Every day, our consultants work with thousands of candidates to help them find the right fit for their next role. Last year, we placed over 0 candidates into permanent roles.

Latest Jobs

• 21 Nov 2018

  QC Supervisor, Raw Material

  Singapore

  Permanent Position

  We are working with a client from Biopharmaceutical Manufacturer (European MNC) and they are looking for a QC Supervisor, Raw Material to join their organisation.
  Job Description

  • Manage all activities establishing and maintaining a raw material lab
  • All testing is performed and documented in accordance with written specifications and in accordance with local/international regulations.
  • Establish and maintain a raw material lab in full cGMP-compliance.
  • Responsible to install lab equipment and qualify/validate lab equipment for intended use in QC raw material lab to support testing of all incoming raw materials.
  • Responsible that training is performed and documented for lab personnel in order that all analysts are qualified to perform the testing under cGMPs.
  • Monitoring and optimization of work flows and methods/procedures, pursue an ongoing quality assurance program
  • Leading Laboratory investigations and facilitates root cause finding.

   

  Expires on 21 Dec 2018

  Posted By

  Axel Lee Kian Heng (Reg No: R1110163)

  Tel: +65 6738 6228

  axellee@pplesearch.com

  apply now

  Share this:

  Requirements

  • PhD or MSc or BS in Pharmacy, Biotechnology, Chemistry or related area or equivalent experience
  • PhD: 6 to 8 years related experience with 2 to 3 years in managing a lab
  • Related experience should be in GMP-regulated industries in Quality Control.
  • Must have a working knowledge of FDA and ex-USA regulatory requirements as well as industry quality management tools, standard, and quality systems.
  • Must have an understanding of pharmaceutical industry trends and practices. Broad cGMP experience is required with knowledge and understanding of manufacturing, quality control, and validation requirements and activities.

  Kindly indicate your current/last salary details and your notice period

  Interested candidates kindly forward your CV to axellee@pplesearch.com (Axel Lee Kian Heng, Reg No: R1110163)
  Feel free to forward this great opportunity to someone who would be a great fit for this role.
   

  All information will be kept strictly confidential. We regret to inform that only successful applicants will be contacted.

  PeopleSearch Pte Ltd
  EA License No: 16S8057

• 21 Nov 2018

  Senior / QA Operations Specialist

  Singapore

  Permanent Position

  We are working with a Biopharmaceutical Manufacturer (European MNC) and they are looking for a Senior / QA Operations Specialist to join their organisation.
  Job Description

  • The Senior QA Operations (Ops) Specialist has responsibility to ensure that all aspects of the operational business comply with cGMP legal and regulatory requirements and Company Manual.
  • Representative of the Operational QA in project teams (e.g. Master Batch records, equipment, cleaning and process validation).
  • Participate in the general QA activities and assist in the different areas of the QA function (Compliance /Release/Change control)
  • Manage quality issues and investigations (e.g. deviations, trends, Out of Specification) with the respective departments
  • Perform review of GMP relevant documents for compliance with Standard Operating Procedures across several customer groups (e.g. TEDI documents, SOPs, documents etc.), including filing and archiving documents owned by QA

  Expires on 21 Dec 2018

  Posted By

  Axel Lee Kian Heng (Reg No: R1110163)

  Tel: +65 6738 6228

  axellee@pplesearch.com

  apply now

  Share this:

  Requirements

  • Masters or Degree in Natural Sciences (Biotech preferred) or related experience in sterile manufacturing
  • Minimum 2 to 8 years experience in pharmaceutical GMP-regulated industries (Biotech preferred), with a minimum of 5 years in Quality Assurance and/or Compliance
  • Strong experience with health authority inspections from major Health Authorities, e.g. USA, EMEA, Canada, Japan, Brazil etc.
  • Related experience should be in GMP-regulated industries in Quality systems and Documentation
  • Must have a working knowledge of FDA and ex-USA regulatory requirements as well as pharmaceutical industry quality systems

  Kindly indicate your current/last salary details and your notice period

  Interested candidates kindly forward your CV to axellee@pplesearch.com (Axel Lee Kian Heng, Reg No: R1110163)
  Feel free to forward this great opportunity to someone who would be a great fit for this role.

  All information will be kept strictly confidential. We regret to inform that only successful applicants will be contacted.

  PeopleSearch Pte Ltd
  EA License No: 16S8057