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Pharmaceutical Testing Jobs (NOW HIRING)

Viatris

Chemist I

Morgantown, WV · On-site

Perform pharmaceutical testing including, but not limited to, HPLC, GC, TLC, UV, dissolution and IR spectroscopy. * Demonstrate ability to understand and perform testing in accordance with all ...

Viatris

Chemist I

Morgantown, WV · On-site

Perform pharmaceutical testing including, but not limited to, HPLC, GC, TLC, UV, dissolution and IR spectroscopy. * Demonstrate ability to understand and perform testing in accordance with all ...

Eagle

Analytical Data Review Scientist

Houston, TX · On-site

Knowledge of emerging analytical technologies and pharmaceutical testing applications. Who We Are Serving customers since 2004, Eagle offers the highest quality in preparation testing for sterility ...

Cardinal Health

Supervisor, Chemistry

Mansfield, MA · On-site

Chemistry performs laboratory testing to characterize the chemical properties of our medical device and pharmaceutical products. This job family develops and executes test protocols using specialized ...

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How much do pharmaceutical testing jobs pay per hour?

As of Jul 14, 2026, the average hourly pay for pharmaceutical testing in the United States is $38.46, according to ZipRecruiter salary data. Most workers in this role earn between $36.54 and $40.38 per hour, depending on experience, location, and employer.

Are there any legit product testing jobs?

Pharmaceutical testing jobs are legitimate roles that involve evaluating the safety and efficacy of drugs and medical products. These positions often require knowledge of laboratory techniques, attention to detail, and sometimes certifications or training in clinical or laboratory settings. Job seekers should verify employers and avoid scams by researching companies and understanding industry standards.

How to become a pharmaceutical QA?

To become a pharmaceutical QA, candidates typically need a bachelor's degree in pharmacy, chemistry, or a related field, along with knowledge of Good Manufacturing Practices (GMP) and quality assurance processes. Gaining experience through internships or entry-level roles in pharmaceutical manufacturing or quality control is common, and certifications such as Certified Quality Auditor (CQA) can enhance prospects. Strong attention to detail, understanding of regulatory requirements, and proficiency with laboratory and documentation tools are essential for success in this role.

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

To excel in Pharmaceutical Testing, candidates typically require a background in chemistry, biology, or pharmaceutical sciences, often with a relevant degree or laboratory experience. Familiarity with analytical instrumentation such as HPLC, GC, and spectrophotometers, as well as Good Laboratory Practice (GLP) certification, is highly valued. Attention to detail, strong problem-solving skills, and effective communication are essential soft skills in this field. These competencies ensure accurate data collection, regulatory compliance, and seamless collaboration within multidisciplinary teams.

What is pharmaceutical testing?

Pharmaceutical testing involves evaluating drugs and medical products to ensure their safety, efficacy, and quality before they are approved for use. It includes laboratory analysis, stability testing, and clinical trials, often requiring knowledge of Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).

What is the highest paying job in pharmaceuticals?

In pharmaceutical testing, senior roles such as Director of Quality Assurance or Regulatory Affairs typically have the highest salaries, often exceeding six figures. These positions require extensive experience, advanced certifications, and leadership skills in managing compliance and testing processes.

What is a Pharmaceutical Testing job?

A Pharmaceutical Testing job involves analyzing drugs, raw materials, and finished products to ensure they meet safety, quality, and regulatory standards. Professionals in this field perform laboratory tests, document results, and comply with industry regulations like Good Manufacturing Practices (GMP). Roles may include quality control analysts, laboratory technicians, or regulatory specialists. These jobs are essential in ensuring that medications are safe and effective for consumer use.

What does a typical day look like for professionals in pharmaceutical testing?

A typical day in pharmaceutical testing often involves preparing and analyzing samples, operating complex laboratory equipment, and accurately documenting results in accordance with regulatory standards. You may work closely with fellow scientists, quality assurance teams, and regulatory specialists to assess the safety, efficacy, and quality of pharmaceutical products. Deadlines and batch release schedules can create a fast-paced environment, but clear protocols and teamwork help streamline the process. This dynamic role combines hands-on lab work with data interpretation and cross-functional communication, offering exposure to multiple aspects of drug development.

More about Pharmaceutical Testing jobs
What cities are hiring for Pharmaceutical Testing jobs? Cities with the most Pharmaceutical Testing job openings:
What are the most commonly searched types of Pharmaceutical Testing jobs? The most popular types of Pharmaceutical Testing jobs are:
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What job categories do people searching Pharmaceutical Testing jobs look for? The top searched job categories for Pharmaceutical Testing jobs are:
Pharmaceutical Testing jobs near you
Infographic showing various Pharmaceutical Testing job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 79% Full Time, 16% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $79,999 per year, or $38.5 per hour.

Senior Quality Control Analyst, QC Technical Resources

Nova Pneuma, Inc.

Fremont, CA

$114K/yr

Full-time

Posted 9 days ago

Job description

Job Summary

Provides scientific and technical, support to the Quality Control Technical Service group while coordinating all aspects of the site’s stability program. Conducts cGMP pharmaceutical testing to ensure regulatory compliance and safety. Assists in method transfers, verifications, and qualifications activities.

Responsibilities

  • Develop and maintain stability protocols, reports, and other related documentation to support the stability program.
  • Manage stability chambers, including qualification, monitoring, and capacity planning.
  • Ensure timely pull points, testing, data review, and reporting for all stability studies.
  • Trend stability data, identify OOT/OOS signals, and support investigation related to stability samples
  • Author, review, and revise QC SOPs, test methods, and technical documentation
  • Develop, validate, and transfer analytical methods as needed, troubleshoot instrumentation such as HPLC, UPLC and GC.

Skills required

  • Deep knowledge of GMP regulations and advanced laboratory techniques.
  • Strong Knowledge of in Empower and OpenLab chromatography software.
  • Strong understanding of stability program requirements (ICH Q1A–Q1E).
  • Familiarity with GMP, data integrity principles, and regulatory expectations.
  • Strong organizational skills and ability to manage multiple studies and timelines.
  • Excellent documentation, communication, and cross-functional collaboration abilities.
  • Knowledge of method validation or lifecycle management.
  • Ability to analyze data trends and contribute to technical investigations.
  • Familiarity with regulatory guidelines (ICH, FDA, EMA)
  • Maintain audit‑ready documentation and support internal and external inspections.
  • Well-organized, capable of multi-tasking and working on complex problems with sound scientific judgement
  • Excellent data analysis skills with attention to detail and interpretation of results
  • Excellent written and oral communication skills
  • Experience with computer software such as WORD, EXCEL and chromatographic workstation systems

Education and experience

  • BS in Chemistry, Biochemistry, Analytical Chemistry or related field
  • Minimum of 8 years of experience in GMP-regulated QC laboratory, preferably in pharmaceuticals or biotech

Physical Requirements

  • Prolonged periods of sitting at a desk and working on a computer
  • Potentially prolonged periods standing
  • Must be able to lift up to 15 pounds at times

Compensation

The base salary for this role starts at $114,000. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, and relevant education or training. Our compensation package also includes diverse health and other benefits and an annual target bonus for full-time positions.