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Pharmaceutical Quality Control Jobs (NOW HIRING)

Must understand and apply cGMP requirements applicable to pharmaceutical quality control laboratory. Must have ability to resolve conflicts between employees both within and between departments.

The company provides its global pharmaceutical customers with a resilient, efficient supply of critical ingredients at scale, while expanding the innovation frontier for new therapeutic development.

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 ...

Bachelor's Degree in science or related field * 8+ years relevant experience in a cGMP pharmaceutical QC environment or 5+ years with a Master's degree Physical Requirements * Prolonged periods of ...

Must understand and apply cGMP requirements applicable to pharmaceutical quality control laboratory. Must have ability to resolve conflicts between employees both within and between departments.

Must understand and apply cGMP requirements applicable to pharmaceutical quality control laboratory. Must have ability to resolve conflicts between employees both within and between departments.

Bachelor's degree with 10 years of pharmaceutical Quality experience (preferably in QC) or an equivalent combination of education and experience Additional Information Applicable only to applicants ...

QC Chemist II - DPI

Hauppauge, NY · On-site

$86K - $95K/yr

Job Title QC Chemist II Organization Name InvaGen Pharmaceuticals Location 7 Oser Ave, Hauppauge, NY 11788 Employment Type (Hourly/ Full Time) Full-Time - Salary/Exempt Benefits In addition to a ...

Bachelor's degree with 10 years of pharmaceutical Quality experience (preferably in QC) or an equivalent combination of education and experience Additional Information Applicable only to applicants ...

Bachelor's degree with 10 years of pharmaceutical Quality experience (preferably in QC) or an equivalent combination of education and experience Additional Information Applicable only to applicants ...

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Pharmaceutical Quality Control information

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$27

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How much do pharmaceutical quality control jobs pay per hour?

As of Jun 16, 2026, the average hourly pay for pharmaceutical quality control in the United States is $27.14, according to ZipRecruiter salary data. Most workers in this role earn between $18.99 and $33.65 per hour, depending on experience, location, and employer.

What are some typical daily tasks for someone working in Pharmaceutical Quality Control?

A typical day in Pharmaceutical Quality Control involves performing laboratory tests and analyses on raw materials, in-process samples, and finished pharmaceutical products to ensure compliance with safety and regulatory standards. You may prepare and calibrate lab equipment, document test results, review batch records, and assist in investigations of deviations or out-of-specification findings. Additionally, collaboration with production, research, and quality assurance teams is common to maintain continuous improvement and address any quality issues quickly. This role is detail-oriented and often includes both routine testing and problem-solving activities, making each day varied and impactful.

What is the role of quality control in pharmaceuticals?

In pharmaceutical quality control, professionals are responsible for testing raw materials, in-process samples, and finished products to ensure they meet safety, efficacy, and quality standards. They use analytical techniques and laboratory equipment to detect contaminants, verify ingredient concentrations, and ensure compliance with regulatory requirements, supporting the production of safe and effective medicines.

Which pays more, QA or QC?

In pharmaceutical quality control, QA (Quality Assurance) roles typically have higher salaries than QC (Quality Control) positions due to their broader responsibilities in process improvement and compliance. QA professionals often require more experience and may hold certifications like ASQ CQE, which can also influence pay. However, salaries vary based on experience, location, and company size.

What are the key skills and qualifications needed to thrive in the Pharmaceutical Quality Control position, and why are they important?

Pharmaceutical Quality Control professionals need a solid background in chemistry, biology, or pharmacy, often supported by a relevant degree and industry knowledge. Familiarity with laboratory instrumentation, Good Manufacturing Practices (GMP), and quality management systems, along with certifications like ASQ or GxP training, is highly beneficial. Attention to detail, strong analytical thinking, and clear communication are key soft skills that drive accuracy and collaboration. These competencies are crucial for ensuring that pharmaceutical products meet strict safety, efficacy, and regulatory standards.

Is Pharma QA a good career?

Pharmaceutical Quality Control (QA) is a vital role in ensuring drug safety and compliance with regulatory standards. It offers stable employment, opportunities for advancement, and requires skills in laboratory testing, documentation, and knowledge of Good Manufacturing Practices (GMP).

Is QC a good career?

Quality Control (QC) in the pharmaceutical industry involves testing and inspecting products to ensure safety and compliance with regulations. It offers stable employment, opportunities for advancement, and requires attention to detail, technical skills, and knowledge of Good Manufacturing Practices (GMP).

