Associate Scientist

Experience Level: Entry-Level

Education: M.S. with 1+ year of experience preferred; B.S. with 3+ years acceptable

We are seeking a motivated and detail-oriented Bioanalytical Scientist with hands-on laboratory experience and strong expertise in HPLC to join our dynamic team. The ideal candidate will have experience in the biopharmaceutical industry, particularly in bioanalytical assays such as Size Exclusion Chromatography (SEC), Ion Exchange Chromatography (IEX), and basic analytical techniques including pH, osmolality, and protein concentration measurements.

This role requires excellent communication skills and the ability to collaborate effectively within a cross-functional team environment.

• Conduct and monitor experiments with minimal supervision, ensuring reproducibility and reliability of results.
• Analyze and interpret experimental data; maintain accurate and organized records.
• Adapt and implement experimental methods from literature; develop and optimize protocols.
• Operate and troubleshoot standard lab equipment and analytical instruments (e.g., HPLC, CE).
• Collaborate in a matrix team environment and communicate findings clearly to colleagues.
• Contribute to technical reports, presentations, regulatory documents, and patent submissions.
• Participate in departmental initiatives such as safety programs and team committees.
• May provide training or supervision to junior staff.

• Education:
  • M.S. in Biochemistry, Analytical Chemistry, Pharmaceutical Sciences, Biology, or related field with 1+ year of relevant experience
  • OR B.S. with 3+ years of relevant experience (M.S. preferred)
• Skills
  • Proficiency in HPLC and other chromatographic techniques (SEC, IEX)
  • Familiarity with basic assays: pH, osmolality, protein concentration
  • Strong analytical and problem-solving skills
  • Excellent communication and teamwork abilities
  • Ability to work independently and manage multiple priorities

• Prior work in a biopharmaceutical or bioanalytical lab setting
• Experience with method development and protocol optimization
• Familiarity with regulatory compliance and documentation standards

Pay and Benefits

The pay range for this position is $25.00 - $33.00/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)

Workplace Type

This is a fully onsite position in Cambridge,MA.

Application Deadline

This position is anticipated to close on Jun 19, 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 ... for other accommodation options.