ORGANISATION

Clinigen Limited 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.

We are currently 1,100 people, headquartered in the UK, with sites in Burton-on-Trent and Weybridge, with global offices in the US, EU, Australia, New Zealand, Japan, Hong Kong, South Africa, and South East Asia. Clinigen has grown rapidly since it began in 2010 and is positioned well for an exciting future of continued growth. To sustain our growth, we’re on the lookout for motivated, ambitious and committed individuals to join our highly successful global team.

ROLE

Job Profile:

Work in a team environment to package, label, and accurately document the creation of clinical trial material.

Key Responsibilities:

• To follow, promote and enforce relevant SOPs, Job Aids, and Company policies and procedures
• Follows step by step instructions to package and label clinical study medication
• Converts 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
• Lead a team of 1-12 employees in packaging runs
• 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)
• Performs other related job duties or responsibilities as assigned

REQUIREMENTS

Role Requirements:

• 6 months experience working within an office setting or medical field preferred
• Preferred experience with Standard Operating Procedures (SOPs), current Good Manufacturing Practices (cGMP), or Good Documentation Practices (GDP)
• High School Diploma or GED required
• 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
• Ability to operate office equipment (telephone, calculator, photocopier, fax, and scanning machines)

BENEFITS