Senior Supplier Quality Engineer

Convatec

Osted, Sjælland
Permanent
Fuldtid

16 dage siden

Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. With around 10,000 colleagues, we provide our products and services in almost 100 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of atrisk skin, to improved patient outcomes and reduced care costs. Convatec’s revenues in
2023 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more about Convatec, please visit http://www.convatecgroup.com.Our search for better is changing the lives of our customers. It’s changing the careers of our people too –creating new challenges and opportunities all the time. We’re a business that never stands still. Join us on our journey to #ForeverCaring as Senior Supplier Quality Engineer, and you won’t either.Job Summary:This is a key role within the Global Quality function, where you will have the objective of supporting the maintenance and improvement of ConvaTec’s Global Supplier Quality program and conducting supplier audits to ensure compliance.About the RoleKey Duties & Responsibilities

Support and lead where appropriate, supplier selection, evaluation, and approval.
Generate appropriate key performance indicators to assess supplier.
Drive resolution of corrective actions.
Raise appropriate questions or concerns regarding regulatory compliance to appropriate authorities regarding Purchasing Control activities.
Demonstrate high commitment to quality and customer service based upon customer needs.
Build strong relationships with customers, suppliers, stakeholders, and support groups worldwide to meet the demands of a changing business environment.
Demonstrate expert technical knowledge and principles in relation to medical devices.
Show project leadership skills for complex and strategic project.

About You:The Ideal Candidate should bring the following qualities to the role:

ISO 13485 or ISO 9001 Auditor Certification and experience in executing audits.
Knowledge of regulatory requirements that affect the medical device manufacturing business and put policies and systems in place to achieve conformance: QSR Part 820, ISO 13485, MDD 93/42, ISO 9001, GMP Parts 201 and 211, EU MDR.
Minimum 3-5 years’ experience in the medical device or pharmaceutical industry.
Robust Supplier Quality knowledge and experience.
Experience in TrackWise, SAP (preferable).
Experience in internal and supplier related CAPA/ NC.
Knowledge and implementation of effective quality control for manufacturing and supply chain operations, particularly in supplier evaluation, selection, auditing, and supplier management programs.
Ability to negotiate and partner with internal and external customers to enhance operational effectiveness.
Knowledge of GxP and relative standards for manufacturing environments.
Ability to work with people / teams in a complex, changing environment, to deliver value-added results to the business.
Demonstrated ability to establish and respond to metrics related to contract manufacturers performance.
Knowledge of quality control principles and their relationship to relevant regulatory requirements.

Travel RequirementsThis position will be required to travel (20%) to ConvaTec and supplier locations (international)Education/QualificationsCertified Quality Auditor - (ISO 9001 or ISO 13485 is required)BS/BA degree in medical engineering, life sciences, manufacturing engineeringWorking Conditions:Hybrid working (2-3 days onsite required; contingent on needs of the business)Language Skills Required:Speaking: Danish/English (required)Writing/Reading: Danish/English (required)Our ambitions will bring the very best out in you. You’ll be pushed to aim higher and really own your work. You’ll be encouraged and supported to make things happen too. It can be challenging. But, as the progress you make will help improve the lives of millions, it’ll be worth it.This is stepping up to a challenge.This is work that’ll move you.#ForeverCaring #ForeverConvatec #WeAreConvatec#LI-DB1#LI-HybridBeware of scams online or from individuals claiming to represent ConvatecA formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address.If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you’re unsure, please contact us at .Equal opportunitiesConvatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.Notice to Agency and Search Firm RepresentativesConvatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.Already a Convatec employee?If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site - Find Jobs". Thank you!

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