Director - Monoclonal Antibody (mAbs) Manufacturing & Central Services

Zoetis is the world's largest Manufacturer and Supplier of Animal Pharmaceuticals.

At Zoetis in Lincoln, NE, we manufacture high quality medicines for dogs, cats, and livestock. Our plant has been recognized as one of the Nebraska's Safest Companies, with a long-standing presence in the Lincoln community. We are a clean, modern site that continues to innovate and grow.

Benefits Include:

4 weeks accrued paid vacation and 13 paid holidays.

401(k) match with company profit sharing.

Tuition reimbursement and Student Loan repayment program.

Great Health, personal, and family benefits starting day 1.

Position Summary

Lead, manage and directly support specific manufacturing functions related to Lincoln Operations Monoclonal Antibodies (mAbs) Manufacturing. Direct the manufacturing of monoclonal antibodies, and related manufacturing support to ensure production of therapeutic, safe, pure, and high quality mAbs. Work with other Zoetis international sites to build a corporate wide best in class mAbs manufacturing capability.

Hours: 1st shift.

Position Responsibilities

• Plans and directs manufacturing resources to produce mAbs in accordance with GMS requirements and approved budgets.
• Plans and implements long range manufacturing plans, policies, and procedures, consistent with strategic goals of the company.
• Develops and reviews operational objectives with all reporting managers. Ensures objectives and goals are clearly understood by all managers/supervisors and mAbs organization.
• Ensures all products produced meet company quality standards. Also, ensures that the facility is operated in conformance with current APHIS Regulations (USDA), European cGMP, US FDA cGMP, Zoetis Quality System Policies (ZQS), and Zoetis SOP's.
• Ensures leadership and clear, concise communication inside and outside the division or departments within the company. Directs the development and training of personnel to enhance effectiveness, coverage, production efficiency, morale, and teamwork.
• Directs the development and implementation of new and innovative manufacturing processes to improve safety, quality, cost, or supply.
• Accountable for pilot scale-up and manufacturing feasibility efforts for new products and improved processes.
• Interfaces with Global Manufacturing Technology (GMT) and Quality Operations (QO) for the transfer of new products to Manufacturing.
• Ensures facilities are operated in a safe, environmentally acceptable manner, and ensures all colleagues are properly trained to work in a safe manner.
• Proposes strategic initiatives to sustain a high performing organization including succession planning and development of colleagues.

Resources Managed

Financial Accountability

• Expense Budget: $12MM

Supervision

• Responsible for supervision of 65 colleagues, in a multi-discipline, 24/7 operation.
• Directly Supervises 5 - 8 colleagues.

Education and Experience

B.S. / B.A. in Life Sciences or Engineering. Minimum of10 years' experience, five years leading a large manufacturing or quality organization with demonstrated ability to develop and achieve long range/operational plans, effectively resolve complex technical issues in a timely manner, prepare and achieve budgets and financial forecasts. Prior experience managing in a biological and/or pharmaceutical manufacturing environment, with increasing levels of leadership responsibility.

Preferred Qualifications:

MBA or Master's Degree in Microbiology, Immunology, Virology, or other relevant advanced technical degree.

Minimum of three years leading a biological manufacturing operation (including aseptic manufacturing

and support systems). Preference given to applicants with mAbs experience.

Technical Skills and Competencies Required

Demonstrated creativity and proven capability to effectively lead and develop others, optimize team and organizational performance, execute strategic and operational plans, lead and manage change, deal with ambiguity, analyze complex issues resulting in appropriate & timely decisions, and promote innovation. Strong commitment to Product Quality, Customer Supply and Operational Excellence. Strong written and verbal communication skills. Demonstrated ability to lead, motivate and develop diverse groups to meet network, site, and departmental objectives. Demonstrated commitment to the Zoetis Cor Beliefs and leadership competencies. Demonstrated ability to interact positively with senior management and related support groups (i.e., Global Manufacturing & Supply (GMS), Supply Chain Management (SCM), Veterinary Medicine Research & Development (VMRD), Human Resources (HR), Quality Operations (QO), etc.) as well as international regulatory authorities (including FDA, USDA, VMD, EPA, OSHA).

Preferred Qualifications:

Prior experience managing a large multi-shift operation (50 ), with responsibility for directing a significant number of colleagues. Successful experience and application of LEAN and Six Sigma Operational Excellence tools.

Physical Position Requirements

• This position requires sitting, standing, and walking with occasional overtime/weekend work.
• Must wear appropriate gowning and PPE (Personal Protective Equipment) in manufacturing/production areas.
• The work conditions for the position are greater than 50% stationary with periodic standing and walking through out the workday(s).
• The colleague(s) may be required to travel and or work greater than 40 hours per week, including weekends and holidays to support the business.

Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume.

Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search.