Packaging Associate - Pharma/GMP
Clinigen, Malvern, AR, United States
Overview
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:
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 towork independently or within ateam
Detail orientedto 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 ahigh regard for confidentialitywhiledealing with all clients, proprietary,and pharmaceutical related information
Computer literate; experience operating with all Microsoft Office software
While at Clinigen, you’ll enjoy: 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.
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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:
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 towork independently or within ateam
Detail orientedto 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 ahigh regard for confidentialitywhiledealing with all clients, proprietary,and pharmaceutical related information
Computer literate; experience operating with all Microsoft Office software
While at Clinigen, you’ll enjoy: 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.
#J-18808-Ljbffr