Job Description
Support quality control activities inclusive of testing and method development. Help perform batch record reviews, CAPAs, and investigations as a part of the quality assurance team. Assist with batch disposition and drug manufacturing processes. Review batch records of internal manufacturing as well as external CMO partners. Help with QC methods and assist with change control activities.
ResponsibilitiesSupport quality control activities including testing and method development.Perform batch record reviews, CAPAs, and investigations.Assist with batch disposition and drug manufacturing processes.Review batch records of internal manufacturing and external CMO partners.Help with quality control methods.Assist with change control activities.Essential SkillsQuality assuranceQuality controlQMSMethod developmentCAPAInvestigationBatch record reviewVeeva VaultCMOElisaSDS PageGMPAdditional Skills & QualificationsBS in a life science7-10 years in a quality capacityPrevious experience in managing CMOsSupporting biologics companies and drug manufacturing companiesExperience working in a QC and QA capacityWork Environment
Work hours are Monday-Thursday 8am-5pm, with work-from-home options on Fridays. You will report directly to the Director and work closely with the QC Departments as well as the internal AD/QC team. This is an individual contributor manager position, not a people manager role. The company values hard-working individuals with good communication skills who can get along with a variety of people. The work environment offers a great culture and the opportunity to contribute to methods that will be used for years to come, with exposure to various molecules at the clinical stage of stage II.
Pay and Benefits
The pay range for this position is $60.00 - $80.00/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 hybrid position in Wellesley Hills,MA.
Application Deadline
This position is anticipated to close on Apr 3, 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.
Diversity, Equity & InclusionAt Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
Hiring diverse talent Maintaining an inclusive environment through persistent self-reflection Building a culture of care, engagement, and recognition with clear outcomes Ensuring growth opportunities for our peopleThe 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 actalentaccommodation@actalentservices.com for other accommodation options.