Analytical Chemist

Job Description

Job Description

Job Title: Analytical Chemist
Job Description

This on-site Analytical Chemist position focuses on performing analytical testing on raw materials and experimental products developed across a global network of product development teams. The role involves routine testing of powders, tablets, and liquid samples, development and validation of analytical methods, drafting and maintaining standard operating procedures (SOPs) related to analytical testing, and supporting the continuous improvement of laboratory practices. The Analytical Chemist collaborates closely with cross-functional stakeholders to deliver accurate, timely data that supports product development and quality decisions.

Responsibilities

• Perform USP dissolution testing of solid oral dosage forms to evaluate both functional and immediate-release film coatings.
• Conduct analytical testing of powders, tablets, and liquid samples in accordance with USP, JP, EP, CP, and other applicable regulatory guidelines.
• Carry out wet chemistry analyses, including titrations and related classical analytical techniques, to support raw material, in-process, and finished product testing.
• Develop, optimize, and validate analytical methods using techniques such as High Performance Liquid Chromatography (HPLC), UV/Vis spectroscopy, FTIR, and dissolution testing.
• Draft, revise, and maintain standard operating procedures (SOPs) related to analytical testing to ensure consistency and compliance.
• Support and enforce cGLP compliance by adhering to internal policies, procedures, and quality standards in all laboratory activities.
• Troubleshoot analytical methods and instrumentation issues, identifying root causes and implementing effective corrective actions.
• Perform raw material monograph testing in alignment with compendial requirements (e.g., USP, EP, JP) where applicable.
• Document all testing activities, observations, and results accurately and in a timely manner in laboratory records and reports.
• Provide clear, concise, and timely project status updates to stakeholders, including interpretation of analytical data and its implications for product development.
• Collaborate with product development and quality teams to support experimental product evaluation and method transfer activities.
• Manage multiple projects simultaneously while meeting required deadlines and maintaining high-quality analytical output.

• Bachelor’s degree in Chemistry, Biology, or a related scientific discipline.
• Minimum of 3–7 years of relevant pharmaceutical laboratory experience; an advanced degree may reduce the required years of experience.
• Demonstrated experience performing dissolution testing of solid oral dosage forms.
• Hands-on experience with High Performance Liquid Chromatography (HPLC) for pharmaceutical analysis.
• Proficiency in UV/Vis spectroscopy for quantitative and qualitative analysis.
• Experience conducting analytical testing of powders, tablets, and liquid samples in accordance with regulatory guidelines such as USP, JP, EP, and CP.
• Working knowledge of wet chemistry techniques, including titration and related classical methods.
• Practical experience operating and interpreting data from FTIR instrumentation.
• Experience supporting raw material, in-process, and finished product testing in a pharmaceutical environment.
• Demonstrated ability to develop, validate, and optimize analytical methods.
• Strong understanding of and adherence to current Good Laboratory Practice (cGLP) standards.
• Ability to manage multiple projects and meet deadlines while maintaining data quality and integrity.
• Effective communication skills to provide clear, concise, and timely updates to project stakeholders.

• Ion Chromatography experience is strongly preferred.
• Familiarity with raw material monograph testing in accordance with compendial requirements such as USP, EP, and JP is preferred.
• Experience working in a pharmaceutical product development or quality control laboratory environment.
• Exposure to analytical method transfer and support of experimental product evaluation.
• Ability to draft and refine standard operating procedures (SOPs) for analytical testing.
• Strong attention to detail and a commitment to maintaining high-quality documentation and records.
• Interest in long-term career growth within analytical and product development roles, including progression to senior and principal scientist levels.

This role is based on-site in a laboratory setting within a pharmaceutical product development environment. The Analytical Chemist works hands-on with a variety of analytical instruments and techniques, including HPLC, UV/Vis spectroscopy, FTIR, dissolution apparatus, and equipment used for wet chemistry and titration. The laboratory operates under cGLP standards, with established internal policies, procedures, and quality systems guiding daily work. The position supports a structured career path with defined progression from Analytical Scientist levels through senior and Principal Scientist roles, offering clear opportunities for professional development and advancement. The work involves close collaboration with cross-functional teams, adherence to compendial guidelines (USP, EP, JP, CP), and consistent use of laboratory information systems and documentation practices to ensure accurate, reliable data.

Job Type & Location

This is a Contract position based out of West Point, PA.

The pay range for this position is $31.25 - $37.50/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

This is a fully onsite position in West Point,PA.

This position is anticipated to close on Jun 22, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email View email address on ziprecruiter.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.