Quality Technician (Braunton, GB, EX33 2DL)
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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
Review batch documentation associated with the manufacture and packaging of products to ensure they meet specification and have been produced in accordance with the MA and GMP. Provide line-side Quality support to Production departments.
Scope of the Role
Reviewing batch paperwork in process for correct completion and compliance to GMP in preparation of QP release.
Reviewing in process test and inspection results to determine product quality.
Supporting the Production departments in determination of actions in the event of a non-conformance (Quality Event) occurring, including decisions to continue production.
Ensuring where a non-conformance has occurred any impacted product and materials are suitably contained and quarantined, including where necessary placing materials on hold and splitting batches as required.
Conducting product sampling and inspection where required in support of non-conformance investigation and process improvements.
Supporting process and quality improvements led by operations teams and Quality Engineer to reduce non-conformance.
Support the implementation of corrective actions as a result of non-conformance investigations.
To undertake such other reasonable duties as may be required from time to time in order to support the Perrigo business.
Experience Required
Minimum 2 years’ experience working in a high volume manufacturing environment, preferably in a regulated industry.
Familiar with the principles of GMP.
Familiar with principles of lean management and continuous improvement, can demonstrate participation in lean management initiatives.
Effective communication – written, verbal & visually – can convey information simply, succinctly, objectively.
Experienced user of computer software programmes such as Excel, PowerPoint & Word is essential. Is able to enter and manipulate data in spreadsheets to sort and produce reports and graphs and analyse data. Can prepare slides in PowerPoint for example to deliver training. Can write a technical report using structure and formatting to improve readability.
Ability to work in a multifunctional team, works collaboratively to find best solution for all.
Eye for detail, is careful and methodical in their work and sets high standards for accuracy.
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
Job details
How this role compares
Computed from every other active Quality role in our database, not just this employer's listings.
We currently track 1528 comparable Quality roles across 148 biopharma companies.
Salary context
276 of 1528 peers report a salary range (USD, annualized)
Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.
Where these roles are based
Top locations among the 1528 comparable roles
+ 46 more countries
Seniority mix
729 of 1528 peers have a known seniority level
Therapeutic area mix
1 of 1528 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
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How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.