Here are our current job openings. Please view the details for more information, and apply from that page if you are interested.
Bausch Health is an equal opportunity employer and supports workforce diversity.
Click column header to sort
The Senior Supplier Quality Specialist -- Systems is responsible for maintaining compliance of Quality Systems utilized to manage Externally Manufactured products and processes throughout the product lifecycle including RX, OTC, Cosmetic and Medical device products.
The Senior External Manufacturing Quality Specialist will support compliant execution of quality-related activities, including but not limited to, new quality system/methodologies implementation, training, CAPA, change management, problem solving, product and process development, acceptance activities.
This position will also work directly with Bausch Health Finished Good (FG)/External Manufacturing (EM) suppliers, as well as medical device/Pharmaceutical product manufacturing facilities, to provide sustaining quality and compliance leadership and routine support related to current commercialized products
In addition the position is responsible for measuring, and reporting key quality metrics to drive quality and efficiency.
This position is responsible for providing customers with prompt, courteous, efficient, high quality service in the areas of order fulfillment and problem resolution needs to ensure a positive customer experience.
Supports U.S. Vision Care customers - must represent company in a professional manner during 100+ daily customer interactions; key member of Customer Resource Center team.
Work schedule: Monday - Friday; 10:00 am - 6:30 pm
Manage the Microbiology Monitoring program for the facility in agreement with all regulatory requirements. Supervise technical staff in connection with routine and project related microbiological testing. Work with Manufacturing and other departments to solve and prevent production related problems.
The Director of Surgical Marketing is team leader for B&L’s cataract equipment and associated accessories, & consumable product lines and responsible for U.S. marketing. This includes: developing the U.S. marketing plans, planning the product portfolio, acting as key strategic interface to R&D and Clinical Affairs in new product development, conducting market research, developing and executing the product(s)’ brand positioning, messaging, and launching new products, product management and sales support, coordinating product life cycle management, and day to day business leadership and support.
Responsible for Supplier Quality Assurance activities for existing supply base, including maintenance of business (MOB) and cost improvement projects (CIP) at the surgical business unit including, but not limited to: product sourcing decision support; advance product quality planning; suppliers assessment/audits and qualification; validation of supplier processes; qualification of services, parts and/or finished products; and managing supplier corrective action activities and concern resolution process leadership.
Additionally, may function in the same capacity to support some new design projects.
Oversee the Metrology Department to assure compliant operations. Measure, track and communicate critical calibration metrics. Communicate status to local management team. Review of all calibration work orders to assure proper range of calibration and accuracy/precision of the instruments. Schedule and provide direction to three (3) Metrology Technicians. Support manufacturing operation by being on call 24/7.
Lead all Metrology related NCR investigations and recommend corrective actions to assure improved instrument reliability. Serve as the cross functional leader in these investigations. Lead RC/CAPA efforts related to the metrology program.
Assist in the review and modification of facility/equipment related PMs on an ongoing basis through participation in Reliability teams and initiatives. On-going evaluation of instrumentation spare parts inventory. Assist in the long-range planning of facility equipment replacement and upgrades. Assist in the development and maintenance of the annual departmental budget.
The HEOR lead will work to ensure quality of design, execution and dissemination of outcomes research studies and tactics across the organization. The purpose of this position is to develop and execute HEOR initiatives that communicate the value of Bausch Health assets to internal and external stakeholders. Reporting to the Vice President of Medical Affairs, the HEOR lead will also work cross-functionally to ensure that HEOR plans are aligned across the organization. Key business partners will be the US medical affairs team, US commercial, and the US Managed Markets team. For the assigned therapeutic area, the Head of HEOR will manage study quality, resources, project plan and vendors and lead customer-facing presentations when HEOR information is requested. This individual will support building HEOR functional excellence in terms of processes, internal training and awareness.
Bausch Health 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 Regulatory Affairs – CMC Senior Director independently manages all regulatory CMC aspects of assigned Bausch Health Company products throughout their lifecycle. This includes Brand, Generics, OTC/Nutritionals, Dietary Supplements and Medical Devices. The Senior Director is responsible for the regulatory CMC strategy of submissions for all products under his/her responsibility as well as managing interactions with regulatory authorities on CMC issues.
The software engineer is primarily responsible for the development of Graphic User Interface (GUI) software, with support / backup responsibility for Cloud API software and Embedded firmware for the Surgical Cataract and Vitreoretinal equipment and eyeTELLIGENCE infrastructure.