Career Opportunity Listings
Ashton Tweed is currently recruiting for a number of excellent opportunities in the life sciences. The following is a representative selection of our open positions. If you are a qualified candidate who is interested in applying for any of these listings, please submit your resume to info@ashtontweed.com and include the job title in the subject line of your email.
- Vice President Global Quality Assurance
Description: This position provides an opportunity to build out a global quality function for a $500 million-plus specialty pharmaceutical and technology company. The successful candidate must have 15-plus years of progressive management experience in quality assurance within the pharmaceutical industry that includes multi-site and global scope. Also must have extensive knowledge of Canadian, U.S., and European good manufacturing practice (GMP), global good laboratory practice (GLP), and clinical quality assurance.
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- Vice President Global Licensing, Pharmaceutical Technologies
Description: Globally maximizing the company’s technologies, this successful candidate will lead the global team that identifies and evaluates new opportunities and structures relationships with pharmaceutical companies. Must have 10-plus years of experience with documented record of business development success with outsourcing drug delivery technologies.
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- Product Development Engineer
Description: A U.S.-based developer, manufacturer and supplier of advanced drug delivery systems is looking for a candidate with a degree in mechanical engineering, industrial design, or a related field. Must have significant mechanical design experience, including the development of new medical products and experience with mechanical and electromechanical systems. Also looking for analytical skills experience (e.g., finite element analysis [FEA], moldflow, geometric dimensioning and tolerance [GD&T], first principles), CAD design experience (e.g., Solidworks), and knowledge of transfer to manufacturing, manufacturing processes, medical device regulations, FDA submissions, testing, and planning.
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- Interim Vice President Quality Operations
Description: The successful candidate will oversee and direct quality operations for company location in Taiwan. Must have a BS in chemistry, pharmacy, biology, life sciences, or related field, as well as 15-plus years of management-level pharmaceutical quality assurance manufacturing experience.
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- Senior Director R&D
Description: The successful candidate must have a Doctor of Veterinary Medicine (DVM) degree and 8 to 10-plus years of companion animal health industry experience in technical services and/or clinical development roles. Also looking for an emphasis in R&D or relevant contract research organization (CRO) experience and experience in execution of clinical trials.
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- Business Development
Description: A drug delivery device company is looking for a candidate with 7-plus years of experience in medical device or pharmaceutical packaging/drug device development. Must have in-depth knowledge of the pharmaceutical industry, particularly parenteral drugs. A bachelor’s degree in science, engineering, marketing, or a related field is required, while advanced degrees in science or engineering and an MBA are strongly preferred.
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- Program Manager
Description: A provider of custom-engineered medical devices located on the East Coast is looking for a candidate with 10-plus years of experience in medical devices, drug delivery, and/or medical diagnostics, as well as 5-plus years of project management. The role includes the management of projects that involve the design and manufacture of custom devices. BS in engineering is required; advanced degree in mechanical engineering or polymer science is preferred.
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- Manager of Regulatory Affairs
Description: This position ensures that new products and changes to current products are prepared and submitted in a timely manner to regulatory agencies in markets. The successful candidate will work with cross-functional teams, regulatory agencies, and other partners, as well as manage other regulatory affairs team members. In addition to managing and developing regulatory staff, the successful candidate will be responsible for managing and prioritizing tasks and projects. Must also formulate 510(k)s in an on-time manner meeting current requirements.
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- Senior Regulatory Affairs Manager
Description: The successful candidate must have at least 7 years of work experience in regulatory affairs in the over-the-counter (OTC) drug, pharmaceutical, dietary supplement, or personal-care industries. OTC experience is critical. Substantial experience in direct interaction with the FDA discussing and/or negotiating submission documents and requirements is also important.
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