Team Lead – TCO

Zoetis•Charles City, IA

11d

About The Position

The Team Leader is responsible for the safe execution of the Charles City production schedule in accordance with Good Manufacturing Practices and other applicable regulatory requirements. Team Leaders actively promotes colleague engagement and development utilizing both site and corporate resources. Conducts all activities and makes decisions that are in accordance with Company policies & SOPs, Zoetis Values, & global regulatory guidelines (including cGMP/cGLP/cGCP), environmental guidelines as appropriate, etc. Update and maintain department procedures including Manufacturing Directions and SOPs using Microsoft Word software. Working Hours: Friday - Monday, 5:00 AM - 3:30 PM

Requirements

BA/BS with 2-4 years of leadership experience OR MBA/MS with 0-2 years of leadership experience OR Minimum of 8 years relevant leadership experience, preferably in a Biologics manufacturing site.
Relevant manufacturing or analytical experience in microbiology, biology, engineering, or other scientific discipline.
Demonstrated commitment to the Zoetis Core Beliefs and leadership competencies.
Demonstrated ability to effectively lead, develop, and motivate individuals and teams.
Demonstrated ability to interact positively with all levels of colleagues including senior leadership.
Demonstrated ability to achieve results.
Extensive knowledge and capabilities with Microsoft Office software including Word, Excel, and PowerPoint
Extensive knowledge and capabilities with SAP Enterprise Resource System
Strong communication (oral and written), interpersonal, and team/group interactive and leadership skills.
Strong commitment to product quality, customer service, and continuous improvement.
Ability to resolve technical issues, troubleshoot manufacturing processes, and investigate process deviations/excursions.
Thorough knowledge of 9CFR and EU regulations, Good Manufacturing Practices (GMPs), and Good Laboratory Practices (GLPs).
Proficient in English, both oral and written, with sound technical writing skills.
Must be able to walk, sit, or stand for long periods of time.
Must be able to wear a respirator.
Must be able to reach above shoulder level, bend/stoop, kneel, push/pull, and handle/grip frequently.
Must be able to work scheduled 40 hours with the ability to work overtime as needed.
Must be comfortable working in varying temperatures.
Frequent lifting and carrying of 5 to 25 lbs.
Regular reaching, bending, stooping, and twisting.
Repetitive motion and substantial movement of the wrists, hands, and/or fingers.

Nice To Haves

Experience using Trackwise (Event Tracking System) Change Request and Investigation Writing software preferred but not required.
Experience using Operational Excellence and problem-solving tools such as DMAIC and Minitab analytical software preferred but not required.

Responsibilities

Manage and own department performance, including leadership and/or participation in floor and lab operations, clean room audits, department meetings, shift changes, etc.
Must be flexible in daily start time to ensure leadership coverage across the shift.
Must be available for on-call support in evenings, nights, and weekends.
Ensure effective utilization of the GMP process for all direct reports, including annual objectives, individual development plans, one-on-one meetings, quarterly and year-end reviews.
Continuously improve the capabilities of the team.
Perform safety related M1 investigations, including initial event summary to site leadership.
Ensure direct reports are compliant with all training requirements.
Perform Human Performance Error Evaluation as applicable.
Continuously develop direct reports to build a strong team and site. This includes the use of performance management tools, improvement initiatives, direct feedback, and open communication.
Continue managing departmental cross training program as part of individual colleague development program.
Effective and timely management of employee relations in accordance with company policies and procedures.
Participate and/or lead special projects as directed by area Manager/Team leader.
Respond to process and/or equipment events by ensuring communication with Process Specialist, Quality, Regulatory, EHS, Finance, Maintenance, and Operational Excellence specialist(s) as necessary.
Compliance and execution of EHS-regulations (Zoetis, US).
Compliance and execution of standards and instructions of company manufacturing specifications and SOPs.
Responsible for completion of Manufacturing Batch Record Review and other applicable department documentation.
Department Specific Responsibilities as indicated.