1,070 Qc Analyst jobs in Singapore

QC Analyst (Lab/ Shift/ Jurong/ 1 Yr Contract)

More information:

• Salary Up to $4,800 depending on experience
• Location : Gul Circle
• Shift Work with shift and transprot allowance
• Immediate Vacancy

Our client, a well known MNC company in BioPharmaceutical Industry, located in the West is looking for QC Analyst.

Job Purpose

• Reporting to QC Chemist, the incumbent will carry out QC analyses in compliance with Laboratory and Analytical Methods ensuring quality, cGMP, heath, safety and environmental standard are met. Assist in other functions such as documentation and preparation of standard operating procedures.

Responsibilities

• Assist in carrying out on the job training of other QC Analysts, incorporating cGMP and safety procedures.
• Perform and carry out analytical testing in compliance with specifications, Analytical Methods, Laboratory Methods and pharmacopoeia requirements.
• Assist in monitor the calibration and maintenance program for laboratory instruments / equipment and ensure compliance with established schedules.
• Assist in qualification of laboratory equipment and validation of analytical methods.
• Ensure that analyses are carried out and reported in accordance with GLP (Good Laboratory Practices). Ensure that analyses are completed on time and are consistent with business requirements.
• Assist in conducting OOS and atypical results investigation.
• To ensure that qualification, preventive maintenance and calibration of laboratory equipment are carried out.
• Report and trend test results.
• Planning and assurance of cGMP compliant quality testing and documentation according to schedule.
• Prepare laboratory reagents in compliance with GLP and laboratory SOP requirements. Source reagents / laboratory consumables keeping in view department budget targets.
• Assist in other functions such as preparation of standard operating procedures and Assist documentation etc and participate in departmental activities as and when required. Maintenance and development of all required laboratory documents (i.e. raw data sheets, log books).
• Responsible for electronic raw data handling in compliance with regulations and guidelines.
• Responsible for inspection and audit preparedness with respect to cGMP and EHS issues.
• Ensure safe working in the laboratory by practicing and communicating safety.
• Other responsibilities that are not included in the above but are related to quality control and in accordance to internal guidelines and SOP

Requirements:

• Preferably possess a years' hands-on anlaytical testing experience in a lab environment, from the pharmaceutical industry.
• Familiar with analytical equipments (eg. HPLC, GC etc)
• Must be willing to work shift on rotational basis.
• Must be analytical, methodical and quality conscious.
• Good knowledge of FDA regulations and cGMP.
• Preferably possess a Diploma in chemistry/ chemical process technology / bio-process technology; or a ITE graduate.

Lim Pey Chyi - Apple.lim@ manpower.com.sg.

Recruitment Consultant (R2090579)

Manpower Staffing Services (S) Pte Ltd

EA Licence: 02C3423

Salary: up to $4500

Duration: 1 year contract

Working Days & Hours: Mon-Fri Office Hours

Location: Tuas (pickup at Tuas Crescent)

Job Description:

Scope will be testing (biochemistry/microbiology) / buffer preparation/paperwork support

Job Requirements: Min Degree in Life Sciences w min internship experience in HPLC and GC in Pharmaceutical industry

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: R21102307

The Opportunity:

• Our client, a MNC Food Manufacturing Company
• Location: Boon lay
• Salary: Up to $2500

Job Responsibilities:

• Perform conformance testing on both raw materials and finished goods to ensure compliance with standards.
• Prepare, update, and manage inspection documentation and quality records.
• Work closely with management to support and implement quality improvement initiatives.
• Liaise with suppliers to address and resolve quality-related matters.

Job Requirements:

• Nitec in any field
• Good team player

Next Step:

• Prepare your updated resume (please include your current salary package with full breakdown such as base, incentives, annual wage supplement, etc.) and expected package.
• Simply click on 'Apply here' to drop your resume.
• All shortlisted candidates will be contacted.

Saw Wei Xiang

Direct Line: 6697 7975

EA License No: 91C2918

Personnel Registration Number: R24123075

Job Description / Responsibilities:
Ensure compliance to statutory and corporate requirements related to Health, Safety, Environment and Quality.
Conduct quality checks on final product according to established procedures.
Keep proper record of all analysis results.
Identify and raise a nonconformance form when the product quality does not meet the specification.
Provide support to the Production, R&D or Sales departments on an ad-hoc basis.
Perform calibration and maintenance of lab equipment as planned.
Properly store and label all retained samples and documentation in the designated storage area.
Qualification and Requirements:
Secondary graduate, Nitec / Higher Nitec, diploma.
No prior experience required.
#J-18808-Ljbffr

