Quality Engineer
Posted:
8 August 2026 (17 hours ago)
Application Deadline:
5 November 2026
Vacancies:
1 Vacancy
Job Summary
Our Work Matters:At Kindeva we make products that save lives ensuring better health and well-being for patients around the Impact You Will Make:This role is joining our dynamic team in Manufacturing Technology (Process & Manufacturing Engineering) where you will be supporting the production and assembly of complex precision components for pulmonary/inhalation drug delivery this role you will support/lead the projects & investigations at Kindeva acrossthe full production lifecycle of MDI valves and cans from raw material production through to finished & Project scope may cover across process production chemical quality project systems and Responsibilities include but are not limited to:Leading product quality investigations including troubleshooting product and process defects and implementing effective corrective of new and existing products and Improvement is the foundation of the company so identifying opportunities and executing projects to reduce costs and improve quality are a significant part of the and prioritising multiple projects or investigations of varying sizes simultaneously communicating with project stakeholders and the wider of data analysis and continuous improvement tools such as Minitab and technical expertise for assigned products and processes including troubleshooting and managing documentation such as SOPs validation protocols reports and change with industry the sites excellent safety record by actively engaging in a safety-first & Experience:2 years experience working in a manufacturing industry or similar to degree level or equivalent in a Manufacturing Chemical Engineering Pharmaceutical Engineering or related of any of the following - GMP working environment Quality Assurance Validation Project management ISO 9001 and working within a of lean manufacturing principles Six Sigma or other continuous improvement methodologies is a understanding of the pharmaceutical industry standards and regulatory requirements (cGMP FDA EMA) is an in managing projects & investigations at the same literate familiar with Microsoft Word and ExcelKey Capabilities:Good organisational interpersonal and time management flexible conscientious and proactive in a positive approach to own training and decision-making and problem-solving verbal and numerical aptitude communication team player with the ability to work we Offer:Attractive compensation pension scheme (up to 10% employer contribution).25 days holiday per year (plus bank holidays) plus service days after 5 Medical sick Assistance Program with 24/7 confidential helpline support for employee and immediate assurance of four times life cover working recognition on-site and cashback at many to work referral Information:Working Hours: 37.5hrs per week (Onsite)Location: Up Brooks ClitheroeAll applicants must be eligible to work in the believe our people make the difference at Kindeva we look for skilled passionate and driven professionals to come and work with us to help us excel in manufacturing technologies and processes which bring lifesaving products to patients worldwide.#LI-AC1
Required Experience:
IC
About Company
Kindeva: A purpose-fueled, people-centric, drug delivery CDMO dedicated to advancing your project, your ambitions and our industry.