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Associate
Director Regulatory -
Veterinary Biologicals
A global veterinary
pharmaceutical company is looking for an Associate
Director -
Veterinary Biologicals - Regulatory to support its
Regulatory and R&D groups. The AD will report to directly to the Senior Director.
The position would
primarily address veterinary biological product
registration needs for the United States. With the
guidance of the Senior Director, and the rest of the
regulatory team, the AD would develop the regulatory
strategy for the team, and be responsible for all US
regulatory submissions for that project.
In addition, the AD would serve as the primary liaison with Biological
Discovery to provide early regulatory input into early
phase Discovery projects. The candidate would
liaise with New Product Marketing to develop label claims,
and product supporting materials. The AD would
liaise closely with EU and CALAR regulatory staff to
facilitate global registration where appropriate.
In addition to project
responsibilities, the candidate would serve as an
alternate Liaison with USDA. Additional
responsibilities would involve obtaining required permits,
and miscellaneous submission as requested by the Senior
Director. Duties would require some travel,
primarily domestic, approximately 2-5 days a month.
No current direct reports are anticipated,
Qualifications:
- MS in biology, animal
science or other related science required, PhD or DVM
preferred
- A minimum of 5 years
experience with veterinary biological products
preferably in regularly affairs or a related area. (10+
yrs exp ideal)
- Strong verbal & written
communication skills
and a demonstrated ability to work in a team
environment
-
Understanding of the veterinary
biological development process and USDA regulatory
requirements desirable. Background knowledge in the
production and testing of veterinary biological products
desirable.
- Background
knowledge in global biological regulatory
requirements, specifically EU and Japan
- Experience
with trade organizations and other industry groups
To confidentially learn
more about these exciting opportunities, please e-mail
your resume in confidence to
resumes@thevetrecruiter.com.
Director
- Clinical
Development
Animal health company is looking for a
Director - Clinical
Development. The
position is principally based in designing and implementing
a clinical development strategy to add new approved
indications for our platform technology and developing and support new regenerative
services and products.
The Director will play a key role in protecting the
safety of our patients and supporting the efficacy of the
products and services.
Requirements:
To find out more about this
exciting opportunity, please
send your resume for immediate consideration to stacy@thevetrecruiter.com.
Manager - Technology
Transfer
A. Position
Specifications
1. Requires a Bachelor of Science degree in
Engineering. A specialization in Process, Industrial
or Chemical Engineering preferred. Experience in
Pharmaceutical manufacturing in a variety of
Supervisory/Management positions within multiple
manufacturing departments, including Product and
Process Development (PPD) and Research and
Development (R&D)...
2. Requires a minimum of 10 years experience in
pharmaceutical manufacturing with a proven track
record in project management and Continuous Process
Improvement. Other beneficial experience/knowledge
includes (but is not limited to) experience working
with small vial parenterals, terminal sterilization
and lyophilization, supervisory/management of a
manufacturing operation (i.e. component and
equipment preparation, sterilization, lyophilization,
quality control, microbiology, quality assurance,
maintenance, manufacturing processes, and
budgeting). Also requires excellent interpersonal,
investigative, and implementation skills.
3. Acts as a full-time Supervisor with
responsibility and authority for discharging the
normal supervisory responsibilities. These include
such matters as scheduling, organizing, assigning
work, maintaining quality, accuracy, quantity of
work; giving advice, guidance, instruction,
direction; developing of detailed internal work
methods; dealing with routine problems; recommending
need for staff changes, initiating recommendations
on personnel matters. Confers with and makes
recommendations to the Director of Manufacturing
when needed.
4. Supervises 1 to 5 employees in the Tech Transfer
area.
5. Controls
and administers the work of the Tech Transfer
department providing leadership to obtain the
cooperation of others on matters which may be of a
controversial nature or require an appreciable
degree of management coordination or control.
For
immediate consideration please send your resume to resumes@thevetrecruiter.com.
Senior/ Principal Scientist -
Monogastric species
A
companion animal
/ pet products
pharmaceutical company is looking for a Senior Scientist -
R&D with experience
as an agricultural nutritionist w/ background in
monogastric species (swine, poultry and fish). Persons
with feed formula experience highly desired. Experience
in the development of treat type products in bird,
small animal and aquatics categories is also desired.
