Product Quality Specialist

Posted 12 Days Ago
Be an Early Applicant
Osted, Lejre, Sjælland
5-7 Years Experience
Healthtech • Manufacturing
The Role
The Product Quality Specialist at Convatec is responsible for documentation validation, problem-solving, deviation management, and process optimization. They play a crucial role in development projects and new product implementation, acting as a link between production, support, project, development, and maintenance teams.
Summary Generated by Built In

Pioneering trusted medical solutions to improve the lives we touch: Unomedical s.r.o. is a member of Convatec which 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. 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. With us, you will not only could influence the production and development of our products - you will also have the opportunity to develop in our QC Support team
We’re a business that never stands still. Join us on our journey to #ForeverCaring as Quality Specialist, and you won’t either.


 

About the role

As a quality Specialist you will be responsible for, the validation of documentation, revalidations, and risk assessments for the specific process. You will also be responsible for systematic problem solving, deviation management, optimization of equipment and processes as well as general support for production and organizational projects. You will have a central and cross-organizational role in connection with development projects and the implementation of new products and act as a link between production, the support team, project team, development, and maintenance.

 

key responsibilities:

  • Improve activities in QC, including facilitation of problem solving.

  • Identify potential improvements by analyzing data in release process.

  • Confident presenter when QC are audited or inspected by customer/authorities.

  • Handle deviations; includes close sparring with operators, technical department, QA etc.

  • Prepare and maintain documentation e.g., risk assessments and periodic evaluation

  • Change Control Request (CCR) with associated documentation

  • QC specialist in connection with development and equipment projects


 About you:

  • A relevant academic background; engineer, chemist, pharmacist or similar, preferably with at least 5 years of experience from a QC specialist role or similar.
  • Experience working with change requests, purchase specifications, validation and deviations using trackside, D2 and SAP.
  • Experience of working in a GMP-regulated environment
  • Academic Profile
  • Knows how to prioritize tasks and deadlines
  • Organize and Planner
  • Fluent in written and verbal competencies in both Danish and English


 

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.

#LI-CH2

#LI-Onsite


 

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 [email protected].

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!

Top Skills

D2
SAP
The Company
HQ: London
5,536 Employees
On-site Workplace

What We Do

At Convatec, #ForeverCaring is our promise to patients & healthcare providers, as we deliver pioneering trusted medical solutions to improve the lives we touch.

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