QA Supervisor
Educational Qualifications:
BSc or equivalent with a minimum of 5 years experience in the pharmaceutical,
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radiopharmaceutical or biopharmaceutical industry
Experience:
Pharmaceutical industry experience or experience within a highly regulated technical
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environment (e.g. GMP)
Demonstrated ability to think strategically and identify a vision along with the plans which need
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to be implemented to meet the end goal
Ability to develop and maintain relationships with internal and external business partners
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Strong communication skills with various levels of the organization
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Proven ability to assess and make risk-based decisions while keeping stakeholders appraised
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Experienced in assessing a situation, identifying issues and developing solutions that result in
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efficiencies or process improvements
Demonstrated leadership capability (ie. takes initiative to lead self and others, lead by example
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and follow through to completion often with minimal direction)
Ability to work with a sense of urgency, prioritize work, meet objective / deadlines with strong
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organizational capability
Successfully demonstrated ability to coach others with a strong self awareness (both strengths and
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opportunities) and ability to self develop
Ability to adapt to change and work flexibly to overcome boundaries
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Strong project management skills with the ability to work independently and within a team
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Ability to adjust work schedule based on business requirements
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To apply please submit a cover letter and resume to: careers@imagingprobes.ca
Attention: Joe McCann, PhD
Centre for Probe Development and Commercialization (CPDC)
1280 Main Street West, NRB-101
Hamilton, ON L8S 4K1
We thank all applicants for their interest, but only those selected for interview will be contacted