Vaga de Site Quality Manager (Sumaré, Brazil)
1 vaga: | Publicada em 16/04
- A Combinar
Sobre a vaga
3M has a long-standing reputation as a company committed to innovation. We provide
the freedom to explore and encourage curiosity and creativity. We gain new insight
from diverse thinking, and take risks on new ideas. Here, you can apply your
talent in bold ways that matter.
Job Description:
3M is establishing two/industry-leading companies, creating value through the spin-off of its Health Care business, while 3M will continue to be a global material science leader, focusing our innovation to win in favorable global megatrends and attractive end markets. This new Health Care Company will be a leading global diversified health technology company with:
Proven category leadership
Exposure to attractive end-markets
Innovation mindset driving improved patient outcomes
Collaborative customer relationships
Deep global regulatory experience
Operational excellence and strong cash flow
Strong sales growth and profitability with significant recurring sales
We expect the creation of the two companies will be completed by the end of 2023.
For now, we will continue to operate as one global company. This role is
positioned to drive the success of the "New Health Care Company.
This position provides an opportunity to transition from other private, public,
government or military experience to a 3M career.
The Impact Youll Make in this Role
As a Site Quality Manager you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by:
Standing up new Quality Management Systems (QMS) for a new medical device
manufacturing site, and obtaining ISO 13485 certification.
Ensuring the suitability and effectiveness of transferred test methods, Device
Master Records (DMR), calibration, and other documents and records.
Hiring and training the Quality Team.
Participating in site Leadership Team ensure the training programs, master
validation plan, software qualification and equipment & facility maintenance plans
are suitable and effective.
Preparing for, managing, and following-up on quality and regulatory
audits/inspections conducted by external agencies, notified bodies, customers, and
internal functions.
Your Skills and Expertise
To set you up for success in this role from day one, 3M requires (at a minimum) the following qualifications:
Pharmacy degree, with the license active in the Pharmacist Council in Brazil
Experience in Regulatory, Quality and/or QMS experience within a heath care
regulated industry
Fluent written and oral communication in both English and Portuguese
Supervision or project leadership experience
Additional qualifications that could help you succeed even further in this role include:
Previous experience establishing a new QMS
Proven ability to lead audit activities
Lean, Six Sigma, and/or Project Manager certification
Work location:
Onsite:
Sumaré, Brazil
Travel:
May include up to:
10% domestic and international
Relocation Assistance:
May be authorized
Learn more about 3Ms creative solutions to the worlds problems at www.3M.com or
on Twitter 3M é um empregador que oferece oportunidades iguais à todos. A 3M
não discriminará nenhum candidato baseado em sua raça, cor, idade, religião,
gênero, orientação sexual, identidade ou expressão de gênero, nacionalidade ou
deficiência.Our approach to flexibility is called Work Your Way, which puts
employees first and drives well-being in ways that enable 3Ms business and
performance goals. You have flexibility in where and when work gets done. It all
depends on where and when you can do your best work.
Please note:
your application may not be considered if you do not provide your education and work history, either by:
1) uploading a resume, or 2) entering the information into the application fields
directly.
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