Analytical Project Manager

1 week ago

Haverhill, Suffolk, United Kingdom EUROAPI Full time

Job Summary

We are seeking a highly skilled Senior QC Analyst to join our Quality Assurance team at EUROAPI. As a key member of our team, you will be responsible for ensuring the highest quality standards in our analytical projects.

Key Responsibilities

  • Own and manage analytical projects, working closely with R&D, clients, and stakeholders to ensure timely delivery and high-quality results.
  • Collaborate with the QC management team to assign and manage project resources, ensuring effective utilization of personnel and equipment.
  • Develop, implement, and maintain analytical methods and procedures, ensuring compliance with regulatory requirements and company standards.
  • Conduct analytical testing and release of API, drug products, and raw materials, ensuring accuracy and precision in results.
  • Write, review, and drive the completion of validation and analytical transfer activities, owning analytical projects within the team and sharing best practices.
  • Develop, train, and report validation and transfer activities within QC for new and existing clients.
  • Lead effective reactive and proactive investigations, driving continuous improvements and ensuring compliance with regulatory requirements.
  • Drive compliance and promote quality standards, working closely with QA and other departments.
  • Ensure effective troubleshooting of equipment or technique failures and problems associated with various analytical techniques.

About EUROAPI

EUROAPI is a leading player in active pharmaceutical ingredients, focused on reinventing solutions to sustainably meet customers' and patients' needs around the world. We have a strong research and development capability and six manufacturing sites in Europe, ensuring API manufacturing of the highest quality to supply customers in over 80 countries.

Requirements

  • Sciences degree.
  • High level of pharmaceutical experience handling HPLC, GC, FTIR, UV, PXRD, DSC.
  • GMP knowledge coupled with proven experience of analytical method validation and transfer principles.
  • Experience of deputizing for senior leadership and working closely with R&D, clients, and stakeholders to manage key analytical projects.

What We Offer

  • Competitive hourly rate and retention bonus.
  • Training and development opportunities.
  • Flexible working hours and a quick turnaround with two interviews and a face-to-face meeting.
  • 23 months contract term.

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