Jobs at TOLMAR

• + Provide strategic and day-to-day leadership for labeling, visual inspection, assembly, tray-pack, and cartoning operations across assigned Windsor manufacturing areas.

Own execution of the production schedule, aligning labor, equipment, materials, training, maintenance, and cross-functional support to meet business and patient-supply commitments.
Establish consistent operating standards and performance-management routines across shifts, including tiered accountability, escalation, shift handoffs, leader floor presence, and effective use of controlled digital or visual-management systems.
Monitor and improve safety, quality, schedule adherence, OEE, throughput, yield, cycle time, right-first-time, labor productivity, deviation, and equipment-reliability performance.
Ensure labeling and packaging operations are inspection-ready and executed in accordance with approved procedures, product and component specifications, serialization requirements, in-process controls, and applicable regulatory commitments.
Maintain clear ownership and timely escalation of constraints involving staffing, components, artwork, recipes, vision systems, inspection, equipment, or quality disposition that could affect schedule or supply.

• Provide site-level compliance leadership by deploying Quality Compliance programs that support company quality objectives and manufacturing operations.
• Serve as a knowledgeable site resource on quality systems, regulatory compliance, and the interpretation of applicable requirements.

• Provide technical support and identify and implement process improvements on automation equipment and systems (including production equipment, utilities systems, and building automation and controls systems).
• Perform necessary functions to monitor and maintain automation equipment and systems in a valid...

• Training Hours may vary
• Perform data review to ensure compliance with published methods, work instructions, compendia, and other standard operating procedures.

• Plan and coordinate validation activities for cross-functional projects, including but not limited to validation plans, protocols, and reports
• Develop and execute validation protocols (IQ/OQ/PQ) for equipment, facilities, utilities, and processes.

• Plan and coordinate validation activities for cross-functional projects, including but not limited to validation plans, protocols, and reports
• Oversee and approve validation protocols (IQ/OQ/PQ) for equipment, facilities, utilities, and processes.

• Support and lead components of the monthly close and Monthly Management Review (MMR) reporting process for R&D and Enabling Functions, including accrual support/validation and variance analysis versus Budget/Monthly Forecast/Prior Year with clear narrative and executive-ready materials.
• Serve as the primary finance partner for assigned cost centers and project portfolios (e.g., cl...

• Serve as the primary technical engineering resource on the manufacturing floor during aseptic bulking, cleaning, milling, and filling activities.
• Actively monitor and verify critical operational steps, environmental controls, and in‑process parameters to ensure compliance with cGMP and aseptic best practices.

• Identify and execute opportunities for cost savings, increased throughput, improved schedule adherence, and workflow optimization across pharmaceutical manufacturing operations, including aseptic and sterile processing environments, while maintaining compliance, product quality, contamination control, and patient safety.

• Participate on cross-functional teams, representing Quality Systems, to drive shared understanding of quality requirements and continuous improvement.
• Drive QMS effectiveness using data and metrics across CAPA, document/records management, training, change control, nonconformance/deviations, and management review.

• Administer the daily operation of Onestream system, ensuring its reliability, availability, and performance.
• Monitor system health and address any issues or errors promptly to minimize downtime.

• Provide leadership in a fast-paced production environment with high quality and regulatory standards; supervise the Validation Engineers.
• Provide direction, mentoring, coaching and development to team members to support personal growth, enhanced job performance and career satisfaction.

• Center on People: We commit to support the well-being of our patients. We are committed to treating our employees and those we serve as valued partners. By placing people at the heart of our actions, we actively engage, invigorate, acquire knowledge, and grow together.​
• Are Proactive & Agile: We embody a culture of engagement and action. With a hands-on appro...

• Support the Supplier Change Notification Program, including completion of impact assessments.
• Own supplier-related quality events (deviations) and supplier corrective action reports (SCARs), including completing investigations and collaborating with technical subject matter experts and suppliers.