Job Description


Responsibilities:

  • Coordination of release system, including the release of incoming raw materials and finished products
  • Perform cross funcational investigations and follow-up with CAPA
  • Perform internal audits and supplier qualification
  • Manage documentation control
  • Coordinate test request and sample workflow
  • Provide quality assurance checks for manufacturing plants
  • Liaise with contract manufacturer on product requirements
  • Coordinate stability programme in accordance to regulatory requirements
  • Support execution of qualification and validation protocols
  • Assist in provision of services as a contract laboratory
  • Support regulatory submissions and external audits
  • Perform any ad-hoc tasks when required
Requirements:
  • A good degree in biotechnology / chemistry / microbiology / pharmaceutical sciences / biomedical science or relevant life sciences
  • Meticulous, driven and resourceful with excellent people skills
  • At least 3 years of experience in a GMP environment
  • Knowledge of qualification / validation is preferred
Please provide the following:
  • Reasons for leaving past & present employment
  • Last drawn/current and expected salaries
  • Your earliest availability
Please email your resumes to jobs@lynkbiotech.com. We regret that only shortlisted candidates will be notified.

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Job Detail

  • Job Id
    JD1311385
  • Industry
    Not mentioned
  • Total Positions
    1
  • Job Type:
    Full Time
  • Salary:
    Not mentioned
  • Employment Status
    Permanent
  • Job Location
    Singapore, Singapore
  • Education
    Not mentioned