Click column header to sort
Position Summary Craft instruments of the highest quality by following verbal and written procedures,
and blue prints.
The Quality Auditor – Suppliers will have responsibility for supplier audit planning, scheduling, execution, documentation, reporting and follow up.
Perform specific duties according to SOP's within the VS3 Assembly/Packaging Department, either by the use of both hands or by using machinery when assigned.
Responsible for the assembly and/or manufacturing of single use, surgical components to create finished goods SKUs in the VS3 Assembly/Packaging area.
All work performed must be completed with the highest Quality standards possible and within the allowed time given in order to maintain the highest efficiencies possible with minimum requirements established for each operation.
Work schedule: Monday - Thursday; 6:00 am - 4:30 pm. Must be able to work overtime as needed, including Saturday's and Sunday's.
Validation of Sterilization processes and equipment including moist heat, dry heat, gamma, and ethylene oxide associated with the manufacture of pharmaceutical or medical devices to assure compliance with cGMP’s, FDA’s and BLP’s guidelines. Job assignments are to be completed without a considerable amount of supervision or coaching.
In addition, Validation of manufacturing equipment, facilities, utilities and computerized systems is highly desirable.
Responsible for the continuous development and maintenance of the compliance status of the activities of the B& L Tampa Pharmaceuticals Organization. This includes the development of strategic and tactical goals based on evaluation of published regulatory and industry trends as well as the evaluation of the relevant quality metrics of the Tampa Organization.
Valeant Pharmaceuticals International, Inc. is a diverse pharmaceutical company that is committed to focusing on our key stakeholders while delivering consistently high performance. Our values provide the overall direction for our company, and provide us with the tools necessary to rise to any challenge by leveraging our collective hard work and effort along with our unwavering competitive spirit. These values help us set goals based on our organization’s potential and what we hope it will become.
Bausch + Lomb, a division of Valeant Pharmaceuticals International, Inc., has one of the best-known and most respected healthcare brands in the world.
Offering the world’s most comprehensive portfolio of eye health products, the company’s core businesses include contact lenses and lens care products, ophthalmic surgical devices and instruments, and ophthalmic pharmaceuticals.
The company began in 1853 in Rochester, New York, and our history of innovation continues today as we invent new materials, engineer new technologies, and create pioneering ways to help people see better to live better.
Valeant Pharmaceuticals International, Inc. is a diverse and decentralized pharmaceutical company that is committed to focusing on our key stakeholders while delivering consistently high performance. Our values provide the overall direction for our company, and provide us with the tools necessary to rise to any challenge by leveraging our collective hard work and effort along with our unwavering competitive spirit. These values help us set goals based on our organization’s potential and what we hope it will become.
The RetinaTerritory Manager is a professional sales position whose primary objective is the presentation, promotion, and sale of the Bausch + Lomb portfolio of retina products such as Stellaris PC Systems, VersaVit, Stellaris PC disposables, Laser Probes, Diamond Dusted Membrane Scrapers (DDMS), Silicone Oil, Retina Disposable Instruments, Pinnacle Instruments, Retina Accessories, and Retina ancillary products. The RTM reports to the Regional Business Director.
This leadership role in Quality Assurance requires the manager to lead the oversight and integrity of Quality systems for Bausch + Lomb devices within the St. Louis site. The individual represents site management quality systems and establishes appropriate standards and guidelines to ensure lasting customer satisfaction.
Supports the development and maintenance of quality assurance programs, policies, processes, procedures and controls ensuring that performance and quality of products conform to establish standards and agency guidelines.
Reviews, analyzes and reports on quality discrepancies related to products manufactured at site and works closely with various key functions to develop disposition and corrective actions for recurring discrepancies.
Works with site management to develop management control requirements and facilitates aspects of management review, complaint review board and compliance requirements based on North American Quality System requirements.
Valeant Pharmaceuticals International, Inc. is a global diversified pharmaceutical company focused in several key therapeutic categories: GI, Dermatology, Ophthalmology, Neurology, Vision Care, Consumer Health, and Dental. Valeant’s corporate mission is to improve the lives of patients with our healthcare products.
The Sr. Director, Information Management will be responsible for developing an Information Management strategy to ensure the proper procurement, implementation, governance, and support of the data assets critical to the Commercial business. This individual will have the autonomy and responsibility for building the Information Management function based on the diverse needs of the function. The person needs to be able to develop and execute a strategy to meet the different needs of a large and diverse product portfolio of both inline and pipeline brands. This person must be comfortable in operating in a fast paced “start up” type environment. This role will be responsible for hiring and leading a 4-6 person team and serving as the face of the function to Commercial Operations leadership, IT, General Managers, the CFO, and CEO. This role reports directly to the Vice President of Commercial Insights & Analytics.
This candidate perform, supervise, or manage a variety of communications and information management (IM) tasks and activities including staff support, publishing, records, administrative communications, and workgroup management