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NSF-DBA is Looking to Grow

Friday the 31st May 2013

As part of their worldwide expansion, NSF-DBA is looking to recruit highly credible Pharmaceutical Professional(s) to support their growing operations.

There are opportunities both in the US and EU:

NSF-DBA www.nsf-dba.com is a part of the rapidly growing NSF Health Sciences Division. We are a high quality provider of Training/Education, Consulting and Audit services to the Pharmaceutical and Biotechnology Industry. Our pedigree and reputation stems from our 25 year history. Since opening our US office in 2008 to service the needs of our growing base of US based clients we have continued to grow both our business and our reputation, despite the current economic climate.

With the recent further acquisitions of Becker and Associates Consulting www.becker-consult.com and IPEA www.ipeainc.com to the NSF Health Sciences Division, we continue to grow the range of high quality services we are able to offer to the industry.

As a result, we are now recruiting to help us manage and develop further both our US and EU activities.

We would like to hear from individuals who are / have operated at the Senior Director/Vice President level or equivalent, who are seeking a new challenge in their careers. Those individuals may still be working in Industry, working in other consultancies, or be working within a regulatory agency.

The US position(s) will be a full-time, salaried role with a generous benefits package. The role would either be based from Boston, or undertaken remotely with a portion of time required at our Boston location. It will involve business development and client liaison activities, as well as some ‘hands-on’ contributions to the delivery of our training/education programs and consultancy / audit services. Our mantra is to proactively help and advise companies to keep ahead of the game, with a focus on Quality Management and Technical subject areas.

Desirable Qualifications/Experience:

  • Experience operating at a Senior Director/ VP level, or equivalent.
  • Proven credibility - either in leadership roles, or in an area of technical excellence.
  • A strong desire to help develop companies and individuals in ‘modern’ Quality thinking and cGMP expectations.
  • Strong connections / networks within industry, regulators, opinion leaders.
  • A minimum of 15 years experience in the Pharmaceutical or Biotechnology area, with a proven track record in a Quality/Manufacturing/Supply Chain/Development/Regulatory role(s) and/or within a Pharma / Biotech regulatory agency.
  • A minimum of a Bachelor’s Degree level qualification in a science based discipline.
  • Experience of working globally and an understanding of cultural differences.
  • Ability to work in a small team environment, often independently.
  • Good interpersonal skills – with clients, colleagues and consultants.

Contact Kate Principe [email protected] if you are interested in this role.

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