Process Analytical Technology Jobs (NOW HIRING)

Description:

Research Scientist III, Analytical Method Development fulfills a critical role in supporting the analytical development and validation of testing methods for the Analytical R&D laboratory. This individual leads analytical development, qualifications, validations for active pharmaceuticals, excipients, dosage forms, release activities and in-process analytical testing services in support of the formulation development department. Independently manages analytical methods development/validation/transfer projects for new products. This individual technically supervises, coaches and reviews the work of analytical development team members. Additionally, this individual helps drive advances in analytical capabilities for all analytical technology, qualifies and maintains analytical equipment.

Essential Functions:

• Performs work at a level considered subject matter expert. 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.
• Development and optimization of 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 supervise and train staff and group members aimed at developing technical capabilities. Expand 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accurate technical documents reporting the results obtained in his/her experiments and the conclusions that can be withdrawn from them including relevant recommendations for next steps.

Additional Responsibilities:

• Stays abreast of new developments in analytical technologies. Contributes to improvement in laboratory operations to increase efficiency and GMP compliance.
• Leads team members on assigned projects, as required.
• Participates and leads scientific discussions on projects with cross-functional team.
• Plan and distribute work plan for the team based on priority as and when required.
• Procurement of necessary requirement to initiate any new project work.

Amneal is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, national origin, age, disability, genetic information, protected veteran status, or any other characteristic protected by applicable federal, state, or local laws. If you require a reasonable accommodation to complete the application process or to participate in any part of the hiring process, please contact us at accommodations@amneal.com. Requests will be handled confidentially and in accordance with applicable laws. 

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)
• 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.

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.