Job Details

ID #51285093
Estado Pennsylvania
Ciudad Philadelphia
Full-time
Salario USD TBD TBD
Fuente Actalent
Showed 2024-03-19
Fecha 2024-03-20
Fecha tope 2024-05-19
Categoría Etcétera
Crear un currículum vítae
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Manufacturing Associate I

Pennsylvania, Philadelphia, 19113 Philadelphia USA
Aplica ya

Description:: Responsible for manufacture of Master and Working Cell Banks andperforming activities within production facilities to support manufacture of Cell &Gene Therapy products, and final product fills according to current GoodManufacturing Practices (cGMPs)Understands aseptic technique concepts Has performed aseptic technique, is able to identify unacceptable practices andmake spot corrections to performance Able to operate and maintain equipment Understands the basic operations and functions of equipment and is able toperform 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 activitiesFollows compliance and regulatory requirements and current Good ManufacturingPractices (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, downstreamTop Skills Details:biologist, biology, mammalian cell, cell culture, protein purification, aseptic, cell banking, GMP, cGMP, cell production, upstream, downstreamAdditional Skills & Qualifications: Associates’/Bachelor’s (science preferred) degree with over 2 years of relevant orequivalent experienceMasters with 0+yrs of industry experienceHands on mammalian cell culture experience is a MUSTExperience working within a Bio Safety Cabinet is a MUST Experience in aseptic processing techniques and some understanding of regulatory requirements for a cGMP manufacturing facilityExperience Level:Intermediate LevelAbout 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 [email protected] (%[email protected]) for other accommodation options.

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