Job Title: Manufacturing AssociateJob Description We are seeking a Manufacturing Associate I to participate in cGMP activities in the cGMP production facility. The Associate will use their training and knowledge of biopharmaceutical manufacturing to execute operations in a cGMP facility. Responsibilities + Dispense raw materials and assemble and move raw materials and equipment into staging or production areas. + Prepare media and buffers and sterilize parts and assemblies. + Stock materials and supplies. + Execute unit operations as described in standard operating procedures, manufacturing batch records, and cGMP guidelines. + Assist in cleaning the facility as directed by the Support Lead. + Perform bioprocess operations including buffer preparation, filtration, and harvest. + Set up, maintain, and use cGMP equipment as directed by standard operating procedures and manufacturing batch records. Essential Skills + Experience with GMP and cleanroom environments. + Proficiency in aseptic techniques and facility sanitization. + Experience in batch record documentation and manufacturing processes. + Ability to handle and work with hazardous materials and chemicals following standard operating procedures and OSHA guidelines. + Good organizational and communication skills, both written and verbal. + Excellent interpersonal skills with the ability to work well in a dynamic and highly collaborative environment. + Ability to prioritize competing tasks. + Ability to lift at least 20kg. Additional Skills & Qualifications + Familiarity with process automation and business quality systems and software. + Knowledge of the biotechnology industry and biopharmaceutical manufacturing is preferred. + 0-2 years of related experience. + A degree in Life Sciences or a technical program, or a High School Diploma. + Ability to work weekends, off-shifts, and overtime as required. + Willingness to work reliably on a flexible schedule, Monday – Friday and some weekends, to meet project demands. Work Environment The work environment requires adherence to cGMP standards and involves wearing hospital scrubs, gloves, safety glasses/goggles, coveralls, and safety toe footwear with shoe covers multiple times per shift. The role involves handling and working with hazardous materials and chemicals according to standard operating procedures and OSHA guidelines. 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.