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A Division
of
GMP
Publications
& FDA.COM
"The GxP Family of
Quality Business"




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"We stand on a higher pillar of excellence!"
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Title |
Location |
Type |
Rate |
Apply |
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Quality Training Manager |
West
Chester PA |
Perm/Full |
$70,000 - $80,000 |
Submit |
Quality Training Manager
Overview:
• Responsible for the organization, content and
administration of Quality Systems-based training
programs for the Brandywine Manufacturing Plant.
Responsibilities:
• Establish methods for identifying quality
system based training needs and ensuring
personnel are trained to adequately perform
their assigned responsibilities.
• Ensure that each employee understands their
job function and the quality system (e.g., FDA
Quality System Regulation) requirements
pertaining to that particular job function,
including how the job relates to the overall
quality system (excluding Manager - Training -
IS).
• Assist trainers / presenters with
instructional techniques that produce the best
results with adult learners.
• Assist trainers / presenters with planning,
designing and evaluating the training
presentations, programs, and/or classes.
• Establish and maintain schedules for quality
system-based training classes.
• Coordinate all aspects of the quality system
training classes (faculty, curriculum, etc.)
• Participate in some of the instruction during
the training classes.
• Consistently strives to improve the quality
system training programs via course evaluations
and critiques.
• Ensure that the required training records are
current and properly maintained.
• Identifies, evaluates, and coordinates outside
quality systems-based training programs.
• Identify need for, and implement programs to
support individual and organizational
development plans.
• Design and develop quality system training and
educational programs.
• Identify learning objectives.
• Evaluate training and development
effectiveness by assessing the performance of
the trainers / trainees.
• Maintain knowledge of training and performance
improvement methods by attending seminars,
reviewing professional publications, and
participating in professional societies.
• Other duties or projects as assigned.
OTHER REQUIREMENTS:
• Excellent writing skills.
• Excellent organization skills.
• Excellent presentation skills.
• Demonstrated office software and computer
skills.
• Demonstrated project management and
coordination skills.
• Proven analytical ability.
• Excellent interpersonal, communication, and
facilitation skills.
• Ability to work collaboratively with team
members to compile information, assesses
problems, and solicits feedback in the
attainment of goals.
• Ability to work with employees at all levels
within the organization.
Qualifications:
• Bachelor's Degree
• Managerial and training experience preferably
in a FDA or similarly regulated industry. Prior
FDA-based Quality Assurance or Regulatory
Affairs experience a plus.
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