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.
To accelerate our growing business, we offer talented individuals who have passion to excel theircareer to apply as:
Quality Control Supervisor (code: QC SPV)
Jakarta Raya
Responsibilities:
- 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.
Requirements:
- 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.
Regulatory (Contract)
Jakarta Raya
Responsibilities:
- Prepare/ Assess existing product documentation (dossier) for medical devices (according to DEPKES/ BPOM/ASEAN requirements);
- Prepare/ Assess existing product documentation (dossier) for bio-science products (according to DEPTAN requirements);
- Prepare/ Assess existing product documentation (dossier) for imported products and chemicals regulated by the government ((according to DEPDAG/ director generals and foreign requirements).
Requirements:
- Candidate must possess at least a Bachelor's Degree of Pharmacy/Pharmacology or equivalent.
- At least 1 year(s) of working experience in the related field is required for this position, but fresh graduates are welcome to apply.
- Good Communication Skills, tidy and sistematic.
- Fluent in english and also familiar with Ms Office (good typing skill).
- Contract positions available (about 3-4 monts).
For further information please check our web:
www.merck.co.id
If you meet the above requirements, please submit your application, CV, related supporting documents, and a recent photograph, mail to:
opportunity@merck.co.id
