Cosette Pharmaceuticals, Inc. is a US-based, fully integrated pharmaceutical company with capabilities in product development, manufacturing, and commercial operations. Cosette has a fast-growing portfolio of branded pharmaceuticals consisting of products in the cardiology, women's health, and migraine markets. Cosette has a long history in quality manufacturing of complex dosage forms including topical creams, ointments, oral liquids/solutions and suppositories, which has led to consistent supply to customers and commercialization success. Cosette has corporate and manufacturing facilities in New Jersey and North Carolina and is supported by more than 300 dedicated employees across all functional areas.

Innovating every day.

• Support the Cosette Complaint Intake and Closure process by interfacing with customers on complaints. Responsible for ensuring timely recognition of critical complaints, adverse events, and communication to Quality Management and Pharmacovigilance. Perform Complaint Investigations into customer complaints by reviewing documentation, examining retain samples, and working with internal departments to arrive at the root cause and recommend appropriate CAPA; perform trending analysis; and respond to the complainants, as required.
• Annual Product Review generation: Prepare Annual Product Reviews according to the scheduled due dates. Perform Statistical Analysis, identify and evaluate product trends, and recommend CAPAs to management as required.
• Participate in Internal Audits including System Audits and Facility Walk-Throughs to assess compliance to cGMPs.
• Support Stability Function by working with Stability Staff to ensure required Stability Studies are Conducted and Reported to Authorities. Work with Stability Equipment and Equipment Vendors to ensure Maintenance of Stability Equipment. Assist with routine Monitoring of Temperature and Humidity of Stability Storage Areas/Chambers, Investigations of Equipment Excursions, and Annual Reviews of all Stability Storage Areas/Chambers storage areas.
• Participate in Regulatory Field Actions: Participate in Field Actions such Recalls, Field Alerts, etc. as required.
• Other Duties as assigned by Manager.

• BA/BS in Chemistry/Biology/related science or Comparable Post Secondary Schooling with applicable industry experience
• At least 5 years industry experience with knowledge of Pharmaceutical Systems.

• Strong problem solving and investigative skills.
• Excellent oral and written communicative skills.
• Understanding of Regulatory Codes
• Good interpersonal skills
• Computer Literacy

• Microsoft Software
• ScienTek Stability System Software
• SAS Software
• Veeva Software

• No PPE's Required
• Ability to occasionally lift up to 50 pounds.
• Ability to withstand short periods at elevated temperatures (hot/cold)

Equal Opportunity Employment

Providing "equal employment opportunity" is one of the most important people policies of Cosette Pharmaceuticals, Inc. Our goal is to do all that we realistically can to provide genuine equal employment opportunity to applicants and employees in all phases of our operation. It is the policy of this Company that there shall be no discrimination with respect to employment, or any of the terms and conditions of employment, because of an individual's race, creed, religion, color, national origin, citizenship, ancestry, age, gender identity or expression, affectional or sexual orientation, marital status, domestic partnership, familial status, atypical hereditary cellular or blood trait, disability (including AIDS and HIV infection), genetic information, liability for service in the United States armed forces or any other legally protected status. The Company is dedicated to ensuring that all employment decisions are in accordance with these principles of equal employment opportunity.