Amneal Pharmaceuticals is hosting a walk-in interview in Rajoda for manufacturing, QMS, and documentation roles. Explore dynamic pharma jobs in India today.

About Amneal Pharmaceuticals

Amneal Pharmaceuticals, Inc. (NYSE: AMRX) is a global leader dedicated to making high-quality medicines accessible worldwide. Backed by a diverse portfolio of over 270 medicines and a team of 7,500+ colleagues, Amneal emphasizes innovation, regulatory compliance, operational growth, and world-class manufacturing standards.

Job Details

• Company Name: Amneal Pharmaceuticals
• Experience: 02 to 12 Years (Varies by role)
• Qualification: Diploma, ITI, B.Pharm, M.Pharm
• Location: Rajoda, Ahmedabad, Gujarat
• Work Type: On-site

Job Description

Amneal Pharmaceuticals is conducting a walk-in interview drive to hire skilled professionals for its OSD manufacturing facility. Opportunities are available across Granulation, Coating, Compression, Capsulation, and QMS departments for operational and leadership roles.

Manufacturing Officer to Senior Executive

• Department: Granulation / Coating / Compression / Capsulation
• Market: OSD Regulated
• Role: Production Supervision & Execution
• Experience: 02 – 12 Years
• Education/Qualification: B.Pharm / M.Pharm

Manufacturing Operator

• Department: Granulation / Coating / Compression / Capsulation
• Market: OSD Regulated
• Role: Machine Operation & Maintenance
• Experience: 02 – 12 Years
• Education/Qualification: Diploma / ITI

QMS & Documentation Executive to Senior Executive

• Department: QMS & Documentation Cell
• Market: OSD Regulated
• Role: Quality Systems & Compliance Management
• Experience: 04 – 10 Years
• Education/Qualification: B.Pharm / M.Pharm

Skills & Qualifications

• Expertise in Granulation, Coating, Compression, or Capsulation machinery
• In-depth knowledge of cGMP, SOPs, BMR/BPR, and regulatory requirements
• Experience with eLogbooks, Deviation, CAPA, and Change Control processes
• Strong understanding of equipment qualification (IQ/OQ/PQ) and audit-trail review
• Hands-on experience in OSD regulated manufacturing environments

Key Responsibilities

• Supervise and execute manufacturing activities as per cGMP and SOPs.
• Operate, monitor, and clean manufacturing equipment and tooling correctly.
• Ensure compliance with BMR/BPR documentation, area cleaning, and safety standards.
• Coordinate SOP training, equipment qualification, and audit-trail review tasks.
• Manage Deviation, CAPA, Change Control, and investigation closure activities.
• Collaborate with cross-functional teams to maintain site Quality Management Systems.

Benefits & Perks

• Exceptional career growth in a expanding global organization
• Continuous learning and development in regulated manufacturing technologies
• Equal opportunity workplace with a focus on safety and inclusion
• Exposure to international quality compliance and cGMP standards

Walk-in Interview Details

How to Apply

Interested candidates meeting the eligibility criteria can attend the walk-in interview directly at the venue with an updated resume. If you are unable to attend, you can share your updated resume via email to [email protected], [email protected], or [email protected].

For more pharmaceutical careers, visit Pharma Recruiter.

Why You Should Join Amneal

Joining Amneal Pharmaceuticals means becoming part of a globally recognized team dedicated to patient health and scientific excellence. Employees benefit from robust career stability, state-of-the-art facilities, continuous skill development, and a culture centered on integrity and compliance.

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