Senior QC Analyst Validation Specialist
1 month ago
As a Senior QC Analyst Validation Specialist at EUROAPI, you will be responsible for ensuring the highest quality of active pharmaceutical ingredients. Your key responsibilities will include owning analytical projects, deputizing for leadership, and working closely with R&D, clients, and key stakeholders to manage key analytical projects.
Our ideal candidate will have a strong background in pharmaceuticals, with a high level of experience handling HPLC, GC, FTIR, UV, PXRD, and DSC. They will also have GMP knowledge and proven experience of analytical method validation & transfer principles.
As a member of our QC Technical Services Team, you will be responsible for sample analysis, release, and testing of API, drug products, and raw materials. You will also be involved in writing, reviewing, and driving the completion of validation/analytical transfer activities.
We offer a competitive hourly rate and retention bonus, as well as training and development opportunities. Our contract term is 23 months, and we work 36 hours per week, Monday-Thursday 9-5.30pm, Friday 9-4pm.
EUROAPI is a leading player in active pharmaceutical ingredients, with a strong focus on reinventing active ingredient solutions to sustainably meet customers' and patients' needs around the world. We are a Contract Development and Manufacturing Organization (CDMO) with six manufacturing sites in Europe.
Our company is committed to taking action for health by enabling access to essential therapies. We have a strong research and development capability and employ over 3,450 people worldwide.
As a Senior QC Analyst Validation Specialist, you will be part of a dynamic team that is passionate about delivering high-quality products. If you are a motivated and experienced professional looking for a new challenge, we encourage you to apply for this exciting opportunity.
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Senior QC Analyst Validation Specialist
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