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Contract Pharmaceutical Scientist Jobs (NOW HIRING)

Local Contract Pharmacist

Philadelphia, PA ยท On-site

$58.75 - $70.75/hr

... of pharmaceutical products. Determinations include medical necessity and benefit decisions ... Sciences is an established provider of healthcare workforce solutions, servicing healthcare ...

MANTECH seeks a motivated, career and customer-oriented Electro-Optical Imagery Scientist to join ... Contract Wage Determination, relevant work experience, skills and competencies that align to the ...

Scientist I

South San Francisco, CA ยท On-site

$135 - $158/hr

We are seeking a highly motivated Preformulation Pharmaceutical Scientist to join our Preclinical ... Experience overseeing formulation or analytical work at contract research organizations.

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How much do contract pharmaceutical scientist jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for contract pharmaceutical scientist in the United States is $42.74, according to ZipRecruiter salary data. Most workers in this role earn between $30.29 and $53.61 per hour, depending on experience, location, and employer.

What is a contract pharmaceutical scientist?

Contract Pharmaceutical Scientists are professionals who work on a temporary or project basis for pharmaceutical companies, research organizations, or contract research organizations (CROs). They contribute expertise in drug discovery, development, formulation, testing, and regulatory compliance. These scientists are hired to fill specific skill gaps, manage workload fluctuations, or provide specialized knowledge for particular projects. Their role may involve laboratory research, data analysis, report writing, and ensuring that products meet industry standards. Contract Pharmaceutical Scientists offer flexibility and can help companies accelerate drug development timelines.

How does a contract pharmaceutical scientist typically collaborate with clients and internal teams during a project?

As a Contract Pharmaceutical Scientist, you will frequently interact with both external clients and internal multidisciplinary teams such as analytical chemists, regulatory affairs, and project managers. Clear communication is essential to align on project goals, timelines, and deliverables. You may be responsible for presenting research findings, discussing experimental design, and adapting protocols based on client feedback. Regular meetings and progress updates help ensure the project stays on track and meets regulatory standards. This collaborative environment offers valuable exposure to diverse scientific and business perspectives.

What are the key skills and qualifications needed to thrive as a contract pharmaceutical scientist, and why are they important?

To thrive as a Contract Pharmaceutical Scientist, you need a solid background in chemistry, biology, or pharmacology, typically supported by a relevant degree and experience in pharmaceutical research. Familiarity with laboratory instrumentation, Good Laboratory Practice (GLP), and data analysis software such as LIMS or chromatography systems is essential. Strong problem-solving, time management, and communication skills help manage multiple projects and effectively collaborate with clients and teams. These competencies ensure accurate, compliant research and efficient delivery of high-quality scientific results in a competitive contract environment.
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Infographic showing various Contract Pharmaceutical Scientist job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $88,899 per year, or $42.7 per hour.

Technical Transfer Engineer (Contract) - Pharmaceutical Manufacturing

Techengpr

Carolina, PR โ€ข On-site

$70 - $90/hr

Other

Posted 11 days ago


Job description

Technical Transfer Engineer (Contract) โ€“ Pharmaceutical Manufacturing
  • Technical Transfer Engineer (Contract) โ€“ Pharmaceutical Manufacturing

We are seeking two experienced Technical Transfer Engineers to support an international pharmaceutical technology transfer project. The selected candidates will collaborate with cross-functional teams in Puerto Rico and China to execute technical transfer activities for solid dosage manufacturing and packaging operations. This role requires strong documentation skills, GMP knowledge, and the ability to work in an English-speaking technical environment.

Key Responsibilities
  • Support technology transfer activities for solid dosage manufacturing and packaging processes.
  • Develop, review, and execute technical transfer protocols.
  • Prepare and manage Change Controls and Risk Assessments.
  • Review and update Batch Records and manufacturing documentation.
  • Support paper-based validation activities and documentation packages.
  • Collaborate with Manufacturing, Quality, Validation, Engineering, and Technical Services teams.
  • Ensure compliance with cGMP, quality standards, and company procedures.
  • Participate in project meetings and provide technical support throughout the transfer process.
  • Travel to China for several weeks during key phases of the project.
Qualifications
  • Bachelor's degree in Engineering, Pharmacy, Chemistry, or a related scientific discipline.
  • Minimum of 3 years of experience in pharmaceutical manufacturing.
  • Hands-on experience with:
    • Technology Transfer
    • Change Controls
    • Risk Assessments
    • Batch Record review and development
    • Validation documentation (paper-based validation)
    • Solid dosage manufacturing and/or packaging operations
  • Strong understanding of cGMP requirements.
  • Excellent written and verbal English communication skills.
  • Ability to work effectively in a multicultural, international environment.
  • Willingness and ability to travel internationally to China for extended periods.
Preferred Qualifications
  • Experience supporting global pharmaceutical technology transfer projects.
  • Familiarity with deviation investigations and CAPAs.
  • Previous experience in regulated pharmaceutical manufacturing environments.
What We Offer
  • Competitive contract compensation.
  • International project experience with global teams.
  • Opportunity to work on a high-impact technology transfer initiative.
  • Initial one-year assignment with a strong likelihood of extension.
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