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Pharmaceutical Operations Shift Supervisor

AbbVieSligo
On-site Full-time

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Experience Level

Experience

Qualifications

Requirements:Bachelor's Degree (Level 8 Qualification) in a relevant science or engineering field. At least 3 years of experience in batch processing operations within an FDA/HPRA regulated pharmaceutical environment. Thorough understanding of cGMP and regulatory requirements. A minimum of 3 years in a highly automated environment. At least 3 years of direct supervisory experience or relevant training. Demonstrated experience in leading teams and engaging in improvement programs. Skills & Attributes:Strong attention to detail and commitment to compliance. Innovative thinker with excellent problem-solving abilities. Results-oriented with the capability to prioritize and meet business demands. Exceptional verbal and written communication skills. Outstanding interpersonal and leadership qualities. Integrity, strong work ethic, and a commitment to a “Right First Time” mindset. Willingness to adapt to business needs, including shift work.

About the job

Join AbbVie as a dedicated and experienced Operations Shift Supervisor in our pharmaceutical manufacturing team. In this pivotal leadership role, you will ensure the safe and compliant production of drug product materials, upholding all regulatory, safety, and organizational standards.

As a leader, you will guide a team of skilled pharmaceutical technicians, drive continuous improvement initiatives, and play a significant role in sustaining AbbVie’s reputation for quality and excellence.

Main Responsibilities:

  • Oversee and execute pharmaceutical processing activities to achieve operational targets.
  • Inspire, motivate, and nurture a team of 4-9 direct reports, ensuring effective communication of objectives and tasks.
  • Plan resources and coordinate training to guarantee safe and efficient operations.
  • Track, report, and manage key departmental performance metrics (yield, rate, usage, attendance, overtime, etc.).
  • Ensure adherence to all safety, environmental, and quality SOPs.
  • Collaborate with fellow shift supervisors and both internal and external stakeholders to facilitate smooth interdepartmental operations.
  • Handle employee relations, performance evaluations, and development plans in conjunction with HR.
  • Maintain accurate personnel records and update manufacturing control systems.
  • Support and implement critical site and departmental strategies.
  • Comply with all EHS (Environment, Health, Safety & Environment) standards and policies.
  • Lead and engage in continuous improvement initiatives.
  • Act as a representative during regulatory inspections and audits.

Leadership & Supervision:

  • Work autonomously, reporting directly to the DP Operations Leader.
  • Establish annual objectives, conduct performance reviews, and oversee team development.
  • Serve as a Subject Matter Expert (SME) for DP Manufacturing issues.
  • Provide technical leadership and collaborate with key stakeholders.

About AbbVie

AbbVie is dedicated to discovering and producing innovative medications that address today's serious health challenges while preparing to tackle tomorrow's medical hurdles. Our mission is to transform lives across key therapeutic areas such as immunology, oncology, neurosciences, ophthalmology, and virology, in addition to our offerings in the Allergan Aesthetics portfolio. We take pride in being recognized as a Great Place to Work.

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