Managing Consultant (Life Sciences Compliance/Validation/Quality)

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Are you an experienced client oriented consultant with a deep passion for developing and growing client relationships? Do you want to take your already proven consulting skills within Quality Management, Compliance and Validation to the next level ? And are you highly motivated to drive business development? If yes, apply your experience as a Managing Consultant with NNIT, one of Denmark’s leading IT consultancies with more than 3,200 employees worldwide.

Join our NNIT Compliance, Test and Validation team in our Søborg, Copenhagenoffice and be part of one of the leading departments in Europe when it comes to providing Compliance and Validation Consultancy services to the Life Sciences industry. With approx. 30 skilled SMEs/consultants in Denmark and about 100 consultants in Europe, China, the Philippines and US, you will be part of a highly international team.

We are passionated people building winning teams with our clients. With deep roots in the pharmaceutical industry, we deliver services that meet the highest requirements for quality, compliance and standardization. Join us in NNIT and Make your mark on a fast-growing IT company.

Your responsibilities as a Managing Consultant

This role will have the following main responsibilities:

Key customer focus

  • Develop and grow key client relationships
  • Plan and execute consulting sales activities to key clients
  • Participate in client management activities and presentations and deliver input to bids and agreements

You will primarily have focus and responsibility for our key Life Sciences customers but it can also be in other regulated industries. In close cooperation with relevant client stakeholders you bring your excellent consultancy mindset, communication skills, and vast project experience into play to identify the required solutions that meet the clients expectations. Every time. From previous positions you have successfully established yourself as a thought leader and trusted advisor. It is important that you can adapt yourself to each client's needs and practices, as these may be very different.

Project delivery

  • Participate in large and complex projects as a CSV Subject Matter Expert ensuring that full compliance and documentation requirements are met
  • Independently orchestrate and manage validation projects
  • Prepare and review project validation documentation
  • Identify and implement process improvements

You will be responsible for developing validation strategies and quality planning, and communicate these to the client. You use your experience in risk-based validation to ensure that validation activities met the clients expectations and fulfill regulatory requirements. You follow up on project milestones and ensure reporting on the validation activities in collaboration with the Project Manager and Excutive Sponsor.

Business Development

  • Continuously contribute to drive our business development including development and adjustment of our services, products, and NNIT Quality Management Winning Solutions
  • As part of the management team provide input to the global department strategy, goals and targets for our Compliance and Validation Consultancy services
  • Responsible for the departments Professional Leads Group/CoP.

Your qualifications and experience

We are looking for an experienced IT Consultant (at least 5 years) who exerts a strong consultancy mindset and who:

  • has experience in fronting clients and provide advisory
  • are motivated by being put in a challenging environment where client stakeholders need to be consulted, advised and led
  • is experienced with Quality Management/Assurance of IT systems and/or infrastructure from previous work in the Life Sciences industry
  • possesses profound knowledge of all phases of the classic V-model and is used to apply current best practices
  • has experience with validation in agile development frameworks (e.g. SAFe)
  • is proactive and havefocus on deadlines
  • can communicate in English on expert level both orally and in writing (Danish language skills are not mandatory but could be an asset)
  • have Management skills
  • is a good team player

What do you bring with you?

You have a higher education and a solid experience in both Client Management and Quality Management, preferably from working in the Life Sciences segment.

You are driven by the Consultant role and thrive to advise clients at a high professional level, where there are challenging requirements for your professional and personal skills. You enjoy being in an environment with clients, where a number of stakeholders need to be consulted.

Work wise, you have intensive experience working with validation of IT systems for external clients or internal in your organization. You like to participate in long-term development projects and in improving the quality of IT. You have a profound experience of all phases of the V-model and you are experienced with working in agile development. Further, you are proactive in your approach to tasks with focus on deadlines.

You will be part of our Global Compliance, Test & Validation team

We are committed to deliver consulting services focused on Compliance, Validation, and Quality Management of IT systems, primarily within the Life Sciences segment. In addition to taking responsibility for complex consulting services in large IT development projects, we also provide clients with strategic advise on compliance with regulatory requirements and process improvements of IT systems, ongoing maintenance and operation.

It is important for us that you continuously develop both personally and professionally. Therefore, we focus on your skills through, relevant professional training, personal development plans, and interesting assignments.

If you can recognize yourself in this description, we encourage you to submit your application as soon as possible. Please notice that we interview candidates continuously, including the period before the application deadline.


Information og data

Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".

Arbejdsstedet er beliggende i København

Jobbet er oprettet på vores service den 30.9.2021, men kan have været deaktiveret og genaktiveret igen.

Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
  • Øvrige
  • København
  • Tirsdag den 30. november 2021

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