Senior Continuous Manufacturing Manager

BioSpace

Rockville (MD)

On-site

USD 135,428 - 145,428

Full time

14 days+

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Benefits offered by this job

Comprehensive healthcare options
Retirement savings
Company-paid time off

Job summary

A prominent scientific organization is seeking a Senior Continuous Manufacturing Manager to oversee and support its pharmaceutical continuous manufacturing strategy in Rockville, MD. The role requires a strong understanding of manufacturing processes and technical expertise to ensure quality standards in pharmaceuticals. Candidates must have a relevant degree and experience in the field, and a commitment to diversity and inclusion is emphasized. Competitive compensation offered.

Qualifications

  • Bachelor's degree or foreign equivalent and 7 years of relevant experience, or Master's with 5 years.
  • Experience in continuous manufacturing processes.
  • Technical expertise in advanced manufacturing technologies.

Responsibilities

  • Support pharmaceutical continuous manufacturing strategy.
  • Identify and implement technical methods for manufacturing processes.
  • Attend seminars and publish research.

Skills

Continuous manufacturing processes
Analytical technologies (PAT)
Flow Chemistry
Regulatory filing
API manufacturing

Education

Bachelor's degree in Chemistry or related field
Master's degree in Chemistry or related field

Job description

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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.

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 workan 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 organizations 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?

Minimum Requirements

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:

  • Requires a Bachelors 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 Masters 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 candidates 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

Seniority level
  • Seniority level
    Mid-Senior level
Employment type
  • Employment type
    Full-time
Job function
  • Job function
    Management and Manufacturing
  • Industries
    Internet News

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