Job Description

About the role:

We are seeking a

female QA Executive

with around

2 years of relevant experience

in the pharmaceutical industry. The candidate will play a key role in ensuring that our manufacturing processes, documentation, and products comply with cGMP and regulatory standards.

Key Responsibilities:

Review and maintain

Batch Manufacturing Records (BMR/BPR)

and related documents. Conduct

in-process quality checks

and ensure compliance with SOPs. Assist in

internal audits

,

deviation handling

,

change control

, and

CAPA implementation

. Participate in

qualification and validation

activities as per QA requirements. Monitor and maintain the

quality management system (QMS)

documentation. Coordinate with production, QC, and regulatory teams for smooth QA operations

Desired Candidate Profile:

Education:

B.Pharm / M.Pharm / B.Sc / M.Sc in a relevant discipline.

Experience:

Minimum

2 years in QA

within a pharmaceutical manufacturing setup (Formulation / API preferred).

Knowledge:

Sound understanding of

cGMP

,

GLP

, and regulatory guidelines (WHO, USFDA, MHRA, etc.). Strong analytical mindset and attention to detail. Good communication and documentation skills. Female candidates are preferred for this position.

To Apply:

Send your updated resume to

hrd@fidopharma.com

Job Type: Full-time

Pay: ₹18,000.00 - ₹30,483.39 per month

Benefits:

Provident Fund
Work Location: In person