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Senior Quality Control Analyst

2 months ago

Haverhill, Suffolk, United Kingdom EUROAPI Full time
Senior QC Analyst Validation Opportunity

EUROAPI is seeking a highly skilled Senior QC Analyst to join our global quality team. As a key member of our QC Technical Services Team, you will be responsible for providing active ingredients that meet the highest pharmaceutical regulatory and compliance standards.

Your Responsibilities
  • Own analytical projects and deputize for leadership, working closely 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, 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.
  • Research, develop, train, and report validation and transfer activities within QC for new and existing clients.
  • Ensure effective troubleshooting of equipment or technique failures and troubleshooting of problems associated with various analytical techniques.
About EUROAPI

EUROAPI is 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.

We are a global company with a strong research and development capability and six manufacturing sites located in Europe. Our Haverhill site in the UK has been established for forty years and employs over 250 people, with a strong reputation in Flow Chemistry, Active Pharmaceutical Ingredient (API) Spray Drying, and as a Contract Development and Manufacturing Organisation (CDMO).

Requirements
  • Sciences degree.
  • 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.
  • Training & development.
  • 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.