Equipment Engineer

2 weeks ago

Brighton, United States Bryllan LLC Full time
Job DescriptionJob Description

Are you interested in an exciting and rewarding career within a growing company? Are you eager to learn and motivated to collaborate with a team to achieve goals? Do you have passion for improving the lives of others?

Bryllan is looking for respectful, empathetic, courageous individuals who are eager to utilize their skills in a rewarding career. Bring the knowledge and experience you've gained from your education and career, along with willingness to continuously learn in the pharmaceutical manufacturing industry. Bryllan LLC in Brighton, Michigan, is a contract manufacturing organization (CMO) with a focus in sterile injectable pharmaceuticals. Bryllan embraces a management philosophy built around the principles of Quality, Integrity, and Service. If you feel invigorated by the thought of contributing to the creation of life enhancing or lifesaving products, this opportunity could be for you


Bryllan is hiring an Equipment Engineer to oversee the design, procurement and qualification of equipment used to manufacture pharmaceutical products. The role requires strong focus on driving quality into production processes, implementation of best practices, and continuous improvement.

An Equipment Engineer is a member of the Engineering team, responsible for all equipment on site.

Skills needed for success in this role:

  • Technical Writing,
  • Validation,
  • Qualification,
  • Protocol Authoring and Execution,
  • Process Automation
  • Project Collaboration

Essential Duties and Responsibilities:

  1. Work closely with the Process Development Team to ensure all equipment meets the technical requirements for the intended processes.
  2. Develop technical documentation required for the qualification of pharmaceutical process equipment.
  3. Coordinate with vendors throughout the design and procurement phases to ensure equipment is correct for the intended purpose and delivered on time to meet the manufacturing schedule.
  4. Provide routine technical support and troubleshooting for resolution of equipment issues.
  5. Provide technical training on equipment as required by Operations.
  6. Act as assigned technical lead and owner of manufacturing process equipment.
  7. Participation in project teams for various new equipment needed in support of manufacturing activities.
  8. Provide engineering solutions and designs for new equipment to be used in the manufacturing of sterile drug product.
  9. Ensure work activities are conducted in strict accordance with safety guidelines and processing standards cGMP's and SOP's

Behavioral Expectations:

  1. Strong work ethic and ability to accomplish tasks without supervision.
  2. Demonstrate leadership both by words and leading by example to foster Bryllan One Team culture.
  3. Ability to juggle multiple projects in a fast-paced work environment.
  4. Excellent interpersonal skills with the ability to communicate effectively.
  5. Basic computer skills (proficient in Microsoft Office applications).
  6. Strong mathematical and organizational skills.
  7. Excellent English communication skills, both written and verbal.
  8. Must possess honesty and integrity, commitment to the highest legal and ethical standards
  9. Ability to treat every person with courtesy and respect
  10. Knowledge of cGMP and regulatory principles

Education Requirements:

Minimum qualification of a four-year Degree in Engineering or Engineering Technologies.

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