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
You will: Own analytical projects and deputize for leadership, working with R&D, clients, and key stakeholders. Work with the QC management team 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 the completion of validation/analytical transfer activities, owning your analytical projects within the team and sharing best practices within the group. Develop, train, and report validation and transfer activities within QC for new and existing clients. Lead effective reactive and proactive investigations, driving continuous improvements. Drive compliance working with QA and promote quality standards. Ensure effective troubleshooting of equipment or technique failures and troubleshoot problems associated with various analytical techniques. Our Company
EUROAPI is focused on reinventing active ingredient solutions to sustainably meet customers’ and patients’ needs around the world. We are a leading player in active pharmaceutical ingredients with approximately 200 products in our portfolio, offering a large span of technologies, while developing innovative molecules through our Contract Development and Manufacturing Organization (CDMO) activities. Taking action for health by enabling access to essential therapies inspires our 3,450 people every day. With strong research and development capabilities and six manufacturing sites all located in Europe (Saint-Aubin-lès-Elbeuf and Vertolaye in France, Brindisi in Italy, Frankfurt in Germany, Budapest in Hungary, and Haverhill in the UK), EUROAPI ensures API manufacturing of the highest quality to supply customers in more than 80 countries. EUROAPI is listed on Euronext Paris. Our Requirements
A high level of pharmaceutical experience handling HPLC, GC, FTIR, UV, PXRD, DSC. GMP knowledge coupled with proven experience of analytical method validation & transfer principles. Experience of deputizing for senior leadership and working closely with R&D, clients, and key stakeholders to manage key analytical projects. What we offer
Competitive hourly rate and retention bonus. A quick turnaround with two interviews (teams interview and face-to-face) and flexibility to offer a quick start date. 23 months contract term. 36 hours per week, Monday-Thursday 9-5.30pm, Friday 9-4pm. Apply Today! Find out more about this exciting opportunity, apply today or contact Marie Meekings.
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You will: Own analytical projects and deputize for leadership, working with R&D, clients, and key stakeholders. Work with the QC management team 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 the completion of validation/analytical transfer activities, owning your analytical projects within the team and sharing best practices within the group. Develop, train, and report validation and transfer activities within QC for new and existing clients. Lead effective reactive and proactive investigations, driving continuous improvements. Drive compliance working with QA and promote quality standards. Ensure effective troubleshooting of equipment or technique failures and troubleshoot problems associated with various analytical techniques. Our Company
EUROAPI is focused on reinventing active ingredient solutions to sustainably meet customers’ and patients’ needs around the world. We are a leading player in active pharmaceutical ingredients with approximately 200 products in our portfolio, offering a large span of technologies, while developing innovative molecules through our Contract Development and Manufacturing Organization (CDMO) activities. Taking action for health by enabling access to essential therapies inspires our 3,450 people every day. With strong research and development capabilities and six manufacturing sites all located in Europe (Saint-Aubin-lès-Elbeuf and Vertolaye in France, Brindisi in Italy, Frankfurt in Germany, Budapest in Hungary, and Haverhill in the UK), EUROAPI ensures API manufacturing of the highest quality to supply customers in more than 80 countries. EUROAPI is listed on Euronext Paris. Our Requirements
A high level of pharmaceutical experience handling HPLC, GC, FTIR, UV, PXRD, DSC. GMP knowledge coupled with proven experience of analytical method validation & transfer principles. Experience of deputizing for senior leadership and working closely with R&D, clients, and key stakeholders to manage key analytical projects. What we offer
Competitive hourly rate and retention bonus. A quick turnaround with two interviews (teams interview and face-to-face) and flexibility to offer a quick start date. 23 months contract term. 36 hours per week, Monday-Thursday 9-5.30pm, Friday 9-4pm. Apply Today! Find out more about this exciting opportunity, apply today or contact Marie Meekings.
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