Key Responsibilities:
Production Implementation: Execute assigned production procedures within defined schedules while maintaining compliance with cGMP regulations.
Safety and Compliance: Ensure a safe work environment by following all site safety procedures and participating as a member of the safety team.
Lab Start-Up and Shutdown: Execute defined lab start-up and shutdown procedures.
Work Environment: Maintain a clean and organized work environment in accordance with defined procedures, ensuring basic lab supply needs are met.
Process Qualification: Qualify and maintain qualifications on all assigned manufacturing processes, which may include synthesis and/or purification equipment cleaning and setup, general solution preparation, column packing, lab cleaning, changeover, start-up, and shutdown procedures.
Routine Monitoring: Conduct routine equipment monitoring, including chart recorders and spectrophotometers, and monitor automated systems, recording operational data.
General Operations: Perform general routine operations such as pH measurements and UV determinations.
Additional Skills & Qualifications:
Biotechnology certificate or college degree preferred.
2-5 years of experience, with previous GMP experience necessary.
Experience with synthesis, purification, and fraction collection is highly valued.
Employee Value Proposition (EVP):This is a great opportunity to get your foot in the door with a growing Contract Manufacturing Organization (CMO) within the biotech industry. We love to promote from within—show good performance, and you can quickly move up the ranks. Pay and BenefitsThe pay range for this position is $30.00 - $31.25/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 TypeThis is a fully onsite position in Milford,MA.Application DeadlineThis position is anticipated to close on Mar 10, 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 & Inclusion At 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 people
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 actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.