Contract Recruitment Specialist | Medical Devices | Quality and Validation | South of the UK & Ireland
Key Responsibilities:
1. Validate new manufacturing processes and equipment by developing requirements based on product specifications, writing test protocols, executing IQ/OQ/PQ testing plans, and analyzing results data.
2. Create quality systems documentation such as SOPs and WIs related to development, qualification, validation, and maintenance of production and process control methods, including statistical analysis tools like Minitab.
3. Set up calibrations by creating calibration schedules and plans according to industry standards, using metrology instruments traceable to NIST/NPL standards.
4. Develop DOE plans to optimize critical-to-quality attributes (CQA), conduct design-of-experiments studies, and perform root cause investigations and analyses.
Additional Details:
* Seniority level: Mid-Senior level
* Employment type: Contract
* Job function: Quality Assurance
* Industries: Staffing and Recruiting, Medical Equipment Manufacturing
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