OverviewLubrizol Life Sciences Health's CDMO business is the leading CDMO for complex formulation development for the pharmaceutical industry, with over 20 years of successful experience and a solid base of clients ranging from the world’s largest pharmaceutical and biotech companies to small VC backed start-ups. As a member of the LLS Health team, you will be working for a company that is engaged in important, exciting, and socially relevant projects. LLS Health is a fast-paced environment that features a variety of projects, technical challenges, and opportunities for growth. To learn more about us, visit www.particlesciences.com and https://www.lubrizol.com/Life-Sciences.We’re always told that one of the best things about working at Lubrizol is the people who work here. Could you be one of them? Responsibilities

Manages daily operations within the Formulation Development department Plans, staffs, leads, organizes and coordinates all activities within the department to ensure progress of internal and contract projects and compliance to cGMP and SOPs Develops and executes strategic business plans for the department Directs the execution of high-profile client projects involving planning and application of methodologies to address pre-formulation, formulation development and physical characterization Provides formulation oversight during production of pre-clinical and clinical trial materials, scale-up and technology transfer to client companies and commercial manufacturing Writes and reviews client reports Develops SOPs and other regulatory documentation Ensures the efficient and effective performance and development of all team members

Qualifications

Minimum of a BS degree in a scientific field At least 10 years of experience in the pharmaceutical industry, including knowledge of cGMPs and clinical manufacturing Previous management experience Proficiency with common PC-based applications, including Microsoft Office Highly developed organization, communication and analytical skills Ability to understand and effectively communicate technical and business information, both oral and written to others, including co-workers, supervisors, subordinates, clients, and vendors Ability to define problems, collect data, establish facts, and draw valid conclusions

Considered a Plus

Pharmaceutical experience that includes program design and management, formulation and all phases of drug product development from inception to scale-up Experience with multiple formulation types (semisolids, solids, liquids, suspensions, controlled release, including sterile and non-sterile) and complex delivery forms (engineered particles, encapsulation, nanotechnology)

Lubrizol offers competitive benefits: Medical, Dental, Vision, 401(k) match, Paid Holidays, Parental Leave, Age-Weighted Defined Contribution Plan, and more. Visit http://benefits.lubrizol.com to learn more. Lubrizol Life Science Health's CDMO business is located in Bethlehem, PA, part of the Lehigh Valley region of Pennsylvania. The region offers access to major markets and a vibrant community with diverse amenities. Lubrizol is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to sex, race, color, national origin, citizenship, age, religion, marital status, military service, sexual orientation, genetic information, gender identity, or any other characteristic or trait protected by federal, state, or local law. Do You Need Assistance? Please let us know if you need an accommodation to proceed with your application. You can call 440-943-4200 or email talentacquisition@lubrizol.com. Nearest Major Market: Allentown Job Segment: Manager, Materials Science, Biotech, Nanotechnology, Law, Management, Science, Legal

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