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Quality Control Pharma Jobs (NOW HIRING)

Catalent, Inc.

Quality Control Analyst

Winchester, KY · On-site

$20.75 - $27.75/hr

Quality Control Analyst Position Summary * Typical working hours are Monday-Friday 3 PM - 11:30 PM ... Other duties as required in support of Catalent Pharma Solutions high performance The Candidate

ThompsonFirstGroup

Quality Control Technician

Easton, MD

$19 - $24.25/hr

Previous quality control or inspection experience in manufacturing (pharma, food, or regulated industry preferred) * Familiarity with GMP, FDA, or ISO standards is a plus * Strong attention to detail ...

Bachem

Quality Control Project Manager

Torrance, CA

$98K - $135K/yr

Bachelor's degree in chemistry or a related life sciences field * 5+ years' QC experience in biotech/pharma * 3+ years' experience in a biotech/pharma CDMO setting * 4+ years of project management ...

QuVa Pharma

Manager, Quality Control Lab

Bloomsbury, NJ

$98K - $135K/yr

Our Manager Quality Control- Lab plays a vital role within our organization. Once you complete our ... Quva Pharma's multiple production facilities and industry-first dedicated remote distribution ...

LGM Pharma, LLC

QC CHEMIST III

Irvine, CA · On-site

$34 - $38/hr

We have an open METHOD VALIDATION / ANALYTICAL CHEMIST III position in our Quality Control ... At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity ...

Us tech Solutions

Quality Control Analyst

Berkeley, CA · On-site

$29.75 - $40/hr

Quality Control Analyst Duration: 12 Months Location: Berkeley, CA 94710 Biological Development ... Pharmacy) (Lead Pharma Technical Recruiter) 10 Exchange Place, Suite 1710, Jersey City, NJ 07302 ...

Us tech Solutions

Quality Control Analyst

Berkeley, CA

$29.75 - $40/hr

Quality Control Analyst Duration: 12 Months Location: Berkeley, CA 94710 Biological Development ... Pharmacy) (Lead Pharma Technical Recruiter) 10 Exchange Place, Suite 1710, Jersey City, NJ 07302 ...

QuVa Pharma

Manager, Quality Control Lab

Bloomsbury, NJ · On-site

$98K - $135K/yr

Our Manager Quality Control- Lab plays a vital role within our organization. Once you complete our ... Quva Pharma's multiple production facilities and industry-first dedicated remote distribution ...

Bachem

Quality Control Project Manager

Torrance, CA · On-site

$98K - $135K/yr

Bachelor's degree in chemistry or a related life sciences field * 5+ years' QC experience in biotech/pharma * 3+ years' experience in a biotech/pharma CDMO setting * 4+ years of project management ...

Astrix Inc

QC Analyst III (Pharma)

Ventura, CA · On-site

$58 - $60/hr

Job type: 6-month contract (possibility of extension or conversion) Job Summary The QC Analyst III is responsible for performing advanced analytical testing, data review, method validation, and ...

Cellares

Manager, Quality Control

Bridgewater, NJ

This position will work with the Quality Control team in supporting our efforts in the GMP ... Partnering with Cellares enables academics, biotechs, and pharma companies to accelerate drug ...

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Quality Control Pharma information

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How much do quality control pharma jobs pay per hour?

As of Jun 27, 2026, the average hourly pay for quality control pharma in the United States is $20.97, according to ZipRecruiter salary data. Most workers in this role earn between $18.03 and $23.08 per hour, depending on experience, location, and employer.

Which pays more, QA or QC?

In the pharmaceutical industry, Quality Assurance (QA) roles generally offer higher salaries than Quality Control (QC) positions due to their broader responsibilities in process oversight and compliance. QA jobs often require more experience, certifications, and strategic skills, which can lead to higher pay. However, salaries vary based on location, experience, and company size.

Is Pharma QA a good career?

Pharma Quality Assurance (QA) is a stable career option in the pharmaceutical industry, focusing on ensuring product quality and compliance with regulations. It often requires attention to detail, knowledge of Good Manufacturing Practices (GMP), and relevant certifications. The role offers opportunities for advancement and job security due to the industry's regulatory nature.

What are the key skills and qualifications needed to thrive as a Quality Control professional in the pharmaceutical industry, and why are they important?

To thrive as a Quality Control professional in pharma, you need a strong background in chemistry, biology, or a related science, along with knowledge of Good Manufacturing Practices (GMP) and relevant regulations. Familiarity with laboratory instruments (e.g., HPLC, GC), LIMS software, and quality assurance certifications such as ASQ or ISO standards is typically required. Attention to detail, analytical thinking, and effective communication help professionals excel in ensuring product quality and regulatory compliance. These skills ensure that pharmaceutical products are consistently safe, effective, and compliant with industry standards.

What is Quality Control in the pharmaceutical industry?

Quality Control (QC) in the pharmaceutical industry refers to the processes and procedures used to ensure that pharmaceutical products meet required standards of quality, safety, and efficacy. QC professionals test raw materials, in-process samples, and finished products using various analytical techniques to verify that they comply with regulatory specifications. The goal is to detect and prevent defects, ensuring that only products that pass rigorous standards are released to the market. QC is essential for maintaining public health and regulatory compliance in the pharmaceutical sector.

