Top Pharmaceutical Operations & Support Jobs

The Quality Manager will build quality systems for implantable neurotechnology, manage risk activities, oversee supplier control, and ensure compliance with Class III medical device regulations.

The Director of Procurement will lead the purchasing strategies, supplier management, team supervision, and continuous improvement aimed at optimizing costs and ensuring compliance. They will report to the CEO and collaborate with various departments to enhance procurement processes.

The Contract and Pricing Strategy Specialist develops pricing models, manages contracts, conducts market analysis, and supports negotiations to ensure financial goals are met.

Lead the regulatory strategies for assigned assets within GSK, ensuring compliance and oversight while guiding global teams and engaging with health authorities.

Assist in tracking tender calls, maintaining a database, developing marketing materials, conducting market research, and performing data analysis. Gain experience in tender management and business development in the pharmaceutical industry.

Lead the Pharmacovigilance function for North America, ensuring regulatory compliance, overseeing medical affairs, managing risks, and engaging cross-functional teams.

The Senior Payor Contract Analyst manages commercial and Medicare Advantage contracts, collaborates with various departments, and conducts financial analysis for negotiations.

The intern will assist the Quality Control department with lab experiments, document work, complete projects, and present findings.

The Sr. Manager, Strategic Sourcing will manage sourcing strategies, collaborate with stakeholders, and oversee supplier relationships to achieve cost savings and ensure compliance with protocols.

The Feasibility Engagement Manager oversees the site selection process for clinical trials, liaises with clients and teams, and ensures efficient communication and coordination. They deliver site capabilities, manage study opportunities, and maintain documentation, all while driving network growth and maximizing award probabilities for clients.

The Regulatory Coordinator I manages the preparation and organization of regulatory documents for clinical trials, ensuring compliance with FDA guidelines and maintaining accurate records.

Lead the transformation of logistics processes within the ERP Modernization Program, focusing on optimizing Warehouse, Transportation, and Trade Management systems for improved efficiency and compliance.

Lead the design and execution of clinical imaging operations in trials, oversee portfolios, ensure compliance and training, and improve processes.

The Operations Plus Manager improves processes, directs operations implementation, leads training, and collaborates with management to achieve goals.

The Maintenance Specialist troubleshoots and repairs manufacturing equipment, performs preventative maintenance, prepares reports, and ensures safety compliance.