Principal Consultant

NNIT; Poland; On-site; PLN 180,000 - 260,000; Full time

Benefits offered by this job

Bonus package

Home internet allowance

Fitness funding

Job summary

NNIT, a leading Life Science consultancy, seeks a Principal Advisory Consultant for Regulatory Affairs. You will join a global Regulatory Affairs team, shaping the growth strategy, and taking lead roles in client engagements, RFPs and business development to expand NNIT's regulatory footprint.

Role emphasizes senior consultancy delivery, cross-functional collaboration, and mentorship, with travel to client sites as required and a focus on expanding relationships with major life sciences clients.

Qualifications

• Bachelor’s degree in a field related to Pharmaceutical Compliance or Regulation with significant experience in Regulatory Affairs.
• Proven consulting experience, ideally in a large life sciences consultancy.
• Strong sales and business development aptitude within a consulting environment.

Responsibilities

• Lead consultancy projects as engagement lead or architect.
• Drive business development, presales and thought leadership activities.
• Develop consultancy offerings and delivery methodologies; train consultants.
• Prepare and deliver RFP responses to win new projects.
• Coach and mentor Regulatory Affairs staff at various levels.

Skills

Regulatory affairs

Business development

Project leadership

Client liaison

Communication

Education

Bachelor's in Pharmaceutical Compliance/Regulation

Master's in Pharmaceutical Regulation (preferred)

Job description

Principal Advisory Consultant – Regulatory Affairs

NNIT is one of the world’s leading consultancies for the past twenty years serving the Life Science industry around the world. We strive to enable our customers to achieve their business goals through digitalization within Quality Assurance, Regulatory Affairs, Clinical, Pharma Production and Laboratory processes.

To further strengthen our Regulatory Affairs team, we are looking for a Principal Consultant with a strong background in the life sciences industry and significant and broad Regulatory Affairs experience across a number of areas.

Your responsibilities:

You will join our Regulatory Affairs team as a Principal Consultant. You will contribute to forming the strategy for growing the Regulatory Affairs business unit, co-responsible for executing this strategy, through business development and thought leadership activities, as well as taking lead consultant roles in client engagements, delivering Requests for Proposal (RFP’s) and driving and taking ownership for sales and business development activities.

• 60% delivering in consultancy projects in advisor, project lead or architect roles, and acting as engagement delivery lead.
• 20% in business development, presales and though leadership activities
• 10% in development of consultancy commercial offerings and related delivery methodologies and consultant training materials
• 5% in the development and delivery of RFP’s to ensure NNIT successfully engages new and additional projects
• 5% in coaching and mentoring of all levels of consultants in the Regulatory Affairs team

Your qualifications and experience:

• A Bachelor’s Degree (or similar) in a field related to Pharmaceutical Compliance or Regulation and significant experience in Regulatory Affairs within a Pharmaceutical company or as a consultant . Other relevant academic qualifications can be considered if you also have highly significant consulting and/or industry based experience in Regulatory Affairs within Life Sciences.
• Proven consulting based experience is an essential requirement for the role, ideally within a large recognised consultancy with a life sciences division or specialism.
• Strong experience of, and an aptitude towards sales and business development within a consulting based environment.
• Experience in managing interactions with clients, partners and vendors and an interest in driving and expanding NNIT client relations as part of business development, pre‑sales and project delivery activities.
• First class documentation, communication, and interpersonal skills, with an ability to liaise effectively and professionally with individuals at all levels.

Preferred requirements:

• A Masters level qualification in a relevant area of study such as Pharmaceutical Compliance or Regulation.
• Deep MedTech and BioTech industry and/or consulting based experience.
• Specific IDMP experience.
• Data and Master Data Management experience.
• Experience bringing new products to market.
• People management skills and a track record of leading teams on complex and multi stakeholder projects.
• Project management experience and a proven history of delivering projects on time and on budget where applicable.

Why should you join NNIT & What we offer to you?

• A dynamic workplace with good working conditions, social activities, team events and work life balance.
• Opportunity to work in a multicultural company with a friendly and dynamic work environment.
• Competitive salary, additional bonus and benefit package (contribution to your home internet, fitness funding, and others).
• An Informal and friendly working culture between NNIT colleagues.
• Opportunity to work with the most significant life sciences clients.
• Diversity of projects, and the possibility of shaping your own career path.
• Personal development model which defines your long-term career goals.

We are hiring into our European team in the following countries: UK, Denmark, Germany, Ireland, Italy, Poland

Fluency in oral and written English is a must. A second language (German, Danish, Italian or French) is desired but not essential.

Travel must be expected, but will be kept to necessary business trips (<10%).

What’s next?