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
The role
The process engineer role focuses on designing, developing, and implementing new or revised production processes for efficient product manufacturing. This includes monitoring and improvement of layout, scrap, waste, inefficiencies for processes and equipment. Additionally, the role acts as a driver and change ambassador in regard to change control request, quality incidents such as NC’s and CAPAs.
Key Responsibilities:
Designing arrangement of manufacturing equipment to ensure most efficient and productive layoutDesigning the sequence of production operations, specifying procedures for the fabrication of applicable tools and equipment, and adapting machinery in response to factory conditionsConducting tests throughout all stages of production to determine control over applicable variables and troubleshooting/solving production problemsProviding guidance to product design engineering on technical specifications that will best utilize equipment and manufacturing techniquesIdentification and reduction of scrapContinuous Improvements of process, equipment and incl documentation – Testing – CCR - ValidationContinuous Improvements of procedures and routinesSupport and execute validation of designated processesEnsuring that documentation of process changes made is compliant with current regulationsAnalyze and focus on critical spare parts in cooperation with responsible techniciansContinuous Improvement on process equipment and processes to increase capacity and stabilityEnsuring adequate level of communication with the team members associated with production personnel and relevant stakeholders to function as smoothly as possibleReporting and presentation of project status and data into Production Management and relevant stakeholdersDriving and owning of NC’s, CAPA’s and CCRs related to the production.Project management / participation in projects related to productionSkills & Experience:
Experience from the Medical Device Industry or other regulated industry (Preferred)Experience with cross organizational projects (preferred)Experience with project management (preferred)Experience with CI on automated processes and production (preferred)Qualifications/Education:
Engineer, produktionsteknolog or similar technical education (required)Knowledge of process validation (required)Knowledge of basic requirements of FDA's QSR, GMP and ISO 13485 or similar (preferred)LEAN or six sigma green belt (preferred)
Our transformation will change your career. For good. You’ll be pushed to think bigger and aim for excellence. Your ideas will be heard, and you’ll be supported to bring them to life. There’ll be challenges. But, stretch yourself and embrace the opportunities, and you could make your biggest impact yet. This is stepping outside of your comfort zone.
This is work that’ll move you.
#LI-ÁN1
#LI-Onsite
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Equal opportunities
Convatec 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 Representatives
Convatec 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.
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