Job Description

Cadchem Laboratories Ltd

API Pharmaceutical Plant

QA Executive

Qualification : BSC / MSC or B.Pharma / M.Pharma

Experience : 1-3 years in Pharmaceutical Company

Key Responsibilities

Quality Assurance Operations

Review and approve

Batch Manufacturing Records (BMRs)

and

Batch Packing Records (BPRs)

. Ensure compliance with

cGMP, ICH, WHO, USFDA, EU GMP

, and other regulatory requirements. Monitor and ensure adherence to

SOPs, policies, and quality systems

. Perform

line clearance

and in-process checks during API manufacturing.
Documentation & Compliance

Preparation, review, and control of

SOPs, protocols, and formats

. Review of

analytical and manufacturing documents

. Ensure proper documentation practices as per

GDP (Good Documentation Practices)

. Maintain and update

Quality Management System (QMS)

documents.
Deviations, Change Control & CAPA

Initiate, investigate, and close

deviations, OOS, OOT, and incidents

. Participate in

root cause analysis

and implementation of

CAPA

. Handle

change control

activities related to processes, equipment, and documents.
Validation & Qualification Support

Assist in

process validation, cleaning validation, and equipment qualification

. Review validation protocols and reports. Ensure compliance of validation activities with regulatory guidelines.
Audits & Inspections

Participate in

internal audits

, vendor audits, and regulatory inspections. Prepare and support

regulatory audits

(USFDA, WHO, EDQM, etc.). Assist in preparation of

audit responses and compliance reports

.
Training & Continuous Improvement

Conduct

GMP and SOP training

for production and QC personnel. Support continuous improvement initiatives in QA processes.
Job Types: Full-time, Permanent

Pay: ₹20,000.00 - ₹25,000.00 per month

Work Location: In person