Pharmaceutical Work, Jobs in Lynmouth, Dev (with Salaries)

Validation Technician
Perrigo —Braunton
- Master's degree
QA Officer
PCI Pharma Services —Bridgend
- Full-time
- Communication skills
Scheme Sales Representative
Accord Healthcare —Barnstaple
- Full-time
- Sales
- Customer service
- Computer literacy
- Free parking
- Health & wellbeing programme
Quick apply
12d
Process Operator (Double Day Shift)
Accord Healthcare —Barnstaple
- £30,000 a year
- Call to connect
- English
- IT
- In-person
Quick apply
Desktop Support Specialist
PCI Pharma Services —Bridgend
- 8 hour shift
- Software troubleshooting
- Customer service
- Microsoft Office
- Annual leave
- Employee assistance programme
4d
BGD_Associate Project Manager - S&D
PCI Pharma Services —Bridgend
- 8 hour shift
- Hybrid work
- Microsoft Office
- Administrative experience
- Maths
- Annual leave
- Employee assistance programme
13d
IV Therapies Homecare Nurse
Lloyds Clinical —Barnstaple
- £43,000 a year
- Travel
- IT
- School
- Annual leave
- Employee assistance programme
Quick apply
Quality Engineering Team Manager
Cytiva —Braunton
- Full-time
- Engineering

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pharmaceutical jobs near lynmouth, dev

Validation Technician

Perrigo -
Braunton

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Job details

Qualifications

Master's degree
Kaizen

Full job description

At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill®, Compeed®, Solpadeine®, NiQuitin®, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.

Join us on our One Perrigo journey as we evolve to win in self-care.

Description Overview

In this role you will be responsible for the preparation and execution of validation protocols according to the Validation master plans and schedules in Process Validation (including Performance Qualification, product hold time and transport studies), Equipment Qualification, Cleaning Validation, Computer Systems Validation, Spreadsheet Validation and execution and reporting of temperature profile mapping for Quality Critical equipment

You will also conduct periodic lifecycle reviews for each of the validation disciplines, and support Improvement projects with technical input and participating in problem solving teams (e.g CAPA, Quality Event, Kaizen).

Scope of the Role

Validation

Generate and assist in the completion of qualification and validation protocols to enable the compliant and efficient introduction of new or changed products, processes, equipment, computer systems, spreadsheets and cleaning procedures.
Report results and findings following execution of protocols.
Conduct lifecycle reviews for products/processes, equipment, cleaning processes, computer systems, spreadsheets and temperature profiles for quality critical temperature-controlled equipment

Process Improvement

Work in collaboration with Quality Engineering and Operational Excellence to provide validation and qualification expertise in improvement initiatives. Provide data via validations to support product control plans and risk assessment processes.
Take an active role in CAPA action teams, QE investigation teams and Kaizen events where required.

Risk Assessment

Identify via risk assessment, validation and qualification requirements for both new and changes to existing products, processes, equipment, cleaning procedures, computer systems and spreadsheets.

Other

Undertake such other reasonable duties as may be required from time to time in order to support the Perrigo business.

Experience Required

Minimum of 2 years’ experience of validation or process engineering roles in the pharmaceutical or other regulated industry
Knowledge of GMP and its application in validation and change management and improvement processes, ability to learn new regulations
Ideally experience of working in an environment employing some elements of lean management, but not essential

Benefits
We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.

Find out more about Total Rewards at Perrigo.

We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more here

Applicants please note: To apply to this position please click the APPLY button at the bottom of the application. (The SAVE button will only save your profile information but not submit an application for this open position.) All application materials, including resumes and CVs, must be submitted in English. Thank you.

We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law. #weareperrigo

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pharmaceutical jobs in lynmouth, dev

Validation Technician

QA Officer

Scheme Sales Representative

Process Operator (Double Day Shift)

Desktop Support Specialist

BGD_Associate Project Manager - S&D

IV Therapies Homecare Nurse

Quality Engineering Team Manager

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