Job Title: Quality Assurance Specialist
Job Summary:
We are seeking an experienced Quality Assurance Specialist to join our team on a 12-month contract. This role is ideal for a skilled professional who wants to expand their expertise in quality management and gain exposure in a regulated environment without committing to a permanent position.
Key Responsibilities:
* Develop and implement quality improvement initiatives to enhance processes, reduce costs, and ensure regulatory compliance.
* Support change controls, risk assessments, and process validations to maintain the highest level of quality standards.
* Analyse data and identify trends using statistical tools to inform quality decisions.
* Write and review corrective action plans (CAPAs), non-conformance reports, and supplier corrective actions to ensure timely resolution of issues.
* Conduct audits and support inspections by regulatory authorities to maintain a strong quality reputation.
* Collaborate with cross-functional teams to embed best practices in quality standards and continuous improvement.
Requirements:
* At least 3 years' experience in a regulated environment - preferably medical devices or FDA/ISO 13485 certified manufacturing.
* Degree in Quality, Science, or Engineering.
* Proficient in MS Excel, Word, and PowerPoint skills.
* Experience with Failure Mode Effects Analysis (FMEA), root cause analysis, and statistical analysis.
* Excellent attention to detail and problem-solving ability.
Benefits:
This contract position offers the opportunity to work on high-profile projects, gain exposure in a regulated environment, and expand your skills without committing to a permanent role.