IPQA, Document Cell, Market Complaints, Market Recall, 00S, 00T, Process, Cleaning Validation, Review of BMR & BPR, Training, QMS.

B.Pharm, M.Pharm, B.E, B.Tech. with 6 to 10 years of experience supervising and controlling production areas like Aseptic Filling, Vial Washing, Autoclave and Lyophilizer. Exposure of machine qualification activity will be added advantage.

This is a non-supervisory position in Reference Standard Laboratory responsible for performing the required tests as part of the project and maintaining the GLP environment in the Laboratory.

Work both independently and as part of intra, inter-departmental teams to ensure that all work is completed in a timely manner to meet both business and quality standards.

Regular reporting in Envision. To maintain the desired call average per month and frequency of calls to be done as expected with respect to Dual Ranking of Customers. Call objectives should be managed to give focus on various Products as agreed.

Support DM Delivery Leads to maintain CDM specified systems and types of deliverables, milestone achievements, risks and mitigations and data transfer agreements, and other study administrative needs.

Diploma in Pharmacy from a recognized University, Institution. Should be a registered Pharmacist under the Pharmacy Act, 1948. 

Master degree in any branch of Chemistry or Pharmaceutical chemistry, Pharmaceutical analysis, quality assurance. 02 years experience in analysis of ASUH drug using sophisticated instruments.

Ph.D. in Biochemistry, Microbiology, Biotechnology, Pharmacology, Life sciences. The candidate must have at least one research publication in SCI-indexed Journals.

B.Sc in Life Sciences, Microbiology, Biotechnology, Biochemistry, or any other relevant discipline from a recognized institution. OR M.Sc. with minimum 60% marks. With experience in size exclusion chromatography, western blotting and Flow Cytometry will be preferred.

Will be responsible for managing Discovery, Development projects end to end. Adept at managing project milestones, budget and stakeholders. Should have excellent communication skills. Must be a good negotiator and must have hands-on knowledge in MS Project, MS Excel.

1 to 4 years in Quality Control, Microbiology, Molebio, Quality Assurance Experience Biosimilars, vaccines, Sterile industry is required.

Having Experience in Environmental Monitoring, Water Testing, In process Sampling, Analysis of Bulk Water, Finished and API by MLT, Bioburden, BET, Sterility, PET and Antibiotic Assay.

To handle all kind of lab instruments and experience to perform AMV and Documentation EM Monitoring, Water testing. Trend preparation, Microbial Testing, SOP and Protocol and other micro related activity

M.Sc. in Organic Chemistry, Analytical Chemistry Or M.Pharmacy in Pharmaceutical Analysis. Experience on the analysis of small organic molecular using various analytical techniques such as HPLC, MS, etc.

Masters in Pharmaceutical Science, Pharmaceutics, Pharmaceutical Technology, Industrial Pharmacy, Analytical Chemistry, with First class or equivalent grade at the preceding degree B. Pharm, B.Sc with a good academic record throughout. The CoE will primarily focus on the development and research of Novel Drug Delivery Systems (NDDS), creating a collaborative platform where academic expertise and cutting-edge research converge to drive innovation in this critical area of pharmaceutical science.

Post graduate degree in any branch of life sciences, biotechnology or Graduate, Post Graduate in any branch of life sciences or biotechnology or Post Graduate in any branch of life sciences, biotechnology selected through National Eligibility Tests-CSIR UGC NET including Lectureship and GATE.

Post Graduate Degree in life sciences OR Graduate, Post Graduate degree in professional course. M.V.Sc, M.Tech, MSc. Degree in Biotechnology Biochemistry, Microbiology, Immunology.

B.Pharm / M.Pharm; To perform equipment qualification, utility qualification activity with proper documentations. To perform Computer system validation. To investigate deviation, change request, OOS, market complaint etc.