As
a Senior Research Scientist, you will play a key and
exciting role in developing and commercializing new
products utilizing sound science, bench-top skills, team
spirit and industry knowledge. You will lead cross
functional team efforts to launch new products via
co-manufacturers as well as in-house locations.
Specific
responsibilities will include:
*
Develop food ingredients and formulas to consumer and
customer needs by leveraging the latest ingredient,
flavor and nutrient technologies, studying trends, and
competitor products.
*
Coordinate and conduct product shelf-life tests, chemical,
and sensory analyses.
*
Prepare raw material and formula specifications.
*
Monitor ingredient and finished product scale-ups and
plant production.
*
Develop experiments and prepare reports by collecting,
analyzing, and summarizing data; Recommend action plans to
implement findings.
*
Regularly interfaces with other members of the
R&D/Regulatory team and cross-functionally with
Marketing, Quality, Purchasing and Manufacturing.
Candidate
must have a Bachelor’s degree, (Masters preferred) and
five to seven years of experience in developing
products in the bird, small animal and aquatics
categories.
To confidentially learn
more about this exciting opportunity, please
e-mail your resume in confidence to resumes@thevetrecruiter.com.
Senior/ Principal Scientist - Food
/ Meat Science
A
companion animal
/ pet products pharmaceutical company is looking for a
Senior Scientist - R&D with
knowledge
and/or experience in the field of Food Science or Meat
Science.
As
a Senior Scientist in our Pet Nutrition R&D group, you
will play a key and exciting role in driving new product
initiatives from concept to commercialization while utilizing
sound science, team and personal leadership skills,
business savvy and industry knowledge.
This
is a key leadership position with the following specific
responsibilities:
*
Provide technical leadership and project management to
deliver business objectives; Lead project teams.
*
Define, initiate and execute projects to develop new
products, to improve product quality, to reduce raw
material and formula costs, and to successfully launch
products.
*
Technically lead development of novel food ingredients and
formulas to meet consumer and customer needs by leveraging
the latest ingredient, flavor and nutrient technologies,
as well as by studying trends, and competitor products.
*
Develop proprietary ingredients, formulas and products
that can be patented and will provide company sustainable
competitive advantage
*
Recommend food manufacturing and blending processes,
systems, and technologies; Provide scale-up and
commercialization support.
*
Develop ingredient, formula and process specifications to
ensure product quality, safety and consistency at lowest
cost.
*
Develop and coordinate experimental designs and testing to
evaluate efficacy, palatability, safety and shelf life of
new products; analyze data, prepare reports and recommend
action plans.
*
Coordinate
sensory, microbiological or chemical analyses, product
shelf-life tests, and off-site research and testing.
*
Regularly interface with Marketing, Regulatory, Quality
and Legal to technically substantiate product efficacy,
attributes and marketing claims.
Candidate
must have a Bachelor’s degree, (Masters preferred) in
Food Science or Meat Science, plus a minimum of five
years of experience in food product development for a
food manufacturer is required. R&D
experience in pet treat development is a plus.
To confidentially learn
more about this exciting opportunity, please
e-mail your resume in confidence to resumes@thevetrecruiter.com.
Associate
Director - Bacterial Process Development
We
have an opportunity for an Associate Director of Bacterial
Process Development to act as an interface between Bacterial
process development, Downstream, Pilot and Manufacturing.
This entails identifying and pursuing strategies to enhance
and align development and commercialization of new
biological products. Incumbent will contribute to
strategic planning, task forces or other initiatives, as
appropriate and will provide innovative solutions that allow
the smooth progress of new Technologies from Discovery to
Pilot and through to Manufacturing. Incumbent will
recommend new and innovative capital solutions that
accelerate the Development process and will track and
monitor progress of projects supported by their group.
Additional
responsibilities include monitoring a budget, providing
technical leadership and expertise to the group,
representing the group on Discovery and Development Teams,
reviewing and approving standard operating procedures,
directly supervising a scientific staff and ensuring that
the group complies with USDA and EU regulatory requirements
including GLP and GMP, health and safety requirements and
company policy.
