Training Coordinator

Description:

Veranova, a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs), is seeking a Training Coordinator to join its Devens, MA site. This role plays a critical part in designing, managing, and delivering training programs that support Veranova’s mission of enabling next-generation therapeutics and improving patient lives. The Training Coordinator will partner with multiple teams, foster professional development, and ensure compliance with industry regulations.

Key Responsibilities:

• Develop, evaluate, and deliver high-quality training programs across all functional areas.

• Design and implement training initiatives aligned with organizational values, compliance standards, and business goals.

• Manage and maintain training systems, including leadership and skills development programs, ensuring accuracy and accessibility of training records.

• Provide leadership to a site Training Committee and collaborate with subject matter experts to create on-the-job training content.

• Oversee controlled training documentation, including periodic review, assignment management, and archival.

• Define, monitor, and report training metrics regularly to the Site Director.

• Ensure ongoing compliance with cGMP requirements and support inspection readiness activities.

• Support QA, EHS, and cross-functional teams in meeting training and documentation needs.

• Develop and maintain participant and instructor training materials (manuals, workbooks, job aids, etc.).

• Administer training plans and track progress using MasterControl or equivalent systems.

• Collaborate with other Veranova sites to share best practices and standardize training programs.

Required Qualifications:

• Bachelor’s degree (mandatory).

• 3–5 years of experience in developing and administrating training programs.

• Strong knowledge of SOPs and GMPs within a regulated environment.

• Experience with MasterControl or similar training/documentation systems.

• Proven organizational skills, attention to detail, and ability to work independently or in teams.

• Proficiency in MS Office (Word, Excel, PowerPoint).

• Strong change management and business process improvement skills.

Preferred Qualifications:

• Experience within the biotech, pharmaceutical, or GMP-regulated industries.

• Demonstrated adaptability in fast-paced and evolving environments.

Compensation & Benefits:

• Competitive salary with performance-based bonuses.

• Defined Contribution Pension program.

• Comprehensive health, dental, and wellness benefits including mental health resources.

• 401(k) plan with company match.

• Paid time off, holiday pay, and generous leave policies.

• Tuition assistance, mentorship, workshops, and LinkedIn Learning access.

• Inclusive work environment supporting diversity and employee growth.