Operations Shift Supervisor

We are seeking a highly motivated and experienced DP Operations Shift Supervisor to join our pharmaceutical manufacturing team. In this key leadership role, you will oversee the safe and compliant production of drug product materials, ensuring all operations meet regulatory, safety, and organizational standards.

You will lead a team of pharmaceutical technicians, drive continuous improvement, and play a crucial part in maintaining AbbVie’s reputation for quality and excellence.

• Supervise and execute pharmaceutical processing activities to meet operational objectives.
• Lead, motivate, and develop a team of 4-9 direct reports, ensuring clear communication of tasks and goals.
• Plan resources and coordinate training to ensure safe and efficient operations.
• Measure, report, and own key departmental performance metrics (yield, rate, usage, attendance, overtime, etc.).
• Ensure compliance with all safety, environmental, and quality SOPs.
• Collaborate with other shift supervisors and internal/external stakeholders to ensure smooth interdepartmental operations.
• Manage employee relations, performance reviews, and growth plans in partnership with HR.
• Maintain accurate personnel records and update manufacturing control systems.
• Support and implement key site and departmental strategies.
• Adhere to all EHS & E (Environment, Health, Safety & Environment) standards and policies.
• Lead and participate in continuous improvement initiatives.
• Represent your area during regulatory inspections and audits.

Supervision & Leadership:

• Operate with a high degree of autonomy, reporting to the DP Operations Leader.
• Set annual goals, conduct performance reviews, and manage team development.
• Act as a site Subject Matter Expert (SME) for DP Manufacturing issues.
• Provide technical leadership and collaborate with key stakeholders.

• Level 8 Qualification in a relevant science or engineering discipline
• Minimum 3 years’ experience in batch processing operations within an FDA/HPRA regulated pharmaceutical environment.
• Detailed knowledge of cGMP and regulatory requirements.
• At least 3 years’ experience in a highly automated environment.
• Minimum 3 years’ direct supervisory experience or relevant training.
• Proven experience leading teams and participating in improvement programs.

• High attention to detail and commitment to compliance.
• Innovative thinker with strong problem-solving skills.
• Results-driven, with the ability to prioritize and meet business demands.
• Strong verbal and written communication skills.
• Excellent interpersonal and leadership abilities.
• Demonstrates integrity, a strong work ethic, and a “Right First Time” mindset.
• Flexible to meet business needs, including shift work.