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.
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The Manager, Sample Operations is responsible for the Sample Accountability/Management under the PDMA guidelines to ensure FDA compliance implemented for any sampling through personal and non-personal promotion. The Manager is also responsible for leading and maintaining sample shipment programs (Representative and Direct to Practitioner) operations and administration with internal departments and the vendor. Vendor management to ensure all guidelines and processes are implemented to adhere to PDMA requirements and Company policies.
Reporting in to the Sr. Director of Research and Development, the R&D Administrative Assistant (AA), is responsible for providing overall comprehensive support for the Sr. Director of R&D, his Staff and others in the Department.
Bausch Health Companies Inc. (NYSE/TSX: BHC) is a global company that develops, manufactures and markets a range of pharmaceutical, medical device and over-the-counter products, primarily in the therapeutic areas of eye health, gastroenterology and dermatology. We are delivering on our commitments as we build an innovative company dedicated to advancing global health. Each day, Bausch Health products are used by up to 150 million people around the world.
Our approximately 21,000 employees are united around our mission of improving people’s lives with our health care products, and we manufacture and market health care products directly or indirectly in approximately 100 countries.
Salix Pharmaceuticals is one of the largest specialty pharmaceutical companies in the world. Founded in 1989, Salix is committed to the prevention and treatment of gastrointestinal (GI) diseases. Salix’s first US commercialized product, Colazal, was approved by the FDA in 2000. We offer effective solutions while continuing to strive to make advancements in patient care.
Every day, our employees around the world strive to improve peoples’ lives with our products. We achieve this by connecting with the patients who use our products and the healthcare professionals (HCPs) who prescribe them. Our therapeutic areas of expertise include management of conditions such as hepatic encephalopathy, irritable bowel syndrome with diarrhea, opioid-induced constipation, and ulcerative colitis.
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We employ dedicated and innovated team members who are driven to solve problems. We improve upon existing treatments, uncover new breakthroughs, and deliver comprehensive practice support to help HCPs provide best-in-class care.
We recognize that our team members are essential to our future. It is our goal to make everyone feel respected and equally appreciated so we are all dedicated and committed to the same cause. Our team members enjoy a dynamic work environment that encourages both professional evolution and personal growth. Each day you spend at Salix, you have the satisfaction of knowing that you are working with dedicated individuals who share a common vision of constant innovation. To ensure that we achieve our goals, our team members are continually learning more about their fields of expertise. We are proud to facilitate this development by providing internal and external professional development opportunities. This commitment to growth helps drive Salix and our employees. Be part of the Salix team dedicated to moving gastrointestinal treatment forward.
This position designs, develops, maintains and troubleshoots embedded software in our medical products. Software will interact with other components through established APIs, control specialized hardware with custom device drivers, control therapy, and interface with the user.
This is an overnight shift from 6pm - 6am Team B.
Assure the purity, strength and safety of sterile and nonsterile products via cleaning, disinfection, and preparation of the aseptic manufacturing areas and equipment. This position required Aseptic Core Gowning Certification, Rinse Water Testing, Disinfection Certification and all related EHS and functional training to maintain GMP requirements.
This is a 2nd shift position (3:00pm - 11:30pm) with some overtime required per business need.
Job requires at least 5 years of packaging or non-sterile/aseptic filling experience. The job functions and responsibilities include proficient operation of filling equipment, including bottle unscramblers, tippers, cappers, conveyance systems, line and equipment cleaning, line clearances, component transfer, line/room disinfection, equipment set up and tear down, equipment troubleshooting, and proper documentation practices. Ability to operate all ointment lines and solution lines. This position requires aseptic gowning certification and line clearance certification. Maintain training requirements including SOP, EHS, and HR. Assume responsibility for the GMP, ISO, EHS awareness and compliance within the respective area. Attend and participate in Lean Improvement initiatives such as reducing costs & OEE initiatives. Responsible for maintaining Quality, OEE, Material Variance and Scrap goals.
The Sr. Manager/Assoc. Director within Nonclinical Safety will support the research and development of new ophthalmic medical device products as well as maintenance of business activities by ensuring that adequate documentation exists for all new and existing products to meet existing and emerging regulatory requirements, particularly the EU Medical Device Regulations (EU MDR) and ISO 10993 series.
The scientist in this role leads the laboratory efforts associated with new and existing products through a strategic and tactical focus on the development and execution of chemical and physical measurements. This role is a team member on development teams and may take the lead on ad hoc teams. The incumbent will have a thorough understanding of the principles that underlie measurements as well as the requirements of regulatory filings.
To provide analytical support and technical leadership to development programs for new product development.
To operate cartoning equipment in a high volume, fast paced environment in accordance with SOP’s, GMP’s and other division specifications.