Associate Specialist Quality Control 1 Year Contract

Singapore, Singapore

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\xe2\x80\x99s 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, acrossReporting 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 API 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 (SOPs) and laboratory test methods.
  • Perform and maintain good laboratory housekeeping (5S), 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.
  • 1 to 3 years\xe2\x80\x99 experience in pharmaceutical analysis is preferred Experience in particle size analyser, HPLC, FTIR, Karl Fischer Titrator with technical competency is preferred.
  • Demonstrated knowledge and understanding of cGMP, GLP, and associated regulatory expectations related to Pharmaceutical Analytical testing is preferred
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
Our Manufacturing & Supply Division is committed to be the most trusted supplier of bio-pharmaceuticals worldwide. Our facilities, along with our external contractors, suppliers, and partners, create an interdependent global manufacturing network that\xe2\x80\x99s committed to delivering a high quality, reliable supply to customers and patients on time, every time.We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another\xe2\x80\x99s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.Current Employees applyCurrent Contingent Workers applySearch Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.Employee Status: Temporary (Fixed Term)Relocation: No relocationVISA Sponsorship:Travel Requirements:Flexible Work Arrangements: Not ApplicableShift:Valid Driving License:Hazardous Material(s):Job Posting End Date: 08/16/2024*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.

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Job Detail

  • Job Id
    JD1442675
  • Industry
    Not mentioned
  • Total Positions
    1
  • Job Type:
    Full Time
  • Salary:
    Not mentioned
  • Employment Status
    Permanent
  • Job Location
    Singapore, Singapore
  • Education
    Not mentioned