Dr.Reddys Laboratories Ltd hiring for Team Lead Quality Assurance-Biologics
Dr.Reddys Laboratories Ltd. (NYSE: RDY) is an integrated global pharmaceutical company, committed to providing affordable and innovative medicines for healthier lives. Through its three businesses – Pharmaceutical Services and Active Ingredients, Global Generics and Proprietary Products €“ Dr. Reddy€™s offers a portfolio of products and services including APIs, custom pharmaceutical services, generics, biosimilars and differentiated formulations. Dr.Reddy’s Laboratories Walk In Interview 2023.Dr. Reddy’s Laboratories Notification full details below. Interested and eligible candidates can attend interview on scheduled time and venue.
Vacancy details:
- Post Name: Team Lead Quality Assurance
- Department: Biologics
- Qualification: B Pharm
- Experienced: 7 to 12 Years
Job Description: Greeting from Dr. Reddy’s Laboratories !!!!
Important Details :
- Work Location: Hyderabad
- Post of date:18/09/2023
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face To Face Interview
- Interview Rounds of Interview: HR
Skills Required Excellent Communication skills, Writing skills, Deep-diving ability on CAPA for problems,
Lead Quality Management Systems, Audit Operations
Key Responsibilities:
Lead and support in hosting all external or internal regulatory, customer, partner audits.
Scheduling the audit readiness meetings & Information sharing on audit readiness for scope, previous learnings, other units or other industry learnings.
Coordinating with the stake holders on having all the relevant information (incidents, complaints, batches, OOSs, OOTs, Excursions and so on) available for audit.
Identifying the team (scribe, scribe receiver, runner, back room, and so on) required for audit management.
Scheduling the opening meetings, daily briefing meetings, audit closing meetings.
Documenting the audit observations, notes, schedules, and audit learnings
Supporting the Documentation Cell ready towards the audit operations for right documents,
Coordinating with the stake holders for compliance assessment on new or revised regulatory guidelines and presenting a strategy plan towards implementation at site.
Leading the Quality Management System for Biologics across the domains including development & operations.
Working towards harmonizing the site’s Quality Assurance procedures with DRL global procedures.
Tracking all the DePex development projects towards Quality Operations and making sure that they are timely implemented at site.
