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Laboratory Scientist

2 months ago

Singapore NUSANTARA PRIME CONSULTING PTE. LTD. Full time
Job Title: Laboratory Analyst

Join our team at NUSANTARA PRIME CONSULTING PTE. LTD. as a Laboratory Analyst and contribute to the success of our organization.

About the Role:

We are seeking a highly motivated and detail-oriented Laboratory Analyst to join our team. As a Laboratory Analyst, you will be responsible for performing biochemistry, analytical, and raw material testing for lot release in accordance with quality standards and procedures.

Key Responsibilities:
  • Perform biochemistry, analytical, and raw material testing for lot release in accordance with quality standards and procedures
  • Responsible for housekeeping duties in the lab, including Quality Tag Out for laboratory equipment
  • Support laboratory operations, including method transfer, equipment qualification, calibration, cleaning, and maintenance, purchase and receipt of reagents and consumables, waste management, reagent and media preparation, critical reagent management, and document management
  • Review lot release data, identify testing discrepancies, and participate in laboratory investigations
  • Participate in inspection and ensure that the laboratory and documents are in a constant state of regulatory compliance and inspection readiness
  • Assist in writing SOP documents, change plans, or change records (document revisions) supporting continuous improvement of test procedures and assay sheet design
  • Carry out completion and review of GMP Documentation of data sheets or LIMS software
  • Carry out QC sample receipt, assay, and release procedures
  • Support Audit preparation and any audit-related activity
  • Read and understand test procedures and requirements per USP, JP, and EP
  • Work 12-hour rotating shifts (Day/Night)
Requirements:
  • Bachelor of Science majoring in Chemistry, Biochemistry, or related scientific degree
  • At least 1-3 years of relevant experience, depending on qualification, preferably in the bio-pharmaceutical/pharmaceutical industry
  • Good working knowledge of cGMP and regulatory requirements related to Quality is preferred
  • Problem-solving and troubleshooting skills
  • Highly motivated and independent
  • Possess good interpersonal and communication skills
  • Knowledge of cGLP/cGMP, FDA, EMA, and ICH guidelines and industry standards for analytical development and characterization
What We Offer:

We offer a competitive salary and benefits package, as well as opportunities for professional growth and development.

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

Please submit your application, including your resume and cover letter, to [insert contact information].