Rullion are currently looking to recruit for the following role:
IQA Technician
ASAP Start
Duration 13 Months initially
Inside IR35
£16.41+ Per hour
Location Sudbury ,UK
Fully site based
Full time hours Monday to Friday
Medical Industry based Role- Point of Care Diagnostics business line.
The IQA Inspector will be responsible for completing inspection, control, and disposition of all incoming materials across the Sudbury manufacturing sites, completing all relevant documentation and traceability processes to applicable quality standards. The IQA Inspector ensures that incoming materials to be used by production meet all quality requirements.
Job Responsibilities:
Carry out inspection of incoming goods across the Sudbury sites using measurement equipment, specifications, and quality control plans (QCP's). Ensuring all incoming materials fully conform to requirements prior to assembly, completing all associated documentation/records and following GDP (Good Documentation Practices).
Provide input to the process for the control and disposition of any non-conforming materials, completing tasks, documentation, and segregating materials as required within documented working practices.
Effectively communicate with both internal & external suppliers/stakeholders. Be point of contact for part quality related enquiries, escalate issues as required, ensuring consistency and adherence to processes.
Complete assigned training within the defined timescales.
Provide support to other Quality functions within Sudbury as required, covering in-process testing and/or inspections and final product release processes.
Provide support for both Internal and 3rd party site audits.
Participate in SQDIP meetings, provide accurate and timely reports, and take responsibility for the achievement of target KPI's for the role.
Establish & maintain supplier 'Quality Approved' samples for relevant attributes (colours, finishes)
Actively use business systems such as CATSWEB, CERDAAC, SAP, Documentum & Learn4U.
Regulatory Requirements
Represent the business in customer audits and regulatory inspections to demonstrate that we have compliant systems.
Maintain compliance with Data Integrity Regulations, GAMP standards, 21 CFR Part 11 and applicable regulatory guidelines.EHS
Ensuring compliance with safety, health and environmental (SHE) legislation.
Driving a safety-first approach maintaining a zero-accident culture, ensure accident prevention and environmental protection regulations of the facility to assure a safe and productive working environment free of any liabilities or defects.Teamwork
Engaging with project teams to help with selection, installation, and commissioning of new equipment.Quality Assurance
Competent in the principles of and practical use of the Quality Management Systems.
Skills and Experience:
You will be able to manage time effectively and possess a desire to succeed.
You will have a flexible approach and ability to adapt according to workload.
You are self-motivated, reliable, able to work on own initiative, manage time effectively and possess a desire to succeed.
You will be an effective team member and able to communicate across functions.
You will be curious - keen to understand, learn and try new things, and possess excellent written and oral communication skills.
Qualifications:
3 or more years' experience in a medical manufacturing environment
In depth knowledge of Quality Management Systems, ISO 13485, 21 CFR 820
IT literate with strong knowledge of Microsoft Office packages.
GDP & GMP (Good Documentation Practices & Good Manufacturing Practices)If avaialble please send CV in and a member of the team will be in touch.
Rullion celebrates and supports diversity and is committed to ensuring equal opportunities for both employees and applicants