Quality assurance Work, Jobs in Cowbridge, Vgl (with Salaries)

QA Officer
PCI Pharma Services —Bridgend
- Full-time
- Communication skills
Quality Officer
Talk Training Ltd —Cardiff
- £30,000 - £35,000 a year
- Full-time
- Hybrid work
- SharePoint
- IT
- Communication skills
- Annual leave
Quick apply
Quality Technician
Seras Energy —Swansea
- Full-time
- Microsoft Excel
- Microsoft Office
- Driving
- Employee discount
- Referral programme
Quick apply
7d
Quality Assurance Lead
MM Group —Newport
- Full-time
- Employee assistance programme
Internal Quality Assurer
Talk Training Ltd —Cardiff
- £29,268 a year
- Full-time
- Hybrid work
- IT
- Annual leave
Quick apply
3d
Quality Technician
Safran —Cwmbran
- Full-time
10d
Senior / Principal Consultant, Air Quality - Cardiff
WSP —Cardiff
- Part-time
- Hybrid work
- Data analysis skills
- Supervising experience
- Project management
- Flexitime
- Work from home
Quality Improvement Lead
Cytiva —Cardiff
- Full-time
- Engineering
- No degree
8d
Quality Technician
Kennametal —Newport
- Microsoft Excel
- Data analysis skills
- Laboratory experience
- Life insurance
- Sick pay
Programme Quality Engineer – Concessions
General Dynamics Land Systems UK —Pentrebach
- £36,000 - £45,000 a year
- Full-time
- Engineering
- Travel
- Communication skills
Principal QA Engineer
Box UK Limited —Cardiff
- Up to £55,000 a year
- Full-time
- Hybrid work
- APIs
- Agile
- Employee discount
- Life insurance
Quick apply
Quality Assurance Engineer
Marshall of Cambridge (Holdings) Limited —Merthyr Tydfil
- Up to £32,000 a year
- Full-time
- Continuous improvement
- In-person
Senior Assistant, Entities Management & Business Relationships (EMBR), Quality Risk and Security Services, 12-month Secondment/FTC
Deloitte —Cardiff
- Hybrid work
- Customer service
- No experience needed
- Microsoft Office
1d
Principal QA Engineer
Box UK —Cardiff
- £55,000 a year
- Hybrid work
- APIs
- Agile
8d
Quality Engineer
Amcor —Swansea
- Full-time
- Engineering
- ERP systems
- Data analysis skills
Senior Quality Technician #RO #UK
CAF Rolling Stock UK —Newport
- Annual leave
- Employee discount
Special Processes Quality Assurance Lead
Safran —Cwmbran
- Full-time
- Engineering
- Travel
- Employee assistance programme
Quality Manager (Blackwood)
Vernacare International Ltd —Blackwood
- Full-time
- Management
- Engineering
- Analysis skills
- Annual leave
- Employee assistance programme
Quick apply
7d
Senior Quality Manager (SQM)
Vishay —Newport
Supplier Quality Engineer
General Dynamics Land Systems UK —Pentrebach
- £36,000 - £39,000 a year
- Full-time
- Engineering
- Travel
- Communication skills
1d

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QA Officer

PCI Pharma Services -
Bridgend

Apply Now

Job details

Full-time

Qualifications

Quality assurance
Communication skills
FDA regulations

Full job description

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.

We are PCI.

Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.

General Purpose of Role:

To perform a Quality Assurance role which supports:

Certification and release of medicinal products in accordance with regulatory, company and project requirements.
Maintain, support and improve the Pharmaceutical Quality System employed within PCI.

Main Responsibilities:

Support the QP in execution of their legal and operational duties.
Administration, control and support core systems within the Pharmaceutical Quality system as allocated by line manager. Including but not limited to Internal audits, vendor management, deviations/complaints, CAPA, change control and document control.
Reporting of metrics for systems within scope of responsibility.
Support and host client audits of the PCI Bridgend facility.
Support delivery of site/departmental projects and objectives.
Support continuous improvement, validation and technical services activities.
Author standard operating procedures.
Provide QA and GMP related training.

Outcomes of Role:

Schedule, host and close out client audits.
Pre-certification assessment of batch records and generation of draft QP certificates.
Post QP certification batch release via the inventory system.
Review and approval of offsite shelf life extension labelling activities.
Pre-approval assessment of change controls and deviations.
Co-ordinate and perform investigations into internal and external quality issues.
Assess temperature excursions during shipment in line with the stability priofile of the product(s).
Approval of completed investigations, CAPA’s and change controls.
Schedule, perform and close out internal and external audits within established timelines.
Pre review of validation/qualification protocols.

Previous Work Experience:

Minimum two years experience in a Quality role within a regulated industry (pharmaceutical, clinical, biotechnology or medical device).
Experience within a regulated industry (pharmaceutical, clinical, biotechnology or medical device).
Holds a qualification in a life sciences subject (HNC, HND or degree or equivalent) in a life sciences subject or suitable experience in a Quality Assurance or technical role within the pharmaceutical industry.
Good GMP knowledge and experience of EU legislation and guidelines; experience with FDA GMP requirements CFR 210 and 211 other regulatory guidelines preferable.
Strong communication skills.
The ability to introduce, co-ordinate, complete and report on projects.
A high level of self-motivation is required.
Able to rationally persuade.
Quality Officers need to be familiar with standard computer applications currently in use by the company.
Interpersonal skills: able to form and maintain relationships at all levels is essential. A Quality Officer must be able to effectively convey potential quality issues and offer constructive advice when required.
Thinking and decision making: a Quality Officer will often need to make decisions and advise on appropriate courses of action in the event of a Quality incident or to agree appropriate Corrective and Preventative actions. A Quality Officer should be able to consider all relevant aspects and possible repercussions are considered regarding these quality issues.

#LI-AT1

Join us and be part of building the bridge between life changing therapies and patients. Let’s talk future

Equal Employment Opportunity (EEO) Statement:
PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

At PCI, Equity and Inclusion are at the core of our company’s purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity – at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

Apply Now

Refine Your Search

quality assurance jobs in cowbridge, vgl

QA Officer

Quality Officer

Quality Technician

Quality Assurance Lead

Internal Quality Assurer

Quality Technician

Senior / Principal Consultant, Air Quality - Cardiff

Quality Improvement Lead

Quality Technician

Programme Quality Engineer – Concessions

Principal QA Engineer

Quality Assurance Engineer

Senior Assistant, Entities Management & Business Relationships (EMBR), Quality Risk and Security Services, 12-month Secondment/FTC

Principal QA Engineer

Quality Engineer

Senior Quality Technician #RO #UK

Special Processes Quality Assurance Lead

Quality Manager (Blackwood)

Senior Quality Manager (SQM)

Supplier Quality Engineer

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