Intas Pharmaceuticals Hiring: Senior Executive to Assistant Manager (Automation & Compliance)
Intas Pharmaceuticals is inviting experienced engineering professionals to join their high-tech manufacturing facility at Matoda. This is a premier opportunity for specialists in Automation and Compliance to advance their careers with a global pharmaceutical leader.
Department: Engineering (Automation and Compliance)
Designation: Senior Executive to Assistant Manager Level
Experience: 7 to 14 years
Qualification: BE / B.Tech
Key skill or job description:
• Design, program, test and implement automated systems (PLCs, SCADA) for manufacturing or laboratory use, ensuring they support FDA-regulated processes.
• Develop and execute validation documentation – including URS, FS, DS – and protocols such as IQ, OQ, and PQ all aligned with 21 CFR Part 11, cGMP, and GAMP standards.
• Ensure compliance with data integrity, user security, disaster recovery, and system backup provisions
• Provide day-to-day operational support, including on-call troubleshooting for upstream/downstream manufacturing systems.
• Lead root-cause analyses for system failures and corrective/ preventive action (CAPA) activities.
• Document process, software versions, maintenance logs, and validation reports to maintain audit trails.
• Support audits; act as subject-matter expert for internal and regulatory inspections.
• Collaborate with process engineers, QA, IT. Production, and external vendors to align automation with operational and compliance requirements.
• Drive continuous improvement through smart manufacturing.
• Maintain enterprise-level cyber resiliency, including OS patching, control system security, and user access compliance.
Who Can Apply
- Candidates with 7–14 years of hands-on experience in Engineering (Automation/CSV).
- Engineers with specific exposure to OSD (Oral Solid Dosage) or Injectable facility equipment.
- Professionals well-versed in USFDA guidelines, 21 CFR Part 11, and GAMP 5.
Why Intas Pharmaceuticals is the Best Choice
Intas is among the top 10 Indian pharmaceutical companies, known for its world-class manufacturing standards and presence in over 85 countries. Working at the Matoda plant offers exposure to cutting-edge "Smart Manufacturing" technologies and a robust regulatory environment (USFDA/MHRA), making it an ideal workplace for career stability and technical growth.
How To Apply
Work Location: Matoda Plant, Ahmedabad.
Application Method: Interested candidates should share their updated CVs via email to Mayur_Parmar@intaspharma.com. Please mention your current CTC, expected CTC, and notice period in the email body.
Frequently Asked Questions (FAQ)
1. What is the job location for this Intas Pharma vacancy?
The position is based at the Intas Pharmaceuticals Matoda Plant, Ahmedabad.
2. Which qualifications are required for this role?
A candidate must hold a BE or B.Tech degree in a relevant engineering field.
3. Is experience in the injectable facility mandatory?
While hands-on experience in OSD or Injectable facility equipment is highly preferred due to the technical nature of the role.
4. What are the key regulatory standards involved?
The role focuses heavily on 21 CFR Part 11, cGMP, and GAMP 5 compliance for automated systems.
5. How do I contact the HR for this position?
You can send your CV directly to Mayur Parmar at Mayur_Parmar@intaspharma.com.
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| Intas Pharmaceuticals Engineering Recruitment 2024 - Matoda Plant. |
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