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2 Oct 2020

Full-Time Senior Manufacturing Engineer

Rebiotix – Posted by annjaclyn Saint Paul, Minnesota, United States

Job Description

Rebiotix Inc, part of the Ferring Pharmaceuticals Group, is a late-stage clinical microbiome company focused on harnessing the power of the human microbiome to revolutionize the treatment of debilitating diseases. Located in Roseville, Minnesota, our goal is to improve the lives of patients and reduce the cost of care associated with complex diseases through our innovative microbiota-based MRT™ drug platform . We are a passionate team of scientists, engineers, and clinical researchers motivated by the opportunity to blaze new trails and create new technologies for today’s medical needs. We are looking for like-minded get-it-done individuals to add to our growing team.


Support day to day manufacturing operations of the RBX7455 product by providing front line support. This includes troubleshooting processing issues, conducting investigations and risk assessments, providing training, and identifying and implementation of process improvements.

Provide technical support and training to manufacturing technicians while determining opportunities for improvement.
Contributes to continual improvement of all manufacturing processes and documentation to ensure they are current, accurate, and clear.
Develop and update Master Batch Records to support manufacturing builds.
Assures product and process quality by designing testing methods; testing finished product and process capabilities; establishing standards; confirming manufacturing processes.
Improves manufacturing efficiency by analyzing and planning work flow, space requirements, and equipment layout.
Reviews and approves Engineering drawings/specifications, layouts, change controls and specifications. Reviews test procedures and plans prior to implementation, conducts failure analysis and inspection on products, processes and materials.
Involved in resolving deviations / non-conformances due to manufacturing related issues
Improve productivity and efficiency by providing ongoing training for new production processes and methods. Make sure the written process translates into efficient and reliable production.
Support product and process development, validation, and tech transfer projects as required.

Bachelor’s degree in Engineering or related field required
Master’s degree in Engineering or related field preferred
Minimum 5 years of manufacturing site engineering experience
Regulated industry experience required, pharmaceutical or biologic experience preferred
Lyophilization experience preferred
Experience in structured problem solving and use of statistical tools
Experience in design for manufacturing, DFMEA, PFMEA, DOE and Validations
Experience with data-based decision making
Ability to apply sound engineering logic to solve complex problems, to properly assess risks, and make decisions accordingly
Can work independently and in team setting
Strong verbal and written communication skills
Follow procedures as written, strong attention to detail, ability to technically write procedures
Proficiency with Microsoft Office programs such as Word and Excel
Resourceful and flexible in finding ways around constraints

We are proud to be an Affirmative Action/EEO Employer. EOE Minorities/Females/Protected Veterans/Disabled. We maintain a drug-free workplace and perform pre-employment substance abuse testing.

How to Apply


Job Categories: LGBT. Job Types: Full-Time. Salaries: 80,000 - 100,000.

Job expires in 23 days.

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