Director of Pharmaceutical Development
April 26, 2012 by admin
Filed under Mid-West, Research & Development
The Director of Pharmaceutical Development will provide overall leadership in pharmaceutical drug development of new veterinary prescription pharmaceuticals in the United States and European Union from product concept through registration.
Responsibilities include:
· providing scientific and regulatory expertise to the Global Project Teams and coordinating production of clinical trial and experimental materials with which to perform studies;
· provide project management for the successful submission and approval of the U.S. CM&C Technical Section to the Food and Drug Administration (FDA) Center for Veterinary Medicine (CVM) and the Part II Section of the European Medicines Agency (EMEA) dossier;
· lead pharmaceutical development conferences with the FDA-CVM and the EMEA;
· manage overall program timelines, budgets, and risk management; and
· edit final reports and regulatory submissions.
Studies will be conducted through Contract Manufacturing and Research Organizations and the individual will guide and assume responsibility for all contractual activities at such facilities on behalf of the organization.
The Director of Pharmaceutical Development is expected to:
· establish and maintain relationships with institutional, government, regulatory agencies, corporate and private authorities and experts in various fields to insure that all operating procedures are in compliance with appropriate regulations and Good Manufacturing Processes (GMP) where appropriate;
· participate in professional organizations; and
· remain current in current research and practices, regulatory laws and emerging technologies by regular interactions with leading scientists, other companies and regulatory authorities to maintain a competitive awareness.
Education: PhD, PharmD or MS and at least 5 years of relevant CMC regulatory and project management experience.
To learn more about this exciting opportunity, please Apply Now
Florida – Boarded Veterinary Criticalist
April 25, 2012 by admin
Filed under South-East, Specialist
Boarded Veterinary Criticalist- for our client who provides mobile ultrasound services. This is a unique opportunity for a veterinary internist to do mobile ultrasound from Vero Beach to Fort Lauderdale, FL. The incumbent will continue to offer and promote services to existing and new clients in South Florida. This includes travel to and from veterinarian offices, scanning of all modalities, interpretations, over reads, marketing, presentations, CE and meetings. All ultrasound equipment will be provided by our client’s organization. This will be a 5 day work week M-F. The incumbent will assist the organization with strategic planning as the company continues to grow.
To learn more about this exciting opportunity, please Apply Now.
Associate Veterinarian – Mississippi
April 25, 2012 by admin
Filed under Generalist, South-East
Wonderful clinic in Oxford looking an Associate Veterinarian with at least 2 yrs experience who has maturity and leadership skills for small animal clientele. Clinic is looking for a somebody who loves Oxford and is committed to the local area.
To find out more please Apply Now
Director – Quality Assurance
April 24, 2012 by admin
Filed under North-East, Research & Development, Technical Services
Our client is a pharmaceutical company which specializes in providing high quality drugs for pets and is searching for a Director of Quality Assurance to be in charge of creating, implementing and overseeing additional quality systems.
The Director must be able to proactively address and lead resolution of compliance issues internally and with external partners and contractors and must have at least 8 years experience in Quality Assurance for a human or animal drug company and will have substantial knowledge of cGMP requirements for multiple dosage forms, along with prior experience with supplier qualification. Additional experience with GDPs and/or GLPs is desirable. International and domestic travel required.
To learn more and/or apply for this opportunity, please Apply Now.
Florida – Boarded Veterinary Radiologist
April 22, 2012 by admin
Filed under South-East, Specialist
Boarded Veterinary Radiologist-(ACVR) for our client who provides mobile ultrasound services. This is a unique opportunity for a veterinary radiologist to do mobile ultrasound from Vero Beach to Fort Lauderdale, FL. The incumbent will continue to offer and promote services to existing and new clients in South Florida. This includes travel to and from veterinarian offices, scanning of all modalities, interpretations, over reads, marketing, presentations, CE and meetings. All ultrasound equipment will be provided by our client’s organization. This will be a 5 day work week M-F. The incumbent will assist the organization with strategic planning as the company continues to grow.
To learn more about this exciting opportunity, please Apply Now.
Vice President / General Manager
April 22, 2012 by admin
Filed under Executive, Sales & Marketing, South-East
The incumbent will lead and manage the day-to-day business operations of the organization to carry out its established strategic direction to achieve the growth and profitability targets. The company plans to more than double sales within the next 5-7 years. The incumbent will meet or exceed annual financial targets as contained in annual operating budgets approved by the CEO and Board of Directors and will prepare and present quarterly reports to the Board of Director’s and at quarterly all-employee meetings. In conjunction with the Corporate Management group, the incumbent will recommend overall strategic direction to the CEO and will lead the management team in annual business planning including strategic planning, establishment of company goals and setting of budgets and will carry out such plans over the course of the year. The GM will serve as a company representative to key customers and industry associations in the Animal Health Industry and keep abreast of industry trends and propose company position and strategy on important industry matters. The incumbent will work within established guidelines and directives, determine company position and make decisions on operating matters including supplier and customer relations, new products, markets, distribution systems, contractual agreements, sales and marketing programs and operating and capital expenditures. The GM will provide direction and support to New Business Development to ensure new product concepts are consistent with the Company’s vision and strategic direction and new products are secured and brought to market timely. He/She will participate in Acquisitions including the search for potential products or companies to acquire, the evaluation and due diligence of products or companies and making recommendations for (or against) such acquisitions and transitioning and integrating the acquisition upon closing. The GM will establish internal and external education and training programs as necessary to ensure the company has a skilled workforce and management ream and will evaluate and provide developmental guidance to the management group thorough quarterly performance reviews and will establish policies, processes and procedures to ensure compliance with all applicable laws and regulations. He/She will ensure the manufacturing facility and quality systems are maintained in accordance with FDA’s cGMP’s and that no major compliance issues exist. This is a leadership role on the Corporate Management team. Travel requirement is up to 50%.
