Research and Development Manager manages and directs the research and development programs to meet organizational needs and to capitalize on potential new products. Develops and implements research and development procedures and techniques. Being a Research and Development Manager oversees complex research projects, analyzes results and provides recommendations based on findings. Assesses the scope of research projects and ensures they are on time and within budget. Additionally, Research and Development Manager may require an advanced degree. Typically reports to a head of unit/director. The Research and Development Manager manages subordinate staff in the day-to-day performance of their jobs. True first level manager. Ensures that project/department milestones/goals are met and adhering to approved budgets. Has full authority for personnel actions. Extensive knowledge of department processes. To be a Research and Development Manager typically requires 5 years experience in the related area as an individual contributor. 1 to 3 years supervisory experience may be required. (Copyright 2024 Salary.com)
Zoetis is a global animal health company dedicated to supporting customers and their businesses in ever better ways. Building on 65 years of experience, we deliver quality medicines and vaccines, complemented by diagnostic products and genetic tests and supported by a range of services. We are working every day to better understand and address the real-world challenges faced by those who raise and care for animals in ways they find truly relevant.
Our name, Zoetis (zō-EH-tis), has its root in zo, familiar in words such as zoo and zoology and derived from zoetic, meaning "pertaining to life." It signals our company's dedication to supporting the veterinarians and livestock producers everywhere who raise and care for the farm and companion animals on which we all depend on.
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. 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.
Role Description
This is an exciting opportunity to join the Supply Chain Manager team in Veterinary Medicine Research and Development. Our managers are critical 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 combines the utilization of 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. Our team also coordinates the acquisition of commercial products used in studies. Our points of interaction include- all teams in Veterinary Medicine R&D, Global Manufacturing and Supply, and third parties.
Some of the main responsibilities include:
Forecasting and Planning:
* Partnering with project team members to ensure that study needs and priorities are understood.
* Reviewing clinical study protocols to determine supply requirements and propose optimal packaging configurations.
* Leading efforts for forecasting and calculating supply needs in conjunction with Clinical, Safety, pharmaceutical and biopharmaceutical scientists.
* Leading efforts for forecasting and calculating sampling needs from the study in conjunction with Clinical, Safety, pharmaceutical and biopharmaceutical scientists to ensure the data gathered from the study is optimized for use across VMRD.
* Designing the import and export pathways that may be needed for global distribution of supplies.
* Providing input to matrix teams on timing, sourcing, and budget projections.
Partner Interface:
* Demonstrating expertise in partnering across multiple functions to deliver results and achieve shared goals.
* Serving as the clinical supply interface with VMRD Clinical teams to develop global supply and procurement strategies.
* Responsible, in conjunction with Regulatory Affairs, for the comparative agent strategy (sourcing and blinding) associated with their candidate responsibilities.
* Working closely with Regulatory and Quality Assurance Groups to enable supply deliverables to meet study needs.
* Managing relationships with worldwide VMRD colleagues and workstreams.
Packaging, Labeling, Distribution, and Destruction:
* Designing a fit-for-purpose packaging, labeling and distribution model to meet the study needs of each unique study.
* Managing packaging, labeling, and distribution activities at the preferred packaging and distribution location (internal or external).
* Managing stock and inventory levels at the preferred packaging and distribution location (internal or external).
* At the completion of studies, manage the returns, reconciliation, and destruction strategy that meets the scientific and regulatory needs for the supplies.
Qualifications:
* Ph.D / M.S. in a scientific Field or B.S. 10 years' experience in a scientific field.
* 5 Years in a Research and Development Environment.
* Ideally, 1 years of 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 a proficiency in using information systems.
* Strong organization abilities coupled with the ability to manage multiple projects
* Can manage multiple tasks in a fast-paced environment
* Ability to balance competing priorities, tactfully
* Excellent in prioritization of various tasks with high level of self-motivation and 'will-do' attitude
* Able and willing to be flexible and adaptable to work in a complex, global environment
* Able to build relationships across the global organization
* Strong sense of customer service and willingness to work with fellow colleagues to obtain the best outcomes for the company