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QC Tech, QC, Jurong

Requisition ID:  35694
Date:  Jul 9, 2021
Location: 

Singapore, Singapore, SG

Department:  Quality

Working at West means having an opportunity to work by the side of our patients and customers, our global team members and the communities in which we operate – which all help contribute to a Healthier World.

At West, we are by the side of patients. The work we do impacts patients’ lives each and every day – our products are a critical part of healthcare delivery and we are proud of the role we play to improve patient health. We work by the side of our team members. We come together as one global team to deliver for our customers and help them address their challenges. We are a diverse, close-knit community of professionals, where everyone has a voice and opportunity to learn and grow through mutual trust and respect. With a 95 year plus history, we have a track record for success, which includes reported sales of $1.84B in 2019. We serve by the side of our community. Giving back is in our DNA—our team members across more than 50 sites globally are involved with hundreds of charities that have special meaning to them through our West Without Borders team member-led giving program.

 

Responsibilities:

  • Perform auxiliary / component incoming inspection per procedure.
  • Perform mold-line in-process inspection per procedure.
  • Perform semi-finish /  finished goods inspection (visual / dimensional / document review) per procedure.
  • Participate in product characteristics trend monitoring and effective escalation and follow-ups.
  • Ensure all inspection activities are accurate and adequately documented (e.g. SAP system, Ms. Office, etc.)
  • Exercise appropriate control to documentation records and retained samples.
  • Ensure all related calibration activities are timely and appropriately performed.
  • Support non-routine assignments initiated by supervisors (e.g. Handle customer complaint, Mold-monitoring activities, etc.)
  • Other duties as assigned by superior.

 

Education and Experience:

  • Min. ‘O’ level, or equivalent qualification.
  • Computer literate (e.g. Ms. Office skills).
  • Good communication & teamwork skills.
  • Self-motivated and positive thinking.
  • Min. 1 year work experience in QA/QC related activities.
  • Added advantage with cGMP and ISO working experience.
  • Preferably with exposure to medical device, pharmaceutical or related manufacturing environment.

West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status.  If you have a disability or special need that requires accommodation, please send an email to peggy.tayloe@westpharma.com. Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening and/or a pre-employment drug screening.

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