Supplier Quality Specialist

4 tygodni temu

Warsaw, Polska ConvaTec Pełny etat
Change is everywhere at Convatec. It’s transforming our business and helping us improve millions of lives. And we’re nowhere near finished. Across every part of our business, we’re pushing for better. Join us on our journey to #ForeverCaring as a Supplier Quality Specialist, and you’ll do the same.

The Supplier Quality Specialist executes and supports supplier quality control activities for external manufacturing business unit and its suppliers within the Global Supplier Quality Team.

Key Responsibilities:

Execution of final release for third party product batches to support base business and to ensure compliance to specifications and documentation requirements.

Support the development, maintenance and execution of training materials, standard operating procedures, and work instructions to support the External Manufacturing Quality processes.

Maintain a strong relationship with Global suppliers to ensure Quality Control and Compliance for daily operations along with New Product Introductions and Base Business Changes.

Maintain strong understanding of quality documentation requirements to provide guidance and solutions for internal and external stakeholders.

Communicate with suppliers to inform and drive correction of errors in product documentation following the appropriate controlled processes

Support the development of and execute Change Control with supplier.

Maintain Monthly Key Performance Indicator (KPI) metrics utilizing strong data mining skills for the Supplier Quality business.

Manage documentation through the document life cycle, ensuring a documented and approved review-and-approval process before being stored.

Provide support during internal and external audits and inspections.

Execution and sign off final release for third party product batches to support base business and to ensure compliance to specifications and documentation requirements.

Skills & Experience:

Minimum 2 years of experience in the medical device industry * Minimum 2 years of experience in quality documentation management / document control is preferred.

Experience in Supplier Quality Management

Basic statistical skills.

Advanced Data mining skills.

Detailed analytical abilities.

Strong prioritization and coordination skills.

Qualifications/Education:

BS/BA degree in medical engineering or life sciences.

Travel Requirements

Position may involve travel up to 10% of the time to Convatec sites and supplier locations globally.

Languages

Speaking: Yes English

Writing/Reading: Yes English

Speaking: Yes Polish

Writing/Reading: Yes Polish

Full time Remote – presence at the local office may be required based on in-country legal requirements and for specific meetings/projects/events.

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-Remote

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 .

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.

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