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Quality Engineer (m/f/d)
Position Summary
For its Quality Engineering department in Munich, Germany, LivaNova is looking for a new innovative, ambitious talent. We are currently hiring for a Quality Engineer (Junior or Level I) to expand and support the advancement of our product portfolio.
You will be a key contributor to the quality strategy for our Cardiopulmonary equipment development and manufacturing processes, being key role for the quality and effectiveness on the device when used to treat our patients.
Your daily tasks will be related to ensure quality as well as compliance of manufacturing processes and sustaining R&D activities within dedicated projects. Furthermore, supporting continuous improvement of products and processes, you will ensure that we meet our superior mission which is “patients first”.
You will support Product Development, Clinical, Manufacturing, and other Quality System activities - locally and globally.

General Responsibilities

• Support and drive product and process quality improvement initiatives by coordinating with cross-functional experts for reducing quality defects
• Support quality operations in local manufacturing, supply chain and product sustenance to maintain quality compliance
• Independently drive non-conformity report activities including but not limited to conducting risk assessments, investigating root cause, and implementing corrective actions
• Collaborate as main stakeholder to define the requirements for design control and design transfer, verification and validation testing, production line testing, and process risk assessment for new generation devices and life cycle management of current devices
• Review product and QMS changes for completeness, accuracy, and safety/effectiveness.
• Support regulatory audits on site
• Perform Quality control (QC) of all products based on established processes
• Perform DHR management and control of all products according to established process and work instructions
• Identify and implement process improvement solutions for DHR document management, data entry traceability and document retrieval, including to conduct solution effectiveness check
• Any other activities and responsibilities as defined by management relevant to the quality engineering function

Skills and Experience

• A minimum of bachelor’s degree in engineering with technical specialization. Preferably in Electronics or Mechatronics. Alternatively, relevant technical job experience in a suitable job area
• A few years’ experience years in relation to described job function would be preferred and university degree is advantages
• Strong Interest in medical devices
• Good verbal and written communication skills in English and German
• Good understanding of quality engineering principles including root cause analysis techniques with ability to show sound engineering skills/knowledge
• Good understanding of basics of statistical tools e.g., Minitab
• Experience in performing risk management techniques /assessments
• Problem Solver: Demonstrated ability to solve problems in an organized and structured approach
• Lean & Six-Sigma skills are advantageous
• Pragmatic and result-oriented: Detail-oriented, and capable to organize and drive activities in alignment with the expectations of stakeholders
• Good team player: open, honest, and appreciative when communicating among peers and management, show strong interpersonal skills
• Show ability to be adaptable, flexible and handle quick changing priorities with a collaborative and relationship building attitude
• Good command of Microsoft Suite tools
• Quality Engineering knowledge is a plus

What we can offer you

In addition to providing you with a supportive, inclusive and collaborative environment where you will feel empowered to take ownership and drive meaningful change, we will reward you with the following:

• A dynamic role in an advanced Medical Device environment interfacing with all worldwide regulatory landscapes supporting your professional career growth
• Exposure to a State-of-the-Art medical device development process, in close co-operation with international clinicians
• Competitive base salary
• Variable short-term & long-term incentives
• Recognition: through our STARS Program, we recognize and celebrate our colleagues’ contributions and achievements

If you like the sound of the above and feel energized by the idea of joining a great brand at a moment of exciting expansion, please apply now. We look forward to hearing from you!
Our commitment to Diversity & Inclusion:
LivaNova values equality and celebrates diversity. We are committed to ensuring that our recruitment process is fair, transparent and free from unlawful discrimination.
Our selection process is driven by the key demands/requirements for the role rather than bias or discrimination on the basis of a candidate’s sex, gender identity, age, marital status, veteran status, non-job-related disability/handicap or medical condition, family status, sexual orientation, religion, color, ethnicity, race or any other legally protected classification.
Notice to third party agencies:
Please note that we do not accept unsolicited resumes from recruiters or employment agencies. In the absence of a signed Recruitment Services Agreement, we will not consider, or agree to, payment of any referral compensation or recruiter fee. In the event that a recruiter or agency submits a resume or candidate without a previously signed agreement, we explicitly reserve the right to pursue and hire those candidate(s) without any financial obligation to the recruiter or agency.
Beware of Job Scams:
Please beware of potentially fraudulent job postings or suspicious recruiting activity by persons posing as LivaNova recruiters or employees. The scammers may attempt to solicit confidential, personal information, such as a social security number, or your financial information. LivaNova will never ask for fees prior/during/after the application process, nor will we ask for banking details or personal financial information in return for the assurance of employment. If you are concerned that an offer of employment might be a scam or that the recruiter is not legitimate, please verify by searching for “See Open Jobs” on
https://www.livanova.com/en-us/careers
, and check that all recruitment emails come from an @livanova.com email address

• Support and drive product and process quality improvement initiatives by coordinating with cross-functional experts for reducing quality defects
• Support quality operations in local manufacturing, supply chain and product sustenance to maintain quality compliance
• Independently drive non-conformity report activities including but not limited to conducting risk assessments, investigating root cause, and implementing corrective actions
• Collaborate as main stakeholder to define the requirements for design control and design transfer, verification and validation testing, production line testing, and process risk assessment for new generation devices and life cycle management of current devices
• Review product and QMS changes for completeness, accuracy, and safety/effectiveness.
• Support regulatory audits on site
• Perform Quality control (QC) of all products based on established processes
• Perform DHR management and control of all products according to established process and work instructions
• Identify and implement process improvement solutions for DHR document management, data entry traceability and document retrieval, including to conduct solution effectiveness check
• Any other activities and responsibilities as defined by management relevant to the quality engineering functio