Clinical Supply Manager at ZOETIS SINGAPORE PTE LTD

Yorba Linda, California, United States -

Full Time

Start Date

Immediate

Expiry Date

13 Feb, 26

Salary

0.0

Posted On

15 Nov, 25

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Supply Chain Management, Project Management, Communication, Negotiation, Inventory Management, Regulatory Compliance, Packaging Design, Forecasting, Relationship Building, Scientific Skills, Adaptability, Self-Motivation, Team Collaboration, Problem Solving, Quality Assurance, Veterinary Medicine

Industry

Pharmaceutical Manufacturing

Description

Location: Michigan Lincoln, NE Role Description: This is an exciting opportunity to join the Supply Chain and Distribution team in Veterinary Medicine Research and Development (VMRD). In this role, you will be accountable for the active development and management of supply plans to guarantee a precise and ongoing supply to companion animal and livestock patients, with a focus on embracing the Zoetis Core Beliefs in your work. Our managers are core members of research and development project teams to ensure that the right material of the right quality gets to the right place at the right time. This role uses your scientific skills to understand not only the production of investigational veterinary materials but also the clinical and safety study plans in which these materials will be evaluated. Responsibilities: Forecasting and Planning: As the Supply Chain Lead, you will: Partner with project team members to ensure that study needs and priorities are understood. Review clinical protocols to determine the requirements for supplies at study initiation and monitor inventories for potential resupply. Propose optimal packaging configurations including coordinating the movement of supplies between manufacturers, third party CROs, field sites, analytical labs, and sample destruction locations. Manage inventory of investigative veterinary products within the VMRD pharmacy and in partnership with the VMRD team across the portfolio. Lead efforts in calculating quantity of drug product and forecasting sample outputs from the study, in conjunction with Clinical, Safety, Biological, Pharmaceutical, and Biopharmaceutical Scientists, to ensure the data gathered are optimized for use across VMRD. Design the import and export pathways of supplies and samples obtained from studies that may be needed for global distribution. Monitor adherence to production schedules and adjust supply plans as necessary. Provide input to matrix teams on timing, sourcing, and budget projections. Partner Interface: As the Supply Chain Lead, you will: Represent the Supply Chain and Distribution and Sample Technologies and Logistics Teams to internal stakeholders and will maintain excellent relationships with external supply partners. Be responsible, in conjunction with Regulatory Affairs, for the comparative agent strategy (sourcing and blinding) associated with their candidate responsibilities. Work closely with Regulatory and Quality Assurance Groups to enable supply deliverables to meet study needs while ensuring adherence to all relevant regulatory guidance, including international requirements. Materials Management: As the Supply Chain Lead, you will: Design a fit-for-purpose packaging, labeling, and distribution model – for supplies and samples – to meet the study needs of each unique study. Manage packaging, labeling, and distribution activities at the preferred packaging and distribution location (internal or external). Manage stock and inventory levels at the preferred packaging and distribution location (internal or external). Manage the returns, reconciliation, and destruction strategy that meets the scientific and regulatory needs for the supplies, at the completion of studies. Qualifications: Ph.D. / M.S. or B.S. + 10 years’ experience in a scientific field, supply chain, or project management. PharmD degree with a license to practice in the state of Michigan, or Pharmacy Tech will also be considered. Desire for experience in a R&D environment and/or demonstrated expertise in managing a partner interface to deliver results and achieve shared goals within the pharmaceutical industry Established skills in project management, communications, and negotiation coupled with proficiency in using information systems. Ability to manage multiple tasks in a fast-paced environment and balance competing priorities tactfully. Takes initiative with a high level of self-motivation and a ‘will-do’ attitude. Able and willing to be flexible and adaptable to work in a complex, global environment. Able to build productive relationships across the global organization. Full time Regular Colleague 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. Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at zoetiscolleagueservices@zoetis.com to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at www.Zoetis.com/careers site, or (2) via email to/from addresses using only the Zoetis domain of “@zoetis.com”. In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis. Join Zoetis – and build your career with a global animal health company dedicated to supporting its customers and their businesses. Why Zoetis Zoetis has more than 60 years of experience in delivering innovative, high-quality products and services that benefit our customers. Zoetis work environment At Zoetis, we take pride in a collaborative spirit and high-performing environment where every colleague is given room to learn and grow. Your opportunities at Zoetis We invest in our people and offer diverse and exciting opportunities to make a difference in a growing global industry while shaping the future of animal health. Results that matter Our colleagues make an impact by working hand-in-hand with those who raise and care for animals to better understand and address the unique real-world challenges they face.

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Responsibilities

The Clinical Supply Manager will develop and manage supply plans to ensure a continuous supply of materials for veterinary studies. This role involves collaborating with project teams and managing inventory to meet study needs effectively.