Duties:
Primary responsibilities for this position include supporting the QC Change Management team with the delivery of activities associated with analytical validation support, CAPA follow up and CC support activities.
Major Accountabilities
Complies with policies and procedures in order to maintain compliance with legal regulations, health and safety, and regulatory requirements as written
Participates in continuous improvement programs to reduce operating costs
Support team members with the archival of documentation, follow up with support teams on key deliverables as needed.
Provide support to the QC specialists as needed to deliver on time closure of changes and CAPAs.
Ensures collaboration of with other functions and departments on changes, CAPAs and Atlas documentation revisions.
Support the compilation of pertinent metrics generated by the team
Skills:
0 Years of Experience required but an interest in the pharmaceutical or biopharmaceutical industry preferred.
Demonstrated effective communication skills both written and verbal.
Strong interpersonal, communication, negotiation, multitasking and problem solving skills.
Keywords:
Bachelor's degree in a scientific field preferred but not required
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Last updated on Jun 5, 2018