Pharmaceutical Equipment Specialist

2 weeks ago

Brighton, Michigan, United States Bryllan LLC Full time

Are you ready to embark on a fulfilling career within a dynamic organization? Do you possess a strong desire to learn and collaborate with a dedicated team to achieve shared objectives? At Bryllan, we are seeking individuals who are respectful, empathetic, and courageous, eager to apply their expertise in a meaningful role. Bring your educational background and professional experience, along with a commitment to continuous learning in the pharmaceutical manufacturing sector.

Bryllan LLC, a contract manufacturing organization (CMO) located in Brighton, Michigan, specializes in sterile injectable pharmaceuticals. Our management philosophy is grounded in the principles of Quality, Integrity, and Service. If you are inspired by the prospect of contributing to the development of life-enhancing or lifesaving products, this opportunity may be the right fit for you.

We are currently looking for a Pharmaceutical Equipment Specialist to manage the design, procurement, and qualification of equipment utilized in the production of pharmaceutical products. This role demands a strong emphasis on ensuring quality in production processes, implementing best practices, and fostering continuous improvement.

A Pharmaceutical Equipment Specialist is an integral member of the Engineering team, responsible for overseeing all equipment on site.

Key Skills Required:

  • Technical Writing,
  • Validation,
  • Qualification,
  • Protocol Development and Execution,
  • Process Automation,
  • Project Collaboration
Primary Responsibilities:
  1. Collaborate closely with the Process Development Team to ensure all equipment meets the technical specifications for the intended processes.
  2. Create the necessary technical documentation for the qualification of pharmaceutical process equipment.
  3. Engage with vendors during the design and procurement phases to ensure equipment is suitable for its intended use and delivered timely to align with the manufacturing schedule.
  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 various new equipment required to support manufacturing activities.
  8. Offer engineering solutions and designs for new equipment to be utilized in the production of sterile drug products.
  9. Ensure that all work activities adhere strictly to safety guidelines 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 words to promote a collaborative team culture.
  3. Manage multiple projects effectively in a fast-paced environment.
  4. Possess excellent interpersonal skills with the ability to communicate clearly and effectively.
  5. Have basic computer proficiency, particularly in Microsoft Office applications.
  6. Show strong mathematical and organizational skills.
  7. Exhibit excellent English communication skills, both written and verbal.
  8. Uphold honesty and integrity, adhering to the highest legal and ethical standards.
  9. Treat every individual with courtesy and respect.
  10. Understand cGMP and regulatory principles.
Educational Requirements:

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

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