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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 at-risk skin, to improved patient outcomes and reduced care costs. Group revenues in 2022 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

As a Sterilization Technician, you will design, construct, validate, and implement new and refurbished sterilization, sanitization, emissions, and monitoring systems. Additionally, you will be responsible for the direct operation of the sterilization or sanitization of products, ensuring that test samples and procedures are in compliance with internal and external requirements. You will also monitor water systems for contamination, write and review documentation for new and current test procedures, and prepare technical reports related to laboratory equipment, products, and/or processes. Furthermore, you will investigate out-of-specification product results and contamination incidents, determining appropriate resolutions including product disposition. Finally, you will set and reinforce product hygiene standards for the organization.

Your key duties and responsibilities as a Sterilization Technician :

It is the responsibility of the Sterilization Technician to support the work that ensure that the company contractual sterilization processes performed at EO sterilization sites are effective and in compliance with all current regulatory requirements.

• Support the management and coordination of the company overall performance in terms of satisfying all the prevailing quality requirements laid down in local documents regarding microbiological control, ISO 13485, and any other relevant regulatory requirements.

• Day-to-day support for sterilization procedures and instructions.

• Participation in Product Development in terms of determination of sterilizability of the new/altered product design to ensure optimal sterilization.

• Participation in Process Development relating to the sterilization process.

• Preparation of validation protocols for sterilization processes within the cycles and products related to Denmark Infusion Device area. Review of protocols and reports from other business units on request.

• Participation in Validation activities on a level to make it possible to review/approve the documents related to the activities such as validation reports.

• Preparation of Procedures and Work Instructions within the sterilization area.

• Perform or participate in internal and external sterilization/production site audits.

• Provide support in connection with product registrations and/or inquiries from authorities and customers, and customer audits.

• Support training of QA/QC staff related to release of sterilized products.

• Participate in projects to support sterilization, sterility assurance, contamination controls and sterilant residue related projects.

About you:

• Experience in the Medical Device Industry.

• Communicative level of English language.

• Proficiency in MS Office.

• Trained in FDA QSR’s, ISO 13485, EU and Canadian medical device regulations.

• Experience with sterilization process technology within gas sterilization.

• Experience with sterilization process technology within radiation sterilization.

• Knowledge of sterilization standards (EN ISO 11135, EN ISO 556).

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.

Note: Please send your CV only in English language.

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Beware of scams online or from individuals claiming to represent Convatec

A 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 careers@Convatec.com .

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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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!