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The Quality Auditor is responsible for ensuring compliance with cGMP, monitoring production processes, conducting documentation audits, and verifying equipment calibrations. They mentor operational staff to improve quality and ensure timely processing of customer orders, maintaining high standards through inspections and checks throughout production.

The Project Engineer is responsible for designing packaging processes and tooling for pharmaceutical products, ensuring compliance with quality standards and customer requirements. Responsibilities include quoting, designing, attending meetings, and supporting validation efforts while adhering to company policies. Occasional travel and overtime may be required.

The AS Team Leader (Dev) is responsible for leading a team within the Analytical Development group, managing team activities, ensuring compliance with regulatory and client requirements, and overseeing method development and validation. The role includes people management, performance appraisals, team training, technical documentation, and project management.

The role involves reviewing and interpreting laboratory data for Analytical Development, ensuring compliance with regulations, and managing data packs for quality assurance. Responsibilities include problem-solving, training staff, prioritizing workloads, and maintaining best practices in documentation and data generation.

The EHS Coordinator assists in ensuring compliance with EHS programs and regulations, conducting inspections and audits, collecting and tracking EHS data, and facilitating meetings. Responsibilities include managing safety-related documentation, supporting incident investigations, and enhancing employee wellness programs. This role involves collaboration with various departments to improve EHS practices and may require overtime or weekend work.

The Cost Accountant is responsible for maintaining cost accounting records, overseeing job accounting processes, and managing inventory values. This role involves preparing financial reports, conducting cost analyses, and ensuring the accuracy of financial metrics. The Accountant will participate in team meetings and contribute to compliance with financial policies.

The Quality Auditor is responsible for ensuring compliance with cGMP regulations by conducting audits on production room documentation, performing real-time batch records review, and ensuring sampling and inspections are performed correctly. They also lead quality improvement efforts and mentor operational teams.