Qualifications include a BS/BA in business or a technical/science degree (engineering, chemistry, etc.). Advanced degree a plus (such as a DVM). 10 years experience as a General Manager or President in private industry with minimum of five years experience in animal health industry. May consider varied high level senior management experience in lieu of GM/President experience dependent upon responsibilities in those positions. The incumbent should have an understanding of financial statements, have strong leadership skills and be highly motivated.
To learn more about this exciting opportunity, please Apply Now
Florida – Boarded Veterinary Internist
April 21, 2012 by admin
Filed under South-East, Specialist
Boarded Veterinary Internist-(ACVIM) for our client who provides mobile ultrasound services. This is a unique opportunity for a veterinary internist to do mobile ultrasound from Vero Beach to Fort Lauderdale, FL. The incumbent will continue to offer and promote services to existing and new clients in South Florida. This includes travel to and from veterinarian offices, scanning of all modalities, interpretations, over reads, marketing, presentations, CE and meetings. All ultrasound equipment will be provided by our client’s organization. This will be a 5 day work week M-F. The incumbent will assist the organization with strategic planning as the company continues to grow.
To learn more about this exciting opportunity, please Apply Now.
Animal Protein Account Manager – Dairy
April 16, 2012 by admin
Filed under Mid-West, Sales & Marketing, South-West
Opportunity for Southwest territory - western OK, northern TX, southeastern CO and western NM
This position entails calling on dairy farms, focusing on primarily 500+ cow herds and the primary products are milk residue test kits, diagnostic test kits, lameness products, foot bath products, cleaners, disingectants, rodenticides and disposable goods. The position is remote and the incumbent will live in the territory and will travel. Company car provided.
To learn more about this exciting opportunity, please Apply Now.
Director of Development and Regulatory Affairs
April 16, 2012 by admin
Filed under Mid-West, Research & Development
The incumbent will act as the primary contact for the FDA and will be responsible for development of strategy, support and execution of our client’s registration portfolio. The successful candidate will possess excellent scientific, written and communication skills and a full knowledge of Food and Drug regulations as they pertain to veterinary products. A minimum of ten years FDA regulatory experience and advanced degree in animal science or veterinary medicine is required. Candidate will be required to ensure that all regulatory submissions meet high quality standards and demonstrate support of regulatory requirements to achieve rapid and successful review and approval by the FDA. The Director will provide regulatory guidance and support to project teams and QA/QC to ensure that the development of all new animal products are conducted in full compliance with all FDA regulatory requirements to achieve timely approval and will assume responsibilities for all current pending FDA regulatory actions.
To learn more about this exciting opportunity, please Apply Now
Laboratory Manager
April 13, 2012 by admin
Filed under Mid-West, Research & Development
Works closely with the Laboratory Director and Assistant Laboratory Director to manage the day to day operations of the lab. Receives requests and processes laboratory samples according to laboratory protocol, assisting clients via phone, email, and fax concerning testing questions, and result interpretation.
Responsiblities
- Organizes daily workload in compliance with sample priority schedule to maximize testing efficiency with regard to time, cost and work distribution.
- Assay quality control sera and monitor results to verify adequate precision of methodology, reagents and instrument functions, monitor test reports for transcription errors to insure that correct data for diagnosing or monitoring patient status is reported.
- Maintains and calibrates instruments daily to insure accurate consistent operation of equipment and to promote increased instrument life span; process is achieved by following instrument manufacturer’s suggested guidelines and/or laboratory maintenance charts.
- Corrects instrument malfunctions within reasonable expectations of training capacity to insure return to continuous operations yielding accurate and precise results and to avoid down time and costly back-up.
- Troubleshoots instrument and reagent problems to determine cause of malfunction maintenance charts.
- Corrects instrument malfunctions within reasonable expectations of training capacity to insure return to continuous operations yielding accurate and precise results and to avoid down time and costly back-up.
- Investigates complaints and deviations from laboratory protocols and reports findings in a Corrective Action Report (CAR).
- Supervises the work performance of the laboratory and accessioning staff; maintains leave and rotational work schedules; completes annual employee performance evaluations; participates in the recruitment and interviews of potential technologists and lab employees.
Requirements:
- 4 year college degree with emphasis on the sciences and MT or PHD in chemistry or biochemistry.
- 5 to 10 years relevant experience in laboratory processing and management.
To learn more about this exciting opportunity, please Apply Now


