India's DMPLOI - Jobs & Networking AppKamla Group of Companies, a leading pharmaceutical manufacturer known for its expertise in injectable medicines, has announced a recruitment drive for the position of IPQA (In-Process Quality Assurance) Officer. Candidates with experience in injectable manufacturing and a strong understanding of cGMP and WHO-GMP guidelines are encouraged to apply.
If you are looking to build your career in pharmaceutical quality assurance, this opportunity offers a chance to work with an organization committed to quality, compliance, and operational excellence.
Job Overview
Particular Details
Company Name
Kamla Group of Companies
Position
IPQA Officer
Department
In-Process Quality Assurance (IPQA)
Job Location
Boisar, Tarapur, Maharashtra
Qualification
B.Pharm / M.Pharm
Experience
2–7 Years
Industry
Pharmaceutical (Injectable Manufacturing)
Educational Qualification
Applicants should possess:
Bachelor of Pharmacy (B.Pharm)
Master of Pharmacy (M.Pharm)
Experience Required
2 to 7 years of experience in Injectable Pharmaceutical Manufacturing.
Good understanding of cGMP, WHO-GMP, and regulatory compliance.
Knowledge of pharmaceutical documentation and quality systems.
Key Responsibilities
Selected candidates will be responsible for:
Monitoring in-process manufacturing activities as per SOPs and BMRs.
Performing line clearance before production operations.
Reviewing manufacturing documentation.
Verifying critical process parameters and equipment status.
Monitoring IPC records during manufacturing.
Ensuring correct use of raw materials, labels, and packaging materials.
Monitoring cleaning, changeover, and sampling activities.
Reviewing and approving in-process and packaging records.
Reporting and following up on deviations until closure.
Coordinating with Production, QA, and QC departments.
Ensuring compliance with cGMP requirements and maintaining data integrity.
Key Requirements
Candidates should have:
Hands-on experience in Injectable Manufacturing.
Strong knowledge of GMP documentation practices.
Understanding of pharmaceutical manufacturing processes and utilities.
Good analytical and problem-solving skills.
Excellent communication and interpersonal skills.
Proficiency in Microsoft Office.
Required Technical Skills
cGMP Compliance
WHO-GMP Guidelines
IPQA Documentation
SOP & BMR Review
Line Clearance
IPC Monitoring
Data Integrity
Deviation Handling
Pharmaceutical Quality Systems
Regulatory Compliance
Why Join Kamla Group?
Opportunity to work with a reputed pharmaceutical company.
Exposure to injectable manufacturing operations.
Professional growth in Quality Assurance.
Collaborative and quality-driven work environment.
Career development in regulated pharmaceutical manufacturing.
How to Apply
Interested candidates can send their updated CV to:
Email: anjali.yadav@kamlagroup.co.in
Contact Numbers:
8956480712
7972964497
Company Website: https://www.kamlagroup.co.in
Technical FAQs
1. What is the primary role of an IPQA Officer in pharmaceutical manufacturing?
An IPQA Officer monitors manufacturing activities in real time to ensure every process follows SOPs, GMP guidelines, and approved Batch Manufacturing Records (BMRs), maintaining product quality throughout production.
2. Why is line clearance important in injectable manufacturing?
Line clearance ensures that production areas are free from previous product residues, labels, packaging materials, and documents before starting a new batch, preventing mix-ups and cross-contamination.
3. What is the difference between QA, QC, and IPQA?
QA (Quality Assurance): Develops and maintains quality systems.
QC (Quality Control): Performs laboratory testing of materials and finished products.
IPQA (In-Process Quality Assurance): Monitors production activities during manufacturing to ensure compliance and quality.
4. What pharmaceutical documentation should an IPQA Officer be familiar with?
An IPQA Officer should understand Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), Standard Operating Procedures (SOPs), logbooks, deviation reports, change controls, CAPA, and equipment qualification documents.
5. What GMP knowledge is expected from candidates?
Candidates should have knowledge of cGMP and WHO-GMP requirements, data integrity (ALCOA+ principles), documentation practices, deviation handling, change control, risk assessment, cleaning validation, and regulatory compliance.
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