Job Description

Description

Duration: 12 months

Salary: Up to 4K

Location: Tuas (With company transport)

Duration: Mon-Fri Office Hours

Job description:

- Perform analytical method transfer in accordance to Standard Operating Procedures (SOPs) and protocol.

- Perform analytical testing accurately and efficiently following Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) requirements.

- Perform cleaning method development and validation

- Able to assess the impact to products based on compendial monograph changes/updates/introduction.

- Perform method validation and verification as per SOP.

- Ability to handle QTS actions and investigations.

- Analytical testing, method transfers and review of test results to meet lead time in a right first time manner;

- Perform testing according to Standard Work Plan as assigned.

- Ensure training records are updated and promptly, are correctly filed to reflect current testing capabilities.

- Method verification in accordance to site or pharmacopeia standards and according to schedule;

- Ensure instrumentation is calibrated / maintained in accordance to schedule as required.

- Execute method equivalency study

- Involve in regular meeting with donating site and facilitate the smooth transfer of the methods.

- Update relevant instrument SOPs as required to ensure it reflects current requirement and practice.

- Compliance to GMP/GLP and Quality Standards (PQS) requirements;

- Understand and comply with Data Integrity and Good Documentation Practices requirements.

- Laboratory safety and housekeeping;

- Contribute to and participate in laboratory housekeeping and 5S program responsibilities.

- Wear Personal Protective Equipment (PPE) as required and observe safety instructions stated in Job Safety Analysis (JSAs), Standard Test Methods (STPs) and Material Application Document (MADs).

- Perform test method validation & cleaning method validation of test methods in accordance to STP and USP/JP requirements

- Complete validation documents reports as required.

- Update SOPs to align with PQS and regulatory requirement (USP, ICH guidelines etc)

- Conduct and document laboratory investigations according to SOPs.

- Raise and complete change controls for changes with GMP impact.

Job requirements:

- Min diploma in Science or Chemical Process Technology

- Has prior QC experience in pharmaceutical industry

Please email your resume at alexgoh@recruitexpress.com.sg

Alex Goh Hock Leong (Alvin)

Recruit Express Pte Ltd (Healthcare & Lifescience)

Company EA Licence number : 99C4599

Personnel EA License: R1763413

alexgoh@recruitexpress.com.sg

Industry

Healthcare / Pharmaceutical / Life Science / Medical Device

Specialization

Chemist / Research Scientist

Location

West

Employment Type

Contract / Temp

Salary

S$2,601 - S$4,000 / mth

If you meet the requirements of this role, please email a detailed resume in Word document to Alex Goh Hock Leong alexgoh@recruitexpress.com.sg.
CEI Registration No.: R1763413
Email: alexgoh@recruitexpress.com.sg
Tel: 67363280
*All information will be treated with strictest confidence. We regret that only short-listed applicants will be notified.

Recruit Express