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 Manufacturing Associate II is a non-exempt position that performs mechanical assembly, electro-mechanical assembly and other value added operations related to Solta’s products.
WORK SCHEDULE: Monday - Friday; 2:30 - 11:00 pm. (2nd shift)
Full-time/Direct Hire - Manufacturing Associate III's
Solta Medical / Bausch Health
11720 N. Creek Pkwy., Bothell, WA 98011
$3,000 Sign-on Bonus
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.
Responsible for providing a high quality and diverse range of services and support to the legal and compliance department. Facilitate a level of excellence throughout the Bausch Health Compliance department, as the Compliance team continues to partner with the business on key initiatives for the overall success of the organization. We are seeking an individual with the utmost degree of professionalism and integrity, capable of handling highly sensitive and confidential matters, and with an industrious and self-motivated approach.
This position provides manufacturing engineering support to a manufacturing operation. This may include designing and implementing new manufacturing processes, designing manufacturing tooling, improving existing manufacturing processes, repairing and coordinating the repair of production machinery, and providing technical guidance to manufacturing personnel.
- The CDS is responsible for optimizing patient outcomes and utilization of B+L premium IOLs by transferring clinical knowledge and valuable skillsets to both surgeon and staff to develop all customers into successful users of our technology.
3rd shift position: Sun, Mon, Tue, Wed: 8pm to 630 AM. Thu: 8pm to 630am (overtime)
Hours and overtime subject to change based on company needs.
Compounding of sterile and nonsterile finished products. This position requires Rinse Water Certification, Aseptic Gowning Certification, Physical, Respirator Certification, Lock-out/Tag-out Certification, Confined Space training, and Cleanroom Certification. Assumes responsibility for the GMP, ISO, environmental health and safety procedure awareness, and compliance within the respective area.
Manages and coordinates activities and resources associated with Quality Assurance overseeing Lab activities and controls to include the approval of incoming and finished product testing data, lab OOS and non-conformance, stability, raw material, component, calibration, and lab equipment qualification.
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.
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 Manager / Senior Manager of Advertising & Promotion, Medical Device Product reviews, approves and monitors product advertising and promotional labeling pieces for compliance with regulatory agencies requirements.
The software quality assurance engineer is responsible for assuring that computerized systems associated with the manufacture of pharmaceutical product is validated in accordance with regional and local procedures and cGMP regulation and guidelines. Job assignments are to be completed without a considerable amount of supervision or coaching.
Technical Operations is the organization within Global Manufacturing & Supply (‘GMS’) responsible for ensuring that externally sourced pharmaceutical products are scientifically robust, manufactured under control and remain in a constant state of validation throughout their product lifecycle in order to maintain a consistent supply of safe and effective products to patients.