Process engineer for development of new products and process improvements for existing products.
Design and support manufacturing process development for sterile and non-sterile solutions, suspensions, and ointments.
Design experiments at pilot scale to support scale-up and transfer to manufacturing environment.
Validate manufacturing processes and equipment cleaning procedures.
Prepare protocols and final reports for executed studies.
Provide technical expertise related to process design and scale-up on development teams.
Conduct investigations to support R&D projects and provide technical support for investigations of commercial manufactured products.
Complying with company cGMP and safety practices and procedures, including, participating in GMP training, FDA audits and fulfilling aseptic gowning requirements.
BS, MS, or PhD in Engineering, or related physical sciences
Minimum of one-year experience in process engineering, technical services and/or validation roles in pharmaceuticals, or FDA regulated industry. Computer literate, and is able to use Microsoft Office software (Word, XL, PowerPoint, Visio, etc.)
Previous experience working in a sterile manufacturing environment and performing cleaning and manufacturing process validation is a plus.
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Bausch Health Companies Inc. is committed to leveraging the talent of a diverse workforce to create great opportunities for our business and our people. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.