What is a Pharmaceutical Quality Control job?

A Pharmaceutical Quality Control (QC) job involves ensuring that medications meet required safety, efficacy, and quality standards before distribution. Professionals in this field conduct tests, analyze raw materials and finished products, and ensure compliance with regulatory guidelines like Good Manufacturing Practices (GMP). They use analytical techniques such as HPLC, spectroscopy, and microbiological testing. QC specialists also document findings, investigate deviations, and collaborate with other departments to resolve quality issues. Their work helps maintain product integrity and patient safety.

More about Pharmaceutical Quality Control jobs
What cities are hiring for Pharmaceutical Quality Control jobs? Cities with the most Pharmaceutical Quality Control job openings:
What are the most commonly searched types of Pharmaceutical Quality Control jobs? The most popular types of Pharmaceutical Quality Control jobs are:
What states have the most Pharmaceutical Quality Control jobs? States with the most job openings for Pharmaceutical Quality Control jobs include:
Infographic showing various Pharmaceutical Quality Control job openings in the United States as of June 2026, with employment types broken down into 98% Full Time, and 2% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $56,447 per year, or $27.1 per hour.
Manager, QC Lab

Full-time

This job post has expired today. Applications are no longer accepted.


Amneal Pharmaceuticals rating

7.3

Company rating: 7.3 out of 10

Based on 9 frontline employees who took The Breakroom Quiz

56th of 71 rated pharmaceutical


Job description

Job Description
Manager, QC Lab:
Responsible for managing the activities of the quality control laboratory to ensure timely delivery of materials for use in production and releases of finished products from the laboratory as committed, ensure testing of stability samples within structure of timelines identified in relevant SOP, ensure laboratory activities on par with compliance expectations, and provide top notch inter- and intra-department customer service. Manage the day-to-day operations of the Quality Control laboratory including setting and communicating priorities based on the production schedule. Maintain knowledge of the potential impact of Quality Control activities on activities in other departments and effectively communicate this information to the appropriate personnel in a timely manner. Manage/Enforce laboratory GMP systems and ensure that they are adequate, sustainable and are being followed. Update Laboratory Procedures (SOPs) and Policies. Interpret SOPs/Methods/Specifications and provide clarity as needed. Manage and perform investigation of out-of-specification laboratory results ensuring that all investigations proceed in a logical, orderly and timely manner and that appropriate corrective and preventive actions are identified, when necessary, review and approve investigation reports. Review and signoff process validation/cleaning validation protocols/reports, method verification/validation reports, annual product review reports. Review certificate of analysis to ensure compliance with the specifications. Develop and implement systems to improve laboratory GMP compliance and/or productivity. Make decisions and implement solutions where deficiencies are found. Provide formal and informal performance feedback to direct and indirect reports including disciplinary action when necessary. Provide input on yearly departmental headcount and turnover of tested samples. Provide input on employee development including promotion and salary increase recommendations. Research and propose capital projects for the laboratory.
Qualifications
Must possess skills in analytical testing involving spectrophotometric analytical techniques, chromatographic techniques (HPLC/GC) employing different data acquisition software, dissolution, dissolution profile and drug release, disintegration, and moisture determination (Karl Fischer, Coulometric, LOD). Must be able to understand and explain compendial (USP/BP/EP/JP) procedures. Must be able to identify problems during the course of analysis and participate in troubleshooting of instrument-related and procedure-related problems. The incumbent must be able to effectively plan and organize multiple tasks with a high degree of complexity in order to complete them in a timely fashion to meet customer needs. Must be able to work in a cross-functional team setting, either as a leader or a member, and with complete understanding of team goals. Must understand and apply cGMP requirements applicable to pharmaceutical quality control laboratory. Must have ability to resolve conflicts between employees both within and between departments.
Education Requirements: Must have at least a Bachelor's degree in Pharmacy or Chemistry or Pharmaceutical Manufacturing.
Experience Requirements: Must have 12 months of experience in the position or in a related position
Salary: $137K-$140K per annum. Hours: 40 hrs/wk 8:30am - 5:30pm Location: Piscataway, NJ
Please contact: Karen Mayen @ 908-227-4220 Ref # 12458
About Us
Amneal is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, national origin, age, disability, genetic information, protected veteran status, or any other characteristic protected by applicable federal, state, or local laws. If you require a reasonable accommodation to complete the application process or to participate in any part of the hiring process, please contact us at accommodations@amneal.com. Requests will be handled confidentially and in accordance with applicable laws.