Apply now and our proprietary system will quickly have you in front of a live recruiter. The Opportunity Description We're looking for a Documentation Specialist II, working in Biotechnology/Medical Devices industry in 1 Discovery Drive, Swiftwater, Pennsylvania, 18370, United States.
- Maintaining and coordinating the Record Retention process of GMP documents for the Viral Platform.
- Onsite and offsite recording retention.
- Updating documents within the Q eDoc system, whether administratively or through a Quality system such as Change Control or CAPA.
- Creation and control of Production logbooks pre, post and during use.
- Creation and control of cGMP forms.
Our Client Our client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models. Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations. Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success - Working knowledge of cGMP
- Good Communication skills both written and verbal
- Proficiency in WORD, and EXCEL, and have a working knowledge of other Microsoft office programs
- Excellent organizational skills
- Sound interpersonal and information gathering skills, being able to relate well to others at all levels throughout the organization and have the ability to work in a team environment, effectively interacting with others
- Work quickly with a high degree of accuracy
What Do You Think? Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible?