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Join our global quality team where you will be responsible for providing active ingredients that meet the highest pharmaceutical regulatory and compliance standards.
This opportunity is for a Senior QC Analyst to join the QC Technical Services Team on a contract basis. The duration of the contract will be 23 months.
Your Responsibilities
* Own analytical projects and deputize for leadership, working with R&D, clients, and key stakeholders.
* Collaborate with QC management to assign and manage project resourcing.
* Sample, analyze, and release API, drug products, test incoming raw materials and drug packaging, provide import testing for drug product batches, CDMO batch testing, in-process samples, cleaning validation, verification analysis, and batch release for raw materials.
* Write, review, and drive validation/analytical transfer activities, owning your analytical projects and sharing best practices within the group.
* Develop, train, and report validation and transfer activities within QC for new and existing clients.
* Lead investigations and drive continuous improvements, both reactive and proactive.
* Ensure compliance and promote quality standards working with QA.
* Research, develop, train, and report validation and transfer activities within QC.
* Troubleshoot equipment or technique failures related to analytical techniques.
Our Company
EUROAPI focuses on reinventing active ingredient solutions to meet customer and patient needs worldwide. We are a leading player in active pharmaceutical ingredients with about 200 products, offering a wide range of technologies and developing innovative molecules through our Contract Development and Manufacturing Organization (CDMO) activities.
With strong R&D capabilities and six manufacturing sites in Europe, EUROAPI ensures the highest quality API manufacturing to supply over 80 countries. Our sites are located in France, Italy, Germany, Hungary, and the UK.
EUROAPI is listed on Euronext Paris.
The Haverhill (UK) site has been established for forty years, employing over 250 people. It is renowned for Flow Chemistry, API Spray Drying, and CDMO activities, including secondary packaging and release of oncology and rare disease medicines. The site also offers contract testing and release services.
Our Requirements
Extensive pharmaceutical experience handling HPLC, GC, FTIR, UV, PXRD, DSC.
GMP knowledge with proven experience in analytical method validation and transfer principles.
Experience deputizing for senior leadership and working closely with R&D, clients, and stakeholders on analytical projects.
What we offer
* Competitive hourly rate and retention bonus
* Quick turnaround with two interviews and a flexible start date
* 23 months contract
* 36 hours/week, Monday-Thursday 9-5.30pm, Friday 9-4pm
Apply Today!
Learn more about this exciting opportunity, apply now, or contact Marie Meekings.
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