Qualifications
include expertise in Bacterial Development, as well as new
technologies, such as DNA process development and
production. The ability to manage across sites is
essential and proven ability to industrialize through Pilot
departments and industrial knowledge is required. MS
or equivalent with relevant experience in Process
Development is required. Desirable skills include
downstream processing of bacterial products along with
purification of biologics to EMEA/USDA/FDA requirements.
Knowledge of registration processes globally is desirable
along with PhD/DVM or equivalent.
For
immediate consideration please send your resume to
stacy@thevetrecruiter.com.
Livestock
Antibacterial Lead In Vivo Modeler
We
are seeking a Livestock Antibacterial Modeler.
This position will lead the in vivo modeling efforts of a
group focused on the discovery of new antibacterial products
for the treatment of livestock diseases. This work
will involve the development and conduct of in vivo models
of bacterial diseases in cattle, swine, and poultry.
This work will also include the development and conduct of
field efficacy programs for further evaluation of new
antibacterial products. The candidate must be able to
interact with other antibacterial team members in order to
develop a successful program for the identification and
evaluation of new antibacterial compounds.
Additionally, the candidate must be willing to work with
other areas of research within the Livestock-Pharmaceutical
group including growth enhancement and reproduction.
The
successful candidate will have a PhD in Microbiology with at
least 10 years relevant industrial experience in an
antibacterial discovery program.
For
immediate consideration please e-mail your resume consideration to
stacy@thevetrecruiter.com.
Product
Development Manager- R&D
The
Product Development Manager is a hands-on position, that
must also be able to strategize, plan, coordinate and
execute present and future activities of cross functional
teams of professionals.
The position requires a person that is experienced,
motivated, disciplined, flexible, action-oriented, results
driven, an effective communicator, and a seasoned problem
solver with uncompromising integrity.
The PDM will prosecute
product development activities culminating in the
registration of new products and actively
engage colleagues in cross-functional settings to set,
drive and achieve Business Objectives outcomes.
Responsibilities:
-
Plan, coordinate and execute development
studies to support product dossiers.
-
Organize and manage Development Teams, CROs,
and third-party contractors to drive successful outcomes.
-
Dialogue with regulatory authorities
throughout the development and post-development life cycles
of products.
-
Estimate resource requirements to support
development objectives.
Prepare and oversee the preparation of
documents (protocols, forms, charts, etc.) for research
studies.
-
Ensure GLP and GCP adherence during the
execution of development activities.
-
Monitor, support, or coordinate the monitoring
of development studies.
-
Audit data and documents supporting
development studies and/or product dossiers.
- Respond to issues and requests by investigators during their
execution of development studies.
- Prepare Final Study Reports
- Coordinate and assist in the QC,
close-out and audit of develompment studies
- Perform Good Clinical Practices (GCP) Quality Assurance Audits for
Development Project studies on raw data or final
reports.
- Work with outside contractors in maintaining compliance with
protocols, and SOPs.
- Participate in the preparation of document packages for submission to
regulatory authorities.
Training
and Education:
- MS, DVM, or PhD in a
Science Curriculum.
- Training and
knowledge of regulations regarding the use of animals in
research.
- Training and
knowledge of Good Clinical Practices (GCPs) and Good
Laboratory Practices (GLPs).
- Training/experience
in Project Management.
Critical
Talents & Skills:
- Working knowledge of
Office Automation Tools in a Microsoft dominated
environment. (e.g.,
Word, Excel, etc.).
- Excellent writing
skills, particularly technical/science writing.
- Excellent verbal and
social skills with an affinity for working in stressful
and fast-paced environments.
- Detail oriented.
- Excellent
organizational skills.
- Able to be effective
as both team member and team leader.
- Working knowledge of
CFRs relevant to FDA/CVM and EPA.
- Working knowledge of
GCPs and GLPs.
Travel:
- Predominantly within
the US, with some Canadian and European potential.
- Normally 10-30%, with
periods as much as 50%.
To find out more about this
exciting opportunity, please
send your resume for immediate consideration to stacy@thevetrecruiter.com.
