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Senior Quality Control Analyst

2 months ago

Haverhill, Suffolk, United Kingdom Euroapi Full time
About the Role

We are seeking a highly skilled Senior QC Analyst Validation to join our Quality Technical Services Team on a contract basis. As a key member of our team, you will be responsible for ensuring the highest pharmaceutical regulatory and compliance standards are met.

Key Responsibilities
  • Ensure effective troubleshooting of equipment or technique failures and investigate problems associated with various analytical techniques.
  • 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.
  • Develop, train, and report validation and transfer activities within QC for new and existing clients.
  • Perform 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 that departmental objectives are implemented in line with the overall Quality/Corporate goals.
  • Comply with all safety and GMP requirements within the Laboratory.
  • Document all testing activities to regulatory standards.
  • Participate in and facilitate improvement programs within the Laboratory.
  • Ensure that all interactions and engagements are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with the client's values.
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 capabilities and six manufacturing sites all located in Europe. Our team of 3,450 people is dedicated to taking action for health by enabling access to essential therapies.

Requirements
  • Sciences degree.
  • Proven pharmaceutical experience handling HPLC, GC FTIR, UV, PXRD, DSC.
  • GMP knowledge coupled with proven experience of analytical method validation & transfer principles.
What We Offer
  • Competitive hourly rate and retention bonus.
  • Training & development.
  • 36 hours per week, Monday-Thursday 9-5.30pm, Friday 9-4pm.