QC Analyst (Pharma/ Shift/ 1 Yr Contract , Renewable)

Manpower Singapore; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A leading company in the pharmaceutical sector is looking for a QC Analyst for a 1-year renewable contract. The role involves performing analyses in compliance with regulatory standards, assisting in training, and ensuring quality control processes. Candidates should have at least 3 years of experience and be knowledgeable in FDA regulations and cGMP guidelines.

Benefits

Completion Bonus

Qualifications

• Minimum of 3 years' hands-on experience in a similar capacity required.
• Good knowledge of FDA regulations and cGMP.
• Willingness to work shifts on a rotational basis.

Responsibilities

• Carry out QC analyses ensuring compliance with quality standards.
• Assist in training new QC Analysts and documentation preparation.
• Manage calibration and maintenance of laboratory equipment.

Skills

Analytical

Methodical

Quality conscious

Resourceful

Team player

Education

Diploma in Chemistry/Chemical Process Technology/Bio-process Technology

Job description

QC Analyst (Pharma/ Shift/ 1 Yr Contract , Renewable)

Location : Gul Circle
Basic Salary (Up to $3800)
Completion Bonus 1 Month

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

• Possess minimum of 3 years' hands-on experience in similar capacity.
• Must be willing to work shift on rotational basis.
• Must be analytical, methodical and quality conscious.
• Good knowledge of FDA regulations and cGMP.
• Must be resourceful, conscientious, dedicated and a good team player
• Preferably possess a Diploma in chemistry/ chemical process technology / bio-process technology; or a ITE graduate.

Lim Pey Chyi - [e-mail]
Recruitment Consultant (R2090579)
Manpower Staffing Services (S) Pte Ltd
EA Licence: 02C3423

Desired Skills and Experience

Possess minimum of 3 years' hands-on experience in similar capacity.
Must be willing to work shift on rotational basis.
Must be analytical, methodical and quality conscious.
Good knowledge of FDA regulations and cGMP.
Must be resourceful, conscientious, dedicated and a good team player
Preferably possess a Diploma in chemistry/ chemical process technology / bio-process technology; or a ITE graduate.

Apple, Pey Chyi Lim EA License No.: 02C3423 Personnel Registration No.: R2090579

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