Alembic Pharmaceuticals Hiring Quality Assurance (QA) – Head (Manager)
- Alembic Pharmaceuticals – A Legacy of Excellence in Pharma Manufacturing
- About Alembic Pharmaceuticals
- Job Position: Quality Assurance (QA) – Head (Manager)
- Location: Indore, Madhya Pradesh
- Qualification: B. Pharma / M. Pharma
- Experience Required: 18-20 years in a regulatory manufacturing plant
- Preferred Background: Candidates with expertise in Oral Solid Dosage (OSD) and Liquid Dosage Forms will be given preference.
- Key Responsibilities
- Eligibility Criteria
- How to Apply?
Alembic Pharmaceuticals – A Legacy of Excellence in Pharma Manufacturing
Alembic Pharmaceuticals Limited, a pioneer in the pharmaceutical industry, is seeking an experienced and dynamic Head (Manager) – Quality Assurance (QA) for its manufacturing facility in Indore. If you have extensive experience in regulatory plant operations and are looking for a leadership role, this could be the perfect opportunity for you.
About Alembic Pharmaceuticals
With over a century of excellence in pharmaceutical manufacturing, Alembic Pharmaceuticals has been at the forefront of innovation, producing high-quality medicines that cater to global healthcare needs. The company is known for its commitment to compliance, quality, and advanced research, making it a preferred employer in the pharma sector.
Job Position: Quality Assurance (QA) – Head (Manager)
Location: Indore, Madhya Pradesh
Qualification: B. Pharma / M. Pharma
Experience Required: 18-20 years in a regulatory manufacturing plant
Preferred Background: Candidates with expertise in Oral Solid Dosage (OSD) and Liquid Dosage Forms will be given preference.
Key Responsibilities
- Lead the Quality Assurance department, ensuring adherence to GMP, regulatory guidelines, and company SOPs.
- Oversee validation, qualification, QMS, market complaints, IPQA, and Lab QA activities.
- Drive quality culture within the organization, ensuring compliance with global regulatory requirements.
- Ensure smooth execution of internal and external audits, regulatory inspections, and compliance activities.
- Implement continuous improvement strategies to enhance the efficiency of QA processes.
- Collaborate with cross-functional teams to achieve operational excellence.
Eligibility Criteria
- Must have 18-20 years of experience in a regulatory pharma plant.
- Should have a strong background in OSD and Liquid Dosage Forms.
- Proven experience in handling regulatory audits such as USFDA, MHRA, TGA, WHO-GMP, etc.
- Excellent leadership and team management skills.
How to Apply?
Interested and eligible candidates can send their updated CV along with current and expected CTC to:
📧 vivek.amishra@alembic.co.in
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