PCT Lead - Injectable Inspection

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a PCT Lead - Injectable Inspection based in the United States.

This leadership role oversees people, technology, resources, and operational activities within a pharmaceutical manufacturing environment.

You will help ensure injectable products meet demanding standards for quality, compliance, safety, cost, and delivery.

The position combines people leadership with technical and operational oversight, continuous improvement, and cross-functional collaboration.

You will work closely with quality, production, procurement, suppliers, and other stakeholders to maintain reliable supply and audit readiness.

The role offers meaningful opportunities to solve complex problems, improve processes, and introduce innovative approaches to manufacturing operations.

You will also develop team capabilities through coaching, performance management, knowledge sharing, and structured development plans.

Based in Kalamazoo, Michigan, this is an on-site position with occasional weekend, shutdown, and holiday coverage.

Accountabilities

• Lead and manage departmental personnel, technology, financial resources, and operational priorities to achieve organizational goals while maintaining quality, compliance, and performance standards.
• Provide day-to-day leadership to production teams, overseeing production cost centers and ensuring products are delivered on time, within budget, and according to required quality standards.
• Establish goals, coach direct reports, assess performance, and identify development needs while creating and executing plans that strengthen both technical and behavioral capabilities.
• Lead and contribute to cross-functional and departmental projects, addressing moderately complex operational challenges and supporting issue resolution beyond the immediate team when required.
• Oversee manufacturing activities and ensure adherence to applicable regulatory requirements, current Good Manufacturing Practices (cGMPs), internal policies, and industry standards.
• Collaborate with quality, production, procurement, suppliers, and logistics partners to maintain supply continuity, prepare for audits, and resolve operational issues.
• Identify and implement opportunities to improve quality, cost efficiency, safety, productivity, and cycle time through continuous improvement initiatives.
• Share technical knowledge and expertise across the department, fostering collaboration, learning, accountability, and a culture of continuous improvement.
• Communicate complex technical and operational concepts clearly, seek stakeholder input, and influence others through well-supported recommendations.
• Anticipate resource requirements, support operational planning, and adapt priorities as organizational needs evolve.
• Explore appropriate AI-enabled tools, including generative AI, to improve problem solving, productivity, and decision-making while applying responsible-use principles.

Requirements

• Bachelor’s degree with at least 4 years of relevant experience, or Master’s degree with at least 2 years of experience; alternatively, an associate degree with 8+ years or a high school diploma/equivalent with 10+ years of relevant experience.
• Demonstrated experience contributing to and leading project teams, managing multiple projects, and balancing ongoing operational responsibilities.
• Knowledge of pharmaceutical manufacturing regulations, cGMP requirements, and applicable organizational policies.
• Previous leadership or people-management experience is strongly preferred, with the ability to set objectives, coach employees, manage performance, and support professional development.
• Strong project management capabilities and the ability to operate effectively within complex organizational structures.
• Experience working collaboratively across functions and cultures, with the ability to build effective relationships with stakeholders at all organizational levels.
• Excellent verbal and written communication skills, including the ability to explain complex concepts and influence decisions.
• Strong organizational, problem-solving, collaboration, and decision-making skills, with a proactive and accountable approach.
• Ability to provide technical leadership in a hybrid or remote collaboration environment and adapt effectively to changing business requirements.
• Master’s degree combined with relevant pharmaceutical industry experience is an advantage.
• Experience forecasting resource needs, setting objectives, and supporting operational planning is preferred.
• Familiarity with AI tools such as ChatGPT or Microsoft Copilot, including the ability to identify appropriate use cases and understand responsible AI practices, risk management, and ethical use.
• Ability to work on-site in Kalamazoo, Michigan, with occasional weekend, shutdown, and holiday coverage.
• Must be authorized to work in the United States for any employer; visa sponsorship is not available for this position.

Benefits

• Annual base salary range of $106,000-$176,600, depending on location and other applicable factors.
• Eligibility for a performance-based bonus with a 15% target of base salary.
• Eligibility to participate in a share-based long-term incentive program.
• Comprehensive medical, prescription drug, dental, and vision coverage.
• 401(k) plan with employer matching contributions and an additional retirement savings contribution.
• Paid vacation, holidays, and personal days.
• Paid caregiver, parental, and medical leave.
• Relocation assistance may be available based on business needs and eligibility.
• Opportunities for professional development, leadership growth, and continuous learning.
• Opportunity to contribute to work that supports the reliable delivery of medicines to patients.
• An environment focused on innovation, collaboration, quality, safety, and continuous improvement.