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 LLC is hiring a Production Associate to execute various operations of pharmaceutical manufacturing at the Brighton facility. Employment for this position will be contingent upon successful completion of an eye exam (with or without the aid of glasses and/or contact lenses) at a vision center of Bryllan's choosing. The eye exam will be provided by Bryllan.

The duties of the Production Associate cover several aspects of production, including but not limited to: Dispensing, Inspection, Labeling, Packaging, and Cleaning/Disinfection of the Controlled Production Area. The Production Associate ensures a clean, safe workplace and quality production of drug product adhering to current Good Manufacturing Practices (GMP's).

A Production Associate is a member of the Operations team, responsible for the safe, efficient, and routine manufacturing of drug product.

Essential Duties and Responsibilities:

1. Follow detailed, written instructions (Manufacturing Batch Record, MBR) and procedures (Standard Operating Procedures, SOP's)
2. Accurately complete production documentation in performance of manufacturing operations.
3. Practice and promote safe work habits while performing job functions in compliance with established company and regulatory safety requirements.
4. Ensure quality standards and best practices are followed throughout the manufacturing process.
5. Maintain functional understanding of cGMP's and the impact of deviation from controlled processes and/or procedures.
6. Perform cleaning/disinfection of the Controlled Production Area (CPA) before, during, or after manufacturing processes.
7. Maintain a clean, orderly work environment that remains stocked with materials and supplies.
8. Demonstrate general knowledge and consistent practice of good aseptic technique.
9. Perform other duties as required.

Specific Position Duties and Responsibilities:

1. Verify identity and quantity of components/materials for use in manufacturing.
2. Record GMP data on controlled documentation accurately, precisely, contemporaneously.
3. Transport hazardous and non-hazardous materials into/out of manufacturing area.
4. Wash, sanitize, and utilize material carts / bins / totes.
5. Complete and maintain training records within expected timelines.
6. Identify and help implement process, procedure, safety improvements.
7. Seek value-added tasks during unplanned downtime.

Behavioral Expectations:

1. Strong work ethic and ability to accomplish tasks without supervision.
2. Ability to understand abstract concepts, such as sterility, contamination, etc.
3. