Randstad, as the EMEA Johnson & Johnson talent acquisition partner, is responsible for finding and contracting talent for the contingent roles at Johnson & Johnson. If you are selected for a role you will be engaged or employed by one of the Randstad recruitment companies in EMEA and will not be an employee of Johnson & Johnson.

Johnson & Johnson

Technical Scientist

Posted Oct 14, 2021
Job ID: JJJP00007882
Location
Cork, County Cork
Hours/week
39 hrs/week
Timeline
1 year
Starts: Nov 8, 2021
Ends: Nov 6, 2022
Payrate range
Unknown
Application Deadline: Nov 8, 2021 12:00 AM

Johnson & Johnson Worksense (via Randstad Sourceright) is responsible for finding, engaging and contracting talent for the Johnson & Johnson contingent workforce.


 

We are currently recruiting a Technical Scientist to join our contingent workforce on a growing team in Janssen Pharmaceuticals for an initial 12 month contract. 


 

The Role:  

We have an exciting opportunity for an Technical Scientist to join our BioTherapeutics Development & Supply (BTDS) API team in Cork. This role will support development projects and manufacturing operations at JSI and be responsible for leading or supporting Process Development, Technical Transfer, Process Validation, Manufacturing investigations, Life Cycle Management and Health Authority Inspections.


 

Key Responsibilities:

  • Supporting early and late phase Technical Transfer activities through generation of protocols/reports, technical writing, execution of laboratory scale studies and participation in manufacturing operations and NPI initiatives.
  • Supporting early and late phase product development activities through generation of protocols/reports, execution of laboratory scale studies and participation in Lean Early Development initiatives as required.
  • Supporting “process fit to plant” during early and late stages of development to provide guidance to both development and manufacturing teams.
  • Supporting “man in plant” by providing support during manufacturing campaigns for new products or during process validation campaigns.
  • Providing expertise to development teams on manufacturing facility design and capabilities, scale-up considerations and GMP operations.
  • Partnering with Project Teams to provide input, review and approval support for BLA submissions.
  • Participating in cross-functional project teams.
  • Interpreting project plans and timelines for CMC projects, and schedule work and experiments to meet these goals.
  • Assisting in manufacturing investigations as required, in particular event, deviations and CAPAs, to help meet product release specifications and timelines.
  • Executing experimental plans and protocols to support product life-cycle improvements, process validation requirements, technical transfer projects and development activities as required.
  • Fostering a culture of Lean and Continuous improvement within the department and with internal and external partners.


 

Candidate Requirements:

  • A minimum of a Bachelor's degree in Biology, Pharmacy or related scientific field is required, advanced degree is preferred.
  • 2+ years’ experience within a regulated biologics or pharma industry
  • Biological process development or commercial manufacturing experience, either cell culture and/or purification.
  • Excellent communication, skills, both oral and written.
  • Capable of planning and executing experiments or projects steps with some supervision.
  • Ability to work well in a team environment, strong collaboration skills and flexibility.
  • Excellent interpersonal skills with the ability to adapt to rapid changes in project priorities and requirements.
  • Acute attention to detail
  • A focus on patients and customers at all times




 

If you meet our requirements and are interested in hearing more about our Technical Scientist , please do not hesitate to apply through the provided link today and a member of our recruitment team will be in touch!


 

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