Job Description

Department:

Manufacturing / Quality Assurance (IPQA)

Experience Required:

2 years in LVP/SVP manufacturing

Qualification:

B. Pharm / M.Sc. in Pharmaceutical Sciences or related field

Immediate Joining Required Before:

30th November 2025

We are seeking an experienced

Manufacturing IPQA Officer

to join our team and oversee critical quality assurance activities in our manufacturing operations. The ideal candidate should have a solid understanding of

LVP/SVP

manufacturing processes and be familiar with

cGMP

and regulatory requirements. This position requires a proactive individual with strong attention to detail and the ability to work in a dynamic, shift-based environment.

Key Responsibilities

Monitor

manufacturing activities

in compliance with

cGMP, SOPs

, and

regulatory requirements

. Conduct

line clearance

to ensure cleanliness and readiness before each batch. Verify

Batch Manufacturing Records (BMR)

and

Batch Production Records (BPR)

for accuracy and completeness. Ensure all

manufacturing operations

are performed according to the

Manufacturing Formula Record (MFR)

. Perform

in-process checks

to monitor product quality and process performance. Document all manufacturing activities, deviations, and quality control measures. Work on a

shift rotation

(three shifts) to ensure round-the-clock manufacturing quality oversight.

Required Skills & Knowledge

Minimum of

2 years of experience

in

LVP/SVP

manufacturing, preferably in the

pharmaceutical

or

biotech

industry. Strong knowledge of

cGMP, SOPs

, and other industry standards. Excellent attention to detail with a focus on

documentation accuracy

. Ability to work efficiently under pressure and in a

team environment

. Familiarity with manufacturing process monitoring,

line clearance

, and

in-process checks

. Strong communication skills, both verbal and written.
Job Type: Full-time

Pay: ₹15,000.00 - ₹30,000.00 per month

Benefits:

Provident Fund
Work Location: In person