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Master of Medical Biotechnology jobs

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    • Assist in resolving data coding discrepancies resulting from the coding of medical events, procedures, and medications.
    • Overseeing the collection, rigorous review, and tracking of all essential site documents required for study activation, including Investigator CVs, medical…
    • View all AbCellera jobs - Montréal jobs - Clinical Study Manager jobs in Montréal, QC
    • Salary Search: Clinical Study Start Up Manager salaries
    • Code medical terms in the clinical database, as required.
    • Ensures that data management documentation is complete and up-to-date in the trial master file (TMF).
    • Pre-employment medical and medical re-examination performed every 2 years or as per Resilience’s SOPs.
    • The role also provides technical support, training, and…
    • Co-lead internal team engagement initiatives and gain structured mentorship from experienced medical strategy leaders.
    • API offers a generous paid time off (PTO) policy that includes vacation days, medical/personal days, and holidays.
    • Maintain documents within QMS systems.
    • Support project execution within medical education programs and assist throughout the brand planning cycle.
    • Manage, maintain, and optimize operational tools,…
    • Experience in regulated industries (life sciences, pharmaceutical, or medical device).
    • Experience using ERP systems (e.g., Oracle) for purchasing, planning, and…
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    • Maintain master recipes and production inventory.
    • Sanofi's global vaccines business unit partners with the public health, medical and scientific communities to…
    • Experience in regulated industries such as medical devices, diagnostics, or biotechnology.
    • Assist in maintaining accurate master data in the MRP/ERP system.
    • Reporting to the Chief Technical Operations Officer, you will support the development and implementation of a project management system and support planning,…
    • Reporting to the Technical Director, you will develop the vascularization strategy for bioengineered cellular medicines.
    • A minimum of three (3) to five (5) years’ experience in Computer Systems Validation within the pharmaceutical/biotechnology GMP environment including authoring…
    • Independently leading research, design verification, validation, and stability studies for new IVD medical devices.
    • Flexible working hours and paid sick days.
    • 8+ years of progressive Quality Assurance experience within the pharmaceutical or biotechnology industry.
    • The manager will ensure that all Active Pharmaceutical…
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