Quality Assurance Specialist

Posted 4 Days Ago
Be an Early Applicant
Tuusula
3-5 Years Experience
Healthtech • Pharmaceutical • Manufacturing
The Role
Quality Assurance Specialist responsible for evaluating customer complaints, analyzing quality data, supporting new product development, and participating in audits. Requires 3+ years of experience in quality engineering, proficiency in Finnish and English, and knowledge of regulatory requirements in the medical device industry.
Summary Generated by Built In


Job Description:

We are now looking for a

Quality Assurance Specialist

to be in charge of various quality assurance activities as part of our QA/RA team in Tuusula.

As a Quality Assurance Specialist, you will have an active and important role in supporting R&D, Maintenance Engineering, Customer Care, Procurement, Product Management and Operations in their efforts to ensure high product quality and global regulatory compliance.

Main Tasks:

  • You will be responsible for evaluating incoming customer complaint data, identifying safety related and potentially reportable complaints and gathering needed information for complaint closure.

  • You will analyze various quality data, identifying production, process or product issues, and coordinating implementation of solutions.

  • You will use problem solving methodologies for in-process, supplier and customer quality issues.

  • The role will also include support for new product development, engineering and manufacturing changes to ensure compliance against regulatory requirements and internal procedures.

  • You will participate in internal and external audits.

  • You will have a great opportunity to further develop and improve our company’s quality management system processes and tools.

#LI-EU1

Job Requirements:

We expect you to:

  • have an Engineering Degree and 3+ years of experience in a quality engineering or quality assurance role

  • have proficiency both in spoken and written Finnish and English

  • demonstrate excellent communication skills across business functions and cultural boundaries

  • enjoy working in a fast-paced, international environment

  • have proficiency in Microsoft Office applications.

Additionally, the following will be considered an advantage:

  • experience in medical device industry and understanding of international medical device standards, regulations and risk management 

  • knowledge and interest in Lean methods and processes.

As a person, you are:

  • Self-motivated and able to work independently, yet an efficient team player, who strives for reaching the goals.

  • You take initiative, learn quickly and enjoy facing challenges and solving problems.

  • You have a sense of urgency and strong attention to detail.

  • You understand the importance of your role in complying with the rigorous regulatory requirements for healthcare technology and ensuring our imaging products fulfill or even exceed the high-quality expectations of our end-users.

We offer you inspiring challenges in a rapidly growing global health-tech business and an opportunity to work within a strong Lean culture. The position offers interesting and varying responsibilities and an attractive opportunity to excel your professional expertise as a part of our global QA/RA team.

Operating Company:

DEXIS

Envista and its family of companies (Envista) will not accept unsolicited resumes from any source other than directly from a candidate. Envista will consider unsolicited referrals and/or resumes submitted by vendors such as search firms, staffing agencies, professional recruiters, fee-based referral services and recruiting agencies (Agency) to have been referred by the Agency free of charge and Envista will not pay a fee for any placement resulting from the receipt such unsolicited resumes. An Agency must obtain advance written approval from Envista's internal Talent Acquisition or Human Resources team to submit resumes, and then only in conjunction with a valid fully-executed contract approved by the Global Talent Acquisition leader and in response to a specific job opening. Envista will not pay a fee to any Agency that does not have such agreement and written approval in place.

The Company
Brea, California
1,933 Employees
On-site Workplace

What We Do

Envista is a global family of more than 30 trusted dental brands, united by a shared purpose: to partner with professionals to improve lives. Envista helps its partners deliver the best possible patient care through industry-leading products, solutions, and technology. Our comprehensive portfolio covers a wide range of dentists' clinical needs for diagnosing, treating, and preventing dental conditions, as well as improving the aesthetics of the human smile.

Our differentiated combination of continuous improvement, a bias toward action and innovation, and a deep respect for the more than one million professionals we serve embolden us to champion dental professionals like no one else can.

The operating companies that form Envista, including Nobel Biocare, Implant Direct, Ormco, DEXIS, Kerr, Metrex, and more represent more than 125 years of dental industry excellence. These brands meet the end-to-end needs of dental professionals worldwide.

We are committed to helping dental professionals improve their patients’ lives by digitizing, personalizing, and democratizing oral care. Every day, our products and solutions are accelerating the future of dentistry. Operating with high sustainability standards guides our decision-making so that we can deliver enhanced outcomes for our people, the environment, and communities.

View our Environmental, Social, and Governance report at https://bit.ly/Envista2022ESG to learn more about our commitment to sustainability.

Learn more at www.envistaco.com

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