Administrative Head
Job Description:
experience in a Pharmaceutical manufacturing company with knowledge of Drugs and Cosmetics Act, and other statutory understanding of HR, Pollution, Fire safety etc.
Key Responsibilities:
Regulatory & Statutory Compliance
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Ensure compliance with the Drugs & Cosmetics Act, Factories Act, and other pharma-specific statutory guidelines.
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Maintain and update all licenses, renewals, and statutory records (GMP, pollution, boiler, fire, factory license, etc.).
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Coordinate with Drug Control Authorities, Pollution Control Board, and other regulatory bodies for inspections and audits.
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Ensure timely submission of statutory reports and returns to government departments.
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Keep management informed on updates or amendments in laws impacting pharmaceutical operations.
Human Resources & Industrial Compliance
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Support in implementation of labour laws and HR statutory requirements (ESI, PF, Minimum Wages, etc.).
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Maintain records related to attendance, overtime, and workforce compliance.
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Assist in recruitment, induction, and training for compliance and safety awareness.
Pollution, Environment & Fire Safety
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Ensure compliance with environmental and pollution control norms (air, water, waste management).
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Liaise with external agencies for renewal of pollution and safety certificates.
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Implement and monitor fire safety protocols, equipment maintenance, and regular fire drills.
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Promote workplace health, hygiene, and safety standards as per statutory guidelines.
General Administration
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Coordinate for facility maintenance, housekeeping, and security arrangements.
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Manage vendor and contractor compliance records.
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Maintain documentation for ISO, GMP, and internal quality audits.
Skills & Competencies Required:
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Sound knowledge of Drugs & Cosmetics Act, Factories Act, and related pharma manufacturing compliances.
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Understanding of HR, labour, fire, and environmental regulations.
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Strong documentation, reporting, and coordination skills.
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Proficient in MS Office, ERP systems, and compliance tracking tools.
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Excellent communication and liaisoning ability with government departments.
Preferred Background:
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Experience in pharmaceutical manufacturing plant administration or compliance function.
Key Skills :
Company Profile
They specialise in manufacturing high-quality IV fluids, capsules and small-volume parenterals, operating from modern WHO-GMP-approved facilities. They combine cutting-edge technology with a disciplined quality culture to serve domestic and export markets reliably.
Apply Now
- Interested candidates are requested to apply for this job.
- Recruiters will evaluate your candidature and will get in touch with you.