Manager of
Regulatory -
Veterinary Biologicals
A global veterinary
pharmaceutical company is looking for a Manager -
Veterinary Biologicals - Regulatory to support its
Regulatory and R&D groups. The
Mgr will report to directly to the Senior Director.
The position would
primarily address veterinary biological product
registration needs for the United States. With the
guidance of the Senior Director, and the rest of the
regulatory team, the Mgr would develop the regulatory
strategy for the team, and be responsible for all US
regulatory submissions for that project.
In addition, the Mgr
would serve as the primary liaison with Biological
Discovery to provide early regulatory input into early
phase Discovery projects. The candidate would
liaise with New Product Marketing to develop label claims,
and product supporting materials. The Mgr would
liaise closely with EU and CALAR regulatory staff to
facilitate global registration where appropriate.
In addition to project
responsibilities, the candidate would serve as an
alternate Liaison with USDA. Additional
responsibilities would involve obtaining required permits,
and miscellaneous submission as requested by the Senior
Director. Duties would require some travel,
primarily domestic, approximately 2-5 days a month.
No current direct reports are anticipated,
Qualifications:
- MS in biology, animal
science or other related science required, PhD or DVM
preferred
- A minimum of 5 years
experience with veterinary biological products
preferably in regularly affairs or a related area. (10+
yrs exp ideal)
- Strong verbal & written
communication skills
and a demonstrated ability to work in a team
environment
-
Understanding of the veterinary
biological development process and USDA regulatory
requirements desirable. Background knowledge in the
production and testing of veterinary biological products
desirable.
- Background
knowledge in global biological regulatory
requirements, specifically EU and Japan
- Experience
with trade organizations and other industry groups
To confidentially learn
more about these exciting opportunities, please e-mail
your resume in confidence to
resumes@thevetrecruiter.com.
Manager
- Clinical
Development Projects - Veterinary Oncology
Leading
animal health company is looking for a Manager - Clinical
Development Projects with an Oncology emphasis. This position will report
directly to VP of R&D.
The
Manager will formulate comprehensive development plans for
each new proposed product, especially in the area of anti-infectives
to treat infectious diseases.
This includes designing and writing of study
protocols, selecting research facilities and researchers to
execute studies, overseeing and monitoring studies,
analyzing and interpreting study results, writing study
reports, and preparing submissions to regulatory agencies.
This positions also provides technical support to commercial
operations and presents results of studies to the scientific
community.
Requirements:
• Ph.D. in an animal health related field or a DVM with special
training in oncology
• Advanced degree (MS or Ph.D.) in clinical veterinary oncology
in addition to a DVM, would be desirable
• Two to five years of experience in product development within
or closely associated with the Pharmaceutical industry is
preferred.
• Must possess the ability to organize and manage a variety of
projects at any one time demonstrating strict attention to
detail.
• Must possess good organizational skills and manage time
efficiently.
• Must be self-motivated, communicative and a problem solver.
• Good interpersonal skills to work within a team environment
To find out more about this
exciting opportunity, please
send your resume for immediate consideration to stacy@thevetrecruiter.com.
Veterinary
Pathologist / Research Leader
Global
pharma company is looking for a Reseach Leader for
pathology section of its the Non-Clinical Drug Safety
department (NCDS) is responsible for all aspects of
pathology from early Discovery support through development
and marketing of the Company’s therapeutics.
The
successful candidate will have the opportunity to evaluate
and interpret outcomes from both discovery and regulatory
toxicology studies. Regulatory work includes the planning,
conduct, reporting and review of toxicology studies,
including peer-reviews. In addition, pathologists
represent the department on discovery and development
project teams. The balance between discovery, regulatory
and team management activities is flexible to match the
needs and talents of the successful candidate
This
position requires a Veterinary/medical degree preferably
with PhD in Pathology or a related field and
Board-certified/eligible by the American College of
Veterinary Pathologists. Familiarity with Good Laboratory
Practice guidelines and 2-5 years experience working in a
regulatory toxicology environment is essential. An
enthusiasm to work with Discovery colleagues to
participate in and develop investigative programs is very
desirable. An ability to balance and constantly prioritize
regulatory work with Discovery projects is critical.
