Lead regulatory strategy and compliance for medical devices and drug-device combination products globally. Serve as SME on FDA, EU MDR and ISO standards, guide program teams on regulatory plans and submissions (NDA/ANDA/BLA/MAA), mentor the regulatory team, and support SaMD classification and global IT compliance.

Support internal audit activities by preparing audit workpapers, analyzing accounting transactions for GAAP compliance, testing controls (including SOX 404), communicating findings, assisting with audit analytics, and helping senior auditors execute audit procedures.

The Regulatory Affairs Officer ensures regulatory compliance, manages product lifecycle, coordinates applications, maintains databases, and collaborates with cross-functional teams to support market availability of medicinal products.

The Statutory Accounting & Controlling Manager leads statutory and compliance accounting for legal entities, oversees monthly and annual reporting, manages audits, and ensures regulatory compliance.

The QC Analyst II performs chromatographic and wet chemistry analysis, supporting validation programs, and ensuring compliance with GMP. This role also involves data review and report writing.

The Sales Representative will provide a great sales experience to GPs and pharmacists, manage territory performance, and achieve sales KPIs through effective communication and strategic planning.

The Regulatory Affairs Lead will direct regulatory strategies, ensure compliance with local regulations, manage a team, and improve regulatory processes through stakeholder engagement.

The Intern, Production Support Engineer will assist with downtime analysis, troubleshooting, performance monitoring, and creating technical drawings for production systems.

The Senior Financial Accountant will oversee financial accounting operations, prepare financial reports, manage compliance activities, and partner with shared services teams to enhance processes.

Support OTC operations across cash application, billing, collections, credit and insurance management. Handle reconciliations, invoicing, dispute management, KPI/CTQ reporting, month-end closings, audits, process improvements and stakeholder collaboration, ensuring compliance with SOPs and GAAP.

The Senior Lead Scientist will assess API suppliers, conduct analytical testing, lead method transfers, and interface with teams to ensure compliance and efficiency in drug development processes.

The Manager, Project Engineering is responsible for overseeing capital projects, collaborating with multiple departments, and ensuring compliance with quality and safety practices.

The Director of Regulatory Compliance will establish and lead the Global Regulatory Affairs Compliance function, ensuring adherence to regulatory processes, managing audits, and evolving the Quality Management System while collaborating with cross-functional teams.

Own end-to-end Polish payroll processing: collect and validate inputs, reconcile outputs, coordinate with HR, Finance and external vendor, ensure legal compliance, respond to employee payroll inquiries, prepare statutory filings, and support continuous improvement and payroll projects.

Lead deployment of Lean 4.0 across production, quality, and labs; coach leaders and teams; run Tier Management, Standard Work, VSM, and Kaizen events; use digital tools and data to identify improvements; collaborate with Quality/Operations and consultants to drive sustained performance and culture change.

The Senior QC Analyst will analyze raw materials and products, review analytical data, conduct method validations, and provide training while ensuring compliance with regulations.

The Director of Regulatory Affairs CMC is responsible for strategic CMC regulatory approaches and managing relationships with stakeholders to ensure compliance and efficiency in regulatory submissions.

The Senior Quality Director oversees quality operations, ensuring compliance with regulatory standards and leading quality management initiatives to ensure product quality.

Prepare and file regulatory submissions for new drugs and variations, maintain drug labeling, and provide regulatory insight during the product lifecycle. Collaborate with regulatory authorities and ensure compliance with regulations.

The Epidemiology Lead is responsible for developing and executing epidemiology strategies throughout the product lifecycle, ensuring evidence generation for clinical development and market access, collaborating with teams, and applying advanced analytic techniques.