Job Description & Requirements
Conducts daily laboratory analysis of raw materials, quality control stability sample testing, in-process testing, finished products and other related testing.
Prepare test solutions, volumetric solutions, standardization of volumetric solutions and reference standards.
Able to plan, schedule and assisting in supervising QC testing for finished product, raw materials & stability products.
Assist to ensure QC testing of products are completed on time, review / approve test report and able to forward the test reports /or samples to QA when required.
Able to conduct laboratory investigation when required.
Ensures and maintains cleanliness and safety of the QC laboratory according to the Good Laboratory Practices.
Performs routine calibration & preventive maintenance for analytical instrument and report any deviation.
Assists the QC team in new assigned projects.
Performs products validation, cleaning validation and method validation.
Conducts microbiological testing and environment monitoring as backup if assigned.
Any other ad hoc tasks assigned.
Requirements:
Minimum Diploma holder in Chemistry / Chemical Engineering / Bioscience / Life Science / Pharmaceutical / QA & QC.
Some prior experience preferred in QA & QC.
Preferred to have experience in HPLC, UV, IR, Dissolution tester.
Other information
:
5 days work week .
Permanent position with 2 years lock-in period.
#J-18808-Ljbffr

Job Description & Requirements

• Conducts daily laboratory analysis of raw materials, quality control stability sample testing, in-process testing, finished products and other related testing.
• Prepare test solutions, volumetric solutions, standardization of volumetric solutions and reference standards.
• Able to plan, schedule and assisting in supervising QC testing for finished product, raw materials & stability products.
• Assist to ensure QC testing of products are completed on time, review / approve test report and able to forward the test reports /or samples to QA when required.
• Able to conduct laboratory investigation when required.
• Ensures and maintains cleanliness and safety of the QC laboratory according to the Good Laboratory Practices.
• Performs routine calibration & preventive maintenance for analytical instrument and report any deviation.
• Assists the QC team in new assigned projects.
• Performs products validation, cleaning validation and method validation.
• Conducts microbiological testing and environment monitoring as backup if assigned.
• Any other ad hoc tasks assigned.

Requirements:

• Minimum Diploma holder in Chemistry / Chemical Engineering / Bioscience / Life Science / Pharmaceutical / QA & QC.
• Some prior experience preferred in QA & QC.
• Preferred to have experience in HPLC, UV, IR, Dissolution tester.

Other information :

• 5 days work week .
• Permanent position with 2 years lock-in period.

This role utilizes microbiology laboratory skills to perform utilities sampling, environmental monitoring, and
microbiological testing for all type of sample/product/materials while ensuring that analysis is performed
according to established Standard Operating Procedures (SOPs), Validated / Verified Methods & current
Compendia

Key Responsibilities:

• Perform routine and non-routine microbiological testing of various samples, products, and materials.
• Ensure proper maintenance and calibration of QC laboratory equipment and systems to maintain full cGMP compliance.
• Support and perform validation of microbiological test methods on laboratory equipment in accordance with cGMP guidelines.
• Prioritize workload to ensure timely completion of documentation and testing activities.
• Provide general support to the microbiology laboratory, including day-to-day operations.
• Assist in laboratory investigations as required.
• Prepare and compile laboratory data for trending and statistical analysis when necessary.
• Contribute to continuous improvement initiatives to optimize testing procedures and improve operational efficiency.
• Ensure project tasks progress according to planned timelines and quality expectations.
• Perform other duties or projects as assigned by the manager.

This role utilizes microbiology laboratory skills to perform utilities sampling, environmental monitoring, and
microbiological testing for all type of sample/product/materials while ensuring that analysis is performed
according to established Standard Operating Procedures (SOPs), Validated / Verified Methods & current
Compendia

Key Responsibilities:

• Perform routine and non-routine microbiological testing of various samples, products, and materials.
• Ensure proper maintenance and calibration of QC laboratory equipment and systems to maintain full cGMP compliance.
• Support and perform validation of microbiological test methods on laboratory equipment in accordance with cGMP guidelines.
• Prioritize workload to ensure timely completion of documentation and testing activities.
• Provide general support to the microbiology laboratory, including day-to-day operations.
• Assist in laboratory investigations as required.
• Prepare and compile laboratory data for trending and statistical analysis when necessary.
• Contribute to continuous improvement initiatives to optimize testing procedures and improve operational efficiency.
• Ensure project tasks progress according to planned timelines and quality expectations.
• Perform other duties or projects as assigned by the manager.

Job responsibilities:

· To provide guidance to warehouse personnel, oversee stock level, purchase orders, schedule agreements, expedite delivery of goods.

· Assist in goods release in batches for distribution or usage

· Oversee quality checks for incoming stocks and ensure quality compliance

· Liaise with laboratory on product non-conformance issue for feedback to supplier

· Conduct returned goods and assist in end-to-end disposition of non-conforming goods

· Schedule and review preventive maintenance for critical equipment

· Provide quality oversight to quality activities in laboratory operations including documentation and validation testing

· Schedule and review Installation, operational and performance qualification.

· Assist and support in regulatory inspections and audits

· Perform audit check on laboratory operations

· Maintain, and biennial review SOP and forms

· Review and approve change control plan

· Review Training and competency adequateness

· Review Corrective and preventive action adequateness

· Non-Conformance and Error trending analysis

Requirements

· Familiar with the standards of Good Manufacturing Practices (GMP).

· Familiar with various test standards or processes, eg. RCPA-FBC, CAP, etc.

· A team player working with teammates under the supervision of Assistant Manager, Quality Management.

· Able to co-operate with colleagues, plan and execute daily tasks according to Standard Operating Procedures (SOPs).

· Willingness to take up other duties required.

· Must be willing to work during rostered weekends and public holidays.

· Degree in biological science is a must.