Proven ability to communicate clearly and effectively and
to foster productive dialog on complex topics is
required as well as the ability to contribute effectively
to sound decision making in a manner that is timely and
consensus based. The ability to introduce new ideas,
practices and technologies to effectively enhance the drug
development process is expected.
For
immediate consideration please send your resume to resumes@thevetrecruiter.com.
Senior
/ Principal Scientist - Animal
Health DD - Immunoendocrinological
Senior
Scientist-Leading Animal Health Pharmaceutical and
Biologicals company has an opportunity for a Senior
Scientist
to help identify potential
immunoendocrinological and endocrinological targets that could
lead to new products. The
successful applicant will be expected to have detailed
scientific knowledge of these fields and a command of how that
knowledge could be applied to treat diseases in a production
setting. She/he
will be expected to lead Discovery efforts within this arena,
suggest new approaches, and evaluate opportunities
Position
requires DVM & MS or PhD. The ideal candidate
will have Board certification, be a graduate in
endocrinology, theriogenology or immunology and have
experience in early phase of research (animal model
development, new substrates, vaccines and
biopharmaceuticals) as well as product registration
requirements (USDA/FDA/EMEA)
To confidentially learn
more about this exciting opportunity, please
e-mail your resume in confidence to resumes@thevetrecruiter.com.
Clinical
Veterinarian / Assoc Director - midwest
Global
R&D company is looking for a Clinical Veterinarian.
Depending on experience, candidate may also be titled as
Associate Director. This position will
manager/supervise a staff of 3 and
will have
oversight of our in-house genetic monitoring program,
development of policies on genetic management of our
commercial colonies, and our genetic testing services and
related veterinary care.
This person will be responsible for providing
training in genetics to our technical services, sales, and
marketing staff. This
position will be responsible for overseeing the review of
breeding histories of commercial colonies and providing
technical input on the genetic management of the
colonies. This position will also have contact with our
customers and support our Director to ensure regulatory
compliance.
This
position requires a DVM and a veterinary medical license for
at least one state. Completion of a residency program
in laboratory animal and ACLAM board certification or
eligibility is highly desired. At least 3 years of
previous research experience is required. Excellent
leadership and communication skills also required.
To find out more about this
exciting opportunity, please
send your resume for immediate consideration to stacy@thevetrecruiter.com.
Senior Scientist - Veterinary
Pathologist
Working
with other dedicated staff, this position will report to
the Toxicology/Target Animal Safety Group Leader in
R&D/Lab Sciences/Metabolism & Safety (M&S) to
serve R&D needs for expertise in pathology,
toxicology, drug development and regulatory submissions.
The
primary focus of this position is to bring pathology and
toxicology experience to the R&D Development and
Discovery teams. As
such, this person will spend much of their time attending
drug discovery and development team meetings to assure
that pathology and toxicology input to the drug
development process in R&D meets all business and
regulatory needs. This
position will also serve to review draft safety study
protocols to be conducted by R&D staff, participate in
pathology peer review of studies conducted by R&D at
company or CRO facilities, potentially monitor safety
studies conducted at CROs for M&S, and potentially
serve as a GLP study director for safety studies conducted
by M&S.
The
position will serve as a peer review pathologist, as
needed, and will participate actively in the formation of
regulatory submissions of compounds for for marketing
status approval worldwide.
This person will likely travel to regulatory bodies
to support drug development plans, as well as the
conclusions of the studies conducted to support the safety
of the drugs developed for R&D.
REQUIREMENTS
At minimum, a DVM, DACVP,
3 years working as a pathologist for GLP safety
studies
Preferably, DVM DACVP, PhD
in pathology. Ten
plus years in the human or animal health pharmaceutical
business with experience serving on Drug Development
teams.
Excellent organizational
skills and communication skills (ie, proactive
communication, scientific dialogue and discussion) are
required.
To confidentially learn
more about these exciting opportunities, please e-mail
your resume in confidence to resumes@thevetrecruiter.com.
