Amneal Hiring QC QMS

BSc MSc MPharm QC QMS Jobs Ahmedabad

BSc/MSc/MPharm QC QMS Investigation vacancies (2–8 yrs) at Amneal SEZ Matoda, Ahmedabad. Apply now.

Amneal Pharmaceuticals is hiring experienced professionals for its Quality Control – QMS Investigation function at its SEZ Matoda, Ahmedabad facility. This opportunity is ideal for candidates with strong analytical writing skills and hands-on experience in pharmaceutical quality systems within a regulated Oral Solid Dosage (OSD) plant.

If you are searching for quality control jobs in Ahmedabad, pharma QMS investigation roles, OSD regulated plant careers, GMP compliance jobs, or pharmaceutical quality assurance opportunities, this position offers exposure to global regulatory standards and structured compliance systems.

Company Overview

Amneal Pharmaceuticals, Inc. (NYSE: AMRX) is a global pharmaceutical company with more than 8,500 colleagues worldwide. The company develops, manufactures, and distributes over 270 high-quality medicines across multiple therapeutic segments.

The SEZ Matoda facility in Ahmedabad operates as a regulated OSD manufacturing plant aligned with international compliance frameworks such as USFDA, EU, and other global regulatory authorities. Quality Control and Quality Management Systems (QMS) teams play a critical role in ensuring data integrity, audit readiness, and regulatory compliance.

Working in such an environment offers professionals:

• Exposure to USFDA-regulated plant systems
• Experience in investigation management and CAPA documentation
• Strong foundation in GMP and data integrity practices
• Cross-functional collaboration in manufacturing, QA, and regulatory teams

Job Role & Responsibilities

Role: Quality Control – QMS Investigation

Qualification: B.Sc, M.Sc, M.Pharm
Experience: 2–8 Years
Location: SEZ Matoda, Ahmedabad
Plant Type: Oral Solid Dosage (OSD) – Regulated Facility

Key Responsibilities:

• Leading and documenting investigations related to quality and operational deviations
• Handling OOS (Out of Specification), OOT (Out of Trend), and deviation investigations
• Drafting comprehensive investigation reports with strong analytical clarity
• Ensuring compliance with GMP, GDP, and ALCOA data integrity principles
• Reviewing and refining official communications, reports, and audit documents
• Supporting internal and external audits with structured documentation
• Collaborating with cross-functional teams for root cause analysis and CAPA implementation
• Maintaining accurate and traceable records of findings and corrective actions

This role demands exceptional analytical writing ability and clear communication skills, as documentation quality directly impacts regulatory audit outcomes.

Eligibility / Qualifications

Educational Qualifications (comma-separated):

B.Sc (Chemistry), M.Sc (Chemistry/Analytical Chemistry), M.Pharm (Pharmaceutics/Quality Assurance/Pharmaceutical Analysis)

Experience Requirements:

• 2–8 years in Quality Control, QMS, or compliance roles
• Experience in regulated OSD manufacturing plants preferred
• Hands-on exposure to deviation handling and investigation documentation

Core Skills Required:

• Strong analytical writing and documentation skills
• Clear spoken and written English communication
• Understanding of GMP, GDP, and data integrity guidelines
• Knowledge of audit preparedness and regulatory inspections
• Root cause analysis and CAPA management

Candidates without regulated plant experience may not meet the role expectations.

Location & Career Growth

Job Location: SEZ Matoda, Ahmedabad, Gujarat

Ahmedabad is one of India’s major pharmaceutical manufacturing clusters. Working in a Special Economic Zone (SEZ) regulated plant provides direct exposure to export-oriented compliance systems and global regulatory standards.

Quality Management System (QMS) investigation roles offer strong career progression toward senior compliance, audit, and regulatory leadership positions.

Compensation will be aligned with experience, regulatory exposure, and current CTC.

Application Process

Interested candidates can share their updated CV at:

chandanid@amneal.com

Application Tips:

1. Highlight investigation handling experience clearly.
2. Mention OOS/OOT and deviation exposure.
3. Include regulatory audit experience if applicable.
4. Specify current CTC and notice period.

Shortlisted candidates will be contacted for further selection rounds.

Important Disclaimer

Amneal Pharmaceuticals does not send job offers from free email services nor does it charge any recruitment fee. Candidates are advised to remain vigilant against fraudulent job communications.

Why QMS Investigation Roles Are High-Value Careers

Pharmaceutical QMS investigation roles are among the most critical compliance functions in regulated manufacturing plants. Poorly handled investigations can lead to regulatory observations, warning letters, or product recalls.

Professionals in this domain gain expertise in:

• Regulatory inspection readiness
• Advanced root cause analysis
• Technical documentation and audit communication
• Risk management and CAPA systems
• Data integrity compliance frameworks

These competencies significantly enhance long-term career stability and earning potential in the pharmaceutical industry.

Frequently Asked Questions (FAQs)

1. Is regulated OSD experience mandatory?

Regulated plant experience is strongly preferred.

2. Are freshers eligible?

No. Minimum 2 years of relevant experience is required.

3. What is the job location?

SEZ Matoda, Ahmedabad, Gujarat.

4. What skills are most important for this role?

Analytical writing, investigation handling, GMP compliance, and documentation control.

5. How do I apply?

Send your CV to chandanid@amneal.com.

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Job Summary

Company	Amneal Pharmaceuticals, Inc.
Vacancies	Quality Control – QMS Investigation
Required Education	B.Sc, M.Sc, M.Pharm
Experience	2–8 Years