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The Operations and Data Excellence Manager is responsible for supporting the business with ownership, accountability and continuous improvement of commercial operations and the functionality of the systems that enable it. Working in close partnership with the Business Unit Directors and wider Leadership Team, they are responsible for driving excellent commercial practices which enable agreed business strategies.
We are seeking a diligent Product Certification Specialist with a firm understanding of the Life Science industry, particularly Medical Equipment/Technology. The individual should be proficient in ensuring our products meet all necessary regulations and standards especially IEC 60601-1 and EMC.
In the role of Fullstack Lead Engineer, you will be responsible for leading and managing a team of skilled engineers to deliver high-quality software solutions for our Life Science and Veterinary departments.
In the role of General Manager, the individual will be entrusted with the responsibility of leading the strategic direction and performance of the business.
The MSL Manager will be responsible for effectively implementing the Field Medical plan and initiatives developed as a part of overall disease area plan during the pre, peri & post launch of any new assets.
This role demands a dynamic Business Development Manager who will be responsible for developing new business opportunities within the medical device sector globally (USA, Europe, Middle East, and Africa, among others).
Play a pivotal role in driving sales growth and market penetration for the pharmaceutical products within a designated territory.
The Procurement Manager Pharma (TGx) will manage and oversee the entire procurement process within the pharmaceutical division and provide strategic direction in purchasing activities.
The Head of HR will be responsible for instituting & reviewing HR policies & SOPs. This role will cover Talent Management, Payroll, Performance Management, Compensation Reviews, Exit Management, among other areas as required.
To support the manufacture of Drug Product (fill finish, device assembly & secondary packaging) of biologics product. The activities range from tech transfer, technical process studies, process validation activities, data analysis to handing change controls, deviations and troubleshooting. Writing and reviewing of DP/Device Assembly/FG validation-related documents and key CMC sections of regulatory dossiers (different countries) are also required for this role.
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