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in Philadelphia, PA
Manufacturing Associate II
Hours | Full-time, Part-time |
---|---|
Location | Philadelphia, Pennsylvania |
About this job
Job Description
Description:
: Responsible for manufacture of Master and Working Cell Banks and
performing activities within production facilities to support manufacture of Cell &
Gene Therapy products, and final product fills according to current Good
Manufacturing Practices (cGMPs)
Understands aseptic technique concepts
Has performed aseptic technique, is able to identify unacceptable practices and
make spot corrections to performance
Able to operate and maintain equipment
Understands the basic operations and functions of equipment and is able to
perform basic troubleshooting
Performs solution and material preparation
Possesses basic technical knowledge and background in the industry
Possesses basic and fundamental engineering and mechanical knowledge
Possesses basic and fundamental facility start-up experience
Has participated in facility start-ups
Participates on and performs technical transfer activities
Assists with the execution of validation activities
Receives and organizes materials
Performs material procurement activities
Follows compliance and regulatory requirements and current Good Manufacturing
Practices (cGMPs) and starts to understand ‘why’ behind the regulations
Follows and executes Standard Operating Procedures (SOPs)
Revises and authors simple SOPs
Follows and executes Batch Records (BRs)
Skills:
biologist, biology, mammalian cell, cell culture, protein purification, aseptic, cell banking, GMP, cGMP, cell production, upstream, downstream
Top Skills Details:
biologist, biology, mammalian cell, cell culture, protein purification, aseptic, cell banking, GMP, cGMP, cell production, upstream, downstream
Additional Skills & Qualifications:
Associates’/Bachelor’s (science preferred) degree with over 2 years of relevant or
equivalent experience
Masters with 0+yrs of industry experience
Hands on mammalian cell culture experience is a MUST
Experience working within a Bio Safety Cabinet is a MUST
Experience in aseptic processing techniques and some understanding of regulatory requirements for a cGMP manufacturing facility
Experience Level:
Intermediate Level
About ActalentActalent 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 & InclusionAt 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.