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Compliance & Quality Specialist NIS/RWE – (F/M)

Paris, Paris, France

Job Description

Cerner Enviza an Oracle company is a leading global healthcare consulting firm and trusted advisor to many of the world’s top pharmaceutical, biotech, and medical device & diagnostic companies. By supporting the work of Cerner Enviza, you will work with world-class healthcare companies, helping them improve global access to medicines by connecting science and research. Cerner Enviza is passionate about our people, our business, and our clients and is proud to foster a culture that contributes to the health and well-being of humankind

With ongoing and ground-breaking developments in Oncology and Rare Disease, an increased focus on more scientific, targeted medicine and continuous integration of technology into development and delivery of medicine, there has never been a more exciting time to work in Life Sciences and, with Cerner Enviza immersed in all of these, there has never been a better time to join us and make a difference to our clients and the lives of patients.

Thanks to our business growth, Cerner Enviza is creating a new role of Compliance & Quality specialist for the Real world Evidence projects with a strong focus on the Non Interventional studies.
Supporting the Compliance & Quality Manager, you act as a key contact with regards to RWE Renewables on queries and issues linked with Compliance & Quality across the business (France, Germany & Brazil)

You will be surrounded by passionate colleagues in an open and engaging environment. You will be given room to work a large variety of topics and grow and continuously develop yourself together with some of the best within their expertise.

  • Dealing with department administrative tasks;
  • Assists with coordination of team meetings, attends meetings, and prepare accurate meeting minutes and action items;
  • Carry out ongoing assessment of compliance policies and procedures and assist in updating new policies to optimize operations or/and internal controls;
  • Contribute to the adherence of the quality policy and ensure that it is understood, implemented and maintained by all;
  • Ensure the effectiveness of all quality actions (CAPA/deviation implementation and follow-up);
  • Create and maintain a library of SOP templates and workflow;
  • Assist with maintaining quality management system documentation (coordinate SOP training and distribution of Quality procedures/documents);
  • Coordinate SOP onboarding for new associates (SOP documentation, SOP quiz, correction and tracking);
  • Participate in audit (internal and external) preparation;
  • Responsible for ensuring completeness of training profiles folders;

Working Environment

Hybrid & Onsite: No Relocation Assistance Offered

This position offers a Hybrid & Onsite working environment. Meaning you will split working time between a Cerner office or client site and remote. If your current geographical location requires relocating, Cerner will not offer relocation assistance to the specified location. #LI-Hybrid

Back to Description

Because It's Personal

Time: 2:57

Additional Information

Working Environment Hybrid & Onsite: No Relocation Assistance Offered
Relocation Assistance Available for this Job: No


  • Higher technical education diploma level Bac +5;
  • Minimum experience of 2 years in either health-related fields (in Clinical or Non-Interventional studies) or in Quality Assurance (audit preparation, deviation/CAPA management, document tracking);
  • Fluent level of English (Oral and Written - Toeic > 900);
  • Strong Administrative skills;
  • Excellent organization skills and attention to detail;
  • Excellent knowledge of Excel / Word;
  • Able to multitask and deal with priorities;
  • Good communication and interpersonal skills, with an ability to engage to different people;
  • A real team player, flexible, co-operative and dedicated to helping the team to deliver a great service;
  • Ability to be proactive and work independently on objectives without permanent supervision;
  • You are flexible: if things do not go as planned, you adapt, and carry on;

All employees must be legally authorized to work in the country where the position is located. Work visa sponsorship is not available for this position.

Cerner is a place where people are encouraged to innovate with confidence and focus on what is important – people’s health and the care they receive. We are transforming health care by developing tools and technologies that make it more efficient for care providers and patients to navigate the complexity of our health. From single offices to entire countries, Cerner solutions are licensed at more than 25,000 facilities in over 35 countries.

Cerner’s policy is to provide equal opportunity to all people without regard to race, color, religion, national origin, ancestry, marital status, veteran status, age, disability, pregnancy, genetic information, citizenship status, sex, sexual orientation, gender identity or any other legally protected category. Cerner is proud to be a drug-free workplace.
If you are an individual with a disability who is unable to use our online tools to search and apply for jobs, and need assistance or an accommodation in the recruiting process, please contact us by calling 866-434-1543 or by emailing

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