. Familiarity with tools like LIMS, CAPA systems, and certifications such as Six Sigma or ISO 9001 are typically important. Attention to detail, problem-solving, and strong leadership skills help ensure effective oversight and continuous improvement. These competencies are crucial for maintaining product safety, regulatory compliance, and operational excellence in pharmaceutical manufacturing.

What is the role of a pharmaceutical quality manager?

A pharmaceutical quality manager oversees the quality assurance and control processes within a pharmaceutical company to ensure products meet regulatory standards and quality specifications. They develop and implement quality systems, conduct audits, and collaborate with production teams to maintain compliance with industry regulations such as GMP. Strong knowledge of quality management systems and relevant certifications are essential for this role.

What does a Pharmaceutical Quality Manager do?

A Pharmaceutical Quality Manager oversees the quality assurance and control processes within pharmaceutical manufacturing. They ensure that all products comply with regulatory standards, company policies, and industry best practices. Their responsibilities include developing quality management systems, conducting audits, and coordinating with production teams to resolve quality issues. Ultimately, they play a crucial role in maintaining product safety and efficacy for consumers.

How much does a QA manager make at Pfizer?

A Pharmaceutical Quality Manager at Pfizer typically earns between $100,000 and $130,000 annually, depending on experience, location, and level of responsibility. Salaries may also include bonuses and benefits related to quality assurance and regulatory compliance roles.
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Pharmaceutical Quality Manager jobs near you
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 10 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/