Search the 15 jobs at Hikma Pharmaceuticals

Seeking a talented and motivated Sr, Specialist, Leave Administrator to assist with the administration of the company's benefits programs, specifically administering the leave of absence programs. Responsible for advising, managing inquiries, generating reports, and ensuring compliance with state and federal laws. Also involves coordination of wellness programs and benefits-related inquiries.

Seeking a Manager, 503B Marketing responsible for overseeing commercial marketing related to 503B compounding. Responsibilities include liaising with sales, marketing, and legal teams, managing marketing content, and collaborating with vendors. Qualifications include 4 years of marketing experience in pharmaceutical industries, a bachelor's degree or higher, and strong communication skills.

Lead projects enabling successful transfers and launches of new and life cycle management of injectable drug products at Cherry Hill. Perform technical evaluation, process development, scale-up, process validation, launch, and lifecycle management. Coordinate quality investigations and project communications.

Oversee Hikma USA's centralized payroll and HR Operations functions for 2000 employees across multiple states. Ensure accuracy of HR data, compliance, efficiency, and positive employee experience. Manage payroll vendor relationships, payroll audits, tax matters, and compliance reporting.

Manager of Trade Operations Analytics at Hikma Pharmaceuticals USA Inc. responsible for managing Order-to-Cash and Supply Chain processes, supporting business segments, providing internal partners with product availability, implementing initiatives, and analyzing data to drive business decisions.

The Senior Analyst, Trade Operations Analytics will manage DSCSA business processes, product allocations, compliance, strategic and analytical reporting, as well as process improvements. They will collaborate across various business functions to ensure efficient operations and customer excellence. The role involves data analysis, reporting, compliance processes, order management, and continuous improvement initiatives.

Analyzing and reporting financial operations, preparing budgets, managing expense reporting, and providing financial support to plant management.

Review and approve GMP documentation, implement documentation changes, maintain document control process, and administer change control process. Responsible for training records, document editing/review, logbook maintenance, QA document file room control, and document distribution.

Responsible for managing manufacturing deviations and investigations in a pharmaceutical setting. Assisting/driving change controls, customer complaints, and annual product reviews. Requires a bachelor's degree in science or engineering, 3-5 years of experience in pharmaceutical processes, and strong organizational and communication skills.

The Manager, Product Transfer at Hikma Pharmaceuticals USA Inc. is responsible for supervising the Product Transfer team at Cherry Hill and leading successful transfers and launches of new products. Key responsibilities include leading the technical evaluation of site capabilities, coordinating quality investigations, and mentoring the team for continuous growth and productivity.

To work directly with operations and engineering departments to develop, lead, and implement new equipment/process projects and production improvement projects. Monitor and improve performance of production rooms/lines by reducing downtime and implementing new solutions. Author and provide assistance with documentation related to production and projects. Support and provide day-to-day process troubleshooting of safety, quality, and productivity-loss related issues.

Designs and configures the SAP systems, specifically PP/QM, with an emphasis on production, planning and Quality management.

Designs and configures the SAP systems, specifically PP/QM, with an emphasis on production, planning and Quality management.

Seeking a Principal Scientist, Product Development/Transfer with extensive experience in pharmaceutical formulation development and filing with USFDA. Responsible for formulation projects, providing technical support, and working on regulatory filings for injectable products.

Seeking a talented and motivated Scientist IV, QC Development & Lifecycle to manage analytical projects, develop and validate analytical methods, and provide leadership in a pharmaceutical company. Responsible for regulatory submissions and new product launches while working closely with various teams and external partners.