Job title: QA Technician (White Shift) Internal Candidates Only
Department: QA
Location: Hamble
Working hours: 40.25 hours per week 7pm to 7am 4 days on 4 days off plus 26.09% shift allowance. ONSITE

JOB SUMMARY – WHAT TO EXPECT:

We have an exciting internal opportunity for a QA Technician to join our QA team on White Shift. Within this role, you will perform measurement and inspection of lenses, auditing of wet paperwork and final release of product, ensuring that lenses manufactured meet the required specifications and regulatory requirements.

You will carry out auditing of the final lot history record to ensure evidence that procedures have been followed has been documented and that the traceability of components and personnel are maintained. You will carry out verification of Sterilisation charts, ensuring all critical parameters in relation to the sterilisation have been achieved prior to lot release. Specifically, you will carry out the following duties:

• Measurement of lenses in line with the Quality Management system.
• Recording true and accurate data for the lenses measured. This is completed either using the electronic system (CVM), Microsoft Excel or controlled paperwork forms available from the eQMS (Agile).
• Verification and releasing of Sterilisation charts – Ensuring Critical parameters have been met.
• Auditing of Lot History Record to ensure traceability of required actions and personnel.
• Authority to Release product on the electronic system (CVM) if all lot testing and auditing meet the set requirements.
• The ability to Raise NCR’s when required, if lots fail to follow standard procedural or sample plan requirements.
• To support the requirement of both routine and non-routine lens measuring activities in UK Manufacturing if required (Investigations/Complaints/Validation/Shelf Life).

• Store quality records and retention samples correctly to enable timely retrieval if required.Support the management, storage, archive and retrieval of Quality Records.

• A full job description is available upon request.

ABOUT YOU:

We are looking for someone who has the following:

• Basic knowledge of use of Word/Excel/Agile/CVM.
• Possess a reasonable understanding of QA and the purpose of the role.
• Ability to work alone as well as part of a team.

• Adaptable and self-starter.Good communicator.

IF YOU LIKE WHAT YOU SEE, TAKE THE FIRST STEP TOWARDS YOUR BRIGHTER FUTURE AND APPLY TODAY! ALL SUITABLY QUALIFIED APPLICANTS WILL RECEIVE EQUAL CONSIDERATION AND OPPORTUNITIES FROM COOPERVISION.

Please view our careers page at https://hcjy.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1 to view all other opportunities.
CooperVision is a global leader in the contact lens industry, dedicated to helping improve the way people see every day. Achieving that goal takes the collaboration of team members with wide-ranging skills; from scientists and researchers, to manufacturing and operations experts, to sales and marketing professionals.
At CooperVision, our effort to improve lives begins with our employees. We are committed to developing people as a key global differentiator and our most important asset. We empower employees to succeed, rewarding great thinking and hard work with competitive pay, comprehensive benefits, and with a special focus on wellness. Our commitment to our core values and a diverse, inclusive, employee-centric culture fuel a deeply engaged, high performing organization.
CooperVision employees pride themselves on being proactive, innovative, flexible and friendly. That’s a strong reflection of our corporate culture—and part of the reason CooperVision may be a great workplace for you.
Job title: QA Technician (White Shift) Internal Candidates Only Department: QA Location: Hamble Working hours: 40.25 hours per week 7pm to 7am 4 days on 4 days off plus 26.09% shift allowance. ONSITE
CooperVision is a global leader in the contact lens industry, dedicated to helping improve the way people see every day. Achieving that goal takes the collaboration of team members with wide-ranging skills; from scientists and researchers, to manufacturing and operations experts, to sales and marketing professionals.
At CooperVision, our effort to improve lives begins with our employees. We are committed to developing people as a key global differentiator and our most important asset. We empower employees to succeed, rewarding great thinking and hard work with competitive pay, comprehensive benefits, and with a special focus on wellness. Our commitment to our core values and a diverse, inclusive, employee-centric culture fuel a deeply engaged, high performing organization.
CooperVision employees pride themselves on being proactive, innovative, flexible and friendly. That’s a strong reflection of our corporate culture—and part of the reason CooperVision may be a great workplace for you

You will carry out auditing of the final lot history record to ensure evidence that procedures have been followed has been documented and that the traceability of components and personnel are maintained. You will carry out verification of Sterilisation charts, ensuring all critical parameters in relation to the sterilisation have been achieved prior to lot release. Specifically, you will carry out the following duties:

• Measurement of lenses in line with the Quality Management system.
• Recording true and accurate data for the lenses measured. This is completed either using the electronic system (CVM), Microsoft Excel or controlled paperwork forms available from the eQMS (Agile).
• Verification and releasing of Sterilisation charts – Ensuring Critical parameters have been met.
• Auditing of Lot History Record to ensure traceability of required actions and personnel.
• Authority to Release product on the electronic system (CVM) if all lot testing and auditing meet the set requirements.
• The ability to Raise NCR’s when required, if lots fail to follow standard procedural or sample plan requirements.
• To support the requirement of both routine and non-routine lens measuring activities in UK Manufacturing if required (Investigations/Complaints/Validation/Shelf Life).
• Store quality records and retention samples correctly to enable timely retrieval if required.Support the management, storage, archive and retrieval of Quality Records