Analytical Science Manager

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Full-time Regular Parsippany, NJ, US

Salary Range: $ To $ Annually

If you are interested in joining an entrepreneurial team, focused on bringing life-saving therapies to market for critical unmet medical needs, consider applying for a role at Cor Medix Therapeutics . The culture at Cor Medix Therapeutics is patient-centered where we feel a sense of urgency to solve some of the most pressing issues in hospital-based healthcare.

Cor Medix Therapeutic’s greatest asset is our people. We have a deeply experienced team and continue to bring on some of the brightest talent that can problem solve and execute with high precision. We are passionate about the work we do and how we do it. We believe in building highly engaged teams that exude integrity, open communication, and innovation. We believe in fostering each employee to reach their highest potential by offering an inclusive environment, opportunities to challenge yourself and grow, and a community of purpose.

We expect that everyone here brings their best selves to work and together, our singular efforts culminate into profound and meaningful breakthroughs.

Cor Medix Therapeutics is a biopharmaceutical company focused on developing and commercializing therapeutic products for the prevention and treatment of life‑threatening conditions and diseases in the United States. Cor Medix is focused on selling and marketing products in institutional settings of care in the US and has field based medical and commercial infrastructure deployed in hospitals, clinics and infusion centers. Rezafungin is currently approved for the treatment of candidemia and invasive candidiasis in adults.

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The Analytical Science Manager‑Technical Operations provides critical technical expertise to support analytical method related activities for both drug substance and drug products. Reporting directly to the Director, the Analytical Science Manager collaborates closely with cross‑functional and external partners to support manufacturing readiness. This role ensures all analytical methods are robust, compliant with global regulatory standards, and optimized for seamless execution in lab.

• Lead analytical method transfers and validation activities for drug substance and drug products.
• Author and review GMP documents such as SOPs, protocols, summary reports, and QMS records.
• Partner with Quality Assurance, Regulatory Affairs, and external test sites to support technology transfers, and analytical method validations.
• Support technical investigations for out‑of‑specification (OOS) results and collaborate with QA to implement corrective actions.
• Serve as department Quality liaison and utilize Veeva eQMS to manage documents, deviations, change controls and quality events.

• In‑depth knowledge of analytical instrumentation (HPLC, GC, LC‑MS), and physical characterization techniques (XRPD, DSC).
• Strong troubleshooting capabilities to resolve complex analytical failures and instrument issues.
• Thorough understanding of global regulatory mandates, including ICH guidelines, cGMP regulations, and industry best practices.
• Strong collaboration and communication skills across cross‑functional and global teams.
• Good organizational and multi‑tasking skills to successfully manage completing projects.

• Masters in Chemistry, Pharmaceutical Sciences, or related field with 5‑10 years of pharmaceutical industry experience.
• Strong expertise in analytical method validation, and global…