324 Lab Analyst jobs in Singapore

Job Description:

• Perform chemical analysis pertaining to product release, project and validation related testing.
• Ensure that all tests are performed in accordance with written procedures.
• Appointed as a trainer on identified subject matter expert. Train new Lab staff.
• Assessment of training effectiveness for new Lab Junior Technicians / Technicians.
• Supervise junior technicians / technicians during testing and that will also include equipment troubleshooting, equipment failure handling and investigation.
• Support Lab consumables purchase, inventory and control expenditure.
• Assist in investigating chemical analysis failure investigation. (not pertaining to Singapore site).
• Conduct or review internal calibration and maintain calibration master list.
• Verify tagging status and certificate of analysis for product release.
• Verification test results obtained by QA Lab Junior Technician / QA Lab Technician.
• Troubleshooting when equipment breakdown or malfunction.
• Ensure and verify chemical mixing process is performed in accordance with written procedures.
• Support routine in-house test requests: Chemical Extraction test if required.
• Any other tasks assigned by superior if required.

Job Requirement:

• Minimum Diploma in Chemical Process Technology/Microbiology or in a related discipline.
• Ability to work independently and willing to perform overtime when required to support the manufacturing operations.
• Able to commit to rotating monthly shifts (8am-5:30pm / 8pm-5:30am)
• Required to work in cleanroom environment.
• Familiar with Microsoft Word, Excel and Access.
• Good communication and writing skill.
• Entry level candidates are welcome to apply.

• Author method validation protocols and execute method validation/ verification for raw material testing.
• Support the laboratory start-up activities, participate in equipment qualification activities including (but not limited to) generation of user requirement specifications, SOPs and configuration specifications.
• Perform QC test for raw material samples including compendial tests and identification tests.
• Perform QC sampling of incoming raw materials.
• Author/ revise raw material specification and other QC related documents.
• Support laboratory activities such as housekeeping and equipment maintenance.

• Bachelor's or Master's Degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biology or related life Sciences or Technology with at least 5-7 years of experience in QC raw material testing.
• Experience in method validation/ verification in the pharmaceutical or biotechnology industry
• Good understanding of good laboratory practices, good documentation practice and data integrity requirements.
• Experienced in routine laboratory operations.
• Experienced/ participated in method transfer, method validation and method verification for raw material testing.
• Experienced in start-ups will be ideal

QC Lab Analyst - Raw Materials (Method Validation/ Verification/ Pharma)

12 Months Contract

Location: Tuas

Up to $6,000 depending on experience

Industry: Pharmaceutical

Our client aims at creating a new manufacturing concept consisting of a new generation of evolutive multi-product facilities, modular, adaptable, and agile, leveraging new disruptive technologies, to better address vaccine business challenges.

Responsibilities:

• Author method validation protocols and execute method validation/ verification for raw material testing.
• Support the laboratory start-up activities, participate in equipment qualification activities including (but not limited to) generation of user requirement specifications, SOPs and configuration specifications.
• Perform QC test for raw material samples including compendial tests and identification tests.
• Perform QC sampling of incoming raw materials.
• Author/ revise raw material specification and other QC related documents.
• Support laboratory activities such as housekeeping and equipment maintenance.

Requirements:

• Bachelor's or Master's Degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biology or related life Sciences or Technology with at least 5-7 years of experience in QC raw material testing.
• Experience in method validation/ verification in the pharmaceutical or biotechnology industry
• Good understanding of good laboratory practices, good documentation practice and data integrity requirements.
• Experienced in routine laboratory operations.
• Experienced/ participated in method transfer, method validation and method verification for raw material testing.
• Experienced in start-ups will be ideal

Lim Pey Chyi -

Recruitment Consultant (R )

Manpower Staffing Services (S) Pte Ltd

EA Licence: 02C3423

Salary: up to $4500

Working Days & Hours: Mon to Fri, office hours

Location: One North

Job Description:

• Support TS&D professionals to collect and analyze lab experimental data in a safe and timely manner.
• Operate construction lab related equipment such as Instron, Sealant mixing pump, aging chambers, dispensing guns. Keep record of customer samples. Perform application testing independently for silicone sealants. Support PMS (project management system) related lab work to ensure timely technical service to Façade and other applications in B&I.
• Support formulation mixing when required, carry out characterizations using analytical equipments, and create test reports by summarizing data
• Participate in lab management tasks such as ensuring 5S laboratory cleanliness, ensuring compliance to chemical storage / handling / waste disposal, create PO/PR for lab supplies, maintaining inventories of consumable materials, chemicals, and supplies.
• Arrange calibrations and preventive maintenance of instruments
• Help TS&Ds for packaging of outgoing sample and arrange shipment
• Actively participate in work group team meetings to address safety, process improvement, problem solving, and other work group, department, and functional topics.
• participate in routine safety check and lab auditing.