Manager of
Toxicology
Global veterinary pharmaceutical company is
seeking a Manager of Toxicology. In this
position, you will manage all
activities to ensure that all toxicology work necessary
for all new and existing drug and pesticide products is
conducted to meet EPA and CVM requirements.
You will be the principal Animal Health liaison
with EPA, CVM and other internal groups such as
development teams, sales, marketing, etc. regarding the
toxicity of all Animal Health products.
You will advise,
develop and manage testing strategies necessary for the
explanation of toxicological effects and to summarize and
communicate large amounts of complex toxicology data in a
clear, simple, concise, and convincing manner.
Qualifications:
•Advanced
degree in toxicology (MS or PhD) plus 10 years experience
in regulatory toxicology. PREFER
Board
certification as a Diplomate of the American Board of
Toxiclolgy
( DVM
or DVM DABVT)
•Knowledge
of the necessary toxicology data to acquire approvals of
animal drugs and registrations for pesticides".
•Ability
to work individually and collaboratively with a team
•Excellent
technical and human relations skills
•Excellent
written and oral communication skills
•Excellent
organizational and document management skills
•Ability
to foresee the consequences of studies or proposed studies,
conducted elsewhere, upon company products
•Experience
in contracting and monitoring toxicology studies to CRO's"
•Experience
in meeting with regulatory authorities such as EPA, CVM and
others".
To confidentially learn
more about this exciting opportunity, please
e-mail your resume in confidence to resumes@thevetrecruiter.com.
Development
Manager / Clinician
The
Development Manager is a key, skilled individual, whose
principal roles are to provide a veterinary perspective to
development teams and be a study director, responsible for the development of non-NADA animal health products
intended for distribution through veterinarians. This
successful Manager will have a technical background, a
strong scientific perspective, and practical knowledge of
veterinary medical issues.
The position will focus on the development of
products that are not subject to formal pre-market
regulatory approval.
Essential Functions:
-
Lead studies generating data to support
product development efforts of
veterinary health products (dermatological, dental,
nutritional, ophthalmic, etc.).
-
Propose, design, organize, manage, and report
scientific evaluations of products undergoing development
for various veterinary uses.
Evaluations include, but are not limited to:
formulation suitability, product safety, and laboratory and
field effectiveness, etc.
-
Provide technical support to multi-functional
product development teams.
Collaborate with colleagues in multinational
development efforts.
-
Provide pre-launch technical support to
Marketing and Professional Services in the form of internal
technical manuscripts, product brochures, and training of
technical and sales staff.
-
Publish and present scientific data in
corporate publications, scientific journals, and at regional
and national veterinary congresses and association meetings.
-
Participate in formulation development and product
innovation efforts.
Provide
formal support and opinions (regulatory implications,
concept feasibility, etc.) to Marketing in the review of
potential product candidates or innovations.
Additional Responsibilities:
-
Assist in
developing labeling in compliance with relevant local,
state, and federal regulations.
-
Suggest
new product candidates based on unfilled needs in the market
place and via line extensions (e.g., formulation
improvements).
-
Manage test
materials and/or marketed product samples in support of
safety and effectiveness studies.
-
Follow up on research and development projects as
necessary.
Knowledge, Skills, and Abilities:
-
Doctor of Veterinary Medicine
preferred;
alternatively, an equivalent combination of education and
relevant experience.
-
Demonstrated ability to effectively communicate
complex scientific information to a variety of professional
and lay audiences
-
Ability
to interact with all members of multi-discipline and
multi-national project teams
-
Ability to work well in team environments to
accomplish shared objectives
-
Demonstrated management skills with a history of
meeting personal and corporate objectives
-
Understanding of product development, research
protocols, research reports, and technical communication
-
Excellent oral and written communication skills
-
Creative thinker with the ability to develop new
product concepts or adapt existing products to fit the needs
of Marketing
-
Working knowledge of applicable regulations
Ability to utilize scientific methods in research and
development
To find out more about this
exciting opportunity, please
send your resume for immediate consideration to stacy@thevetrecruiter.com.
Chief
Clinical
Veterinarian - California
Growing
company with state-of-the-art facility is looking for a
Chief Veterinarian. This is an excellent opportunity
to combine DVM with business management skills.
