Cell Medica: Vacancies

Vacancy

Cleanroom Associate

Cell Medica is seeking an experienced Cleanroom Associate for the GMP manufacture of novel cell therapy products.

Full time post. Salary depending on experience.

Summary of responsibilities and activities

Cell Medica, a cellular therapeutics company developing and providing clinical grade cell-based products for treatment of immuno-compromised patients is seeking an experienced Cleanroom Associate for the GMP manufacture of novel cell therapy products. The Cleanroom Associate will support our team in central London in the GMP manufacturing of cellular therapeutics and will be responsible for cleanroom day to day maintenance.

The cleanroom associate reports directly to the GMP Production Manager.

Identified activities for the position

(as required by the company, activities may be amended, appended or removed through agreement with your line manager; appropriate training will be provided where applicable)

The activities will include

  1. Perform established GMP manufacturing processes for Cell Medica’s cellular therapeutics.Support GMP implementation and validation of new processes.
  2. Perform supporting procedures like e.g. sample preparation, preparation of manufacturing materials, accurate documentation.
  3. General Cleanroom maintenance according to defined standards
  4. Keeping an accurate stock check of reagents and consumables in the cleanroom facility.
  5. Maintaining manufacturing equipment through cleaning, servicing and maintaining records for cleaning and servicing of equipment.

Skills and experience relevant to the position

(internal training will be provided as necessary)

  1. A degree in biological science, preferably with a focus on immunology.
  2. At least 2 years experience working with blood-derived cellular products -
    experience with cell culture and flow cytometry would be highly beneficial.
  3. At least 2 years experience in cleanroom processing of cellular products - preferably in an industrial environment.
  4. Ability to record information and manage data to GMP/GCP standards.
  5. Maintaining document systems and batch records in accordance with regulatory requirements.
Where
Cell Medica
Closing date
31st January

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