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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.
• Primary areas of responsibility include raw material dispensing, assembly and movement of raw materials and equipment into staging or production areas, preparation of media and buffers, preparation and sterilization of parts and assemblies, stocking of materials and supplies
• Execute unit operations described in standard operating procedures, manufacturing batch records, and cGMP guidelines
• Assist in the cleaning of the facility as directed by the Support Lead
• Perform bioprocess operations that include buffer preparation, filtration, and harvest
• Setup, maintenance, and use of cGMP equipment as directed by standard operating procedures and manufacturing batch records
Additional Skills & Qualifications:
• Familiarity of process automation and business quality systems and software
• Ensure work executed in compliance with company and regulatory quality policy and systems
• Familiar with biotechnology industry and biopharmaceutical manufacturing is preferred
• 0-2 years related experience
• Must be able to work weekends, off-shifts, and overtime as required. Applicant must be willing and able to work reliably on a flexible schedule, Monday – Friday and some weekends, to meet the demands of the project
• Must be able to don gowning in the form of hospital scrub, gloves, safety glasses/goggles, coveralls and safety toe footwear with shoe covers multiple times per shift
• Handle and work with hazardous materials and chemical per standard operating procedures and OSHA guidelines
• Good organizational and communication skills, both written and verbal, and the ability to prioritize competing tasks
• Excellent interpersonal skills with the ability to work well with others in a dynamic and highly collaborative environment. Ability to interact constructively with peers and support groups
• Ability to lift at least 20kg
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 for other accommodation options.
