Packaging Associate - Pharma/GMP

Clinigen; Malvern (Chester County); On-site; USD 45,000 - 60,000; Full time

Job summary

A global specialty pharmaceuticals firm in Chester County is seeking a detail-oriented individual to package and label clinical study medications. The role requires adherence to Good Manufacturing Practices and involves converting client documents to internal formats. The ideal candidate should have experience in a regulated environment, excellent communication skills, and the ability to work independently as well as within a team. This position offers a supportive culture that values inclusivity and continuous improvement.

Qualifications

• Experience in a cGMP, GDP, and SOP environment preferred.
• 6 months experience in an office or medical field.
• Detail oriented and capable of producing accurate work.

Responsibilities

• Package and label clinical study medication.
• Convert client documents to internal formats.
• Inspect products for defects and uniformity.

Skills

Attention to detail

Communication skills

Self-motivation

Tools

Microsoft Office

Job description

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.

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)

Requirements

• Experience working in a cGMP, GDP and SOP environment, preferably within the Pharma industry
• 6 months experience working within an office setting or medical field preferred

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
• Computer literate; experience operating with all Microsoft Office software

Benefits

The culture.

Thanks to our diverse opportunities for engagement and involvement, every colleague's Clinigen experience can be a bit different, and we're proud of that. We work hard to ensure our company culture is inclusive to people from all backgrounds and social styles.

The transparency with leadership.

All colleagues can share anonymous feedback with leadership on a weekly basis through our employee engagement platform. We use this feedback to inform our actions and decisions. We've been able to take steps to continuously improve how we do things at Clinigen.

The benefits.

We take pride in having a broad range of activities, systems, and programs that provide a competitive benefit offering and build a culture of celebrating success.

EEO. Clinigen is an Equal Opportunity Employer and is committed to providing equal employment opportunities to all applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, or any other characteristic protected by applicable law.