Job Overview
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Date PostedMarch 12, 2024
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Location (State / UT)
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Expiration dateMarch 14, 2025
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Experience10 Years
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GenderAny
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Desired QualificationBachelor Degree, Master’s Degree
Job Description
Roles and Responsibilities:
- Able to run the whole Sterile operation individually.
- He should have Sterile Regulatory knowledge.
- Lead role in facing the Audits
- Able to Handle validation, and media fill operation.
- Analytical skill
- Drafting skills of Investigation, QAMS
- Handling of All CFT requirements with respect to sterile operations Including all above Expertise.
Desired Key Skills:
- Sterile SME
- Able to handle Investigation and QAMS activity.
- Impart training to Teams for Sterile operations and Behaviors.
- Budgets skill
- Impact evaluation/Risk assessment
- All-time Audit Readiness
- Meet Market requirements (C vs A)
- Adhere to cGMP AND Safety norms.
Must Skill:
- Good Communication & Presentation Skills
- Interpersonal Skill
- Have worked in a USFDA plant.
- Result-oriented mindset.
- Analytical thought process
- Decision-Making Skill
Qualification: B. Pharma, M.Pharma
Experience: 12-16 Years