Quality Assurance Associate

GENinCode Predictive Genetics; Greater London; On-site; GBP 60,000 - 80,000; Full time

Job summary

A leading genetic testing organization in the UK is looking for a full-time Quality Assurance & RA Associate to support quality management processes in an innovative environment. The ideal candidate must hold a degree in Science and have strong interpersonal and communication skills. Responsibilities include ensuring compliance with regulatory standards and conducting quality assurance activities. The role offers flexible working patterns and is ideal for individuals who thrive in a fast-paced environment.

Benefits

Flexible working patterns

Excellent company benefits

Qualifications

• Good knowledge of regulations for In-Vitro Diagnostics Devices.
• Understanding of Medical laboratories Requirements.
• Ability to work cross-functionally and under supervision.

Responsibilities

• Conduct quality assurance and control activities.
• Support Quality Management System processes.
• Analyze processes for improvement opportunities.
• Perform internal and external audits.

Skills

Interpersonal skills

Communication skills

Adaptability

Knowledge of ISO 15189

Microsoft Office proficiency

Fluent English

Education

Degree or equivalent in Science

Job description

FULL TIMEQA& RA Associate _IN-VITRO DIAGNOSTIC MANUFACTURING (GENETIC TESTING). SALARY NEG DEPENDANT UPON EXPERIENCE + BENEFITS

Company Description

GENinCode is a leader in advanced genomic technology, offering innovative solutions for the prediction and management of cardiovascular disease, thrombosis, and familial hypercholesterolemia. Leveraging both traditional clinical measures and genetic information, the company provides comprehensive risk assessments and clinical guidance to healthcare professionals.

Role Description

This is a full-time, on-site role located in Hammersmith for a Quality Assurance Associate. The responsibilities include conducting quality assurance and quality control activities, implementing quality management processes, and ensuring compliance with regulatory and operational standards. The role involves analyzing processes and systems to identify areas for improvement, maintaining documentation, and actively supporting the continuous enhancement of quality standards within the organization.

Duties and responsibilities

• Support the company Quality Management System (QMS) processes such as Complaints, Non-conformance, CAPA, Change Control and Risk Management processes liaising with internal subject matter experts as applicable.
• Support manufacturing andanalytical method validation activities as and when required, writing and / or reviewing validation plans and reports as assigned.
• Provide guidance to the rest of the organization for effectively implement and ensure compliance with the requirements of the applicable regulatory agencies, standards, and regulations
• Work with the Development team to ensure smooth and timely introduction of new products, participating in the product design stages including design reviews and product verification and validation for both, reagent kits and bioinformatics pipeline.
• Support external computerised systems validation program.
• Perform internal and external audits as required.
• Manage Post-market surveillance program, liaising with appropriate stakeholders, and compiling the annual Product Reports for GENinCode assigned products, including those manufactured by external contractors.
• Attend meetings and participate in new projects as designated by line manager.

The Candidate

You will join the corporateQA& RA team, providing support to all GENinCode sites in UK, EU and US.

You MUST have

• A degree or equivalent in Science.
• Good knowledge of applicable regulations for In-Vitro Diagnostics Devices or Medical Device (software)
• Good Knowledgeof Medical laboratories Requirements (ISO 15189) and laboratory processes

Skills Required

• Good interpersonal and communication skills. Personable and able to communicate with staff of all levels. Able to work cross-functionally.
• Work effectively, independently and under supervision, being able to adapt to fast pace rapidly changing environment. Flexible approach to work and the tasks to be undertaken.
• Fluent in English (oral and written)_main language used within the company for internal communications and all QMS documents.
• Other EU spoken languages desirable.
• Essential Microsoft Office package knowledge.

The Package

• Neg salary subject to experience
• Full Time Permanent Role / flexible working patterns available.
• Excellent company benefits.
• Leading genetic testing organisation.

PLEASE NOTE – ONLY SHORTLISTED APPLICANTS WILL BE CONTACTED