MSD Associate Specialist Quality Control - One Year Contract 

Singapore, Singapore 

164737965

Job Description

THE OPPORTUNITY

• Be part of the team that ensures sustainable products meets standard quality and committed to deliver to customers worldwide!
• Based in Singapore , the regional hub for Asia Pacific (AP) and top-ranked biopharmaceutical company on the Straits Times and Statista’s list of Best Employers in Singapore for three consecutive years (2021, 2022, 2023).
• Join the premier biopharmaceutical company that has been in Singapore for more than 25 years and in AP for over 60 years.

Our Quality group ensures every single material inside our products is manufactured, processed, tested, packaged, stored and distributed aligned with our incredibly high standards of quality and meets all regulatory requirements. Partnering across our internal manufacturing facilities, external contract manufacturers and suppliers we create an interdependent global manufacturing network committed to deliver a compliant, reliable supply to customers and patients on time, every time, across

Reporting to Lab Manager, Quality Control, the Chemist is responsible for performing and reviewing laboratory testing of raw materials, in-process samples, intermediates, final drug substances and stability batches in Active Pharmaceutical Ingredients Laboratories.

WHAT YOU WILL DO:

Critical responsibilities but not limited to:

• Ensure tests and other tasks assigned are performed in a timely manner in compliance to Standard Operating procedures, requirements specified in our company Quality and Safety Standards, regulatory dossiers and pharmacopoeia.
• Manage and perform calibration, maintenance and qualification of laboratory equipment.
• Participate in laboratory efficiency improvement tasks, analytical method transfer, development, validation and equipment qualifications activities.
• Conduct and support Laboratory investigation on laboratory equipment failure, OOT and OOS and identify the root cause and its report writing.
• Review and revise Standard Operating Procedures and laboratory test methods.
• Perform and maintain good laboratory housekeeping, inventory and in-house stock control, reference standards, chemical reagents, and consumables.

After one year on the position, you will be competent to perform most of the laboratory testing following cGMP, data integrity and GLP requirement. You will have been trained to use various laboratory equipment ranging from such as particle size analyzer, FTIR, UV-Vis spectrometer, microscope, Empower CDS, HPLC, GC, etc.

WHAT YOU MUST HAVE

• Bachelor Degree in Chemistry / Biochemistry with prior working experience preferred
• 0 – 3 years’ experience in pharmaceutical analysis is preferred. Fresh graduates with relevant internship experience will be considered
• Experience in particle size analyser, GC, HPLC, FTIR, Karl Fischer Titrator, Potentiometric titrators with technical competency is preferred
• Demonstrated knowledge and understanding of cGMP, GLP, and associated regulatory expectations related to Pharmaceutical Analytical testing is preferred
• Position can be on regular hours or 12 hours rotating shift (night/day including Sat/Sun). If on shift, shift allowance will be provided

WHAT YOU CAN EXPECT

• Limitless opportunities across various areas in Manufacturing; well-structured career path
• A state-of-the-art facility that delivers solution to its customers world-wide

Current Contingent Workers apply

Temporary (Fixed Term)

No Travel Required

Not Applicable

*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.

A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.