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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, 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 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 facility
Experience Level:
Intermediate Level
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.
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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.
Other
$37k-46k (estimate)
02/10/2023
05/04/2024
The job skills required for Biopharmaceutical Manufacturing Associate include Written Communication, Regulatory Compliance, Initiative, etc. Having related job skills and expertise will give you an advantage when applying to be a Biopharmaceutical Manufacturing Associate. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Biopharmaceutical Manufacturing Associate. Select any job title you are interested in and start to search job requirements.
The following is the career advancement route for Biopharmaceutical Manufacturing Associate positions, which can be used as a reference in future career path planning. As a Biopharmaceutical Manufacturing Associate, it can be promoted into senior positions as a Pharmacy Technician II that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Biopharmaceutical Manufacturing Associate. You can explore the career advancement for a Biopharmaceutical Manufacturing Associate below and select your interested title to get hiring information.