April 2008 

If you are a life sciences company looking to hire professionals who are currently available for interim or fixed duration roles, please review the selection of Ashton Tweed candidate profiles below. To learn more about any of these available candidates or if you have another permanent or interim human capital need we can help with, please email us at partners@ashtontweed.com or call 610-725-0290 to speak with one of our life sciences partners.

If you are a candidate with a life sciences background and/or the skills matching the descriptions below, please submit your resume to info@ashtontweed.com.

Regulatory

Senior Director of Regulatory Affairs with 30 years of hands-on/multi-discipline experience with pharmaceuticals, biologics and in-vitro diagnostics. Expertise on US, Canadian, and EU registration processes from beginning to end including direct agency interactions. Developed regulatory compliance programs and regulatory strategy at all stages of development for therapeutic biologics, in-vitro diagnostics and new chemical entities for both US and EU registrations.

Strategic Regulatory- Ph.D.

Regulatory Affairs executive with demonstrated success developing strategies to move products through the regulatory approval process and market rollout. Proven expertise in FDA preparation and application submission for drug and bio-medical devices. Effective FDA negotiator with experience working with international cross-functional teams to achieve global regulatory requirements. 

Process R&D/ Manufacturing- Ph.D.

Pharmaceutical executive with 25+ years industrial experience in chemical process R&D and pharmaceutical development with in-depth knowledge of organic chemistry and chemical kinetics. Well-published advocate for emerging technologies that enhance productivity of lab experimentation in support of process development. Proven ability to learn new scientific areas and solve challenging technical problems. 

Pharmaceutical Manufacturing/ Drug Delivery- Ph.D.

Pharmaceutical executive with 25+ years experience in technology R&D, product development and business/corporate development. Experienced in all phases of technology and product development from discovery support through commercial manufacturing with a particular focus on novel drug delivery technologies. Successful leadership record in both established and start-up pharmaceutical enterprises. 

Pharmaceutical QA- Ph.D.

Pharmaceutical executive with 20+ years experience in research and development, CMC regulatory, QA/QC, technical operations, business development, new technology development and project management in corporate, academic and government organizations. Provided leadership and support for rheumatoid arthritis and cancer drug BLA submissions. Experienced in successfully supporting regulatory audits and leading the development and validation of analytical methods, bioassays and processes. Responsible for vaccine manufacturing and the development of new biologics and vaccines.

Marketing

Skilled senior global marketing/management professional with 20+ years experience in pharma, diagnostics, clinical development, patient recruitment, reimbursement, and research products. Adept in developing licensing strategies, primary and secondary market research and building medical advisory boards and independent thought-leader consulting relationships. Key strengths include new product and technology positioning, internal consensus building, team building and management, and financial expectations modeling.

Many of the candidates above are also available for permanent placement, and our partners can create a custom designed search for interim or permanent candidates to meet your specific needs. To learn more, please contact us at partners@ashtontweed.com or at 610-725-0290.

Jim Rudman- x 422
James Laird- x 423
Jordan Warshafsky- x 441
Ashton Tweed
620 Lee Road, Suite 130
Wayne, PA 19087
Phone: 610-725-0290
partners@ashtontweed.com