QC Chemist (Pharma/Biotech)

NUSANTARA PRIME CONSULTING PTE. LTD.; Singapore; On-site; SGD 20,000 - 60,000; Full time

Job summary

A contract-based laboratory firm located in Singapore is seeking a candidate with a Bachelor of Science in Chemistry or Biochemistry for laboratory operations. Responsibilities include performing biochemistry and analytical testing, assisting in quality compliance, and supporting equipment maintenance. Fresh graduates are welcome to apply, and candidates must be able to work rotating 12-hour shifts. The position has a contract length of 12 months with options for extension based on performance.

Qualifications

• Fresh graduates are welcome to apply.
• Good working knowledge of cGMP and regulatory requirements preferred.
• Must be able to work rotating 12-hour shifts.

Responsibilities

• Perform biochemistry and analytical testing for lot release.
• Support laboratory operations including method transfer and equipment maintenance.
• Assist in writing SOP documents and continuous improvement.
• Carry out QC sample receipt, assay, and release procedures.

Skills

Problem-solving skills

Communication skills

Interpersonal skills

Education

Bachelor of Science in Chemistry, Biochemistry or related field

Job description

Responsibilities

• Perform biochemistry, analytical and raw material of in-process and marketed products for lot release in accordance with quality standards and procedures


• Responsible for housekeeping duties in the lab. Perform Quality Tag Out for laboratory equipment such as freezer, water bath, etc.


• Support laboratory operations including but not limited to 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


• To assist in writing SOP documents, change plan or change records (document revisions) supporting continuous improvement of test procedures and assay sheet design


• To carry out completion and review of GMP Documentation of data sheets or LIMS software


• To carry out QC sample receipt, assay and release procedures


• Support Audit preparation and any audit related activity


• Reading and understanding the test procedure and the requirements per USP, JP and EP

About You

• Bachelor of Science majoring in Chemistry, Biochemistry or related scientific degree


• Fresh graduate are welcome to apply.


• 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 guidance and industry standards for analytical development and characterization


• Must be able to do rotating 12-hour shift work (day and night shifts)

Job Type: Contract

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