Qc Analyst jobs at Msd in Singapore, Singapore

Job Description

Organizational context

Reports to Director - Animal Health IT Manufacturing and Supply Contacts

Responsibilities

• Safeguards and drives the adoption of the Global SAP Template
• Reviews and approves changes before they are executed
• Build strong relationship with Local Business Process Owners (LBPO’s) and Key Users / SME’s
• Delivers input to the Global Business Process Owners (GBPO) and Team Manager for Projects and changes
• Manages medium complex projects
• Participate in workshops, support design, realization testing, training and go-live
• Support second line support team
• Connect with EPM colleagues to understand end-to-end processes and aim for improvements or impact of existing change requests

Experience / knowledge

• Broad general IT knowledge and experience
• In depth knowledge of SAP Warehouse Management (WM) solutions in an Manufacturing Environment and SAP Manufacturing (PP/MM)
• Five years or more hands on experience with SAP customizing in WM, PP and MM and preferably other Manufacturing Modules and management of medium complex projects.
• Demonstrated track record as an ERP Specialist in a batch managed industry. Pharmaceutical or Life Science is preferred.
• Knowledge and experience in computer system validation is preferred.
• Knowledge of methods and techniques for the adjustments and implementation standard software.

Education

• Higher educational or academic level
• SAP R/3 relevant modules at customizing level
• Project management certification (eg PMI) and Lean Six Sigma green belt certification is preferred

Skills

• Strongly developed analytical skills
• Excellent communication skills
• Shows drive to deliver quality work
• Customer-oriented way of working
• Can maintain contacts with people from a wide variety of backgrounds
• Mature business partner
• Fluency in English (speaking and writing)
• Creative problem solver

Other requirements

• Travel: 20-25%

What we look for …

Current Contingent Workers apply

*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.

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

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.