Bharat Serums and Vaccines Released Excellent Job Opportunity

Bharat Serums and Vaccines Released Job Openings On 21/07/2022.Our belief in Bringing Life to Life is anchored to a passion that has made us preserve, protect and enhance quality of life. For over four decades, we at BSV have used scientific resources to develop a range of biological, biotech and pharmaceutical products. Today, we have the privilege of working in close partnership with our customers and stakeholders to make a sustainable impact.Application form link provided at the end of post.

Vacancy Details:

Bharat Serums and Vaccines Recruiting MS/M.Sc(Science) in Biotechnology with 10-12 years experience for Manager – R & D Position.Complete Details for the Manager – R & D as follows.

Important Details :

• Location : Mumbai
• No of Vacancies:01
• Details of Salary: Not Disclosed by Recruiter
• Opening date for online Application: 21/07/2022
• Mode of application :Online
  
• How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps

Related Job:  Pharmacovigilance FRESHER And Experienced Openings At TCS,Accenture,Sun Pharma,Icon Clinical Research 

Job Description/Skills Required

Roles and Responsibilities

• – Process Development of Equine Biologicals & Human Biologicals-Drug Substance & Drug Product-Commercial molecules, Under Development molecules & Third-party manufacturing.
• – Scale up of the processes from Lab scale to Manufacturing scale.
• – Technology transfer of Equine Biologicals & Human Biologicals Inhouse and Loan license.
• – Execution of Engineering Batches, Pre-clinical batches, R & D stability batches, Process Validation batches.
• – Alternate vendor development of Critical materials/Consumables-Enzymes, UF DF cassettes, Chromatography Resin, Filters, Virus Filters, RM -PM.
• – Preparation of Project Budget and adhering to Project timelines given to management
• Unit operations:
• – Hands on Experience in handling of Unit operations -Precipitation, Ultrafiltration, Column chromatography, Virus Filtration, Lyophilization.
• Documentation:
• – Preparation of Documents -MMF, PDR, Chromatography Resin Validation, BMR, SOP, URS, Study protocol, Study report, Risk Assessment.
• – Should be able to handle Deviation, Change control, CAPA.
• – Preparation of documents for Test license, CMC Documentation, should be able to handle regulatory queries.
• – Execution of Non GLP & GLP Virus clearance studies.
• – Co-ordination with Cross functional teams
• Additional responsibilities:
• – Training of staff and overseeing general lab activities
• – Sound knowledge of SEC HPLC, SDS PAGE, Protein content estimation.

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