AbbVie Hiring for Manufacturing Supervisor: Mon-Fri (6am-2:30pm) at Worcester, Massachusetts Full Time

As a Manufacturing Supervisor at AbbVie, you will play a vital role in overseeing the production process and ensuring that all operations run smoothly. In this position, you will be responsible for developing weekly goals, schedules, and priorities for staff, and reviewing production schedules to determine unit assignments and critical actions. You will also provide on-the-floor training to support formalized technical and GMP training, and monitor operator training files to ensure compliance with industry standards.

As a Supervisor, you will work closely with QA and Subject Matter Experts to resolve exceptions and review new batch records and SOPs. You will also work interdepartmentally to resolve work orders, dispensing, preventative maintenance, QC, and documentation issues, ensuring that direct materials budgets and overtime budgets are met. Additionally, you will provide supervision primarily to skilled non-exempt and junior level exempt employees, evaluating staff performance and acting as a mentor for less senior personnel.

If you are a highly motivated and experienced manufacturing professional seeking a challenging leadership role, we encourage you to apply for this exciting opportunity to play a crucial role in our organization. Join our team and contribute to our success as we strive to deliver high-quality products to our customers.

Responsibilities:

• Develops weekly goals and schedules and set priorities for staff. Reviews weekly production schedule and priorities to determine unit assignments and critical actions.

• Reviews all materials and batch records required to support shift and any off shift needs for the day.

• Provides on the floor training to support formalized technical and GMP training. Check that operator training files match and support the processes they are required to carry out.

• Monitors operator training files and work with compliance specialist to keep files up to date.

• Works with QA and Subject Matter Expert (Tech Ops or Process Sciences) to resolve exceptions. Reviews new Batch records and SOPs.

• Works with technology transfer team to incorporate new processes in the plant.

• Works interdepartmentally to see that work orders, dispensing, preventative maintenance, QC, and documentation issues are resolved and enhances communications at all levels.

• Ensures that direct materials budgets and overtime budgets are met.

• Requires a Bachelor’s degree or equivalent; Eight plus years’ experience in all aspects of manufacturing/ production processes

• Computer proficiency and scheduling experience required, good writing skills

• You should have a strong understanding of GMP requirements, as well as experience working with quality systems and batch record review

• Working knowledge of safety and quality systems required

• Familiarity with industrial automation (e.g., distributed control and PLC-based systems

• Familiarity with equipment and facilities validation

• As a supervisor, you should have exceptional leadership and communication skills, with the ability to motivate and mentor staff to achieve their full potential.

• You should be comfortable working cross-functionally, collaborating with other departments to resolve issues and ensure that production goals are met

AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community, and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.