Lead Scientist, Analytical R&D

About the role

Fulfills a critical role in supporting the analytical development and validation of testing methods for the Analytical R&D laboratory. Supports the formulation development department with analytical testing services.

Responsibilities

• Drives research strategy including independently managing analytical method development/validation (mostly LC and GC) for active pharmaceutical ingredients, excipients and dosage forms to be used in the analytical R&D laboratory for routine analysis.
• Leads high-visibility technical projects with focused deliverables.
• Develops and optimizes new and existing analytical methods for qualification and release testing of products.
• Interpret and communicate complex experimental results, present technical findings to internal R&D & management teams and document findings in internal technical reports and/or external publications.
• Responds to internal and external inquires by performing advanced data generation, analysis and complicated problem solving independently.
• Technically supervises and trains staff and group members aimed at developing technical capabilities.
• Expands analytical capabilities of the Analytical Group.
• Conducts independent assessment of method performance to address scientific questions or problems.
• Drives scientific and technical innovation, including through external collaboration and partnership.
• Generates well-structured, accurate technical documents reporting the results obtained in his/her experiments and the conclusions that can be withdrawn from them including relevant recommendations for next steps.

Qualifications

• Education: Master Degree (MS/MA) in chemistry or other relevant pharmaceutical sciences - Required. Ph. D. in Pharmaceutical sciences or other relevant field - Preferred.
• Experience: 9 years or more in pharmaceutical experience (with Masters Degree) or 5 years or more in pharmaceutical experience (with Ph.D.).
• Specialized Knowledge: Broad knowledge of modern analytical equipment and techniques. Extensive experience in cGMP laboratory testing. Hands-on experience with HPLC, GC, TLC, and MS. Method development and validation experience. Experience writing the standard operating procedures (SOPs) and test methods. Experience with regulatory document compilation. Knowledge of Raman, ICP-MS, Mastersizer - Preferred. Inhalation/nasal product testing - Intermediate. Knowledge to ACI, NGI and other analytical techniques for inhalation drug products - Preferred.

Benefits

The base salary for this position ranges from $110,000 to $140,000 per year. Amneal ranges reflect the Company's good faith estimate of base salary that Amneal reasonably believes that it will pay for said position at the time of the posting. Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, geographic location and other relevant skills. At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement. We also promote employee well-being with programs that helps you enjoy your career alongside life’s many other commitments and opportunities.