With an office in Horsham, Endo International is a global specialty pharmaceutical company focused on improving patients’ lives while creating value. Endo develops, manufactures, markets, and distributes quality branded and generic pharmaceutical products as well as over-the-counter medications through its operating companies. Endo employs approximately 6,000 people worldwide.

Analytical Services Associate Director

This position is responsible for the QA technical oversight of all QC analytical activities in support of commercial Xiaflex Bulk Drug Substance manufacturing. He/she is also responsible for managing all analytical method development, optimization, transfer, and validation activities for the site. The person will prepare, review, and approve Risk Analyses/Assessments related to analytical projects, investigations and change controls.

The ideal candidate will possess a Master’s Degree in Biochemistry, Chemistry, or Biological Science, and have at least 12 years of combined experience in commercial and R&D bio-analytical operations. Broad experience in a development, quality, and manufacturing environment is required.

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Senior Process Engineer

This position works in a hands-on capacity in the cGMP fermentation and production support areas to manufacture and support the equipment and process for manufacture of Collagenase Clostridium histolyticum (CCH) bulk drug substance (BDS). He/she will lead engineering initiatives as they pertain to the manufacturing facility and utility areas, including new equipment and/or systems installations, and equipment, systems, and process improvement initiatives.

The ideal candidate will possess at least a Bachelor’s Degree in Chemical Engineering, Bioengineering, or Biological Sciences. He/she should have a minimum of five to seven years of working in biopharmaceutical cGMP manufacturing environment, technology development, technology transfer and/or validation.

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Purification Scientist

This position will provide protein purification expertise in support of commercial manufacturing activities. Key areas of focus are execution of scale-down models of purification process for process improvement, process trouble-shooting, and resolution of deviations, validation studies, and development and optimization of product purification from bacterial fermentation processes.

The ideal candidate will possess at least a Bachelor’s Degree in Biological Sciences, Biotechnology, or Biochemical Engineering. He/she should have a minimum of five to ten years working in purification process development and/or process validation laboratories. General experience in a development, quality, or manufacturing environment is preferred.

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