5835 jobs - 12 added today
Recruiting? Call us on 01772 639610
Email me jobs relevant to my job search
2 months ago
only 22 days until close

Validation Quality Assurance (QA) Engineer


Abbott
Location: Witney
Job type: Permanent
Sector: Manufacturing
Category: Inspection Jobs
Apply
Select how you want to share:
View similar
United Kingdom - Witney





JOB DESCRIPTION:

Known globally for the development of revolutionary technologies, Abbott Diabetes Care designs, develops and manufactures glucose monitoring systems for use in both home and hospital settings.

We have a Centre of Excellence in Witney for the manufacture of electrodes and biosensors used by patients and healthcare professionals for the day-to-day management of diabetes. As a result of strong business growth and industry-leading product development in the biosensor business we have an opportunity for a Validation Quality Assurance (QA) Engineer to join our Technical Quality Assurance team.

Serving as a primary representative for the quality assurance function on project teams, and supporting the R&D/Technical Services, Engineering and Operations areas, you will provide Quality Assurance expertise and guidance to ensure the validation of site products, processes and systems meets customer, business and regulatory requirements.

Responsibilities include:

Define and support the validation strategy associated with varied site projects covering facilities, utilities, equipment and processes.
Develop process validation and equipment qualification requirements (IQ, OQ, PQ) as part of design transfer activities.
Review validation protocols with responsibility across equipment, production, facilities & utilities, analytical methods, sterilisation and shipping studies.
Ensure the status of site validation system is established and maintained in accordance with internal procedures, regulatory requirements and industry guidance / standards.
Support the implementation of change control documentation.
Assist in completion of risk management reports utilising risk analysis tools such as FMEA and Root Cause Analysis.
Maintain an awareness of regulatory and industry best practice trends, hot topics and changes in relation to validation.

To be successful, you will bring with you previous experience of validation processes, change control and risk management, ideally gained within the Medical Device or Pharmaceutical industry. You will also offer knowledge of cGMP, ISO13485, and 21 CFR 820. The ideal candidate will be a proactive individual who takes initiative and is able to work independently as well as part of a high performing cross functional team within a regulated, quality-driven environment.

This is a fantastic opportunity to become a valued member of a highly skilled Technical Quality Assurance team working in a fast growing area of our business.

As you’d expect from an innovative global healthcare company, we offer an excellent starting salary, and a competitive range of benefits including a defined contribution pension scheme, private healthcare, life assurance, and a flexible benefits scheme.

We politely request that Recruitment Agencies do not make contact in regard to this position.

JOB FAMILY:
Operations Quality

DIVISION:

LOCATION:
United Kingdom > Witney : Production Facility

ADDITIONAL LOCATIONS:

WORK SHIFT:
Standard

TRAVEL:
Yes, 5 % of the Time

MEDICAL SURVEILLANCE:
Not Applicable

SIGNIFICANT WORK ACTIVITIES:
Not Applicable
United Kingdom - Witney





JOB DESCRIPTION:

Known globally for the development of revolutionary technologies, Abbott Diabetes Care designs, develops and manufactures glucose monitoring systems for use in both home and hospital settings.

We have a Centre of Excellence in Witney for the manufacture of electrodes and biosensors used by patients and healthcare professionals for the day-to-day management of diabetes. As a result of strong business growth and industry-leading product development in the biosensor business we have an opportunity for a Validation Quality Assurance (QA) Engineer to join our Technical Quality Assurance team.

Serving as a primary representative for the quality assurance function on project teams, and supporting the R&D/Technical Services, Engineering and Operations areas, you will provide Quality Assurance expertise and guidance to ensure the validation of site products, processes and systems meets customer, business and regulatory requirements.

Responsibilities include:

Define and support the validation strategy associated with varied site projects covering facilities, utilities, equipment and processes.
Develop process validation and equipment qualification requirements (IQ, OQ, PQ) as part of design transfer activities.
Review validation protocols with responsibility across equipment, production, facilities & utilities, analytical methods, sterilisation and shipping studies.
Ensure the status of site validation system is established and maintained in accordance with internal procedures, regulatory requirements and industry guidance / standards.
Support the implementation of change control documentation.
Assist in completion of risk management reports utilising risk analysis tools such as FMEA and Root Cause Analysis.
Maintain an awareness of regulatory and industry best practice trends, hot topics and changes in relation to validation.

To be successful, you will bring with you previous experience of validation processes, change control and risk management, ideally gained within the Medical Device or Pharmaceutical industry. You will also offer knowledge of cGMP, ISO13485, and 21 CFR 820. The ideal candidate will be a proactive individual who takes initiative and is able to work independently as well as part of a high performing cross functional team within a regulated, quality-driven environment.

This is a fantastic opportunity to become a valued member of a highly skilled Technical Quality Assurance team working in a fast growing area of our business.

As you’d expect from an innovative global healthcare company, we offer an excellent starting salary, and a competitive range of benefits including a defined contribution pension scheme, private healthcare, life assurance, and a flexible benefits scheme.

We politely request that Recruitment Agencies do not make contact in regard to this position.

JOB FAMILY:
Operations Quality

DIVISION:

LOCATION:
United Kingdom > Witney : Production Facility

ADDITIONAL LOCATIONS:

WORK SHIFT:
Standard

TRAVEL:
Yes, 5 % of the Time

MEDICAL SURVEILLANCE:
Not Applicable

SIGNIFICANT WORK ACTIVITIES:
Not Applicable
Apply

Email me jobs relevant to my job search

  Back to the top