Par Formulation Pvt. Ltd.
Assistant Manager / Deputy Manager – Technical Services
Packaging Development & Operations | Par Formulation Pvt. Ltd.
🏢Company: Par Formulation Pvt. Ltd.
📍Location: Chennai, Tamil Nadu
💼Department: Technical Services (Packaging Development & Operations)
🎓Qualification: B.Pharm / M.Pharm / B.Tech (Packaging / Packaging Development)
📅Experience: 10–16 Years
🕐Employment: Full-Time
Job Overview
Par Formulation Pvt. Ltd. is seeking experienced professionals for the role of Assistant Manager / Deputy Manager – Technical Services (Packaging Development & Operations). The selected candidate will be responsible for packaging development, validation, regulatory compliance, artwork management, vendor qualification, and packaging process optimization for pharmaceutical products.
Key Responsibilities
- Review and approve packaging artwork in compliance with regulatory and marketing requirements.
- Coordinate with QA, Regulatory Affairs, and external vendors for timely artwork approval and implementation.
- Design and develop primary, secondary, and tertiary packaging configurations along with validation strategies.
- Manage packaging change controls, feasibility studies, and support new product introductions (NPI).
- Handle Material Approval System (MAS), including vendor sample evaluation and qualification activities.
- Prepare, review, and maintain packaging specifications, MPRs, SOPs, and other cGMP-compliant documentation.
- Conduct shipping validation studies to ensure packaging integrity during transportation and distribution.
- Execute Packaging Validation (PV) activities and support Equipment Qualification (IQ/OQ/PQ).
- Perform Moisture Vapor Transmission Rate (MVTR) studies to evaluate packaging barrier properties.
- Monitor shop-floor packaging operations, support troubleshooting activities, and ensure compliance with global regulatory requirements including USFDA, EU, and WHO guidelines.
Required Skills
Packaging Development & ValidationPackaging Artwork ManagementShipping ValidationEquipment Qualification (IQ/OQ/PQ)MVTR StudiesVendor Qualification & Material Approval System (MAS)cGMP DocumentationRegulatory Compliance (USFDA, EU, WHO)Packaging Process TroubleshootingCross-functional Team Coordination
Why Join?
- Opportunity to work with a leading pharmaceutical organization.
- Exposure to global regulatory and packaging compliance standards.
- Involvement in packaging innovation, validation, and new product development projects.
- Collaborative and growth-oriented work environment.
How to Apply
Email: Nagarajan.patchaiappan@endo.com
WhatsApp: +91 70106 60108
