In this role, you will:

  • Lead and manage people, technology, and financial resources within the department, ensuring alignment with short-term goals.
  • Actively share knowledge and collaborate within and across departments to foster innovation and continuous improvement.
  • Identify and implement potential improvements in processes or products, taking calculated risks to develop innovative ideas.
  • Solve moderately complex problems within your area of expertise and assist with cross-functional issues, providing technical guidance and oversight.
  • Oversee operational activities, manage multiple projects, and ensure compliance with regulations and GMP through effective execution of unit operations.
  • Manage the performance of direct reports through goal setting, coaching, mentoring, and ongoing assessment, recognizing and addressing development needs.
  • Solicit input, explain complex concepts, and persuade others to adopt a point of view, building alignment across manufacturing assets.
  • Own human performance event investigations as Lead Investigator, making autonomous decisions with minor impact and escalating significant decisions.
  • Form, lead, and facilitate cross-functional teams to execute key processes, ensuring accountability for the production activities of numerous Pfizer products.
  • Assist with short-range and long-range planning, including scheduling operations and staff, and coordinating facilities shutdowns and preventive maintenance.

Here Is What You Need (Minimum Requirements)

  • BA/BS with at least 4 years of experience OR MBA/MS with at least 2 years of experience OR PhD/JD with any years of experience OR Associate’s degree with at least 8 years of experience OR High School Diploma (or Equivalent) with at least 10 years of relevant experience
  • A robust grasp of industry knowledge and business operations, such as financial basics, enterprise systems like payroll and inventory management
  • Proficiency in administrative, managerial, and technical report writing skills
  • Effective written and oral communication skills
  • Strong computer and presentation capabilities
  • Experience in people management
  • Knowledge of GMP and regulatory requirements

Bonus Points If You Have (Preferred Requirements)

  • Certifications in Continuous Improvement or Project Management
  • Familiarity with Local Environmental Health and Safety standards
  • Excellent interpersonal and communication skills
  • Experience in motivating and developing team members
  • Strong leadership and decision-making skills

Physical / Mental requirements

  • Requires the moving of heavy equipment and the ability to lift ~40 pounds.
  • Strong problem-solving skills in a structured environment

Non-Standard work schedulem travel or environment requirements

  • Supports a 24/7 facility. M-F 10:00PM-6:30AM.
  • Ability to work 1st shift until GMP operations start.
  • Ability to support operations and training in other shifts when needed.
  • Ability to work weekends when needed

Other job details

  • Last day to apply: August 5th, 2025
  • Employee Referral Bonus eligible
  • Work Location Assignment: On Premise

Apply Now

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