QC S&T Analyst (Pharma/Biotech)

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Nusantara Prime Consulting Pte. Ltd.
Singapore
SGD 60,000 - 80,000
Be among the first applicants.
2 days ago
Job description

Responsibilities:

  • Supports team tasks to support laboratory operation and infrastructure in areas such as equipment, data systems, and methods.
  • Participates in the management of laboratory equipment and computerized systems in the QC laboratory to ensure business continuity and system data maintenance (e.g., Empower, LIMS, SAP) and that equipment maintenance/calibration is in a state of compliance.
  • Participates in method technology transfer and laboratory equipment technological refresh/introduction activities into the QC Laboratory within project timelines.
  • Engages in QC laboratory long-range planning to secure laboratory infrastructure needs and ensure a data integrity plan is in place to support business and laboratory compliance.
  • Authors and executes qualification and equipment qualification documentation/method transfer (e.g., reports, protocols, change control, related quality documents or procedures) in compliance with cGMP and corporate/site or regulatory requirements.
  • Supports and ensures timely escalation/handling of lab events or related quality actions (e.g., NCR, lab investigation, CAPA).
  • Assists in the preparation and participation in internal/external audits and audit responses to enable successful audit outcomes.
  • Participates in EHS, business compliance, cGMP, and all other compliance-related matters, where applicable. Leads/supports CI initiatives to enable laboratory performance metrics.
  • Carries out any other tasks as assigned by the Line Manager.

About You:

  • University degree in a science-related discipline (e.g., chemistry, biology, pharmaceutical sciences, or equivalent experience).
  • Minimum of 1-3 years of pharmaceutical experience in a Quality Control function.
  • Experienced in regulatory/pharmaceutical requirements.
  • Analytical thinking with basic problem-solving and writing skills.
  • Motivated and independent.
  • Basic GMP knowledge/experience with QC lab equipment and method transfer.
  • Good communication skills and strong ability to work in cross-functional teams.
  • Ability to work towards timelines.
  • Based in Tuas.

Job Type: Contract

Contract Length: 12 months. Option to extend/convert subject to performance review.

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