Clinical Management
- The
Chief California Veterinarian is responsible for
providing direction on the use, care and management of
all animals that are used for studies and/or housed at
the Company in California.
- Manage/supervise
the Veterinary Technical Staff
- Support,
problem-solve and interface with new and existing
clients during the initiation of in-vivo studies and
during studies while clients are on site.
- Establish
policies and procedures related to the humane needs,
care and management of study animals.
- Provide
education and training as necessary to assure the
highest quality services are provided by Veterinary
Technician and Animal Husbandry staff.
- Provide
anesthesia, pre and post-operative care.
- Provide
veterinary care-preventative, interventional and acute
for all animals on site and those that are housed
remotely.
- Represent
the Company with regard to animal use and care to
clients, vendors and outside agencies.
- Keep
the Chief Operating Officer and Institutional Official
apprised of significant issues related to animal care
Business
Management
The
Chief California Veterinarian is responsible and
accountable for the continuity and growth of Earnings
(along with Sr. Team) by:
- Collaborating
with Client Services, Sales, and Accounting on
invoices and scheduling, and stewarding close and
continual coordination between these groups and the
Clinical Staff.
- Working
with Client Services, Sales, and Accounting to achieve
continuity and, over time, improvement in the margin
between Pricing and Core Surgical Costs.
- Client
interaction including sales meetings, and building of
client goodwill and client base.
- Participating
in Service Agreement (client contract) discussions
seeking volume commitments and term agreements where
opportunities exist, and helping to deal with
situations where a valued Client wants to pay an
amount that is ‘under baseline cost.’
- Collaborating
with Client Services to achieve accurate and prompt
recording of preliminary invoice data at time of
check-out (use of labor, equipment, staff overtime,
staff double-time, professional services, key
supplies, etc…).
Requirements
The
Attending Veterinarian must have the following:
-
Current
license to practice veterinary medicine within the United
States.
-
Board
Certification or board eligibility preferred for ACLAM,
ACVECC, or ACVA
-
Must
have received DVM at least two years ago.
-
Proven
experience in managing staff of at least eight employees.
-
Proven
clinical, surgical and expertise.
-
Ability
to work in fast paced environment.
-
Ability
to positively interact with clients and staff at all
levels, including speaking at meetings, trainings and
trade shows
-
Experience
in working with start-up and/or fast growing business a
plus.
-
Available
for some evenings and weekend shifts
Senior Scientist - Veterinary
Pathologist
Working
with other dedicated staff, this position will report to
the Toxicology/Target Animal Safety Group Leader in
R&D/Lab Sciences/Metabolism & Safety (M&S) to
serve R&D needs for expertise in pathology,
toxicology, drug development and regulatory submissions.
The
primary focus of this position is to bring pathology and
toxicology experience to the R&D Development and
Discovery teams. As
such, this person will spend much of their time attending
drug discovery and development team meetings to assure
that pathology and toxicology input to the drug
development process in R&D meets all business and
regulatory needs. This
position will also serve to review draft safety study
protocols to be conducted by R&D staff, participate in
pathology peer review of studies conducted by R&D at
company or CRO facilities, potentially monitor safety
studies conducted at CROs for M&S, and potentially
serve as a GLP study director for safety studies conducted
by M&S.
The
position will serve as a peer review pathologist, as
needed, and will participate actively in the formation of
regulatory submissions of compounds for for marketing
status approval worldwide.
This person will likely travel to regulatory bodies
to support drug development plans, as well as the
conclusions of the studies conducted to support the safety
of the drugs developed for R&D.
REQUIREMENTS
At minimum, a DVM, DACVP,
3 years working as a pathologist for GLP safety
studies
Preferably, DVM DACVP, PhD
in pathology. Ten
plus years in the human or animal health pharmaceutical
business with experience serving on Drug Development
teams.
Excellent organizational
skills and communication skills (ie, proactive
communication, scientific dialogue and discussion) are
required.
To confidentially learn
more about these exciting opportunities, please e-mail
your resume in confidence to resumes@thevetrecruiter.com.
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