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Viatris
Every day, we rise to the challenge to make a difference and here’s how the QA Executive Level II role will make an impact:
Key responsibilities for this role include:
Perform detailed batch record review of finished products prior to QP/QA release.
Assist with the maintenance of the incident report system, supplier non-conformance system and the CAPA system.
Perform detailed technical / quality review of all updated artwork.
Approve final printed labelling (where applicable) and update master artwork files and packaging batch records.
Quality Oversight for site Packaging Operations.
Assist in the management of Customer Quality Complaints/Medical Device Vigilance systems.
Prepare monthly/quarterly/annual KPI/Management review data. Prepare annual product quality review reports. Maintain and deliver quality related training to Viatris personnel.
Maintain the companies incoming inspection program.
The minimum qualifications for this role are:
Minimum of a Bachelor's degree (or equivalent) in a Science related discipline and 2-4 years’ relevant experience within a pharmaceutical company with a minimum of 1 years’ experience within a Quality Assurance role.
Experience of sterile manufacturing desirable but not essential. However, a combination of experience and/or education will be taken into consideration.
Knowledge and or experience of all quality system aspects including: Deviation management, CAPA, complaint handling, auditing, change management, supplier qualification, batch release.
Experience of Trackwise or similar electronic document management systems is desirable but not essential.
Excellent communication (oral & written) and interpersonal skills.
Ability to handle multiple tasks in a fast paced environment with strong organisational and time management skills.
Experience of working with various IT systems and software packages with strong working knowledge of Microsoft Office (word, Excel, powerpoint etc.)
Bachelor's degree
