Merck Job Vacancy

PT Merck Tbk. is a leading multinational company in the pharmaceuticals and chemicals business in Indonesia. Founded in 1970, PT Merck Tbk. went public in 1981. The majority of the shares are held by the Merck Group, headquartered in Germany, which is the oldest pharmaceuticals and chemicals company in the world.
In pharmaceuticals, we manufacture and market well-known pharmaceutical brands such as Neurobion®, Sangobion® and Glucophage®. In the Chemicals business, Merck markets a whole range of laboratory reagents, pigments and other specialty chemicals.

Our vision is to make a difference in the lives of people globally through our innovative medicines, vaccines, biologic therapies, consumer health and animal products.  We aspire to be the best healthcare company in the world and are dedicated to providing leading innovations and solutions for tomorrow.

We have made it our mission to provide innovative, distinctive products and services that save and improve lives and satisfy customer needs, to be recognized as a great place to work, and to provide investors with a superior rate of return.

Merck and Schering-Plough merged in November 2009 to create a new company. Today, we are the second-largest healthcare company in the world. We also are a global leader in consumer products and animal care.

Both Merck and Schering-Plough have a long and rich history of working to improve people's health and well-being. Through the years, our researchers have helped to find new ways to treat and prevent illness - from the discovery of vitamin B1, to the first measles vaccine, to cold remedies and antacids, to the first statins to treat high cholesterol. Our scientists also have helped develop many products to improve animal health, including vaccines and antibiotics.

While we are proud of our past, we are enthusiastic about the future of this new company and we are excited to help create a healthier, brighter future for people around the world.

Quality Control Supervisor (code: QC SPV)
Jakarta Raya

  • Ensure  that quality and HSE system & procedures (SOPs) are implemented in QC activities  inline with  quality standards/ cGMP, GLP, ISO14001 & OHSAS 18001;
  • Ensure that the QC‘s SOPs, Testing Procedures, Specifications and other QC document are proper and valid;
  • Ensure that the Out of Specification procedure is implemented  & reported;
  • Responsible to coordinate the QC activities, improve productivity and efficiency;
  • Responsible to review testing results of products & monitoring and ensure that the results comply with the specifications before forwarding to QC Manager;
  • Responsible for Analytical Method Validation and completeness of Analytical Method Validation Report.


  • Bachelor degree from a reputable university, major Chemisry, Pharmacy;
  • Experienced in Pharmaceutical industry / QC Laboratory;
  • A Pharmacist with at least 3 years experiences in QC Laboratory (Chemical, Instrumentation and Microbiological);
  • At least 2 years experiences as a QC Supervisor;
  • Knowledge on GLP, cGMP standard and knowledge on work safely in QC Lab. 
  • Knowledge on QC Instrumentation such as HPLC, Spectrophotometer, etc.
  • Knowledge related to QC test methods, e.g. microbiological test, titrimetry, chromatography, spectrophotometry, etc. and equipment calibration. 
  • Good communication skill, good team work and able to lead and develop people.

QA Compliance Supervisor
Jakarta Raya

  • Ensure regulatory compliance for all preparation and review of all regulatory dossier (including all technical supporting document), for new and existing products (local and export).
  • Packaging material development coordinator, ensure timely packaging material artwork preparation (new or changes) up to OK for printing. QA Review for packaging material artwork.
  • Coordinate and excute vendor monitoring system based on approved Standard Procedure Supplier Quality Management for all GxP vendors, including vendor audit.
  • Coordinate Raw Material and Packaging Material new source qualification activities, monitor the progress, coordinate the sample testing, trial, stability study, prepare trial order report and assesment for the next step in coordination with Purchasing, Development, Production, QC and SCM Pharma
  • Technical agrrement master data and preparation.
  • Stability study monitoring and review for all routine and non routine stability.
  • Prepare all Standard Operating Procedure as above responsibilities, review periodically and ensure the validity.
  • Prepare regular monthly and annual status reporting for all above responsibilities.


  • Candidate must possess at least a Bachelor's Degree, Master's Degree / Post Graduate Degree from Pharmacy/Pharmacology or equivalent.
  • Required language(s): English
  • At least 3 year(s) of working experience in the related field is required for this position.
  • Preferably Coordinator/Supervisors specializing in Quality Control/Assurance or equivalent.
  • Knowledge on current Health Authorithy regulation and basic GMP requirement
  • Knowledge on ACTD requirements
  • ERP Master data maintenance knowledge
  • Posses computer skill, e.g. Mocrosoft Office, etc
For further information please check our web:

If you meet the above requirements, please submit your application, CV, related supporting documents, and a recent photograph, mail to:



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