Pharmaceutical Equipment Specialist

2 weeks ago


Brighton, Michigan, United States Bryllan LLC Full time
Job Overview

Are you looking for a fulfilling career in a dynamic organization? Do you have a strong desire to enhance the lives of others through your work? Bryllan LLC is seeking dedicated and compassionate individuals to join our team.

As a contract manufacturing organization (CMO) specializing in sterile injectable pharmaceuticals, Bryllan LLC in Brighton, Michigan, values Quality, Integrity, and Service. We are currently in search of an Equipment Engineer to manage the design, acquisition, and validation of equipment essential for pharmaceutical production. This role emphasizes quality assurance in production processes, the adoption of best practices, and ongoing enhancements.


The Equipment Engineer will be an integral part of the Engineering team, overseeing all equipment operations on site.

Key Skills Required:

  • Technical Writing
  • Validation Techniques
  • Equipment Qualification
  • Protocol Development and Implementation
  • Process Automation
  • Collaborative Project Management

Primary Responsibilities:

  1. Collaborate with the Process Development Team to confirm that all equipment fulfills the technical specifications for the designated processes.
  2. Create the necessary technical documentation for the qualification of pharmaceutical process equipment.
  3. Engage with vendors during the design and procurement stages to ensure equipment suitability and timely delivery in alignment with the manufacturing timeline.
  4. Provide ongoing technical support and troubleshooting to resolve equipment-related issues.
  5. Deliver technical training on equipment as required by Operations.
  6. Serve as the designated technical lead and owner of manufacturing process equipment.
  7. Participate in project teams for the introduction of new equipment to support manufacturing operations.
  8. Develop engineering solutions and designs for new equipment utilized in the production of sterile drug products.
  9. Ensure that all work activities adhere strictly to safety protocols and processing standards, including cGMPs and SOPs.

Behavioral Expectations:

  1. Exhibit a strong work ethic and the ability to complete tasks independently.
  2. Demonstrate leadership through actions and communication to promote a unified team culture.
  3. Manage multiple projects effectively in a fast-paced environment.
  4. Possess excellent interpersonal skills for effective communication.
  5. Have basic computer proficiency, particularly in Microsoft Office applications.
  6. Show strong mathematical and organizational abilities.
  7. Exhibit excellent English communication skills, both written and verbal.
  8. Maintain honesty and integrity, adhering to the highest legal and ethical standards.
  9. Treat all individuals with respect and courtesy.
  10. Possess knowledge of cGMP and regulatory principles.

Educational Qualifications:

A minimum of a four-year degree in Engineering or Engineering Technologies is required.



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