Job Requirements: Min Diploma/Degree in Chemistry/Chemical Process Technology/Chemical Engineering/Material Science or similar w min 2 yrs of relevant chemical lab experience

Interested candidates, please submit your resume to:

Ally Audrey Lok Xin Woon

Recruit Express Pte Ltd (Healthcare & Lifescience)

Company EA Licence number : 99C4599

Personnel EA License: R

• Supports team task to enable adequate resources to support laboratory infrastructure (E.g.:

Equipment, Method, System) needs

• Participates in the management of laboratory equipment and IT systems in QC laboratory to ensu business continuity and system data maintenance, equipment maintenance/calibration is in a stat of compliance

• Participates in method technology transfer and laboratory equipment technological refresh/introduction activities into QC Laboratory within project timeline

• Participates in QC laboratory long range planning to ensure laboratory infrastructure needs is secured and Data integrity plan is in place to support business and laboratory compliance

• Author or Review (If assigned) method transfer/qualification and equipment qualification documentation (E.g.: Reports, Protocol, change control, related quality documents or procedures) are in GMP compliance to corporate/site or regulatory requirements

• Supports and ensure timely escalation/handling of lab events or related quality actions. (E.g.:

NCR, Lab Investigation, CAPA)

• Acts as QC SME/ Supports preparation and participate in internal/external audit, audit responses, to enable a successful audit outcome

• Participate in EHS, Business Compliance, GMP and all other compliance-related matters, where applicable. Lead/supports Cl initiatives to enable laboratory performance metrics

• Carry out any other task as assigned by Supervisor

Interested applicants, please email your updated CV to or WA for more information.

We regret to inform that only shortlisted candidates will be contacted.

EA Personnel No: R

EA Personnel Name: Lim Ruo Yi, Rachel

Company EA license No.: Recruit Express Pte Ltd (99C4599)

• Author method validation protocols and execute method validation/ verification for raw material testing.
• Support the laboratory start-up activities, participate in equipment qualification activities including (but not limited to) generation of user requirement specifications, SOPs and configuration specifications.
• Perform QC test for raw material samples including compendial tests and identification tests.
• Perform QC sampling of incoming raw materials.
• Author/ revise raw material specification and other QC related documents.
• Support laboratory activities such as housekeeping and equipment maintenance.

• Bachelor's or Master's Degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biology or related life Sciences or Technology with at least 5-7 years of experience in QC raw material testing.
• Experience in method validation/ verification in the pharmaceutical or biotechnology industry
• Good understanding of good laboratory practices, good documentation practice and data integrity requirements.
• Experienced in routine laboratory operations.
• Experienced/ participated in method

• Author method validation protocols and execute method validation/ verification for raw material testing.
• Support the laboratory start-up activities, participate in equipment qualification activities including (but not limited to) generation of user requirement specifications, SOPs and configuration specifications.
• Perform QC test for raw material samples including compendial tests and identification tests.
• Perform QC sampling of incoming raw materials.
• Author/ revise raw material specification and other QC related documents.
• Support laboratory activities such as housekeeping and equipment maintenance.

• Bachelor's or Master's Degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biology or related life Sciences or Technology with at least 5-7 years of experience in QC raw material testing.
• Experience in method validation/ verification in the pharmaceutical or biotechnology industry
• Good understanding of good laboratory practices, good documentation practice and data integrity requirements.
• Experienced in routine laboratory operations.
• Experienced/ participated in method transfer, method validation and method verification for raw material testing.
• Experienced in start-ups will be ideal

• Testing of raw material, in-process control samples and final product
• Implement and maintain cGMP
• Effectively perform various laboratory techniques
• Ensure all equipment is used and maintained in GMP environment

Requirements:

• Minimum Diploma in any science related courses or above
• Experience in HPLC / GC
• Familiar with GMP / GLP environment
• Able to start immediate or within short notice period

If you meet the requirements of this role, please email a detailed resume in Word document to Cindy Wong

CEI Registration No.: R

Email:

*All information will be treated with strictest confidence. We regret that only short-listed applicants will be notified.

EA License No: 99C4599

EA Personnel No: R

EA Personnel Name: Cindy Wong Xin Yi