ZipRecruiter

Log In

1

Pharmaceutical Analysis Jobs (NOW HIRING)

Merck & Co.

$39K - $111K/yr

Our Pharmaceutical Analysis and Digital Technology (PADT) and Large Molecule Analytical (LMA) departments in Rahway, NJ, West Point, PA, Boston, MA, and South San Francisco, CA are seeking co-ops who ...

Merck & Co.

$39K - $111K/yr

Our Pharmaceutical Analysis and Digital Technology (PADT) and Large Molecule Analytical (LMA) departments in Rahway, NJ, West Point, PA, Boston, MA, and South San Francisco, CA are seeking co-ops who ...

Creative G C

Nitrosamine Researcher

Saint Louis, MO · On-site

A master's degree in a science-related area (chemistry or pharmaceutical science preferred) with a minimum of two (2) years of experience in pharmaceutical analysis; or a doctoral degree in a science ...

next page

Showing results 1-20

All JobsScience JobsResearch JobsScientist JobsPharmaceutical Analysis Jobs

Pharmaceutical Analysis information

See salary details

$34

$38

$41

How much do pharmaceutical analysis jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for pharmaceutical analysis 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.

What is pharmaceutical analysis?

Pharmaceutical analysis is the process of identifying, quantifying, and purifying the chemical components in pharmaceutical substances and products. It involves a range of analytical techniques to ensure the safety, efficacy, and quality of drugs, from raw materials to finished products. This field plays a vital role in drug development, manufacturing, and regulatory compliance by detecting impurities, verifying concentrations, and confirming product stability.

What are the key skills and qualifications needed to thrive in pharmaceutical analysis?

To thrive in Pharmaceutical Analysis, a strong background in chemistry, analytical techniques, and a relevant degree (such as in pharmacy, chemistry, or related fields) is essential. Familiarity with technical tools like HPLC, GC, UV-Vis spectrophotometry, and compliance with regulatory standards such as GMP and GLP are typically required. Attention to detail, critical thinking, and effective communication help professionals accurately interpret results and collaborate with cross-functional teams. These skills ensure the reliability of drug testing, regulatory compliance, and the safety and efficacy of pharmaceutical products.

What are some common challenges faced by professionals working in pharmaceutical analysis, and how can they be addressed?

Professionals in pharmaceutical analysis often encounter challenges such as maintaining strict compliance with regulatory standards, ensuring the accuracy and reproducibility of analytical results, and managing tight project deadlines. Addressing these challenges requires meticulous attention to detail, ongoing training on regulatory updates, and effective communication within multidisciplinary teams. Utilizing robust quality control procedures and leveraging advanced analytical technologies can also help maintain high data integrity and streamline workflows.

What is the difference between Pharmaceutical Analysis vs Quality Control Analyst?

AspectPharmaceutical AnalysisQuality Control Analyst
CredentialsDegree in Chemistry, Pharmacy, or related field; certifications like ASQ or GMP trainingDegree in Chemistry, Biology, or related field; GMP and lab safety certifications
Work EnvironmentLaboratories, research facilities, pharmaceutical manufacturing plantsQuality control labs within pharmaceutical manufacturing facilities
Job FocusDeveloping and validating analytical methods, testing drug samples, ensuring product qualityPerforming routine testing, inspecting raw materials and finished products, ensuring compliance

Pharmaceutical Analysis involves developing and validating analytical methods to test drug quality, while Quality Control Analysts focus on routine testing and inspection to ensure products meet standards. Both roles require similar credentials and work in laboratory settings within the pharmaceutical industry, but their specific responsibilities differ.

More about Pharmaceutical Analysis jobs

What are popular job titles for Pharmaceutical Analysis?

Popular job titles for Pharmaceutical Analysis:

Pharmaceutical Analysis jobs near you
Infographic showing various Pharmaceutical Analysis job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 85% Full Time, 12% Part Time, and 2% Contract. Highlights an 80% Physical, 4% Hybrid, and 16% Remote job distribution, with an average salary of $79,999 per year, or $38.5 per hour.

Associate Scientist, Pharmaceutical Analysis-Microbiology

Exton, PA • On-site

Frontage Laboratories
Pharmaceutical and Medicine Manufacturing • 201 - 500 employees
Learn more about Frontage Laboratoriesexternal

Full-time

Medical, Dental, Life, Retirement

Re-posted 9 days ago

Job description

                      Associate Scientist, Pharmaceutical Analysis-Microbiology

Full-time

Exton, PA


Frontage Laboratories:

Frontage Laboratories Inc. (Frontage) is a global contract research organization with broad expertise in supporting pre-clinical and clinical drug development. Frontage operates out of several different locations within the USA, Canada, and China. Frontage’s core competencies include drug metabolism, pharmokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.

Analytical Chemistry-CMC:


We specialize in analytical services and method development, validation and transfer for product development and clinical trial materials (CTM) manufacturing support, as well as commercial product release and stability testing.


Position Summary:

Performs routine and non-routine microbiology sample analysis (specifically, MLT/Bioburden, Endotoxin, Environmental Monitoring, Sterility, and AET) and a variety of tasks to support product development, ensuring agreed timelines.

Responsibilities:

  • Performs method development and validation under supervision.
  • Prepares study protocols, reports, investigation reports, and generates cGMP documents as needed.
  • Performs quality checks of data, laboratory notebooks, and other scientific documentation as required.
  • Maintains qualification and compliance of instruments, and conducts technical and equipment troubleshooting as needed.
  • Reports and resolves any unexpected issues under supervision.
  • Complies with all relevant cGMP regulatory requirements while carrying out assigned studies.
  • Collaborates with team members (Analytical Scientists, Quality Assurance, Material Coordinators, and Manufacturing Technicians) to meet timelines for drug product delivery.
  • Identifies opportunities for improvement in quality of services, and works with the team to implement.

Requirements:

  1. B.S. in Biology or related discipline with 1-3 years relevant experience in pharmaceutical or related industry (CRO experience is a plus).
  2. Experience in pharmaceutical product and facility testing (MLT/Bioburden, Sterility, Endotoxin, Environmental Monitoring, AET).
  3. Experience working in a BSL2 laboratory is a plus.
  4. Capable of setting priorities based in a fast-paced, changing environment.
  5. Excellent oral and written communication skills, attention to detail and data quality, and experience working on diverse collaborative teams.

Salary and Benefits:

Frontage Laboratories offers a competitive compensation and benefits package including health and dental insurance, a 401(k) plan, disability insurance, and life insurance.

Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.