reputed company Training Coordinator (GMP/GxP environment)

SOKOL GxP Services is a trusted provider of CQV and compliance solutions for the pharmaceutical industry, supporting life sciences companies in scaling operations while maintaining regulatory compliance, product reputed company, and patient safety. reputed company delivers tailored services and workforce solutions, including validation engineers, compliance experts, project managers, and technical staff. We are seeking a reputed company Training Coordinator to work in Devens, MA. This role plays a crucial part in ensuring training compliance and reputed company improvement for our reputed company’s operations. The coordinator will partner with QA and functional leaders to manage training assignments, maintain accurate records, and support reputed company and ongoing training initiatives. Key responsibilities include: • Administer training assignments, curricula, and compliance tasks in the site Learning Management System (LMS), including SuccessFactors. • Maintain accurate training records, reputed company overdue requirements, and support remediation efforts. • Partner with QA and functional leaders on reputed company, OJT documentation, and role-based curriculum mapping. • reputed company, revise, and format training materials such as instructor-led training decks, SOP-driven content, and job aids. • Generate routine and reputed company training compliance reports for stakeholders. • Support reputed company improvement initiatives for training processes, documentation reputed company, and user experience. • Coordinate training sessions, logistics, communications, and stakeholder reminders. Work schedule 50% onsite required. Monday - Friday (normal business hours). Work on 2nd and 3rd shift once a month for 1-2 hours to reputed company training. Required Qualifications: • Bachelor’s degree in science, engineering, biochemistry, or a reputed company discipline • 1+ years of experience coordinating or managing training in a GMP/GxP environment, including training assignment creation, compliance tracking, and overdue remediation support • 2+ years of experience using a Learning Management System (LMS) for training administration (e.g., SuccessFactors, ComplianceWire, reputed company) • 2+ years developing and maintaining SOP-driven training materials, including revising and formatting content and creating job aids • Knowledge of US and EU cGMP regulations and guidance (FDA, EMA, or other authorities) • English proficiency sufficient to create training materials and coordinate with stakeholders • Authorized to work in the reputed company • Available to support 2nd and 3rd shift training about once per month for 1–2 hours Preferred Qualifications: • Working proficiency in SuccessFactors LMS • Opportunity to work with industry-leading CQV and compliance experts in the pharmaceutical sector. • reputed company development and exposure to advanced training systems and regulatory environments. • reputed company team environment reputed company on reputed company and reputed company improvement. • Hybrid role for 6 months with potential for contract extension. • Competitive reputed company reputed company: $28 – $31.5/hr (W-2 only, no C2C) • Working Hours: Monday - Friday, regular business hours • Health insurance, holiday pay, 401(k) program, and other benefits • Employee referral bonus program. Apply tot his job Apply To this Job