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Contract Pharmaceutical Scientist Jobs (NOW HIRING)

Eurofins

Pharmaceutical Robotics Scientist

Groton, CT · On-site

... Contract Research Organisation services. It is one of the market leaders in certain testing and ... We are seeking an associate scientist to join the Smart Lab within Drug Product Development. The ...

MSD Malaysia

$117 - $184/hr

Our company's Pharmaceutical Sciences and Clinical Supply organization translates molecules to ... Outsource/coordinate formulation development or clinical manufacturing at Contract Development or ...

Posted today

Eurofins Scientific

Scientist, Data Review

Columbia, MO · On-site

... pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation ... THIS IS NOT A DATA SCIENCE POSITION* Eurofins BPT-Columbia is looking for a Associate Scientist ...

Synerfac Technical Staffing

Quality Chemist

Horsham, PA · On-site

$35 - $40/hr

M-F, 8-4 Our client is a contract pharmaceutical manufacturer looking to add a quality chemist to ... science or engineering field Must have cGMP knowledge/background within a lab and QMS experience ...

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How much do contract pharmaceutical scientist jobs pay per hour?

As of Sep 6, 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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Contract Pharmaceutical Scientist jobs near you
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, 81% Full Time, 14% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $88,899 per year, or $42.7 per hour.

Scientist, Analytical Development (Contract)

Vertex Pharmaceuticals Incorporated

Boston, MA • On-site

$62/hr

Other

Posted 11 days ago

Vertex Pharmaceuticals rating

6.5

Company rating: 6.5 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

78th of 86 rated pharmaceutical

Job description


Scientist, Analytical Development
Position Summary
We are seeking a talented and highly motivated (Scientist), Analytical Development to support analytical strategy and method development for complex therapeutic programs, with an emphasis on biologics and cell and gene therapy. This individual will play a key role in developing, optimizing, qualifying, and transferring analytical methods used to characterize product quality, purity, identity, and stability.
The ideal candidate will have strong technical expertise in HPLC, LC-MS, and biophysical characterization techniques, including DLS, SEC-MALS, and CE, as well as the ability to work effectively in a cross-functional, fast-paced development environment.
Key Responsibilities
  • Develop, optimize, qualify, and support transfer of analytical methods for characterization of therapeutic materials, intermediates, and final products
  • Apply and troubleshoot analytical techniques including HPLC/UPLC, LC-MS, DLS, SEC-MALS, and CE
  • Perform biophysical characterization to assess critical quality attributes such as purity, aggregation, size distribution, molecular weight, and heterogeneity
  • Generate, analyze, interpret, and clearly communicate analytical data to cross-functional teams
  • Support product and process development through analytical testing for comparability, formulation, stability, and process-related investigations
  • Author and review technical documents including protocols, reports, method qualification summaries, and development reports
  • Collaborate closely with partners in process development, manufacturing, quality, regulatory, and research functions
  • Support collaboration activities with external contract organizations as needed
  • Maintain accurate and complete documentation in accordance with applicable quality and compliance standards. Prior experience with Electronic Lab Notebook (ELN) documentation is preferred.

Required Qualifications
  • Bachelor's, Master's, or PhD in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, Molecular Biology, or a related scientific discipline
  • Relevant industry experience in analytical development, pharmaceutical development, biotechnology, or a related field
  • Strong hands-on experience with HPLC/UPLC and LC-MS, including method development, optimization, and troubleshooting
  • Prior experience with biophysical characterization techniques, including DLS, SEC-MALS, and CE is beneficial but not required
  • Demonstrated ability to interpret complex analytical data and draw scientifically sound conclusions
  • Strong written and verbal communication skills, with the ability to present findings clearly to technical and cross-functional audiences
  • Strong organizational skills and ability to manage multiple priorities in a dynamic environment

Preferred Qualifications
  • Experience supporting cell and gene therapy programs, biologics, or other advanced therapeutic modalities
  • General knowledge of analytical considerations for complex biologics or cell and gene therapies
  • Experience with analytical method qualification, comparability studies, stability studies, and technology transfer
  • Familiarity with work in regulated environments, including GLP/GMP practices
  • Proven ability to work collaboratively across multidisciplinary teams

Core Competencies
  • Analytical rigor and scientific problem-solving
  • Strong technical troubleshooting skills
  • Attention to detail and commitment to data quality
  • Effective cross-functional collaboration
  • Clear communication and technical writing
  • Ability to adapt in a fast-paced research and development environment

Pay Range
%60-$62/HR
Requisition Disclaimer
This job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals ("Vertex"). The individual selected for this role will be offered the role as an employee of a third- party agency partner; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements
By applying for this position, you agree to the Atrium Terms and Conditions and you direct Atrium to share your application materials, which may include your CV/Resume, email address or phone number, with Vertex. For more information on how Vertex handles your personal data related to your job application, please see Vertex's Careers Privacy Notice. Agreeing to the Atrium Terms and Conditions, includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employment to notify you of job openings, profiles, articles, news, and other employment-related information, as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners
(collectively, "Atrium Alerts"). Atrium Alerts may be sent by email, phone, or text message. Your personal information will be safely stored within the Atrium & Vertex databases. Atrium does not sell your personal information to third parties. Text message and data rates may apply. To OPT OUT of text messaging or to modify your communication preferences for Atrium Alerts at any time, please contact Atrium at privacyadministrator@atriumstaff.com.
If you do not agree with the Atrium Terms and Conditions, you can still complete your application for this position by emailing your resume to our team at tempstaffing@vrtx.com. Please include the job title in the subject of your email.
No C2C or Third-Party Vendors

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