The role involves ensuring GMP compliance, managing quality systems, conducting supplier audits, supporting QA activities, and handling documentation in a pharmaceutical environment.

The QC Bioassay Manager leads a team in analytical testing for proteins and nucleic acids under GMP, overseeing personnel development and project management.

Assist in quality assurance tasks including GMP training management, document archiving, and supplier management to ensure compliance in a biopharmaceutical setting.

The Director of Corporate Accounting will oversee accounting operations, ensure compliance with financial regulations, optimize reporting processes, manage audits, and lead an international accounting team.

The role involves supporting the QA Operations Team with administrative tasks, reviewing and approving quality-related documents, and assisting in the preparation of quality documentation for clients.

The Senior Business Controller leads financial planning and analysis, oversees budgeting and forecasting processes, develops financial models, and provides strategic insights to enhance business growth, working closely with cross-functional teams.

The Vice President of Business Development is responsible for managing strategic accounts, driving sales, developing account plans, leading customer engagements, and coordinating internal stakeholders to foster business growth in the biopharmaceutical sector.

The Director of Business Development will drive sales across Europe by identifying clients, negotiating contracts, and implementing sales strategies to achieve revenue growth, collaborating with internal teams, and participating in regional marketing activities.

The Assistant Controller oversees accounting operations, ensures compliance with IFRS, manages financial reporting, audits, and tax activities, and collaborates across departments for financial analysis and efficiency improvements.

The Project Manager oversees project progression, manages timelines, coordinates with clients and teams, ensuring projects meet goals and budgets.

The Scientist in Upstream Early-Stage MSAT will oversee technology transfer for upstream processes, ensuring compliance and collaboration across teams in biopharmaceutical manufacturing.

The Senior Engineering Planner coordinates maintenance and calibration activities, ensuring compliance and reliability within manufacturing operations. Key responsibilities include planning schedules, monitoring performance, and improving processes.

The Quality Systems Supervisor coordinates the Quality System Compliance team, manages GMP documentation, oversees quality KPIs, and acts as a subject matter expert in inspections.