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Manufacturing Quality Engineer

Unomedical s.r.o.

Information about the position

  • Place of work: Priemyselný park 3, Michalovce
  • Basic wage component (gross) and other rewards: 1 100 EUR/monthminimum 1100€ / monthly (depending on experiences and quality of the candidate) + quarterly bonus and other benefits in compliance with social benefit program of the company
  • Start date: by agreement
  • Contract type: full-time

Job description, responsibilities and duties

At ConvaTec, our vision is to develop pioneering trusted medical solutions to improve the lives we touch. We are a global medical technology business focused on serving people and care givers in the areas of advanced wound care, ostomy care, continence and critical care and infusion care. We devise, develop and manufacture innovative products and services that support people with deeply personal and challenging medical conditions, helping to improve care for them and giving them greater confidence, freedom and mobility.

We are guided by our five core values, that shape the way we work, every day: Improve Care, Deliver Results, Grow Together, Own It and Do What’s Right. We are a global Group, with over 9,900 employees and in 2020, our Group generated revenues of over $1.894 billion. To learn more about ConvaTec, please visit www.convatecgroup.com.


Every day, our products improve the lives of millions of people around the world. We’re hugely proud of this, which is why we’re transforming our business to reach millions more. Join us as a Manufacturing Quality Engineer, and you’ll drive progress that really means something.


About the role:
This is a brand new position in Michalovce plant and is part of the Sustaining Engineering Group.
Manufacturing Quality Engineer role manages the performance of the Engineering aspects of the site’s Quality System and Quality Control processes in achieving all established user requirements and all applicable requirements.
The role ensures compliance with Corporate Quality System procedures during Process Development, Design Transfer, Process Validation, Launch and Engineering Change activities.
Collaborates with internal suppliers and customers to establish product quality requirements.

Your key duties and responsibilities:
• Actively supports and influences technology transfer teams in the translation of product Design Requirements into Manufacturing Requirements
• Assures work is complete, meets standards and requirements appropriate for the type of product
• Supports the introduction of new equipment into production, providing guidance and enforcing high quality standards throughout the respective project
• Supports the implementation of continuous improvement activities by assessing impact on the Quality system
• Investigates process and product performance issues and leads or participates in multifunctional evaluation of products in the market.
• Evaluates data using statistical tools. Lead or support Complaint investigations through Root Cause Analysis and effective Corrective or Preventive Actions (CAPA). Lead or actively support Product Change Control
• Supports manufacturing, providing guidance to ensure high quality standards are maintained
• Provides leadership as subject expert in Risk management and Control plan activities
• Maintains risk management procedures, ensuring alignment with relevant regulatory standards
• Provides leadership as subject expert in validation, completes assessment of validation requirements associated with a change in the process
• Maintains validation procedures, ensuring alignment with relevant regulatory standards and leads revalidation assessments

Employee perks, benefits

• Quarterly bonus after the trial period - max. 10% from the monthly salary of the employee (based on the results of the production plant)
• Large corporation with representation and manufacturing plants in the world
• Very stable employer for Michalovce city and its surroundings
• Corporate culture – Underpinning everything we do are our values:
- Improve care
- Deliver results
- Grow together
- Own it
- Do what´s right
• Meals in the amount of 0.17 Eur per one meal unit / day
• Supplementary pension plan after the trial period with the employer's contribution
• Free bus transport within Michalovce city
• Social fund (various support and perks for employees)
• Flexible working hours
• Development trainings
• Career opportunities for internal employees
• Various events / team building activities for employees (no pandemic situation)
• Various employee discounts by vendors within Michalovce city

Information about the selection process

Note: Please send your CV only in English language.

Only candidates who meet our requirements will be invited for the interview. Data of not selected candidates will be deleted in compliance with GDPR and data protection law.
Information about personal data processing of job seekers is located on link: www.convatec.sk/o-nás/kariéra/

Requirements for the employee

Candidates with education suit the position

University education (Bachelor's degree)
University education (Master's degree)

Educational Specialization

Degree in an engineering or scientific discipline is desirable

Language skills

English - Upper intermediate (B2)

Number of years of experience

3

Personality requirements and skills

About you:
• Demonstrated experience in a quality engineering or a similar role
• Experience in a production company – required
• Experience in medical devices or life sciences technology driven company – preferred
• Demonstrated application of change control processes in a complex and regulated manufacturing environment
• Experience with all phases of the product development lifecycle including concept, design, implementation, verification, and validation activities necessary for product commercialisation
• Regulatory and compliance knowledge and expertise in quality systems
• Project management expertise including managing multiple projects


Education / Qualifications:
• Degree in an engineering or scientific discipline is desirable
• Proficient with software such as Word, Excel, Powerpoint, and Project, as well as statistical tools (e.g. Minitab)
• Successful candidate must be able to manage own workload, managing multiple projects at the same time
• Knowledge and experience of working with a Quality Management System within Medical Device manufacturing
• Green belt six sigma certified – preferred
• Project management – preferred
• English - Upper intermediate (B2) – preferred (not required). A lower level of English language is acceptable with further development.


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.

Advertiser

Brief description of the company

At ConvaTec, our vision is to develop pioneering trusted medical solutions to improve the lives we touch. We are a global medical technology business focused on serving people and care givers in the areas of advanced wound care, ostomy care, continence and critical care and infusion care. We devise, develop and manufacture innovative products and services that support people with deeply personal and challenging medical conditions, helping to improve care for them and giving them greater confidence, freedom and mobility.

We are guided by our five core values, that shape the way we work, every day: Improve Care, Deliver Results, Grow Together, Own It and Do What’s Right. We are a global Group, with over 9,900 employees and in 2020, our Group generated revenues of over $1.894 billion.

To find out more please visit https://www.convatecgroup.com/careers/ - thanks for your interest!

Number of employees

500-999 employees

Company address

Unomedical s.r.o.
Priemyselný park 3
071 01 Michalovce
www.convatec.sk