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>> CAREERS: VALIDATION SPECIALIST
Title:
Validation Specialist
Duties:
We are currently looking for a dedicated and hardworking individual
to join
our Team as a Validation Specialist. As a Validation Specialist,
you will
provide computerized system validation consultation, training
and evaluation. You will develop, implement and support Validation
Plans and develop and execute test scripts. You will lead and
manage software validation projects by preparing validation
protocols, reports, and test plans.
You will interview engineers and developers and in doing so will be
responsible for developing clear, concise, professional
documentation for all phases of the development life cycle, such as
user guides, installation guides, functional specification
documentation, and technical specification documentation in
accordance with established plans and quality standards. You
must be well versed in the regulations governing the life sciences,
such as FDA, TPD and GxP.
Ideal Person:
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Degree in Engineering, Computer Science, Science or related
field required
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Demonstrated success and 5 years of software validation and test
development experience in a medical device or pharmaceutical
industry
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Strong knowledge, understanding and application of principles,
concepts and practices of software validation procedures and
regulations
-
The ideal candidate has experience in life science systems such
as; ERPs, spreadsheets, process control systems, lab instruments
and quality systems.
-
A dynamic, fun approach to business, a high energy level, and
the ability to thrive and excel in a fast paced, changing
environment
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Excellent interpersonal, organizational and analytical skills as
well as the ability to be a strong leader, team-builder and
coach.
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Bilingualism is an asset
- Travel
is REQUIRED
Contact Information
Compliance Associates Inc.
HR Department
T (905) 738-3773
F (905) 738-2447
8000 Jane Street,
Suite 402, Tower A
Concord, Ontario L4K 5B8
http://www.complianceassociates.ca
Mail resume to:
careers@complianceassociates.ca
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