Process Validation Engineer to Oticon Medical

Oticon Medical is part of William Demant Holding with more than 8.000employees across the world and revenues of over DKK 8 billion. Oticon Medical is the fastest growing manufacturer of bone anchored and cochlear implant hearing systems for children and adults.  At Oticon Medical we combine more than a century of experience in audiology and sound processing from Oticon with decades of pioneering experience in hearing implant technology. Our connection to Oticon gives us unique access to knowledge, resources and technology that we use for developing innovative and life-changing implantable hearing

Would you like to work with products that actually change the lives of people worldwide and do it in a fast growing company? Then you may be a good match for Oticon Medical. Right now we are looking for a dedicated and highly skilled Process Validation Engineer to support our fast growing business and international expansion. 

The position is situated in our Gothenburg office working with bone anchored solutions. This is a new position and you will have the opportunity to influence and change our internal validation procedures.

 

Job Describtion

You ensure an efficient and secure flow of our Titanium implants

In your new job, you will be responsible for the development and maintenance of the validation plan related to our main processes concerning titanium implant manufacturing, cleaning and sterilization. In this regard, you implement and document all validation activities.

You will be working in projects in the development organization to ensure that critical process parameters are defined, planed, documented and executed.

Responsibility for projects and initiation and execution of necessary improvements and corrections will also be important aspects of your working day.

Finally yet importantly, you will be ensuring compliance regarding internal and regulatory requirements.

Team wise, you can look forward to joining the Operations team consisting of 4 dedicated and highly skilled colleagues. The team is responsible for all aspects of the process from purchase to returns. Besides your closest colleagues you will also be working closely together with other functions in different projects. 

 

Competence

We are looking for someone with a passion to work with process validation and have worked at least 3 years as a process validation engineer in the medical device industry. Basically you have an engineering degree and experience with GMP and ISO 13485. You stimulates by managing and coordinating your own work but also by working as a team with your colleagues.

Your professional style is characterized by your ability to work structured and focused in a technical and professional manner - no matter the deadlines or the pressure you experience.

• Besides that, we expect that you re pragmatic and strive for efficiency in all that you do


Think and act holistically and like to take responsibility
re a skilled in creating and maintaining good relations to all parts of the organization

• Know how to benefit from multi-site and multi-cultural development teams


Besides the above mentioned, we prefer flexible candidates who are able to travel up to 40 days per year

 

Application

In this recruitment we are working with PS Partner AB. To apply for this position please visit www.pspartner.se and attach your CV and personal letter in English. For more information please contact consultant Gabriella Christiansen at +46 707962917 or Johan Sjöberg +46 761709851.

We are looking forward to hearing from you!