Job Description

Job Title:

IPQA Officer (In-Process Quality Assurance)

Department:

Quality Assurance

Industry:

Pharmaceuticals

:

We are seeking a detail-oriented and proactive

IPQA Officer

to join our Pharmaceutical Quality Assurance team. The ideal candidate will be responsible for ensuring in-process compliance with cGMP, regulatory guidelines, and company SOPs during manufacturing and packaging operations.

Key Responsibilities:

Monitor and ensure compliance with

cGMP, SOPs, and regulatory requirements

during manufacturing and packing activities Perform

in-process checks

for tablets, capsules, liquids, ointments, etc. Review and verify

Batch Manufacturing Records (BMR)

and

Batch Packing Records (BPR)

Ensure proper

line clearance

before and after production and packing operations Verify

critical process parameters

and in-process control results Monitor adherence to

data integrity

practices Handle

deviations, change controls, OOS, and CAPA

related to IPQA activities Ensure proper labeling, coding, and packaging compliance Support

regulatory audits

, internal audits, and customer inspections Coordinate with Production, QC, and Warehouse teams for quality-related matters Maintain accurate documentation and records as per regulatory norms

Qualifications:

B.Pharm / M.Pharm / M.Sc

1-5 years of experience in

IPQA

within a pharmaceutical manufacturing company Sound knowledge of

cGMP, WHO-GMP, and regulatory guidelines

Skills & Competencies:

Strong attention to detail and documentation skills Good understanding of pharmaceutical manufacturing processes Ability to identify deviations and ensure corrective actions Effective communication and teamwork skills Knowledge of data integrity and compliance standards
Jobtype: Permanent

Arbejdssted: Personligt fremm?de