Naxcuure Healthcare Pvt. Ltd., a growing pharmaceutical organization committed to quality, innovation, and healthcare excellence, has announced an exciting career opportunity for experienced professionals in the Quality Assurance domain. The company is currently hiring IPQA Officers for its OSD (Oral Solid Dosage) Manufacturing Plant located in Jhulasan, Kadi, Mehsana, Gujarat.

This opportunity is ideal for candidates with strong knowledge of GMP compliance, in-process quality monitoring, deviation handling, and pharmaceutical documentation.

About Naxcuure Healthcare Pvt. Ltd.

Naxcuure Healthcare Pvt. Ltd. focuses on delivering high-quality pharmaceutical products while maintaining strict regulatory compliance and quality standards. The company promotes a culture of innovation, collaboration, integrity, and continuous learning, making it an excellent workplace for pharmaceutical professionals seeking long-term career growth.

Job Details

Particulars Details

Company Name

Naxcuure Healthcare Pvt. Ltd.

Position

IPQA Officer

Department

Quality Assurance (IPQA)

Experience Required

3 to 5 Years

Qualification

B.Sc. / M.Sc.

Industry

Pharmaceutical Manufacturing

Plant Type

OSD (Oral Solid Dosage)

Location

Jhulasan, Ta: Kadi, Mehsana, Gujarat – 382705

Application Mode

Email

Email ID

hr@naxcuure.in

Key Responsibilities of IPQA Officer

The selected candidate will be responsible for maintaining quality standards during manufacturing operations and ensuring compliance with regulatory guidelines.

Major Responsibilities:

In-Process Quality Monitoring during manufacturing and packaging activities.

Line Clearance Verification before batch initiation.

Batch Manufacturing Record (BMR) and Batch Packaging Record (BPR) review.

GMP Compliance monitoring across production areas.

Handling deviations and participating in investigations.

Coordination of sampling and testing activities.

Monitoring process adherence as per approved SOPs.

Documentation review and compliance verification.

Ensuring data integrity and regulatory compliance.

Required Skills

Candidates should possess expertise in:

In-Process Quality Assurance (IPQA)

GMP & GDP Compliance

Line Clearance Activities

Batch Documentation Review

Deviation Handling & Investigation

Pharmaceutical Manufacturing Processes

Sampling & Testing Coordination

SOP Compliance

Regulatory Audit Readiness

Quality Risk Management

Educational Qualification

Candidates must possess:

Bachelor of Science (B.Sc.)

Master of Science (M.Sc.)

Preference will be given to candidates having pharmaceutical manufacturing experience in OSD facilities.

Experience Requirement

Applicants should have:

Minimum: 3 Years

Maximum: 5 Years

Relevant experience in IPQA activities within pharmaceutical manufacturing plants is preferred.

Why Join Naxcuure Healthcare?

Opportunity to work in a growing pharmaceutical company.

Exposure to regulated manufacturing environments.

Professional development and career advancement opportunities.

Collaborative and innovation-driven work culture.

Hands-on experience with quality systems and regulatory compliance.

How to Apply?

Interested and eligible candidates can send their updated resume to:

hr@naxcuure.in

Subject Line: Application for IPQA Officer

Candidates are advised to mention their current CTC, expected CTC, notice period, and total experience in their application.

Technical FAQs

1. What is the role of an IPQA Officer in a pharmaceutical company?

An IPQA Officer monitors manufacturing activities in real time, performs line clearance, verifies GMP compliance, reviews batch records, and ensures products are manufactured according to approved procedures and regulatory requirements.

2. What is Line Clearance in pharmaceutical manufacturing?

Line Clearance is the documented verification process performed before starting a manufacturing or packaging batch to ensure that equipment, materials, labels, and documents from previous operations have been removed.

3. Why is GMP compliance important in OSD manufacturing?

Good Manufacturing Practices (GMP) ensure product quality, safety, consistency, and regulatory compliance. GMP helps prevent contamination, mix-ups, documentation errors, and quality defects.

4. What is deviation handling in Quality Assurance?

Deviation handling involves identifying, documenting, investigating, and resolving any departure from approved procedures, specifications, or processes to maintain product quality and compliance.

5. What documents are typically reviewed by an IPQA Officer?

An IPQA Officer reviews:

Batch Manufacturing Records (BMR)

Batch Packaging Records (BPR)

Logbooks

Equipment Usage Records

Cleaning Records

SOP Compliance Documents

Deviation Reports

Change Control Documents

Conclusion

Naxcuure Healthcare Pvt. Ltd. offers an excellent opportunity for experienced Quality Assurance professionals to join its OSD manufacturing facility as an IPQA Officer. Candidates with 3–5 years of experience, strong GMP knowledge, and expertise in in-process quality assurance should consider applying for this promising role and become part of a team dedicated to advancing healthcare quality and innovation.