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Responsible for handling finished product and packing material section for sterile and OSD. Includes planning and completion of analysis, investigations, document review, and safety procedures. Requires good communication skills, compliance knowledge, and exposure to FDA inspections.
Seeking a Research Associate with 3-6 years of experience in testing and validation of Injectable Packaging Materials. Responsibilities include analysis of packaging materials, operation of testing instruments, knowledge of regulatory requirements, and drafting communication skills.
Review and approve laboratory records, Ensure compliance with standard operating procedures and regulatory requirements, Initiate QMS elements like Deviations and Change Control, Prepare/review SOPs, Testing results, Calibration records, Validation protocols and reports
Serialized Product Traceability encompasses a set of Serialization and Track & Trace initiatives aimed at securing the supply chain to ensure safe, authentic products reach every patient. The Serialization Process Specialist at Endo USA, Inc. is responsible for accuracy and completeness of Serialization transactions, compliance with global serialization regulations, and managing serialization efforts with internal and external partners. Key responsibilities include system monitoring, gap identification, compliance maintenance, onboarding partners/products, troubleshooting issues, collaboration with external partners, and communication across functions for compliance.
The Senior Financial Analyst at Paladin Pharma is responsible for financial and management accounting, financial reporting, and internal control procedures. This role involves analyzing trends, preparing financial statements, collaborating with departments, and recommending process improvements. The ideal candidate has a CPA designation, 4+ years of relevant experience, attention to detail, data analysis skills, and proficiency in French and English.
Responsible for packaging operations, cleaning, troubleshooting, and preventive maintenance of packaging equipment. Executes documentation procedures and supervises cleaning activities during routine operations.
Senior Associate for Qualification and requalification of Utility systems.
Responsible for performing audits globally for vendors and service providers in the field of sterile manufacturing, ensuring GMP compliance, and managing documentation related to vendor qualification. Must have a Master's in science (Microbiology) or Master in Pharma with 10-14 years of experience in sterile formulation and vendor auditing.
This Compensation Manager role at Endo involves shaping the culture of the company through rewards and recognition programs. Responsibilities include developing and implementing compensation programs, providing consultative support, and ensuring compliance with policies and regulations. The position also involves managing base pay, incentive compensation, and stock compensation.
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