Is QC a high paying job?

Quality Control (QC) roles in the pharmaceutical industry typically offer competitive salaries that increase with experience, certifications, and location. Entry-level positions may have moderate pay, while senior QC specialists or managers can earn higher wages, especially with specialized skills and regulatory knowledge.

What is the work of QC in pharma?

A Quality Control (QC) professional in pharma is responsible for testing raw materials, in-process samples, and finished products to ensure they meet quality standards and regulatory requirements. They use analytical techniques and laboratory equipment to identify defects, verify compliance, and document results to maintain product safety and efficacy.

What is the difference between Quality Control Pharma vs Quality Assurance Pharma?

AspectQuality Control PharmaQuality Assurance Pharma
Primary FocusTesting and inspecting raw materials, in-process, and finished products for complianceDeveloping and maintaining quality systems and processes to prevent defects
CertificationsGMP, GLP, relevant laboratory certificationsGMP, ISO 9001, quality management system certifications
Work EnvironmentLaboratories, testing facilitiesQuality departments, documentation, audits
Common Employer RolesPharmaceutical companies, contract labsPharmaceutical companies, regulatory agencies

While both roles aim to ensure product quality, Quality Control Pharma focuses on testing and inspection, whereas Quality Assurance Pharma emphasizes establishing systems and processes to prevent issues. Understanding these differences helps in choosing the right career path or job focus within the pharmaceutical industry.

What are some of the common challenges faced by Quality Control professionals in the pharmaceutical industry?

Quality Control professionals in pharma often face challenges such as staying updated with evolving regulatory standards, managing tight timelines for product release, and ensuring accuracy in complex analytical testing. They must also coordinate closely with production and R&D teams to address any discrepancies or deviations quickly. Maintaining meticulous documentation and effectively handling audits are essential parts of the role, making attention to detail and strong communication skills particularly important.
More about Quality Control Pharma jobs
What cities are hiring for Quality Control Pharma jobs? Cities with the most Quality Control Pharma job openings:
What states have the most Quality Control Pharma jobs? States with the most job openings for Quality Control Pharma jobs include:
What job categories do people searching Quality Control Pharma jobs look for? The top searched job categories for Quality Control Pharma jobs are:
Quality Control Pharma jobs near you
Infographic showing various Quality Control Pharma job openings in the United States as of June 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 100% In-person job distribution, with an average salary of $43,612 per year, or $21 per hour.
Quality Control Analyst

Quality Control Analyst

Catalent, Inc.

Winchester, KY • On-site

$20.75 - $27.75/hr

Full-time

Life, Retirement, PTO

Posted 17 days ago

Catalent rating

7.4

Company rating: 7.4 out of 10

Based on 51 frontline employees who took The Breakroom Quiz

53rd of 73 rated pharmaceutical

Job description

Quality Control Analyst
Position Summary
  • Typical working hours are Monday-Friday 3 PM - 11:30 PM.
  • This position is 100% on-site in Winchester, Kentucky.

Catalent's Winchester location is the flagship US manufacturing location for large scale oral dose forms, with integrated analytical and development services. With 28 years of expertise in product development, technology transfers and commercial manufacturing, and roots in industry-leading Glatt technology.
The Quality Control Analyst performs the basic and critical experimental work of day-to-day analysis, including generation and analysis of data. The Quality Control Analyst works "hands on" in an analytical lab that requires analytical testing, computer operating, record keeping, and report writing abilities.
The Role
  • Perform efficient/reliable/high quality analytical testing in accordance with USP/NF/EP/JP/FCC/etc. or customer supplied guidelines. Typical testing may include Dissolution, Titration, Polarimetry, Loss on Drying, Viscosity, Residue on Ignition, Heavy Metal Content, FTIR, HPLC, and GC, etc.
  • Maintain accurate written records of all analysis performed.
  • Accurately interpret and effectively communicate analytical results and issues.
  • Schedule daily tasks in an organized and efficient manner.
  • Calibrate and maintain lab equipment and instrumentation.
  • Responsible for operating in a safe manner, must be familiar with basic laboratory and chemical hygiene practices
  • Perform peer review of analytical testing and write up. Write SOPs on an as needed basis.
  • Other duties as required in support of Catalent Pharma Solutions high performance

The Candidate
  • Bachelor's degree in a scientific field required (Chemistry or Biology preferred). Alternate degrees in a non-scientific field may be accepted with at least 2 years of relevant experience in a material testing laboratory.
  • 2+ years in Quality, Laboratory, Clinical, or Chemical manufacturing role preferred.
  • Assisting with other personnel with lifting of liquid containers and all objects of greater than 50 lbs. Operating safely in a dynamic environment which includes mobile and fixed equipment and changing conditions while completing job tasks that range from simple to complex and/or multi-tasking.

Why You Should Join Catalent
  • Several Employee Resource Groups focusing on D&I
  • Tuition Reimbursement - Let us help you finish your degree or earn a new one!
  • Generous 401K match
  • 152 hours accrued PTO + 8 paid holidays

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.

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About Catalent

Sourced by ZipRecruiter

Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Somerset, NJ, US

Year founded

2007

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