Verification Scientist IV

Who is USP

The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the worlds top authorities in health and science to develop quality standards for medicines dietary supplements and food ingredients. USPs fundamental belief that Equity Excellence manifests in our core value of Passion for Quality through our more than 1300 hardworking 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

This is a nonsupervisory position within the Verification department of USPs Global Laboratory and Technical Operations (GLTO) division. The incumbent will be responsible for conducting and implementing activities related to current Good Manufacturing Practice (cGMP) site audits quality control and manufacturing (QCM) product documentation reviews and test design for conformance to applicable compendial standards.

How will YOU create impact here at USP

In this role at USP you contribute to USPs public health mission of increasing equitable access to highquality 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.

You will serve as the primary and/or secondary contact for participants in the verification program(s) and will manage verification projects working closely with participating companies and with fellow staff throughout the verification process to ensure timely completion of work. You will be responsible for the preparation and/or evaluation of cGMP site audits/reports QCM documentation/reports and test data/results regarding facilities and products undergoing verification. In addition you will help develop and implement new tools procedures and techniques for the verification department to meet USPs objectives and the needs of the verification programs participating companies in order to support continued growth of the verification services as a center of excellence within USPs fastpaced rapidly changing organization

The Verification Scientist IV has the following responsibilities:

• Conducts thorough review and evaluation of QCM i.e. quality control and manufacturing documents and other data received from pharmaceutical ingredient and dietary supplement manufacturers to ensure compliance with verification requirements. Prepares reports on observations made during the review and corresponds with participants of the programs with the intent to ensure acceptable corrective actions are taken where needed.
• Ensures compliance with verification procedures and requirements in the preparation of summary reports and approval letters for the final disposition of products undergoing verification.
• Works collaboratively with all parties to create a work schedule with verification staff other USP departments contract auditors and testing laboratories on matters relating to the verification programs.
• Conducts audits and/or coordinates with USP GMP auditors at USP Rockville and at USP international sites to provide necessary assistance to enable the auditor(s) to conduct a thorough audit of program participants manufacturing facilities for the manufacture of drug substances excipients dietary ingredients and/or dietary supplements.
• Conducts surveillance activities for participants to ensure that surveillance audits/internal audits and surveillance documentation review and product testing are conducted according to program requirements.
• Develops and revises standard operating procedures (SOPs) and participant manuals.
• Performs other duties as assigned.

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:

Education and Experience:

• M.Sc. degree in food science analytical chemistry biochemistry or related fields.
• Minimum of five 5 years of relevant experience or equivalent combination of education and experience (e.g. B.S. degree with a minimum of seven 7 years of experience).
• Experience working in current Good Manufacturing Practice (cGMP) facilities involved in the manufacturing and/or QA/QC of foods pharmaceuticals and/or dietary supplements/ingredients.

Industry Experience:

• Proven experience in establishing quality systems compliance within the above fields.
• Willingness to travel approximately 10 domestically and internationally

Additional Desired Preferences

• Extensive knowledge of FDA regulations pertaining to cGMP requirements.
• Knowledge of and experiences with GMP audits using 21 CFR parts 111 and 117 are desired.
• Proficient with regulation and guideline interpretation audit procedures proper documentation and Quality Assurance.
• Certificate from the American Society for Quality (ASQ) as a Certified Quality Auditor (CQA) is desirable.
• Working knowledge of the International Conference on Harmonization (ICH) quality guidelines and multidisciplinary guideline on the Common Technical Document (CTD) for APIs is desirable.
• Regulatory CMC submission experience and/or industry experience in the establishment of quality systems compliance is desirable.
• Knowledge of and experience with analytical methodologies.
• Good organizational planning and excellent verbal and written communication skills.
• Detail oriented; able to deal with multiple changing priorities; and able to work with minimal supervision.
• Effective and efficient project management experience is desirable.
• Thirdparty quality certification/verification experience in the pharmaceutical or dietary ingredient/supplement industry is a plus but not required

Supervisory Responsibilities

None this is an individual contributor role.

Benefits

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

Compensation

Base Salary Range: USD $85500.00 $111250.00 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 jobrelated 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.