<p>Job Description</p> <p>The Sr. Manufacturing Technician is responsible for executing all cell culture manufacturing and aseptic techniques. The role includes documenting all operations in electronic batch records in compliance with GMP and SOPs, and involves reviewing and revising production documents as needed. The technician will also conduct OOS investigations and batch record reviews.</p> <p>Responsibilities</p> <ul> <li>Perform all cell culture manufacturing and aseptic techniques. </li><li>Document all operations in electronic batch records in compliance with GMP and SOPs. </li><li>Review and revise production documents as needed. </li><li>Conduct OOS investigations and batch record reviews. </li><li>Complete other duties as assigned. </li></ul> <p>Essential Skills</p> <ul> <li>Experience in cleanroom environments. </li><li>Knowledge of cell therapy, cell culture, and mammalian cell culture. </li><li>Familiarity with GMP regulations and SOPs. </li><li>Proficiency in 5S and lean manufacturing principles. </li></ul> <p>Additional Skills & Qualifications</p> <ul> <li>Bachelor's or higher degree in Life Sciences or related field with 5+ years of cGMP experience in the biotech or pharmaceutical industry. </li><li>Biotechnology certificate with 6+ years of cGMP experience in the biotechnology or pharmaceutical industry. </li><li>Experience with cell culture and following SOPs. </li></ul> <p>Work Environment</p> <p>This is a 100% onsite position with an initial training period of 3-4 months from Monday to Friday. Following training, the schedule will shift to Wednesday through Saturday, 6:30 am to 5:00 pm. The role will initially split time between Cambridge, MA and Burlington, MA, eventually moving full time to the new plant in Burlington. The dress code is business casual.</p> <p>Additional Skills & Qualifications</p> <p>Bachelor's or higher degree (Life Sciences or related field) or equivalent with 4-5+ years of experience working in a cGMP environment in the biotech or pharmaceutical industry.</p> <p>Biotechnology certificate with 6+ years of experience working in a cGMP environment in the biotechnology or pharmaceutical industry or GED or equivalent with 8-10+ years of cGMP experience</p> <p>Experience with cell culture</p> <p>Follow up all SOPs</p> <p>Experience Level</p> <p>Expert Level</p> <p>Job Type & Location</p> <p>This is a Permanent position based out of Cambridge, MA.</p> <p>Pay and Benefits</p> <p>The pay range for this position is $60320.00 - $74800.00/yr.</p> <p>They will receive a 10% bonus and RSUs as a part of the offer.</p> <p>Workplace Type</p> <p>This is a fully onsite position in Cambridge,MA.</p> <p>Application Deadline</p> <p>This position is anticipated to close on Mar 13, 2026.</p> <p>About Actalent</p> <p>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.</p> <p>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.</p> <p>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 for other accommodation options.</p>