QA Manager / AM / Executives

GLOBAL CALCIUM; Krishnagiri District; On-site; INR 600,000 - 900,000; Full time

Job summary

GLOBAL CALCIUM in India invites applications for Quality Assurance roles across multiple levels. The team focuses on QMS, regulatory compliance, and documentation to support pharma manufacturing. Strong communication and adherence to cGMP are essential as you may engage in audits and cross-functional collaboration.

We seek candidates with B.Pharm/M.Pharm/MSc (Chemistry or related field) and relevant QA experience; candidates with API/pharma exposure preferred. Immediate joiners encouraged.

Qualifications

• B.Pharm / M.Pharm / MSc in Chemistry or relevant field.
• Experience ranges across levels: Trainee 0–5 years; Executive 3–10 years; Assistant Manager 8–12 years; Manager 10–20 years.

Responsibilities

• Implementation and maintenance of Quality Management Systems (QMS).
• Handling of Deviations, CAPA, Change Control, OOS, OOT.
• Preparation, review and approval of SOPs, BMR, BPR, protocols, and reports.
• Ensuring compliance with cGMP, regulatory guidelines (USFDA, WHO, MHRA, etc.).
• Conducting internal audits and supporting external audits.
• Review of analytical and manufacturing documents.
• Handling investigations and root cause analysis.
• Coordination with cross-functional departments (Production, QC, etc.).
• Training and mentoring junior team members (for senior roles).

Skills

Pharmaceutical QA

Regulatory audits

Documentation

Communication

Education

B.Pharm

M.Pharm

MSc (Chemistry)

Job description

Job Summary

We are hiring for multiple positions in the Quality Assurance (QA) department across various levels. Candidates with experience in pharmaceutical manufacturing and strong knowledge of QMS, regulatory compliance, and documentation are preferred.

Key Responsibilities

• Implementation and maintenance of Quality Management Systems (QMS)
• Handling of Deviations, CAPA, Change Control, OOS, OOT
• Preparation, review, and approval of SOPs, BMR, BPR, protocols, and reports
• Ensuring compliance with cGMP, regulatory guidelines (USFDA, WHO, MHRA, etc.)
• Conducting internal audits and supporting external audits
• Review of analytical and manufacturing documents
• Handling investigations and root cause analysis
• Coordination with cross-functional departments (Production, QC, etc.)
• Training and mentoring junior team members (for senior roles)

Eligibility Criteria

• Qualification: B.Pharm / M.Pharm / MSc (Chemistry or relevant field)
• Experience Range:
  • Trainee / Officer: 0–5 years
  • Executive / Sr. Executive: 3–10 years
  • Assistant Manager / Deputy Manager: 8–12 years
  • Manager: 10–20 years

Key Skills Required

• Strong knowledge of pharmaceutical QA processes
• Experience in regulatory audits
• Good documentation and communication skills
• Exposure to regulated plants preferred

Preferred Candidates

• Immediate joiners or candidates with shorter notice periods
• Experience in API / Pharma manufacturing industry

How To Apply

Interested candidates can apply through Naukri or share profiles to:

[e-mail]