Overview
Be part of the team that ensures sustainable products meet standard quality and are committed to delivering to customers worldwide.
Based in Singapore, the regional hub for Asia Pacific (AP) and a 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.
Responsibilities
Ensure tests and other tasks assigned are performed in a timely manner in compliance to Standard Operating procedures, 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 requirements.
You will be trained to use various laboratory equipment ranging from particle size analyzer, FTIR, UV-Vis spectrometer, microscope, Empower CDS, HPLC, GC, etc.
Qualifications
Bachelor Degree in Chemistry / Biochemistry with prior working experience preferred
0 – 3 years’ experience in pharmaceutical analysis 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 solutions to its customers world-wide
Our Manufacturing & Supply Division is committed to be the most trusted supplier of bio-pharmaceuticals worldwide.
Our facilities, along with external contractors, suppliers, and partners, create an interdependent global manufacturing network delivering high quality, reliable supply on time, every time.
We are proud to be an equal opportunity employer, committed to fostering an inclusive and diverse workplace.
This posting has been created to pipeline talent for prospective roles that we anticipate will be needed soon in our organization.
By applying to this Pipeline Advertisement you will be submitting your interest to be contacted for roles similar to what is described in the Pipeline Advertisement.
Requisition Details
Requisition ID: P-
Seniority level: Not Applicable
Employment type: Temporary
Job function: Quality Assurance
Industries: Biotechnology Research, Pharmaceutical Manufacturing, and Veterinary Services
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