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Position Summary: This position is responsible for performing operations related to the manufacturing and/or packaging of pharmaceutical products through equipment set-up, operation, clean-up and maintenance in compliance with all regulatory cGMP requirements and company policies and procedures. Area of manufacturing specializes in injection molding, extrusion and creams manufacturing.
Monday through Thursday nights. 8pm to 6:30am.
The Material Handler I is the entry level material handler that will focus on gaining the knowledge and understanding to successfully provide released components to the production areas.
Shift: Monday –Friday 7:30am to 4:00pm
Primary purpose and function of this position:
The purpose of the Regional Manager is to integrate and direct implementation of Teva Neuroscience sales plans, and objectives within the geography.
This territory includes:
North: Burlington, Vermont
South: Bronx, NY
East: Worchester, MA
West: Schenectady, NY
The ideal place(s) to live are: Connecticut or western Massachusetts would work as well.
The Technician participates in installation and troubleshooting of system operating equipment. The primary task is, however, the safe and reliable operation of the equipment. The Technician also performs preventive and predictive maintenance tasks including, but not limited to, cleaning, repair, adjustment and lubrication as well as modification of equipment. This task phase will be scheduled in a way as to not interfere with the operation of the facility.
This is a FIRST shift opportunity working 7:00 AM to 3:30 PM Monday through Friday. The position also includes a rotational "On-Call" schedule.
This role will drive the evolution of global Teva Consumers Solutions and Commercial IT integrated multi-channel capabilities through a series of strategic projects across a complex enterprise. This individual will lead large scale IT program engagements and projects to successful completion while demonstrating excellent project management and system development best practices. They will engage with business leadership to ensure proper expectation setting and partner with stakeholders to ensure proper strategic planning, alignment, integration and visibility. He or she will need to drive consensus and decision-making with business, IT, Teva Consumer Solutions with executive management to balance competing priorities. They will oversee direct reports and lead matrixed teams while maintaining visibility of day-to-day activities with project teams to mitigate risks and addressing program and operational obstacles as needed. This individual will provide status reporting to internal and external stakeholders while closely managing project financials. They will also recommend options or solutions that meet new and evolving business needs and lead the selection the most relevant tools/techniques to meet specific requirements. He or she will lead the development and implementation of strategic solutions to business problems in-line with the overall global commercial IT architecture through application of personal experience, industry knowledge and validate solutions with subject matter experts. This position requires excellent communication, collaboration, presentation and relationship management skills. The ideal candidate should possess a successful track record of obtaining results in a large corporate, matrixed environment.
The Chargeback Processing Sr Specialist will be responsible for the timely review and validation of debit memos submitted for chargebacks through Revitas CARS with complete accuracy. The incumbent will also resolve chargeback errors, communicate with wholesalers on a daily basis and manage chargeback accounts resulting in more than $12B in annual chargebacks. Proper issuance of chargebacks allows for indirect sales data to reflect accurate data used for sales and customer incentives and profitability analysis.
Publishing Associate I is responsible for the publishing and dispatch of basic lifecycle management submissions and troubleshooting document issues. The Publishing Associate I follows defined standards and works in close collaboration with senior staff and operational team members to ensure the creation of accurate, timely and technically competent regulatory submissions.