Noronic Hiring QA Officer

B.Pharm QA Officer Vacancy Ahmedabad

B.Pharm QA Officer vacancy in Ahmedabad at Noronic Pharma. 6 months–2 years QA experience required. Apply now.

Noronic Pharmaceutical Pvt. Ltd. is inviting applications for the position of Quality Assurance Officer at its Ahmedabad facility. This opportunity is ideal for early-career pharmaceutical professionals who want hands-on exposure to GMP documentation, batch record review, process validation, and stability studies in a regulated manufacturing environment. Candidates with prior QA experience in pharmaceutical manufacturing will be given preference.

If you are actively searching for pharmaceutical QA jobs in Ahmedabad, B.Pharm quality assurance vacancies, GMP documentation roles, or process validation executive openings, this position offers structured career growth in a compliance-driven environment.

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Company Overview

Noronic Pharmaceutical Pvt. Ltd. is a growing pharmaceutical manufacturing company committed to delivering quality-driven formulations. The organization operates under current Good Manufacturing Practices (cGMP) and follows structured Quality Management System (QMS) procedures to ensure product safety, regulatory compliance, and batch-to-batch consistency.

Quality Assurance plays a central role in pharmaceutical manufacturing. From documentation control to validation review, QA ensures that every batch released meets defined regulatory standards and internal quality benchmarks. Noronic Pharma emphasizes documentation integrity, data accuracy, and systematic compliance aligned with regulatory expectations.

Professionals joining the QA department gain direct exposure to real-time manufacturing documentation, deviation control systems, and stability monitoring practices, which are critical for long-term career growth in regulated pharmaceutical industries.

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Job Role & Responsibilities

Designation: Quality Assurance Officer

Experience: 6 Months to 2 Years

Location: Gota, Ahmedabad

Working Hours: 09:30 AM – 06:00 PM

The selected candidate will be responsible for maintaining pharmaceutical quality systems and ensuring batch compliance as per GMP guidelines.

Core Responsibilities

• Preparation and review of Batch Manufacturing Records (BMR).
• Preparation and review of Batch Packaging Records (BPR).
• Support process validation documentation activities.
• Assist in stability study documentation and monitoring.
• Ensure compliance with SOPs and internal quality systems.
• Maintain documentation accuracy and traceability.
• Coordinate with Production and QC teams for batch documentation closure.

Compliance & Quality Exposure

The role includes hands-on exposure to:

• GMP documentation practices
• Process validation protocols
• Stability chamber documentation
• Batch release documentation workflows
• Regulatory documentation audit readiness

This position strengthens expertise in pharmaceutical quality systems, data integrity practices, and documentation lifecycle management.

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Eligibility / Qualifications

Required Educational Background

B.Pharm, M.Pharm, B.Sc (Chemistry), M.Sc (Chemistry), Diploma in Pharmacy.

Experience Requirement

• 6 months to 2 years of experience in Pharmaceutical Quality Assurance.
• Freshers without QA exposure may not be considered.

Preferred Skills

• Good documentation skills.
• Understanding of cGMP and QMS systems.
• Basic knowledge of validation and stability protocols.
• Strong coordination and communication skills.

Female candidates are preferred as per current organizational requirement.

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Location & Salary

Location: Gota, Ahmedabad, Gujarat
Salary: As per industry standards. Compensation will be based on candidate experience and documentation exposure in pharmaceutical QA functions.

Ahmedabad remains one of India’s leading pharmaceutical manufacturing hubs, offering long-term career opportunities in QA, QC, Production, and Regulatory Affairs domains.

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Application Process

Interested candidates should share their updated resume at:

Email: hr@noronicpharma.com

Ensure your resume clearly mentions:

• Current CTC
• Expected CTC
• Notice Period
• Relevant QA experience details

Shortlisted candidates will be contacted for further evaluation.

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Why Consider a QA Career at Noronic Pharma?

Quality Assurance is one of the highest-growth functions in pharmaceutical manufacturing. With increasing global regulatory scrutiny, companies require strong QA professionals skilled in:

• Batch record review
• Data integrity compliance
• Validation documentation
• Stability data management
• Deviation and CAPA systems

This role provides foundational exposure to pharmaceutical compliance systems that are critical for career advancement into Senior QA Executive, QA Manager, Validation Specialist, or Regulatory Affairs positions.

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Frequently Asked Questions (FAQs)

1. Is prior QA experience mandatory?
Yes, candidates should have 6 months to 2 years of pharmaceutical QA experience.

2. Are freshers eligible?
Only candidates with some QA exposure are preferred.

3. What qualifications are accepted?
B.Pharm, M.Pharm, B.Sc, M.Sc, and Diploma in Pharmacy.

4. Is this a production role?
No, this is strictly a Quality Assurance documentation and compliance role.

5. What type of exposure will I gain?
Hands-on experience in BMR/BPR review, validation documentation, and stability study compliance.

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Career Growth Perspective

Pharmaceutical Quality Assurance is a high-demand domain due to increasing regulatory requirements from WHO, CDSCO, and international agencies. Professionals with strong documentation and validation expertise often move into higher-paying roles in:

• Validation & Qualification
• Regulatory Affairs
• Audit & Compliance
• Quality Systems Management

Early exposure to structured QA documentation significantly enhances long-term career stability in pharmaceutical manufacturing.

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Summary

Company	Noronic Pharmaceutical Pvt. Ltd.
Vacancies	Quality Assurance Officer
Required Education	B.Pharm, M.Pharm, B.Sc (Chemistry), M.Sc (Chemistry), Diploma in Pharmacy
Experience	6 Months – 2 Years (Pharma QA Preferred)

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