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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.
This role focuses on leading the sales and marketing strategies of the company's API sales for ROW markets (APAC, LATAM, Africa).
Looking for person in Financial Account and Controls with hands on skills in SAP FICO Functional. Preferred Candidate: CA + FICO certified professional with 12-14 years experience in leading SAP FICO Practice.
This role is for an IT Security Consultant, who will be responsible for identifying and managing potential risks related to IT security within the Organisation.
Lead the legal department at an industry-leading life science company, providing strategic advice and ensuring company-wide legal compliance.
The Marketing Lead will be responsible for managing and executing marketing strategies, and driving growth within the Medical Devices sector.
The Commercial Finance head will be responsible for overseeing all the commercial & financial planning decision-making processes, and providing strategic insights to boost profitability.
The role is for a Product Manager based in New Delhi, for a leading diagnostics company in India. The ideal candidate will have 10+ years of experience in product management, preferably in the IVD or life sciences industry.
This role involves managing both short and long-term borrowing from financial institutions, overseeing investment activities, coordinating with auditors and rating agencies, administering bank accounts, and facilitating payment processing across units, while also preparing and presenting comprehensive management reports on treasury operations.
As a Clinical Data Manager, the candidate will play a crucial role in ensuring that Real World Evidence studies collect accurate and complete data that meets regulatory requirements, enabling researchers to develop innovative treatments and therapies that could save lives. They will lead the development and implementation of Electronic Data Capture (EDC) systems, which enable the collection of patient-reported outcomes (ePROs) and case report files (eCRFs).
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