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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Bausch Health Companies 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 responsibility of the Regional Business Director is to provide leadership, strategic direction, and drive towards attainment of quarterly and annual sales goals for the Americas Organization and specified Region.
As directed by the supervisor and/or group leader perform functions to fulfill orders for shipment to customers. This may include but is not limited to customer service support, replenishment, cycle counting, picking, packing, and manifesting. Employee may be trained in any or all of the required disciplines depending on business needs. Employee must work all assigned hours and may also be required to perform other duties as directed by the supervisor and or group leader.
Hours - Sunday-Friday - 11:30pm-7:30am
The Regulatory Senior Manager handles regulatory development and post-approval/regulatory compliance for assigned products. Participates on the product development/life-cycle management team to provide regulatory guidance for assigned pharmaceutical Prescription products. Manages relevant regulatory strategy components and interactions with Regulatory Authorities for these products. May perform due diligence efforts on new product opportunities.
Leads the development of generic pharmaceutical products. Main area of focus would be topical (Skin and ocular), parenteral and liquid oral product development:
- Experimental design and laboratory troubleshooting
- Set-up, preparation and execution of R&D trials and cGMP activities
- Drafting, reviewing and approving stability protocols and reports
- Preparation of technical presentations
- Interpretation of data
- Internal and external communications with other operating functional groups (Quality, Regulatory, Stability, Supply Chain, Management, contract research organizations (CROs), and others
- Product transfers and scale-up activities
- Physical and chemical characterization of selected prototypes
- Set-up, preparation and execution of laboratory activities
- Preparation and execution of R&D and cGMP manufacturing activities
- Supervision of technician
- Development team composed of technicians and/or junior chemists (Chemists I-III)
- Performance evaluations of team members
- Scientific discussions/training
- Intellectual property opportunities
Documents laboratory work in compliance with company policies, government regulations. Provides general support to Formulation and Process Development Department. Supervise technicians. Provide leadership in laboratory maintenance activities.
The Principal System Engineer confirms Solta products meet functional system requirements, coordinates activities involved in system level specification, testing, and development for medical device products in the aesthetic space. The applicant must be a hands-on self-starter, who has the ability to work collaboratively with a multi-disciplinary product development team in accordance with the standards IEC 62304, IEC 62366, IEC 60601, and ISO 13485.
Bausch Health is a progressive, exciting place to work - a place where opportunities abound for new and current employees. At Bausch Health, we have a strong belief that the company's success coincides with employee achievement of personal and professional goals. We are always looking for new employees who will become part of the success of our company. Bausch Health offers a competitive salary, benefits, and a work environment that fosters and respects the contribution of each individual.
In this newly created role, the selected candidate’s primary responsibility will be to provide financial support to the IT lead implementing SAP globally. This person will assist in preparing, maintaining and monitoring the global SAP financial budget and forecasts for both capital expenditures and operating expenses. This person will also assist with the preparation and distribution of reports to IT and Senior Management, highlighting and reporting on variances from budget and prior forecast. S/he will be expected to resolve any financial queries that are raised, including timely communication of risks or opportunities relative to the budget/ forecast. The candidate will be expected to produce quality work in an organized, timely and efficient manner.
Manufacturing Machined parts to the highest quality by following verbal and written producers and blueprints.
Bausch Healthcare 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.
Sr. Manager/Director, Medical Affairs position is a role within Bausch + Lomb with responsibility for Medical Affairs of surgical programs. This position reports to the head of medical affairs.
This is a 2nd shift position (3:00PM-11:30pm) with 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.