Seeking a Quality Control Chemist for 6+6 months for a pharma company in Singapore

Project status
Project posted
15th February 2016
Project duration (approx.)
6.0 Months
Budget (approx.)
$300 / day
Industry
Pharmaceuticals
Area of expertise
Operations
Consultant location
On-site
Location
Singapore

Background & Objectives

Seeking a Quality Control Chemist to work on a 6 month project (can be extended to 12 months) for a pharma company in Singapore.

Planned start date: 4th April

Please apply by 17 Feb to be considered.

Key deliverables

Responsibilities:
• Write and review working procedures, SOPs and OJTs for the laboratory.
• Perform analytical testing of QC stability samples promptly in accordance to procedure and annual stability report is published.
• Conduct OOS investigations.
• Perform maintenance and troubleshooting of laboratory equipment.
• Perform equipment qualification and analytical method validation.
• Perform laboratory equipment verification and calibration in accordance to procedures.
• Perform basic microbiological testing such as total microbial count, endotoxin level in water and products.
• Act as back up for QC Analyst as and when required.
• Conduct routine checks and inspections on assigned tasks eg. Chemical store, safety equipment, calibration of equipment etc.
• Ensure all documentations and quality records are conducted in accordance to GMP/GLP requirements and that they are filed in accordance to existing policies.
• Participate actively and contribute to company teams/projects eg. LIMS, CDS, Safety, WIP, Analytical Method Transfer Exercise etc.
• Train fellow colleagues on written procedures and SOPs pertaining to equipment operation, test methods and general laboratory operation
• Perform review and approval of testing in LIMS
• Proactive trending of test results
• Prepare test results for Annual Product Review Report reporting.
• Provide QC support in testing of Production and Stability samples, troubleshooting for OOS results, calibration and maintenance of laboratory equipment and review of quality documents

Consultant requirements

•Degree in Chemistry or a Diploma in Chemical Process Technology with at least 5 years of relevant experiences.

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