We are a global leader in the development and manufacturing of active pharmaceutical ingredients, focused on specialist niches with expertise in highly regulated and complex chemistries. Formerly part of Johnson Matthey, we have over 50 years of experience navigating the challenges of the global healthcare industry, and nurturing long-standing, trusted customer relationships. Operating within two divisions, Generics and Originators, we deliver a differentiated service offering to pharma and biotech customers for every stage in the drug development lifecycle.

Perform chemical testing of raw materials, intermediates, and Active Pharmaceutical Ingredients (APIs) in support of process research, GMP production, and stability testing. Responsible for utilizing common analytical techniques such as: HPLC, GC, UV-Vis, KF, FTIR, NMR, and wet chemical methods such as titrations.

Your responsibilities:

• Applies basic scientific knowledge to perform routine analysis and to solve simple analytical problems encountered during production support.
• Learns and applies Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMPs).
• With guidance, revises SOPs, test methods, and other GMP documents.
• Conducts analysis and interpret results.
• Transfers, modifies, and improves analytical methods with guidance from experienced team members.
• Reviews analytical data for raw materials.
• Performs testing for the qualification of reference standards.
• Performs cleaning verifications and with guidance performs cleaning validations.
• Calibrates instruments and contribute to laboratory organization and compliance.
• Volunteers to assist with task not directly related to a specific project.
• Participates in self-development activities.
• To carry out any other duties which are within the employee’s skills and abilities whenever reasonably instructed.

• Bachelor’s Degree or Associate's degree in Chemistry or related field
• Minimum one (1 year) experience in a quality control environment
• Able to operate standard QC laboratory equipment (HPLC, GC, FTIR, UV, KF, etc.) desirable
• Proficiency in Microsoft Office desirable

Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state or local law.

All applications are carefully considered and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice.