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Career Opportunities...
... Within the Food & Nutrition
Group
... Within the Pharmaceutical & Healthcare Group
... Within the Chemicals Group
... Within the Agri, Biotech & Consumer Products Group
Senior Scientific
& Regulatory Consultant
The Food & Nutrition Group of Cantox has a challenging
opportunity for a Senior Scientific and Regulatory Consultant in our head office
in Mississauga, Ontario, Canada. Qualified
candidates will be expected to lead scientific studies with a view to resolving
complex scientific problems; to direct the day-to-day work of and mentor the
career development of scientists within the Food & Nutrition Group and to
identify, develop and maintain successful, long-term business relationships
between Cantox and representative companies in the global food industry.
As a member of the Food & Nutrition Group, you will:
- Direct and manage resources,
activities and timelines to ensure that projects are effectively executed to
meet client and business objectives.
- Be responsible for the management and
quality control of complex scientific projects.
- Act as an in-house scientific advisor
on complex scientific issues.
- Supervise, manage, mentor, coach,
develop, provide training, and conduct performance planning and review for
regulatory personnel.
- Keep abreast of
scientific trends and changes by participating with scientific agencies and
attending scientific conferences.
- Act as a major corporate spokesperson
in high profile situations, identify new business opportunities and generate new
projects and build and maintain effective long-term client relationships.
- Join a complement of 15 scientists
led by Drs. Ashley Roberts and Ian Munro.
Qualifications and Experience
- Requires a PhD/MD (toxicology
preferred) with at least 10-15 years experience as a leader within the food
& nutrition industry
- Demonstrated leadership, management,
interpersonal and communication (verbal, written, listening and presentation)
skills in fast-paced, dynamic and changing environment
- Strong planning, organization and
decision-making capabilities; must be able to prioritize and manage multiple
tasks simultaneously, resolve conflicts and solve problems with minimum
supervision
- Persuasive, effective and flexible in
personal interactions at all levels
- Ability to lead and work in
cross-functional teams with a style that builds alliances and emphasizes
integrity, results, collegiality and effective teamwork
- Willingness to travel to
lead interaction with scientific government authorities, meet clients, present
at international conferences, market the skills and expertise on Cantox’s
internal regulatory affairs staff.
Scientific
& Regulatory Consultant
The Pharmaceutical & Healthcare Group at our head office in Mississauga,
Ontario,
Canada
has an immediate opening for a Scientific & Regulatory Consultant.
This individual will advise and work with in-house Toxicology and
Regulatory Affairs professionals and Pharmaceutical & Healthcare Group
client’s, assist with the development of strategic guidance in complex
scientific areas, including product development issues, and will be responsible
for reviewing scientific advice provided to clients by the Group.
As Scientific &
Regulatory Consultant in the Pharmaceutical & Healthcare Group, you will:
- Provide scientific
consulting services to Pharmaceutical & Healthcare Group clients,
provide strategic guidance in complex scientific areas, and be responsible
for the quality of scientific advice provided to clients by the Group.
- Play a key role in the
identification, development and maintenance of successful, long-term
business relationships between Cantox and representative companies in the
global pharmaceutical industry.
- Mentor the longer-term
career development of those employed in the Pharmaceutical & Healthcare
Group.
Qualifications and Experience:
- A PhD in a related
field, with minimum 3-5 years experience as a leader within the
pharmaceutical and healthcare industry (Product Development experience and
Regulatory Affairs knowledge a must; DABT certification a definite asset).
- Strong planning,
organization, and decision-making capabilities; must be able to prioritize
and manage multiple tasks simultaneously, resolve conflicts, and solve
problems with minimum supervision.
- Persuasive, effective,
and flexible in personal interactions at all levels, including with clients
and regulatory agencies.
- Willingness to travel
to lead interactions with scientific government authorities, meet clients,
present at international conferences, and market the skills and expertise of
Cantox’s Pharmaceutical & Healthcare Group.
Toxicologist
As a
Toxicologist at Cantox, you will:
- Critically review relevant information to
formulate assessments and to draw scientific conclusions,
- Manage small projects; effectively coordinate
multiple projects simultaneously,
- Participate in business meetings, as required.
Qualifications and Experience:
- B.Sc. in Toxicology (Toxicologist I)
- B.Sc. in Toxicology, with 2 years
experience, or a M.Sc. (Toxicologist II)
- Ability to retain clear picture of project
goals, plus understanding how projects are structured,
- Ability to multitask and effectively
prioritize,
- Ability to guide the work of less experienced
staff,
- Ability to communicate effectively (strong
writing skills).
Toxicologist
II
As a
Toxicologist II at Cantox, you will:
Scientific
studies:
Work within a team, where each person is assigned a
component or part of a project (project specific, location specific) and/or
assigned to manage complete projects.
NOTE: The incumbent may also be responsible for duties
outlined in the position description for Toxicologist Is, especially in times of
low staff availability.
- Provide support to numerous projects pertaining to drugs
and foods by:
- Meeting with team/project manager to define scope of
project/deadlines, budgets, etc.
- Prepare search requests for search team; review searches or
have TI review searches
- If on the search team
- conduct searches as requested
- ensure objective(s) of requested search are
well-defined to ensure efficient search
- Search for information required to prepare report (or your
section of the report) using various sources such as library, intranet,
databases
- Review, evaluate and summarize various toxicological
studies on drugs, food products, nutraceuticals, functional foods, etc. This
requires reviewing and interpreting a wide array of toxicological studies
such as pharmacokinetic, acute, subchronic, and chronic toxicity,
genotoxicity, reproductive toxicity, and carcinogenicity studies. In
addition to reviewing and interpreting this information, it is required that
a critical analysis of this information be performed to assess the
credibility of these studies and evaluate if the information is acceptable
for reporting.
- Reviewing other relevant information
(>non-toxicological@), i.e., regulatory, dietary exposure data,
analytical studies which may be required for drafting a report.
- Organize pertinent information according to project
requirements and outlining the format of the document, which may require
some consultation with the project manager.
- Reporting this information and ensuring that the report
identifies all required issues which may include forming an opinion, and
making conclusions based upon the scientific information that has been
reviewed.
- Writing brief summaries (abstract) of a large body of
information so that all key elements and conclusions are presented.
- Incorporate information scientific/non-scientific from
various sources in order to draft reports for client/publishing
- Review summaries for accuracy- Review draft with senior
project manager (be prepared to defend material in draft)
- Re-write, as requested by project manager
- Assume responsibility for the quality (scientific accuracy, completeness, writing style
of the initial draft) of own work
- Assume responsibility for tracking time and
staying within allocated time to perform duties required
Qualifications and Experience:
- B.Sc. (1-4 years experience)
- Formal scientific training and additional experience
- Experience in your area of expertise (e.g., proven ability
of applying toxicological knowledge)
- Critically evaluate scientific papers
- Ability to work on a number of different aspects of one
project and evaluate and integrate work from a number of sources into the
project
- Ability to retain clear picture of project goals, plus
understanding how projects are structured
- Ability to multitask
- Ability to guide the work of less experienced staff
- Ability to communicate effectively
- Developing written skills as a professional scientist
- Proficient with computer skills e.g., Word, WordPerfect,
Excel, Quatro Pro, Internet Explorer, MS Project (if required) Basic
coaching and feedback skills
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