Intertek · Publicerad 6 dec

Intertek are looking for thorough individuals, focussed on delivering accurate and robust audits within agreed timeframes and experienced within the medical device area, to take on the role as auditors within Intertek's Swedish Notified Body for MDD (93/42/EC). If you want to be part of our journey, we would love to hear from you!

Please send your application consisting of a CV and personalised cover letter as soon as possible.

Arbetsuppgifter

The Notified Body within Intertek Semko AB is accredited to certify companies according to the EU Medical Device Directive (MDD). Reviewing documentation, assessing products, performing quality management system audits and unannounced audits are part of the certification and the Notified Body.

As an auditor in our Notified Body, you will perform audits of our customers within the medical device industry. Our customers are primarily based in Sweden, but we do also work with other parts of the world. You can therefore expect a significant amount of travelling.

In addition to the auditing, you will be required to coordinate audit activities with the audit team, assist customers with questions relevant to the audit and / or certification process, write audit reports, follow up on audit findings, participate in audit meetings and work on ad hoc projects, relevant to the job, that may arise.

We are currently expanding our area and therefore looking for a number of auditors. Today we are 12 employees at the Notified Body eager to optimise our processes, work more efficiently and expand our knowledge and competencies.

As an auditor you can expect to interact, on a frequent basis, with internal and external personnel including our customers, other members of the Notified Body team and management.

The role is permanent and based in Stockholm or Gothenburg.

Utbildning/erfarenhet

At least 3 years' experience in the medical-technical industry e.g. within auditing, quality management, regulatory affairs, research & development or production/service.
Experience in one or more of the following is a distinct advantage:
  • Notified Body / Medical Device Directive
  • Technical File Review
  • Auditing
  • Medical-technical industry
  • Electrical, sterile, dental or implantable devices
  • Software
  • Health care
  • Risk management
  • Scientific literature or clinical trials
  • Medical device regulations
  • Industry practice and standards
Higher education, MSc, and/or equivalent experience in either Health Science, Engineering or Quality/Regulatory disciplines related to the Medical Device or Pharma industry sectors.

As a person you are independent, organised, analytical, thorough and results-oriented. You have a keen eye for detail but can also take a step back to see the bigger picture when required. You are able to react effectively in stressful situations, have strong communication and interpersonal skills and the ability to define problems, collect data, establish facts and draw valid conclusions. Effective time management is also essential to the role.
Lastly, you have good working knowledge of Office systems, and speak and write Swedish and English fluently.

Förmåner

Intertek is a safe workplace with collective agreements, benefit package with pension, health care contributions and parental leave allowance. We have flexible working hours and encourage a good working climate and happy employees.
+ Läs mer om jobbet
Om företaget
Intertek is the trusted advisor to many of the world's leading brands, companies and governments, and has earned a reputation for accuracy, reliability, integrity, and technical competence. Our services take us into nearly every field, from textiles, toys and electronics, to building, heating, pharmaceuticals, petroleum, food, cargo scanning and medical devices.
In a world where a company's success depends on its reputation for quality, safety, and socially responsible products and processes, Intertek employees make a difference.
Join the team at Intertek and work with some of the best, brightest, and most inspiring people in the testing, inspection, and certification industry.
+ Läs mer om företaget
Sista ansökningsdag
31 jan
Anställning
Tillsvidareanställd
Omfattning
Heltid
Antal Tjänster
1
Yrkesområde
Teknik & Ingenjör
Rekryteringen hanteras av
Poolia

Inga fler liknande jobb tillgängliga