At a Glance
- Tasks: Prepare and execute validation protocols for quality-critical equipment and processes.
- Company: Perrigo is a leading player in self-care solutions, committed to enhancing wellbeing for all.
- Benefits: Enjoy competitive pay, hybrid working options, and career development opportunities.
- Why this job: Join a collaborative culture focused on personal responsibility and making a positive impact.
- Qualifications: Minimum 2 years in validation or process engineering; knowledge of GMP is essential.
- Other info: Flexible hours and a commitment to diversity and inclusion make this role unique.
The predicted salary is between 30000 - 42000 Β£ per year.
At Perrigo, we are driven by our mission to make 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. 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.
Description Overview
- 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.
- Conduct periodic lifecycle reviews for each of the validation disciplines.
- Support Improvement projects with technical input and participating in problem-solving teams (e.g., CAPA, Quality Event, Kaizen).
Scope of the Role
- 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
- To undertake such other reasonable duties as may be required from time to time in order to support the Perrigo business.
- Consistently views product quality and GMP compliance as a personal responsibility.
- Takes ownership for quality in their area and/or activities conducted by them and does not assume that errors will be caught by someone else.
- Only carries out tasks they are trained to complete and proactively highlights quality issues and potential solutions to their leader.
Experience Required
- Flexibility to work varied hours as needed β although it is not envisaged that this will be a regular or frequent occurrence.
- Minimum of 2 yearsβ 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.
Hybrid Working Approach
We love our offices and the setting they provide for in-person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles.
We are proud to be included in the Forbes list of 'America's Best Employers by State 2024'.
We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law.
Validation Technician employer: Perrigo Company plc
Contact Detail:
Perrigo Company plc Recruiting Team
StudySmarter Expert Advice π€«
We think this is how you could land Validation Technician
β¨Tip Number 1
Familiarise yourself with the specific validation protocols mentioned in the job description, such as Performance Qualification and Cleaning Validation. Understanding these concepts will help you engage in meaningful conversations during interviews.
β¨Tip Number 2
Network with professionals in the pharmaceutical industry, especially those who have experience in validation roles. Attend industry events or join relevant online forums to gain insights and potentially get referrals.
β¨Tip Number 3
Research Perrigo's products and their commitment to quality and compliance. Being knowledgeable about their brands and mission will demonstrate your genuine interest in the company during interviews.
β¨Tip Number 4
Prepare to discuss your experience with risk assessment and process improvement initiatives. Highlight any relevant projects you've worked on that align with the responsibilities of the Validation Technician role.
We think you need these skills to ace Validation Technician
Some tips for your application π«‘
Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of the Validation Technician role at Perrigo. Tailor your application to highlight relevant experience in validation or process engineering.
Highlight Relevant Experience: In your CV and cover letter, emphasise your minimum of 2 yearsβ experience in validation or process engineering roles, particularly in regulated industries. Mention any specific knowledge of GMP and how you've applied it in past roles.
Craft a Strong Cover Letter: Write a compelling cover letter that connects your skills and experiences to the job description. Discuss your familiarity with validation protocols and your ability to work collaboratively on improvement projects.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial for a role focused on quality and compliance.
How to prepare for a job interview at Perrigo Company plc
β¨Understand the Role
Make sure you thoroughly read the job description and understand the key responsibilities of a Validation Technician. Be prepared to discuss how your previous experience aligns with these tasks, especially in areas like validation protocols and quality compliance.
β¨Showcase Your Knowledge of GMP
Since knowledge of Good Manufacturing Practices (GMP) is crucial for this role, be ready to explain how you've applied GMP in your past work. Share specific examples that demonstrate your understanding and commitment to quality standards.
β¨Prepare for Technical Questions
Expect technical questions related to validation processes, risk assessments, and problem-solving methodologies. Brush up on relevant concepts and be ready to discuss how you've contributed to process improvements in previous roles.
β¨Emphasise Team Collaboration
Perrigo values collaboration, so highlight your experience working in teams, especially in cross-functional settings. Discuss any projects where you worked alongside Quality Engineering or participated in CAPA action teams to show your ability to contribute effectively.