Current Opportunities

Tracking # 62 Industry Pharmaceutical Jobs Job Title Manufacturing Supervisor Location Northern New Jersey Salary Open Job Description Our client is one of the world's leading players in the development, manufacture, and sale of generic pharmaceuticals. Founded over 65 years ago, they have more than 10,000 employees operating in over 40 countries around the globe. The Company has development and manufacturing facilities in the US, Europe, and Asia. The plants produce a variety of products in different formulations including tablets, capsules, injectables, suppositories, sprays, steriles, powders, oral liquids and semi-solids. They offer one of the broadest product portfolios and strongest pipelines in the industry—around 800 products on the market, over 320 products under development and pending registration, and current products are registered in more than 60 countries. This high impact role assuring that products manufactured comply with cGMPs, SOPs, and other applicable regulations. Responsibilities The incumbent will: Supervise the direct processing of materials and the associated hourly workforce to ensure attainment of business results. Effectively collaborate with and manage a work team with specific responsibility for motivating others, ensuring performance, schedule execution, task coordination, equipment and area preparation and effective administration of personnel policies and procedures. Manage conflict and effect resolution to technical and personnel challenges is key as is openness to change and the ability to effect positive change. Because our clients business is dynamic and advances in science and technology require new methods of production we are looking for individuals who can do the following: Collaborate with team members in the identification and implementation of continuous improvement initiatives and action plans. Support activities in the areas of cost containment, efficiency, productivity, energy conservation, waste minimization, operational excellence and lean practices. Demonstrate integrity, credibility and flexibility in their daily performance so as to motivate others to do the same. Assure compliance with safety and environmental practices, cGMPs and SOPs in the work area. Participate in external and internal audits and inspections. Initiate the investigation when a quality or safety event occurs during the shift. Work with members from Quality and Technical Operations to properly handle unplanned events. Ensure that corrective actions are implemented. Ensure that personnel under his/her supervision are properly trained in cGMPs, procedures, good documentation practices and regulatory matters. Participate in design and implementation of training and development programs. Perform performance management and disciplinary process. Ensure materials receiving and verification in the work area, equipment cleaning, set-up and area cleaning and verification are completed according to procedures. Assure that materials are properly handled and equipment is properly operated according to SOPs, guidelines, and regulations. Maintain control of processes and product quality by ensuring compliance with cGMPs, safety and environmental regulations. Monitor the manufacturing processes during the shift. BS in Engineering or Science preferred. 2+ years of experience in Pharmaceutical or Chemical industry. Relocation Package No Interview Expenses Yes Benefits Package Yes