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Title:  Manager- CAPA Effectiveness

Date:  Feb 21, 2025
Location:  Tandalja - R&D
Company:  Sun Pharmaceutical Industries Ltd

                         

                                                                        Job Description                             

 

 

Position:

Manager: CAPA Effectiveness

 

 

Job Title:

Manager: CAPA Effectiveness

Job Grade:

G10

Function:

Global Quality and Compliance

Sub-function:

Corporate Quality Audit

Manager’s Job

Title:

Lead – CAPA Effectiveness

Skip Level Manager’s Title:

 

Function Head

Title:

 

Location:

Tandalja (Baroda R&D)

No. of Direct Reports (if any)

 

 

 

                         

Job Summary

 

Areas of Responsibility

  • To conduct the CAPA effectiveness review activities at manufacturing sites of Sun Pharma as per the review plan
  • To perform CAPA effectiveness review for CAPAs provided to Regulatory Authorities.
  • To perform review of implementation status of “Global CAPA” across Sun manufacturing sites.
  • To inform CAPA effectiveness review outcome to Lead / HOD and prepare CAPA effectiveness review report within stipulated timeline.
  • Participate in Regulatory Audit Review activities of manufacturing sites of Sun Pharma, need basis.
  • Sound knowledge of current regulatory requirements/expectations
  • Effective interpersonal, communication and organizational skill
  • Participate and support project work as allocated by reporting authority

Travel Estimate

 

 

 

Job Scope

Internal Interactions (within the organization)

 

External Interactions (outside the organization)

 

Geographical Scope

 

Financial Accountability (cost/revenue with exclusive authority)

 

 

 

Job Requirements

Educational Qualification

 

 B. Pharma or M. Pharma

Specific Certification

 

 

Skills

 

 QA Background, Knowledge of QMS or Compliance, US FDA experience is require.
OSD and Sterile experience is require - sterile will be preferable

 

 

 

 

 

Experience

10 to 16 years of work experience.

Experience in a pharmaceutical organization with good exposure of Quality and Manufacturing Operations.

A strong knowledge of GMP’s and regulatory audits, CAPA assessments in international regulatory environments.

 

 

Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification.  It is not designed to contain or be interpreted as a

comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to

this job.  Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).

 

 

 

 

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