Training Manager

Posted 3 Days Ago
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Waterford, MI, USA
In-Office
63K-84K Annually
Entry level
Healthtech
The Role
Lead GMP-compliant training programs across a pharmaceutical plant. Responsibilities include developing curricula, identifying training needs, delivering sessions, monitoring completion, evaluating effectiveness, updating materials, leading continuous improvement, supporting regulatory inspections and audits, managing the training team, and contributing to QMS processes such as deviations, CAPA, and change control. The role also represents the site in global training communities and supports regulatory compliance and operational excellence.
Summary Generated by Built In

Job title: Training Manager

  • Location: Waterford, Ireland

  • Full-Time, 6-Month Fixed Term Contract

About the job

As a Training Manager, you will lead the development and delivery of comprehensive GMP-compliant training programs across the plant, ensuring all personnel are qualified and equipped to meet regulatory standards and operational excellence. You will partner with department heads to design customized curricula, manage the training team, drive continuous improvement initiatives, and serve as the site's training representative in global Communities of Practice while supporting regulatory inspections and QMS processes.

Main responsibilities:

  • Developing and implementing annual training programs to ensure compliance with Good Manufacturing Practices (GMP) and other regulatory standards
  • Collaborating with department heads to identify training needs and developing customized training plans
  • Supporting the managers in the establishment of the curricula for the different areas
  • Conducting training sessions for new hires and existing employees on specific topics as necessary
  • Monitoring the completion of the training plan to identify risks and weaknesses
  • Evaluating training effectiveness through assessments, feedback, and performance metrics
  • Ensuring update of training materials to reflect changes in regulations, procedures, and best practices
  • Leading continuous improvement initiatives to enhance training material and processes
  • Providing support during regulatory inspections and audits by presenting training records, training process and material
  • Managing the training team and ensuring their proper qualification for their activities
  • Contribute to QMS processes related training activities (e.g., Deviation, CAPA, Change Control) for the site
  • Representing the site in the training CoP led by global and, if requested, participating in the CoE and ensuring local communication

About you

Required Experience & Capabilities:

  • Experience in quality management systems in the pharmaceutical industry ensuring compliance with GMP and other regulatory standards and experience in developing, implementing, and evaluating training programs, particularly those related to quality systems and regulatory compliance
  • Ability to create effective training programs and materials that meet the needs of the organization and comply with regulatory standards
  • Proficiency in evaluating training effectiveness through data analysis, assessments, and feedback to continuously improve training programs
  • Strong understanding of regulatory requirements and the ability to ensure training programs align with these standards
  • Expertise in planning, organizing, and managing training projects, including setting timelines, allocating resources, and monitoring progress
  • Excellent verbal and written communication skills, with the ability to effectively convey information, collaborate with various departments, and present training outcomes to senior management

Why choose us?

  • Bring the miracles of science to life alongside a supportive, future-focused team 
  • Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally 
  • Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact 
  • Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave 

#LI-EUR

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

The salary range for this position is :€63 200,00 - €84 267

Final compensation will be determined based on demonstrated experience, skills, location, and other relevant factors. Employees may be eligible to participate in Company employee benefit programs.

Skills Required

  • Experience with quality management systems in the pharmaceutical industry and compliance with GMP and other regulatory standards
  • Experience developing, implementing, and evaluating training programs related to quality systems and regulatory compliance
  • Ability to create effective training programs and materials aligned with organizational needs and regulatory standards
  • Proficiency evaluating training effectiveness through data analysis, assessments, and feedback
  • Strong understanding of regulatory requirements and ability to align training programs with those standards
  • Experience planning, organizing, and managing training projects, including timelines, resource allocation, and progress monitoring
  • Excellent verbal and written communication skills, collaboration skills, and ability to present training outcomes to senior management

Sanofi Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Sanofi and has not been reviewed or approved by Sanofi.

  • Retirement Support Retirement support stands out through a notably strong 401K matching structure (e.g., 150% match up to a 6% contribution), which materially boosts total rewards for long-tenured employees.
  • Parental & Family Support Parental and family support is positioned as unusually robust, including a global gender-neutral paid parental leave standard (14 weeks) and added supports such as childcare assistance and adoption/surrogacy/infertility help.
  • Equity Value & Accessibility Equity participation is made more accessible via an Employee Stock Purchase Plan that includes a meaningful purchase discount and matching/free-share mechanics, increasing perceived total compensation beyond base pay.

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The Company
HQ: Paris
85,000 Employees
Year Founded: 1973

What We Do

We are Sanofi, an innovative global healthcare company. We chase the miracles of science to improve people’s lives. Our team, across some 100 countries, is dedicated to transforming the practice of medicine by working to turn the impossible into the possible. We provide potentially life-changing treatment options and life-saving vaccine protection to millions of people globally, while putting sustainability and social responsibility at the center of our ambitions. Interactions with this account must comply with the Terms: https://bit.ly/sanofi-terms

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