About The Position

Our breakthroughs would not make it to the hands of patients without our dedicated and agile pharmaceutical manufacturing team. Understanding the importance and impact of their role in Pfizer's mission, they ensure that patients and physicians have the medicines they need when they need them. Colleagues like you, who take pride in their work and always strive to improve outcomes, are essential. Your commitment helps to guarantee that our innovations reach those who need them most, reinforcing the critical role you play in our mission.

Requirements

  • Must have a bachelor's degree with at least 5 years of experience; OR a master's degree with at least 3 years of experience; OR a PhD with 0+ years of experience; OR an associate's degree with 8 years of experience; OR a high school diploma (or equivalent) and 10 years of relevant experience.
  • Demonstrated expertise in applying statistical methodologies to enhance manufacturing processes and quality control test methods.
  • Proficiency in the MS Office Suite, including Word, Excel, PowerPoint, SharePoint, and Visio.
  • Exceptional verbal and written communication skills.
  • Strong presentation abilities.

Nice To Haves

  • Experience in a GMP environment.
  • Previous management experience.
  • Strong problem-solving skills.
  • Ability to work collaboratively in a team environment.

Responsibilities

  • Lead or co-lead moderately complex projects, effectively managing time and resources.
  • Apply skills and knowledge to contribute to departmental work and resolve moderately complex problems.
  • Make decisions guided by policies in non-standard situations and operate independently in ambiguous scenarios.
  • Work independently on assignments, seek guidance on complex issues, and review your own and others' work.
  • Utilize judgment and experience to become a resource for others and mentor colleagues.
  • Troubleshoot and resolve on-site issues, collaborating with site operations to ensure continuous audit readiness.
  • Identify high-risk areas, implement improvements, and interface with engineering and technical operations to enhance processes.
  • Manage changes in the area, guide operational teams, prepare resource forecasts, and identify improvement opportunities.
  • Facilitate agreements between teams, lead clinical production efforts, and ensure timely, injury-free, and defect-free execution.
  • Develop Operations Specialists' skills, review area Change Controls, strengthen compliance culture, and enforce safety regulations while sustaining lean management practices.
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