Global OTC Program Coordinator in New Jersey

Title: Global OTC Program Coordinator

Reports to: Head of Quality

Department: Quality Assurance/ Quality Control/ Regulatory

Responsibilities:

• Facilitate communication between the three OTC Factories (Sites) to support smooth, quick sharing of OTC Quality and Regulatory information, data, results and reports.
• Facilitates the timely and accurate response to each Factory’s requests with regards to Quality / GMP documents, samples management, and communications as it relates to quality responsibilities, including the release of RMs, intermediates, bulk & FGs; and regulatory communications.
• Ensure accuracy and completeness of all quality documents forwarded to each Factory.
• Review and facilitate the forwarding of samples to testing sites, communication of test reports, mediation to resolve missing documents or test requirements, and follow-up to...