Officer / Senior Officer - Research & Development

Officer / Senior Officer - Research & Development

1 Nos.
69898
Full Time
3.0 Year(s) To 6.0 Year(s)
3.00 LPA TO 4.50 LPA
Engg Design / R&D / Product Mgt
Chemicals/PetroChemical
B.Sc - Chemistry; M.Sc / MS Science - Chemistry
Job Description:

? HPLC/GC Analysis of In-process, Intermediates, raw material, packing material and Finish
Product samples as per defined test procedure.
? Chemical Analysis of In-process, Intermediates, raw material, packing material and Finish
Product samples as and when required.
? Sampling of intermediate, finished product and raw material samples as and when required.
? To maintain Raw Data Sheet and log book.
? Responsible for qualification of working standard, Impurity standard and Intermediate
standard as and when required.
? To ensure Housekeeping in Lab and maintain GLP practices.
? Perform all the activities in laboratory as per defined procedure and as per GLP requirements.
? Responsible for procurement, qualification and maintenance of Intermediate standard,
working standard.
? If any instrument should be not done well then inform to Incharge of Quality control
department.
? Analysis should be done as per time to time based on production requirement.
? Responsible for on the job training given to new Joinee employee & Lab attendent as and
when required.
? Analysis of R & D sample and sample of process development material.
? Activity of process development work and analysis for the PD lab sample

Key Skills :
Company Profile

--- --- --- engages in the development of Active Pharmaceutical Ingredients (API) and New Chemical Entities (NCE), API intermediates, Regulatory Starting Materials (RSM), Basic Starting Materials, Key Building Blocks, and Xanthine Derivatives for use in clinical testing and commercial production. In addition to process R&D, we provide stability studies, scale-up and process optimisation, process validations, and commercial manufacturing.

Our six manufacturing plants receive innovations from our two R&D centres. These cutting-edge manufacturing facilities have received accreditation from a number of agencies, including the USFDA, EU GMP, EDQM, KFDA, and COFEPRIS.

This enables APL to deliver our entire range of services to our international clientele for their needs in API and drug substance manufacturing in India.

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