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Quality Control, Pharma Industry, R and D, CSIR, Food Industry, Pathology, Medical Writing, coding

Required Research Associate-Early-stage Ph.D. or M.Sc. in Biotechnology, Microbiology, Molecular Biology, Genetics, or Life Sciences.

Dr. D. Y. Patil Dental College & Hospital, DPU, Pune is hiring  Research Associate Detail are provided below  1. Position:  Research Associate 2. Job Type : Full-time (Immediate Joining) 3. Remuneration:  ₹ Commensurate with qualifications and institutional norms 4. Key Responsibilities:  -Execute nucleic acid extraction, PCR/qPCR, gel electrophoresis, and biobanking. -Ensure preventive maintenance of equipment and quality upkeep as per GCLP norms. -Manage the EQA program and NABL documentation. -Assist with grant applications, publications, and manuscript drafting. -Collect, code, process, and document clinical samples as per GCLP norms. -Maintain experimental databases, laboratory records, and inventory files. -Coordinate workflows with clinicians, scientists, and postgraduate students. 5. Qualification and Skills :  Education:  Early-stage Ph.D. or M.Sc. in Biotechnology, Microbiology, Molecular Biology, Genetics, or Life Sciences. C...
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Required Executive Production Mammalian - B.Tech in Biotechnology / Post Graduation in Biotechnology

Lupin is hiring for Executive Production Mammalian for Pimpari Chinchwad Pune Maharashtra 
Details are provided below 
1. Position: Executive Production Mammalian
2. Company: Lupin Pharma 
3. Job Location: Pimpari Chinchwad Pune 
4. Job Description: 
-Act as shift supervisor, lead, train and mentor the downstream team.
-Buffer preparation for small and large-scale operations, IPQC operation of buffer and protein intermediate samples.
-CIP of chromatography systems, TFF systems and process vessels.
-SIP of TFF systems and process vessels.
-Operation of chromatography systems, TFF systems, Virus Filtration System, DS filtration for protein purification.
-Monitor key process parameters.
-Preparation, execution and maintenance of SOP's, BPRS, qualification documents and other facility related documents.
-Co-ordinate with QC/QA teams on day-to-day activities of production operations.
-Review of executed BPR's.
Raw material and consumables inventory planning and maintenance.
-Operation, maintenance of sterile and decontamination autoclave.
-Deviation identification, initiation and investigation assistance for the facility related deviations.
-Preparation of GMP documents like- Qualification and validation protocols and other process or facility related documents for media preparation and cell culture operations.
5. Work Experience: 
3-8 years of mammalian manufacturing experience.
6. Education: 
B.Tech in Biotechnology or Biotechnology / Post Graduation in Biotechnology or Biotechnology
7. Competencies: 
Strategic Agility
Developing Talent
Result Orientation
8. How to Apply: 

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