Manager – Pre-Clinical Development

February 9, 2010 by admin  
Filed under Mid-West, Research & Development

The incumbent will formulate pre-clinical (target animal safety, toxicology and pharmacokinetic) development plans for new products in development and will work collaboratively within and across project teams to adhere to time schedules and meet critical deadlines. Read more

Manager of Clinical Development – Animal Health

February 9, 2010 by admin  
Filed under Mid-West, Research & Development

The primary responsibility of this role is to develop and execute comprehensive plans for products in clinical development. Key responsibilities include designing and writing study protocols, selecting veterinary investigators to execute clinical trials, overseeing and monitoring studies, and interpreting study results, writing study reports and preparing submissions to regulatory agencies. The positions also provide technical support to commercial operations and presents results of studies to the scientific community.

Qualifications include a DVM and/or a PhD in an animal health related field. An advanced degree (MS or PhD in addition to a DVM is desirable.

To find out more please Apply Now.

Principal Scientist – Veterinary Surgery

February 7, 2010 by admin  
Filed under Research & Development, Specialist

The Principal Scientist will partner with cross-functional teams including marketing, R&D, medical/clinical and regulatory to develop evidence strategies leading toward successful market approval and acceptance of novel, minimally invasive medical devices. Read more

Principal Scientist – Veterinary Surgeon

February 2, 2010 by admin  
Filed under Research & Development, Specialist

This position will be a key member of the Preclinical Research organization helping teams develop innovative surgical solutions. Read more

Director of Regulatory Affairs

January 29, 2010 by admin  
Filed under Mid-West, Research & Development, South-West

The Regulatory Affairs Group is critical for the ongoing support of a wide range of existing products, and the development of new products. The regulatory affairs group consists of a team of skilled professionals working to meet Regulatory, Operational, Business and Scientific objectives.

The Director of Regulatory Affairs is the principal source of regulatory information and advice for the company, in addition to being a working manager, providing guidance to the other regulatory affairs staff, and overseeing the regulatory affairs group.  Read more

Director of Regulatory Affairs

January 29, 2010 by admin  
Filed under North-East, Research & Development

Animal health company is looking for a Director – Regulatory Affairs to be responsible for directing its regulatory affairs activities associated with registration of veterinary pharmaceutical products in North America.

Responsibilities:

  • Coordinate all licensing procedures with the FDA, EPA, etc
  • Provide representation on regulatory/technical committees of the trade association AHI
  • Provide leadership by guiding staff in the management of submissions.
  • Communicate emerging legislation and its consequences within the regulatory affairs group and across other functions
  • Initiate product stewardship activities for existing product line in the US

Read more

Corporate Affairs Director (DVM)

The Director of Corporate Affairs is responsible managing the activities of the Corporate Affairs Department which includes Technical and Customer Service, Regulatory Affairs, Corporate Communications, and Quality Assurance teams.

The Director will also provide scientific support and direction as needed by each of the teams. The Director will assist with Technical Services in resolution of difficult complaints by providing scientific guidance relating to customer issues. The Director will work with the Regulatory Affairs Manager to provide guidance to other departments for compliance of regulations. The Director is responsible for ensuring all packaging, external communications, marketing materials and collateral materials are consistent in messaging and adhere to the company’s philosophy. The Director is responsible for providing content for technical marketing pieces as needed. The incumbent will also direct quality communications to the market for providing feedback from the market on quality issues to QA and the management team. In addition the Director will provide scientific articles to external publications to promote the reputation of the company. They will work with QA on quality issues, will set up standard operating procedures regarding quality complaints, will provide responses based on findings in QA investigations and will assist in training the team on quality assurance and food safety.

Qualifications include: Doctor of Veterinary Medicine or other advanced degree. It is preferable to have board certification. Excellent communication and presentation skills (oral and written), excellent PC skills (Excel, Word, Power Point) required. Outgoing personality and the ability to function as a team leader.

To learn more about this exciting opportunity, please  Apply Now.

Environmental Regulatory Manager

December 9, 2009 by admin  
Filed under Research & Development

A global provider of specialty chemicals in carefully focused markets including Animal Health Pesticides, Electronic and Wood Treatment chemicals is looking for an Environmental Regulatory Manager.

Duties include managing environmental regulatory matters for products, including registration and registration reviews, product development regulatory support, planning, budgeting, and direct management of regulatory specialists, compliance, etc.

Qualifications 

  • M.S. or PhD. preferred in a technical field such as Engineering, Chemistry, Biology, Industrial Hygiene, Safety or Environmental/Public Health.
  • Minimum 5 years experience in Pesticide Regulatory Affairs or Animal Health Regulatory Affairs
  • Knowledge of federal and state environmental regulations and procedures, including knowledge of U.S. laws pertaining to the regulation of pesticides under the Federal Insecticide Fungicide and Rodenticide Act (FIFRA), knowledge of pesticide laws.
  • International regulatory experince a big plus
  • Excellent written communication and presentation skills
  • Spanish and/or Portuguese language skills would be desirable

 To apply for this opportunity, please  Apply Now.

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