Senior Software Engineer - CMS (Critical Manufacturing System)

Role Overview

As Senior Software Engineer you are responsible for ensuring the stability, reliability,

and continuous improvement of Manufacturing and Laboratory Systems for ConvaTec. You will be providing support, maintenance, and enhancements for global systems including Maximo CMMS, Critical Manufacturing MES, Labvantage LIMS, Labelling & Artwork Management Systems and Delmia Apriso MES.

This is to enable efficient production operations and rapid issue resolution. The ideal candidate combines technical troubleshooting skills with a strong understanding of manufacturing processes and a commitment to delivering excellent service to business users.

NOTE: Role will support EU/US timezones. Flexibility in working hours will be expectedKey responsibilities and authority

• Deliver second-line support for key manufacturing and laboratory platforms, addressing incidents, service requests, and user queries in a timely manner.

• Troubleshoot, debug, and resolve system issues, escalating complex problems as needed.

• Perform routine system maintenance, upgrades, and patches to ensure optimal performance and compliance.

• Collaborate with cross-functional teams (Production, GQO, QA, IT) to analyze and resolve issues.

• Support System Owners with Application Delivery project activities, ensuring project timelines are met.

• Document support activities, solutions, and system modifications for traceability reporting and compliance.

• Participate in root cause analysis and implement corrective/preventive actions for recurring issues.

• Develop or configure new or updated system functionalities.

• Write clean, efficient, and maintainable code for systems when required, adhering to best practices and coding standards.

• Provide training and support to users and support teams, promoting best practices and system adoption.

• Stay updated on the latest vendor software developments and recommend improvements and upgrades.

• Contribute to the testing and deployment of new system functionalities and integrations.

• Assist in task estimation, planning, and continuous improvement initiatives.

• Apply agile methodologies and principles to manage projects and deliver value quickly and efficiently.

About You

• At least 5 years of experience in applications of IT support, with a focus on regulatory and Quality Solutions.

• Hands on experience with Critical Manufacturing System, Maximo CMMS or Delmia Apriso is preferred

• Experience supporting and maintaining manufacturing or laboratory platforms

• Proficient communication skills to align with Business Users

• Proficient in troubleshooting, debugging, and resolving software and system issues in a manufacturing environment.

• Strong understanding of manufacturing processes and workflows.

• Familiarity with database technologies (e.g., SQL), scripting, and integration with shop-floor equipment.

• Knowledge of ITIL (IT infrastructure Library) or similar service management frameworks is an advantage.

• Experience with software development methodologies (e.g., Agile) and version control systems (e.g., GitHub).

• Proficient in one or more programming languages relevant to MES systems (e.g., Python, Java, C#, JavaScript/TypeScript)

• Excellent problem-solving, analytical, and communication skills.

• Ability to document technical solutions and provide user training.

• Team player with strong collaboration skills across technical and non-technical stakeholders.

• Willing to participate in on-call support rotations and respond to urgent production issues when required.

Qualifications & education

• Bachelor's in Engineering, Software development, Information technology, or a related field. Advanced degrees or certifications are a plus.

• ITIL 4, GMP or Database technologies is a plus

At Convatec, we’re pioneering trusted medical solutions to improve the lives we touch. If you’re ready to make a real impact, apply today and help us bring our Forever Caring promise to life.

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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.

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!About Convatec 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 over 10,000 colleagues, we provide products and services in around 90 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention, treatment for hard to heal wounds, at-risk skin and ulcerated tissue to supporting debilitating conditions, improved patient outcomes and reduced care costs. Convatec's revenues in 2025 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more please visit: http://www.convatecgroup.com.