• Senior Continuous Manufacturing Manager

    The US Pharmacopeial Convention (USP) (Rockville, MD)


    Description

    Who is USP?

     

    The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world's top authorities in health and science to develop quality standards for medicines, dietary supplements, and food ingredients. USP's fundamental belief that Equity = Excellence manifests in our core value of Passion for Quality through our more than 1,300 hard-working professionals across twenty global locations to deliver the mission to strengthen the supply of safe, quality medicines and supplements worldwide.

     

    At USP, we value inclusivity for all. We recognize the importance of building an organizational culture with meaningful opportunities for mentorship and professional growth. From the standards we create, the partnerships we build, and the conversations we foster, we affirm the value of Diversity, Equity, Inclusion, and Belonging in building a world where everyone can be confident of quality in health and healthcare.

     

    USP is proud to be an equal employment opportunity employer (EEOE) and affirmative action employer. We are committed to creating an inclusive environment in all aspects of our work—an environment where every employee feels fully empowered and valued irrespective of, but not limited to, race, ethnicity, physical and mental abilities, education, religion, gender identity, and expression, life experience, sexual orientation, country of origin, regional differences, work experience, and family status. We are committed to working with and providing reasonable accommodation to individuals with disabilities.

    Brief Job Overview

    **Senior Continuous Manufacturing Manager** **, The United States Pharmacopeial Convention, Rockville, MD.** Support the organization’s pharmaceutical continuous manufacturing (PCM) strategy. Develop services for manufacturers. Identify and implement technical and scientific methods including process analytical technologies (PAT) for continuous pharmaceutical manufacturing processes. Create materials to inform on development processes and solutions for manufacturers. Identify research projects to aggregate and curate knowledge. Implement training in drug substance and drug product areas. Innovate methods to support market development, adoption, and improve continuous manufacturing technologies. Work with cross-functional teams and partners to solve both technical and process-related issues. Attend scientific seminars and conferences, publish research, and make presentations.

     

    How will YOU create impact here at USP?

     

    In this role at USP, you contribute to USP's public health mission of increasing equitable access to high-quality, safe medicine and improving global health through public standards and related programs. In addition, as part of our commitment to our employees, Global, People, and Culture, in partnership with the Equity Office, regularly invests in the professional development of all people managers. This includes training in inclusive management styles and other competencies necessary to ensure engaged and productive work environments.

     

    Who is USP Looking For?

    The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience:

    Minimum Requirements:

    + Requires a Bachelor’s degree, or foreign equivalent degree, in Chemistry, Chemical Engineering, Pharmaceutical Science, or a related field and seven (7) years of post-bachelor, progressive and related work experience. In the alternative, the employer will accept a Master’s degree, or foreign equivalent degree, in Chemistry, Chemical Engineering, Pharmaceutical Science, or a related field and five (5) years related work experience.Requires five (5) years of experience with the following:

    + Continuous manufacturing processes and analytical technologies (PAT);

    + Technical expertise in advanced manufacturing technologies in the pharmaceutical industry;

    + Utilizing Flow Chemistry or Control Strategy Development for continuous manufacturing pharmaceuticals;

    + Conducting regulatory filing for a product developed and manufactured using Continuous Management;

    + Leveraging knowledge in API manufacturing; and

    + Assessing supply impact of quality-assured pharmaceuticals and medical products.Up to 15% domestic and international travel required.Telecommuting permitted within the Washington D.C. metropolitan area.Employer will accept any suitable combination of education, training or experience. **reference code: MD0022**

     

    Benefits

     

    USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected.

    Compensation

    Base Salary Range: USD $135,428.00 – $145,428.00 annually.

     

    Target Annual Bonus: % Varies based on level of role.

     

    Individual compensation packages are based on various factors unique to each candidate’s skill set, experience, qualifications, equity, and other job-related reasons.

     

    Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP.

     

    Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities

     

    This employer is required to notify all applicants of their rights pursuant to federal employment laws.

     

    For further information, please review the Know Your Rights (https://www.eeoc.gov/poster) notice from the Department of Labor.

     

    **Job Category** Technical Programs

    **Job Type** Full-Time