Intertek Group

Manager, Toxicology - Mississauga, ON

Intertek Group$95K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • B.Sc., M.Sc. or Ph.D. in Toxicology or a relevant field.
  • Specialization in a relevant toxicology area (e.g., molecular toxicology, pharmacology).
  • Strong expertise in regulatory toxicology and drug development processes.
  • Proven project management skills with complex projects.
  • Excellent verbal and written communication skills.

Responsibilities

  • Understand project needs and develop scientific approaches for deliverables.
  • Prepare and review toxicology/safety risk assessments and advise on studies.
  • Lead project teams while managing project phases effectively.
  • Develop client relationships and identify new project opportunities.
  • Support leadership in achieving goals and help develop junior staff.

Benefits

  • Paid time off and holidays.
  • Medical, dental, and vision insurance.
  • Life and disability insurance coverage.
  • RRSP with company match.
  • Tuition reimbursement opportunities.
Full Job Description
Job Description

Manager, Toxicology (Consultant)

Intertek is searching for an Manager, Toxicology (Consultant to join our Assuris team in our Mississauga, ON office. This is a fantastic opportunity to grow a versatile career in consulting!

The Manager, Toxicology is responsible for:

What you'll do:
  • As a scientist, understand the needs of the project and possible issues, and the vision of the deliverable (report, regulatory dossier, research, risk assessments, nonclinical program design or analysis, etc.) and how best to conduct the project efficiently with respect to scientific and writing activities and the project scope. Exercise judgment and be principally involved in deciding the approach needed to resolve the problem. Review and interpret published/unpublished scientific materials and synthesize findings into reports and address the implications of the findings given the regulatory and toxicology questions at issue. Prepare toxicology/safety risk assessments for active substances, excipients, impurities, and other compounds and advise on, guide, and monitor toxicology studies and whole programs, including data review and issue resolution. Know and apply regulatory agency guidelines and expectations for pharmaceuticals and healthcare products of various types to client product development programs and be aware of industry standards. Review internal reports and be responsible for the quality and scientific accuracy of the final deliverable to internal reviewers and, depending on the complexity of the project, to the client.
  • Where required (e.g., in complex projects), use powers of analysis and lateral thinking skills to identify "out of the box" solutions in/across the different dimensions of the problem.
  • As a project manager, provide leadership to project teams, oversee the work of assigned team. Depending on the size and complexity of the project, lead or support all project phases from set-up (scope, budget and proposal preparation, administrative elements) to initiation (address project requirements depending on size and complexity; design tasks and envision deliverables), through project maintenance to manage progress and client relationships, and project deliverables focused on the client's needs (supported by senior staff).
  • Be a consultant, both in-house and to outside clients. Interact and develop relationships with clients on most projects to ensure smooth communication regarding project scope, timing, and other parameters. Identify new project opportunities with existing clients, participate in marketing initiatives and sales discussions. Work typically involves balancing needs of and resolving potential conflicts among several projects or programs typically of major complexity.
  • Support leadership in meeting goals and objectives and contribute to the development of junior staff.

What it takes to be successful in this role:

Desired Qualifications:
  • B.Sc., M.Sc. or Ph.D. with experience in the pharmaceutical or relevant industry/sector. Education degree should be in Toxicology or a relevant field.
  • Additional specialization in an area of toxicology, e.g., molecular toxicology, physiology, metabolism, pharmacology, anatomy, chemistry, regulatory knowledge, etc.
  • Subject matter expertise: scientific acumen and expertise to a level that can be expected to undertake and understand most standard studies within the overall field of toxicology. Able to critically review information and present a mature scientific argument. Additionally, an understanding of the role of regulatory toxicology in drug development and ability to solve increasingly complex scientific problems.
  • Excellent communicator and manager, able to practice effective time management and able to manage complex projects in order to meet client expectations related to project deadlines and deliverables. Enjoys working within a team including more senior and more junior team members.
  • Clear and skillful writer, able to draw together key points, identify and include relevant details, and prepare a clean and persuasive document.

Personal Characteristics:
  • Excellent communication skills in both verbal and written format; able to develop persuasive, clear arguments and rationales.
  • Well organized and structured; able to pay attention to detail.
  • Excellent customer service and interaction skills.
  • Enjoys the challenge of analyzing and solving problems.
  • Able to self-motivate to meet project or submission timelines, process information, and work independently in a fast-paced, multi-tasking environment, but also a team player able to contribute work on a number of different parts of a project.
  • Able to work in an office in Mississauga, Ontario, Canada (remote/home-based work could be discussed in due course).

Salary & Benefits Information

Salary will be up to $95K. Individual compensation packages are based on a variety of factors unique to each candidate including skill set, experience, qualifications, and other job-related reasons. In addition to competitive compensation packages, Intertek employees are eligible for a variety of benefits including paid time off, paid holidays, medical, dental, vision, life, and disability insurance, RRSP with company match, tuition reimbursement and more.

This position is a replacement.

*Intertek does not accept unsolicited approaches from agencies and will not pay a fee for any placement resulting from the receipt of an unsolicited resume.

About Intertek Group

Intertek Group plc is a British multinational assurance, inspection, product testing and certification company headquartered in London, United Kingdom. It is listed on the London Stock Exchange and is a constituent of the FTSE 100 Index. Intertek operates in over 100 countries and has more than 46,000 employees. The company provides services such as testing, inspection, auditing, certification, quality assurance, advisory, and outsourcing services to various industries such as aerospace, construction, consumer goods, food, healthcare, and more.
Learn more about Intertek Group
Size
46,000 employees
Industry
Founded
1996

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