Lupin Limited Walk In Interview 2023 .Lupin Limited Notification full details below..Intrested and eligible candidates can attend Interview on scheduled time and venue.Lupin Limited is one of India’s largest manufacturers of bulk actives and formulations. The principal bulk actives manufactured by it include Rifampicin, Pyrazinamide, Ethambutol (anti-TB), Cephalosporins (anti-infectives) and cardiovasculars. The company also possesses competencies in phytomedicines, in which medicines are made out of plant and herbal resources supported by the discipline of modern medicine.
Vacancy details:
- Role: Officer – QC(Biotech)
- Qualification: M.Sc. Microbiology
- Total Experience – 2 – 5 Years.
Job Description: Greeting from Lupin Limited !!!!!!!!!!
Important Details :
- Location: India- Pune Biotech, MH, IN
- Post of date 19/09/2023
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Fact to face Interview.
- Rounds of Interview: HR
JD –
1) Candidate should have good knowledge about all microbiological related activity, Environmental monitoring of classified area, Water analysis,
Bioburden Analysis, BET.
2) Sampling, testing of water samples. Media Preparation required for different analysis. Sub-culturing, serial dilution of cultures and CPT. To perform population determination of biological indicators. To perform the organism identification.
3) To prepare microbiology related SOPs/STPs, EOPs and GTPs/QRMs/
Investigation summary etc.
4) Operation of Daily pH, balance calibration, autoclave, DHS, Incubators, Air
Samplers, and non-viable particle counter.
5) To report any deviation/out of specification results and safety risks to the supervisor as and when observed.
6) Qualification of equipment, autoclave, DHS etc.
7) The candidate should be familiar with cGMP requirements, Change control, Deviation, Out of Specifications, Sample Management, Stability Management and investigation tools.
8) Review of environmental monitoring and water analysis trends, and daily reports.
9) To ensure cGMP compliance and maintain the laboratory in audit ready condition.
