Mylan Laboratories Ltd (VIATRIS) Walk In Interview 2023 . Mylan Laboratories Ltd (VIATRIS) Notification full details below..Interested and eligible candidates can Send Resume On Hr Mail.Mylan is a global healthcare company focused on making high quality medicines available to everyone who needs them. Our heritage of being a provider of generic pharmaceuticals goes back to our founding in West Virginia in 1961. Today, we are passionate champions for better health around the world with a platform unmatched in the industry.
Vacancy details:
- Post Name: Officer - IPQA ( Injectable )/Officer - Injectable Manufacturing
- Qualification: B. Pharmacy / M. Pharmacy / M. Sc/Bsc
- Experienced: 02 to 7 years
Job Description: Greeting from Mylan Laboratories Ltd (VIATRIS)!!!!
Important Details :
- Location: Ahmedabad( Sanand )
- Post of date:03/6/2023
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to Face interview
- Interview Rounds of Interview: HR
Officer - IPQA ( Injectable )
Roles and Responsibilities
- To perform IPQA activities at shop floor in each and every stage of sterile manufacturing and packing.
- QA overview for clean room behavior and aseptic activity.
- Review of batch processing records.
- Review of all documents relating to the manufacturing, Packaging & analysis report prior to batch release.
- QA overview for receipt of material from warehouse to production.
- IPQA of Dispensing, Manufacturing, Packaging and Dispatch activities.
- Review and Control of SOPs, Specification, BPR issuance, Master Formulae and Records.
- Preparation & Review of process validation protocols and reports.
- Executing the validation/revalidation activity in the absence of authorized person.
- Responsible for regulatory audits with exposure equivalent to WHO Geneva PQ/USFDA
Desired Candidate Profile
- Execute IPQA Excellence by setting clear benchmarks.
- Smart Thinker and displays smart/ tactical moves & mental agility.
Apply Online
Officer - Injectable Manufacturing
Roles and Responsibilities
- Experience required only Injections and Parenteral Production
- Preparation and maintaining (log books, BMR/BPR) and online documentation.
- Manufacturing the batch and aseptic filtration of the batch manufactured after QC release.
- To participate in aseptic process & Sterilization of equipment assemblies, storage containers, aseptic area garments, filling area accessories, machine tools any other autoclavable materials used in aseptic area.
- Proper unloading, storage, and handling of aseptic area articles.
- To ensure cleaning of pre-filter (return riser, LAF, garment cabinet, pass box) as per schedule.
- To perform product filter integrity and vent filter integrity as per schedule.
- Line clearance to start any line operation.
- Quality management through In-process checking at different stages.
- Up-keeping of areas for cGMP audits and visits.
Desired Candidate Profile
- Good communication skills.
- Ability to manage the team efficiently.
Apply Online
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