Deputy Manager - Manufacturing QMS

Amneal Pharmaceuticals LLC

Ahmedabad District

On-site

INR 800,000 - 1,100,000

Full time

14 days+
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Job summary

RXinsider LTD. Ahmedabad invites an experienced Supervisor to oversee sterile manufacturing operations, ensuring SOPs, change control and CAPA are prepared, reviewed, revised and implemented effectively.

You will also prepare essential documents such as CCF, SOP, Investigation reports, risk assessments and protocols, coordinating with quality and compliance teams to maintain audit readiness.

Qualifications include MSc or B.Pharm/M.Pharm with 8–11 years of experience.

Qualifications

  • Qualification: MSc / B.Pharm / M.Pharm
  • Experience : 8 - 11 years

Responsibilities

  • Supervisor is responsible for preparation, review, revision, control and implementation of standard operating procedures activity, Change control and CAPA of Sterile manufacturing department
  • Document preparation like CCF, SOP, Investigation, Risk Assessment, Protocol etc.

Skills

Quality Management Systems
CAPA
Regulatory Compliance
Change Control Management
Report Writing
Audit & Inspection Readiness
Capability Development
Manufacturing Process and Equipment
Communication & Collaboration

Education

M.Sc
B.Pharm
M.Pharm

Job description

Key Responsibilities
  • Supervisor is responsible for preparation, review, revision, control and implementation of standard operating procedures activity, Change control and CAPA of Sterile manufacturing department
  • Document preparation like CCF, SOP, Investigation, Risk Assessment, Protocol etc.
JOB DESCRIPTION
  • Supervisor is responsible for preparation, review, revision, control and implementation of standard operating procedures activity, Change control and CAPA of Sterile manufacturing department
  • Document preparation like CCF, SOP, Investigation, Risk Assessment, Protocol etc.
Skills
  • Quality Management Systems | Mastery
  • CAPA (Corrective and Preventive Actions) | Mastery
  • Regulatory Compliance | Expert
  • Change Control Management | Expert
  • Report Writing | Expert
  • Audit & Inspection Readiness (Internal & External Audits) | Expert
  • Capability Development | Expert
  • Manufacturing Process and Equipment Understanding | Expert
  • Communication & Collaboration | Expert
Qualifications

Qualification: M.Sc B.Pharm / M.Pharm

Experience : 8 - 11 years

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