Packaging Specialist - (Pharma/GMP) job opportunity at Clinigen Group.

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Date2026-03-05T18:03:15.842Z bot
Clinigen Group Packaging Specialist - (Pharma/GMP)
Experience: General
Pattern: Full-time
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loacation Malvern, United States Of America
loacation Malvern....United States Of America

Clinigen is a rapidly growing global specialty pharmaceutical and services company with a unique combination of businesses. Our divisions operate in a complex global regulatory environment and ensure that vital medicines are delivered securely on time and wherever they are needed in the world. The primary objective of this position is to ensure the accurate packaging, labeling, and documentation of clinical trial materials in accordance with established protocols and regulatory requirements. Your role at Clinigen : Follow step by step instructions to package and label clinical study medication Convert client documents to internal company documents Works with other team members to create consistent and uniform products Compares printed labels to the original proof to ensure they match character for character and with proper spacing Inspects products for defects and uniformity Works with supervisor and the quality department to investigate and correct documentation errors Learns and adheres to Good Documentation Practices (GDP), current Good Manufacturing Practices (cGMP), and CSM’s Standard Operating Procedures (SOPs) To be successful in this role you should have: Strong cGMP, GDP and SOP experience, preferably within the Pharma industry 6-12 months experience working within an office setting or medical field We’re excited about you if you have: Ability to work independently or within a team Detail oriented to produce timely and accurate work Excellent oral, written, and interpersonal communication skills with active listening ability Self-motivated with exceptional time management skills to prioritize work and efficiently react to change in a fast paced environment Maintain a high regard for confidentiality while dealing with all clients, proprietary, and pharmaceutical related information Highly computer literate; experience operating with all Microsoft Office software

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