Job Title: Biomanufacturing TechnicianJob Description The Biomanufacturing Associate I is a vital part of the gene therapy manufacturing team, utilizing biological, bioprocess, manufacturing, and mechanical principles in a cGMP and GLP environment to ensure the production and release of high-quality products according to client specifications. This role involves performing various routine and semi-routine tasks, requiring judgment to resolve issues or make recommendations, with guidance when necessary, in order to effectively execute manufacturing protocols within a regulated setting. Responsibilities + Apply and adhere to SOPs, cGMP, GLP, Quality, and basic Safety requirements under guidance. + Perform routine and semi-routine tasks according to SOPs in areas such as upstream activities, downstream activities, and fill-finish activities. + Follow verbal and written instructions in alignment with the batch record during planned manufacturing activities. + Utilize basic quality documents and apply Good Documentation Practices with guidance. + Document, review, and check work accurately to prevent errors prior to submission. + Identify, record, and report observed process variances/deviations in real time. + Operate equipment and complete process tasks by following SOPs, safety guidelines, and manufacturing instructions. + Prepare, clean, and maintain equipment and tools. + Recognize common safety issues and report incidents immediately. + Adhere to safe working practices and comply with site-based guidelines, including cleanroom and aseptic procedures, PPE and gowning requirements, and safe handling of biological specimens and hazardous materials. + Ensure 100% on-time completion of the training plan. + Be punctual and flexible with work schedule to support business demands. + Perform other responsibilities as required. Essential Skills + Experience with cGMP, GLP, and SOPs. + Knowledge of aliquoting, cell culture, chromatography, Tangential Flow Filtration (TFF), fill finish, and GDP. + Strong attention to detail and ability to recognize deviations. + Good analytical, critical thinking, and problem-solving skills. + Proficiency in MS Word, Excel, Teams, and databases. Additional Skills & Qualifications + High School Diploma or equivalent with high grades in science courses and 2 years of related experience, or an A.S. with 1 year, or a degree in biology/life sciences, bioengineering, or related discipline with 0-1 years of related experience. + Ability to work in accordance with established values and as a team player. + Positive attitude, professional tone, and effective collaboration skills. + Willingness to continuously learn and improve. + Pass/maintain aseptic/gowning qualifications & media fill activities. + Ability to work in a cleanroom for at least 4 hours/day. Work Environment The work environment is a laboratory setting where the technician will engage with advanced technologies and equipment. The role involves working in a cleanroom, adhering to strict gowning and aseptic procedures, and ensuring safety protocols are followed for handling biological specimens and hazardous materials. Pay and Benefits The pay range for this position is $23.50 - $23.50/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 Rockville,MD. Application Deadline This position is anticipated to close on Jun 20, 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 (%20actalentaccommodation@actalentservices.com) for other accommodation options.