Qualifications include a Ph.D +/-DVM in Molecular Biology or equivalent with 2+ years of experience or Masters in Molecular Biology or equivalent with 5+ years of relevant experience. The incumbent should have expertise in the bioinformatic analysis of microbial genomes and potentially host transcriptomes. This analysis will aid in diagnostic analysis and both autogenous and USDA licensed product development.

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Qualifications include a Doctor of Veterinary Medicine degree, preferred board-certification, MBA or extensive business and leadership training, minimum of 7 years as a leader in an animal welfare/health organization, experience in marketing and corporate relations , solid knowledge of the animal welfare/health industry, ability to develop business strategies in line with the organization’s goals, must bridge diverse areas of expertise: medicine/surgery, toxicology, behavior, research, business strategy and marketing. Leadership and staff development skills are key, experience working with unions is helpful.

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Qualifications include a DVM with 3-5 years of veterinary practice experience. A PhD is a plus as well as someone who is a trail-blazer and champion of identifying new technologies and technology improvements.  Will need to have mastery at handling complex tasks & projects as well as multiple projects concurrently and will apply knowledge of technical and medical fields within category teams and peers.  The incumbent will aggressively seek new technology and IP protection and will stay abreast of new developments and opportunities.  Will need to represent the company via the media, web, conferences and veterinary outreach and will need to be an excellent technical writer and have a track record of publishing in peer reviewed scientific journals.  Will need the abiilty to design protocols for clinical trials whereby the outcome will support product claims.

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The Research Coordinator will communicate with and travel to designated study sites to conduct pre-study site evaluations, study initiation, interim monitoring and study close out visits for preclinical and clinical studies. The incumbent will establish rapport with subcontractors and study site personnel to facilitate communication and compliance with all study activities. Reviews the study records, casebooks and Investigator’s notebooks to ensure contents are current and complete including verification of owner consent, existence and maintenance of source documents and inventory of test supplies. Facilitates clarifications, corrections and data query resolution with study sites or data management, subcontractors and assists with responses to quality assurance audits. The incumbent will assist in management of study test article inventories and other related study materials. Depending on qualifications, may assist in the appropriate response to, and documentation of, adverse events. May serve as Project Manager and have oversight of all communications with a client for a specific clinical study. As Project Manager will coordinate the allocation of monitoring and quality control resources to best meet client needs, including scheduling and oversight of Clinical Research Coordinators. Serves as an ambassador for the company to generate new business and new business leads.

Qualifications include DVM or VMD. Good communication skills, good active listening skills. Experienced in GCP trials, 3-5 years of practice experience. Excellent interpersonal skills. Ability to travel 75% of the time. Basic computer skills, valid driver’s license with clean driving record, willingness to travel. Minimum Experience in data management, quality control and/or quality assurance is helpful.

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International Territory Manager-Animal Safety-Caribbean, Latin America, Miami, Puerto Rico, The incumbent is responsible for maximizing sales, increasing market share and building a strong international distributor network for our client’s animal safety productions internationally. The incumbent will call on customers and prospects to identify customer needs and inform them of new and existing products and services. Other responsibilities include developing lists of prospects, communicating with customer base, achieving or exceeding sales budgets, developing and recommending pricing strategies, representing company and analyzing industry trade shows and meetings to promote products and services, increasing market and competitive knowledge and identifying new product for distribution. The incumbent will develop long and short term profit driven business plans, develop long-lasting relationships with key customers and industry influencers and will work with marketing on advertising and promotional activities for product lines. The incumbent will work with technical support and will help execute sales and marketing programs, participates in the annual budgeting process, keeps management up-to date on market conditions and competitive situations.

Qualifications include college degree in animal science, agricultural business, international business or related field. Sales experience (5 or more years preferred)

Incumbent will work closely with department heads and develop and share metrics across the organization to build financial understanding and achieve aggressive growth plans. CFO will build a lean finance team as the company grows.

Incumbent will ensure strong financial controls, including managing audits, while supporting an entrepreneurial and performance driven culture.

CFO will be energetic, stellar communicator as well as an open and supportive team builder.  CFO will enjoy learning the business, from our manufacturing partners to our key customers and will be passionate about building a company and its infrastructure to listen to customers: companion animal veterinarians.

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Key Responsibilities include:

• Prepare and submit highest quality NADA, ANADA and DIN submissions to the FDA’s CVM and the Canadian VDD.
• Maintain current knowledge of FDA and Health Canada regulations and guidance related to CMC, NADA, ANADA, INAD and DIN filings; compiling and reviewing documents for preparation of submissions.
• Develop and manage project plans for submissions in conjunction with consultants, communicating with internal departments to obtain documents, and identifying potential issues that may affect timing schedule and submission quality.
• Prepare and submit annual reports to Regulatory Authorities; identify and address regulatory and compliance risks and solutions.
• Implement and maintain an adequate Quality System including Pharmacovigilance and Recall Procedures

 Requirements:

• Strong interpersonal skills
• Sound knowledge of the US & Canadian regulatory requirements for animal health products.
• Ability to deal with scientific and other complex matters.
• Bachelor’s degree in a scientific discipline or equivalent.
• Regulatory affairs specific qualification would be an advantage
• Experience in interfacing with relevant regulatory authorities.
• Five to ten years of regulatory experience in the animal health or pharmaceutical industry, with product sourced from abroad.