Quality Assurance Supervisor IDAP 2nd Shift

QA Supervisor IDAP 2nd Shift

WHO?

INCOG are looking for a Quality Assurance Supervisor - IDAP to join their rapidly growing team. Working closely with the Manager of Quality, the Quality Assurance Supervisor - IDAP will be instrumental in in championing and developing our organization’s Quality Mindset and a culture of efficiency, attention to detail, and delivery on time.

This position is on Second (2nd) shift (2pm to 10:30 pm) with occasional weekend support, dependent on operations’ needs.

WHAT?

The Supervisor will need to successfully navigate and identify operational and quality gaps. They will will exemplify excellent interpersonal skills and develop productive, customer-centric working relationships with subordinates and colleagues, customers, suppliers, and partners.

The role responsibilities are, but are not limited to:

• Recruit, build, and lead a QA Operations team, specifically focused on Inspection, Device Assembly and Packaging operations.
• Responsible for training and maintaining an engaged work force competent in both theory and application of Quality processes.
• Lead through coaching, mentoring, and maintaining an on-the-floor presence in operations to ensure rigorous quality work standards and quality product manufacture.
• Prioritize and coordinate QA resources to balance production timelines and needs.
• Lead and support development of processes for inspection, device assembly and packaging operations.
• Lead strategy and direction of the Quality Assurance team to partner with Operations in the performance of on-the-floor batch record review and corrections.
• Establish an ongoing state of readiness in the exercising of rapid decision-making in the preliminary evaluation of the scope and impact of deviating events, requirements for product segregation, and the implementation of initial corrective actions.

YOU!

Ideally, candidates will have a Bachelor’s degree in a scientific discipline, along with 5 years of GMP experience. Of that experience, a minimum of 2 years should come from Quality Assurance within biopharma or a similar regulated industry. It is preferrable that this candidate will also possess 2+ years of experience as a people leader or supervisor.