Are you our new Senior Quality Assurance Specialist?

Arbeidsgiver
Abbott Norge AS
Stillingstittel
Senior Quality Assurance Specialist
Frist
Snarest
Ansettelsesform
Fast
Bli kjent med Abbott Norge AS

About Abbott

Abbott is a global healthcare company devoted to improving life through the development of products and technologies that span the breadth of healthcare. At Abbott, we're committed to helping you live your best possible life through the power of health. For more than 125 years, we've brought new products and technologies to the world - in nutrition, diagnostics, medical devices and branded generic pharmaceuticals - that create more possibilities for more people at all stages of life.

 Today, 109,000 of us are working to help people live not just longer, but better, in the more than 160 countries we serve. Our mission is to understand that the first step to living your best life is good health. Everything we make is designed to help you do just that. That’s our commitment to building life-changing technologies that keep your heart healthy, nourish your body at every stage of life, help you feel and move better, and bring you information, medicines and breakthroughs to manage your health.

 

The position of Senior Quality Assurance Specialist Nordics is with our Commercial Affiliate within Cardiometabolics and Informatics business unit located in Oslo, Norway. This role will provide quality assurance support to various functions within the Nordics business and be responsible for maintaining an effective Quality System.

 

Responsibilities and Duties

  • Support the multi-site ISO 9001 Quality Management System
  • Independently lead groups and projects to resolve complex issues. Analyze complex problems and identify their impact. Establish probabilities. Draw conclusions reflecting broad business needs. Ensure compliance.
  • Cross-functionally lead Quality System process improvements which may include training, corrective action and preventive action (CAPA) activities, equipment maintenance, product and process planning, quality audits, validation.
  • Responsible for completing documentation in a timely manner and in accordance with business standards.
  •  Make timely and effective decisions related to business issues within scope of responsibility; appropriately elevate high risk issues/decisions; identify and quantify risks and their consequences relative to the success of a project/task; recommend appropriate action
  • Monitor and maintain quality processes that assure compliance to all applicable regulations, standards and divisional policies.
  • Assist in external and internal audits
  • Understand and be aware of the quality consequences which may occur from the improper performance of their specific job.


Required Qualifications

  • Degree preferably in science, engineering or a closely related discipline, or an equivalent combination of education and work experience.
  • Minimum 5-7 years of relevant experience, such as Quality, Compliance, Engineering, within a regulated environment, such as medical device, diagnostics or pharmaceutical industries, to develop the competence required to meet the skills and responsibilities of the position.


Preferred Qualifications

  • Strong knowledge of ISO 9001 or ISO 13485
  • Knowledge of applicable Quality System Requirements and other relevant regulations for medical devices.
  • Knowledge of quality management techniques and the application and principles of quality engineering. Strong knowledge and application of concepts, practices and procedures. Ability or aptitude to work on problems that are complex in scope where analysis of situations or data involves multiple competing factors. Understanding of statistics.
  • Previous experience with regulatory body
  • Previous experience working in a distribution environment


Personal Characteristics

  • Effective communicator, excellent interpersonal skills with the ability to achieve results through influencing others. Demonstrated ability to maintain positive people relationships and build strong links with all departments
  • Self-starter, possesses flexibility and ability to work under pressure in a fast-changing environment and ambiguous situations
  • Positive attitude, capable of applying critical thinking, pragmatic and goal oriented team player with a high level of initiative, energy and enthusiasm
  • Excellent organisation, facilitator and presentation skills
  • Responsible-minded with a high persuasive power


What can we offer you?

 Abbott provides a varied, challenging and international position in a dynamic and pleasant working environment. In our organization, you can count on excellent primary and secondary benefits, a positive working atmosphere, a personal growth plan, extensive training opportunities and good career perspective. We are in the business of advancement, both in health solutions and in the lives and careers of our employees. Our work across the world and in many areas of healthcare provides a rich environment for our employees to explore career paths, interests and opportunities.

 

How to apply?

Apply by following the link in the ad. All applications must include CV and cover letter.

We review applications ongoing.


Om arbeidsgiveren

Abbott is a global leader in in vitro diagnostics and offers a broad range of innovative instrument systems and tests for hospitals, reference labs, blood banks and clinics.

Sektor
Privat
Sted
Kjelsåsveien 161, 0884 Oslo
Hjemmekontor
Delvis hjemmekontor
Bransje
Farmasi og legemiddel,
Medisinsk utstyr og rekvisita
Stillingsfunksjon
Dokumentasjon,
Kontor og administrasjon,
Kvalitetssikring
Arbeidsspråk
Norsk,
Engelsk

Nøkkelord

QA, Kvalitet, Quality Assusrance, Commercial, Kvalitetssystem

Spørsmål om stillingen

Kontaktperson
Oyku Aktas
Stillingstittel
Talent Acquisition Specialist
Følg firma
941 følger dette firmaet

Kjelsåsveien 161, 0884 Oslo

Annonseinformasjon

FINN-kode 352477669
Sist endret 10. mai 2024 13:06

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