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Cell Culture Associate

Cell Culture Associate

The primary focus of the Cell Culture Associate role will be supporting cellular therapeutic manufacturing during process transfers, routine production, and technology improvements.

Employee Responsibilities:
  • Production of blood component lots through cell culture, harvest, and cryopreservation
  • Supports aseptic product manufacturing, including media preparations, plant support, and other duties required for cellular therapeutic manufacturing
  • Weighs and measures in-process materials to ensure proper quantities are added/removed
  • Performs patient process unit operations and support operations described in SOP and batch records
  • Adheres to the production schedule ensuring on-time, internal production logistics
  • Records production data and information in a clear, concise, format according to proper GDPs
  • Assists in setting up manufacturing areas and equipment/fixtures and performs facility and equipment commissioning activities (i.e. routine maintenance and cleaning of rooms and equipment)
  • Works in a team based, cross-functional environment to complete production tasks required by shift schedule
The Ideal Candidate would possess:
  • Ability to work with the physical demands of the position which include:
    • Standing/walking for several hours at a time
    • Carry, lift, push, and/or pull up to 50 pounds
    • Climbing ladders or stairwells several times a day
    • Bending or kneeling several times a day
    • Overhead reaching
    • Repetitive use of arms/wrists/hands while setting up equipment and processing
  • Experience working in a cleanroom environment and performing aseptic processing
  • Comfort working with human blood components and in close proximity to strong magnets
  • Strong computer, scientific, and organizational skills
  • Excellent communication (oral and written) and attention to detail
  • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
  • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
Minimum Qualifications:
  • High School diploma or equivalent is required, but Bachelor's degree in relevant science or engineering discipline, is preferred or equivalent work experience
  • 2+ years of relevant work experience in pharmaceutical, biotechnology, and/or sterile production environments required, but an equivalent combination of experience and education is acceptable
  • Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing, is desirable
  • Authorization to work in the United States indefinitely without restriction or sponsorship
What we offer:
  • Excellent full time benefits including comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays
Position is full-time, working 12 hour shifts. Operations are 24/7, so position may be for any one of several shift schedules. Candidates currently living within a commutable distance of Bothell, Washington are encouraged to apply.

Eurofins Lancaster Laboratories Professional Scientific Services ® (PSS) is a global, award-winning insourcing solution that places our people at our clients' site dedicated to running and managing laboratory services while eliminating headcount, co-employment and project-management worries.

We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR and great place to work best practices, to recruit, hire, train and manage highly qualified scientists to perform laboratory services using our client's quality systems and equipment.

Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer .


 
Published 2 days ago
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