Operations Night Shift Manager
Our breakthroughs would not make it to the hands of patients without our pharmaceutical manufacturing team. We rely on a team of dedicated and agile members, who understand the importance and impact of their role in Pfizer’s mission. Patients need colleagues like you who take pride in their work and always look to improve outcomes. You will help to ensure that patients and physicians have the medicines they need, when they need them.
ROLE SUMMARY (WHAT YOU WILL ACHIEVE)
The successful candidate will be the Leader of one of two Night Operations shifts, leading a team of operations colleague engaged in the Filling, Visual Inspection and Packaging of aseptic pharmaceutical Drug Products.
You will have complete, single-point responsibility and Business ownership of the assigned values streams for the night shift that you are accountable for. You will act as the Process Centric Team Lead across all value streams on shift responsible for aspects of sterile Equipment Preparation, sterile Filling, packaging and VI of Injectable product.
You will support our patients' needs by maintaining impeccable regulatory compliance and developing behavioral and technical competencies for the organization within an environment of continuous improvement.
As a Manager, your breadth of knowledge on internal or external business challenges will help us improve our products, processes and services. You will be responsible for meeting objectives and preparing forecasts for resource requirements. Your risk-taking ability will help us advance new concepts and methodologies. You will provide technical guidance and oversight to team members and help in problem solving.
It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe.
You will be responsible for all aspects of Safety, Quality of product, Financial performance and Supply to markets from your value stream. The Night Shift manager will lead the team on Tier 1 visual management cadence, metrics and guide the team to achieve results.
You will indirectly lead a team of 7-10 supervisory colleagues and indirectly lead a cross functional team of 200+ colleagues in support of manufacturing activities across your assigned shift.
ROLE RESPONSIBILITIES (HOW YOU WILL ACHIEVE IT)
The successful candidate will act as coach and mentor to transform production units into a cohesive, harmonized team. You will be responsible for counseling colleagues to ensure their development, mediate conflicts within the team and provide corrective and performance management actions when necessary. The Operations Manager is also responsible for timely performance feedback and appraisals for all team members through their direct managers. You must operate within established HR policies and basic colleague relations guidelines.
You will provide an environment that encourages creativity, innovative ideas, and engagement. You must also drive a high sense of urgency and accountability within your team to safely produce high-quality critical Drug Product to our patients.
You will be fully responsible and accountable for deploying the Pfizer Lean Production System (iMEX -Integrated Manufacturing Excellence) including Continuous Improvement program, Total Productive Maintenance, Visual Management, Standard Work and Gemba process in your shift. Candidate will lead Operational Excellence initiatives (i.e. Kanban, M1 investigations, GB certification, etc.), develop OpEx skills of colleagues, and drive a culture of continuous improvement with their team utilizing IMEx principles.
You will be responsible for leading the team in identifying and implementing Continuous Improvement projects to improve efficiency, safety, quality and cost improvements.
You must possess the ability to critically analyze manufacturing processes for reproducibility, ruggedness, and root cause failure investigations of day to day operations. Requires developing strategies and systems to improve process performance. You will troubleshoot and solve production process problems which requires understanding of compliance, pharmaceutical, pharmacological, biological, biochemical, medical device, controlled substance and microbiological factors.
You must provide solutions to a wide range of problems which require the regular use of ingenuity, innovation, and creativity. May refer to precedents and policies. Able to gather, analyze and interpret information and identify cause and effect relationships. You must ensure solutions are imaginative, practical, thorough, and in line with organization objectives.
You must be able to adapt and respond positively to situations and people in order to meet changing work unit priorities.
You will be accountable for all financial aspects within your shift including absorption, expense, waste/MUV and Cost of Poor Quality. You must provide input to the preparation of and attainment to annual budget & revisions to product costing.
You will demonstrate personal leadership, initiative, judgment and accountability in day-to-day work activities in addition to exhibiting planning and organizational skills.
You must possess strong communication skills and demonstrate integrity and cooperation in working with diverse colleagues and groups.
You will participate on multiple cross disciplinary teams and interface with multiple levels of Pfizer colleagues as well as senior leadership.
- Bachelor's degree plus 5+ years of experience in GMP manufacturing/engineering/quality function.
- Master's degree plus 3+ years of experience in GMP manufacturing/engineering/quality function.
- At least 2 years in a People Leadership position.
- Experience in an aseptic/FDA-regulated manufacturing environment and working knowledge of cGMP requirements is required.
- Knowledge of continuous improvement methodologies, including experience deploying lean/6-sigma skills and Operational Excellence.
- Comprehensive, demonstrated skills in communicating (oral and written) effectively with diverse individuals/groups; facilitating trust, understanding, growth, empowering and enabling employee, business and customer relationships.
- Proven track record of delivering results consistently and fostering an engaged culture.
- Sterile Injectable experience preferred.
- Pharmaceutical process development, exposure to multiple aseptic sites and practices.
- Medical Device background and related manufacturing experience preferred.
- Project Management experience highly desirable.
- Demonstrated experience driving transformational change or remediation in Operations.
- Prior front-line leader supervision experience.
Must be available for weekend/off-shift escalations and support if needed. The role spends significant time on the shop floor standing/walking and interacting with colleagues.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Work Schedule: work schedule is a night shift, 6 pm to 6 am on a 3/2/2 schedule. Given production demand, work hours may need to adjust (including nights and weekends) from time to time (e.g., OTE all-colleague meetings, time of increased project activity requiring leadership presence, etc.).
Travel: travel to other sites, or to above-site locations with corporate/enabling functions may be required infrequently.
Other Job Details:
- Last Date to Apply for Job: 8/6/21
- Eligible for Relocation