Analytical Chemist

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Analytical Chemist | remote/part-timePosition Summary

We are seeking a motivated and detail-oriented Part-Time Analytical Chemist to support analytical development activities from preclinical through clinical stages. This role involves close collaboration with contract manufacturers and service providers to ensure the integrity and quality of analytical data in compliance with regulatory standards. The ideal candidate will possess strong organizational skills, a keen eye for detail, and the ability to work independently in a dynamic, fast-paced environment.

Key Responsibilities

• Conduct QC review of analytical data for starting materials, intermediates/in-process controls, drug substances, and drug products, including batch release and stability testing.
• Review documentation and results related to reference standard qualification; oversee shipment, tracking, and inventory of reference standards.
• Support analytical development efforts at external contract manufacturing organizations (CMOs) and service providers.
• Collaborate with internal and external stakeholders to resolve data discrepancies and ensure regulatory compliance.
• Maintain accurate records, reports, and correspondence to support analytical development.
• Ensure adherence to applicable quality, safety, and compliance standards.
  
  

Qualifications

• Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field.
• 1-3 years of industry experience in analytical chemistry or a pharmaceutical laboratory setting.
• Basic understanding of analytical techniques such as HPLC, GC, dissolution testing, and spectroscopy.
• Strong attention to detail with proven ability to interpret and review analytical data.
• Proficiency in Microsoft Office, especially Excel.
• Excellent communication, organizational, and problem-solving skills.
  
  

Key Skills - Must-Haves

• Quality Control (QC)
• Analytical Chemistry
• In-Process Controls (IPC)
• Reference Standard Qualification
• Small Molecule Analysis
  
  

Secondary Skills - Nice-to-Haves

• Chemistry, Manufacturing, and Controls (CMC)
• High-Performance Liquid Chromatography (HPLC)
• Laboratory Operations
• Gas Chromatography (GC)
• Spectroscopy
• cGMP Compliance
• ICH Guidelines
• FDA Regulatory Compliance
  
  

Preferred Attributes

• Familiarity with cGMP, ICH, and FDA regulatory guidelines.
• Experience working with CMOs or CROs.
• Ability to manage multiple tasks and timelines in a collaborative team environment.
  
  

Pay and Benefits

The pay range for this position is $35.00 - $50.00/hr.

Requirements

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)
  
  

Workplace Type

This is a fully remote position.

Application Deadline

This position is anticipated to close on Sep 12, 2025.

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 due to a disability, please email actalentaccommodation@actalentservices.com ( actalentaccommodation@actalentservices.com) for other accommodation options.

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