MQ Shift Supervisor (12 Hour Day & 12 Hour Night Shifts) Job in Rocky Mt, North Carolina US

Aspire...to save others' lives, while shaping your own.

What We Are Made Of
Hospira, Inc. is the world's leading provider of injectable drugs and infusion technologies. Through its broad, integrated portfolio, Hospira is uniquely positioned to Advance WellnessTM by improving patient and caregiver safety while reducing healthcare costs. The company is headquartered in Lake Forest, Ill., and has approximately 14,000 employees. Learn more at www.hospira.com.

The Rocky Mount operations has over 2500 employees and is one of the largest manufacturers of generic specialty injectables, including small and large volume parenterals, in the world. Rocky Mount offers a wide range of very rewarding and fulfilling careers. If you're a highly motivated individual with strong career aspirations and you believe your professional goals are in alignment with Hospira; then you're ready to advance wellness at the Rocky Mount operations.

What We Are Proud Of
We at Hospira, Inc. feel rewarded by our hard work and take pride in knowing we're on our individual career paths with a shared goal:

Advancing wellness™, through the right people and the right products

As an equal opportunity and affirmative action employer, Hospira, Inc. embraces diversity of thought and cultural perspective and fosters an environment of empowerment, fairness, and respect.

Why It's a Great Place
Employees are offered an agile yet balanced work atmosphere, incentive compensation and the benefits that you'd expect from an industry leader.

Who You Can Become
At Hospira, Inc. you can have the opportunity to help continue our tradition of excellence, build upon it and contribute to its success. Empower yourself to use all of your skills to reach your goals - so that you can allow patients worldwide to reach theirs.

The MQ Supervisor will be responsible for supervising a select shift to ensure that all manufacturing and packaging operations are operating within a state of cGMP compliance. This individual will supervise and coordinate the quality functions within Small Volume Parenterals (SVP) or Large Volume Solutions (LVS) manufacturing and will communicate effectively and provide direction to employees on the shifts. The MQ Supervisor will be accountable for ensuring that all products manufactured meet registration and cGMP requirements in accordance with all regulatory requirements, and for also ensuring that the shift is working within the parameters of Hospira's quality systems. The MQ Supervisor has the ability to shut down a production line if product is not meeting quality standards. The MQ Supervisor will ensure that when quality-related issues arise, these issues are quickly elevated, so that sufficient resources are applied to correctly investigate, document, and lead to corrective actions.
Responsibilities:
1. Provide daily supervision of MQ employees working on a specific shift.
2. Work in conjunction with management to ensure that all aspects related to site GMP compliance are followed.
3. Work with the MQ Manager to ensure that all manufacturing, control procedures and specifications are followed as they relate to production, processes and equipment.
4. Assure that the appropriate resources are utilized on a specific shift as they relate to CAPAs, root cause analysis, preventive actions, trending results and corrective actions, in accordance with facility standards and GMP compliance.
5. Direct manufacturing staff to uphold quality and determine when manufacturing lines need to be shut down to investigate production issues.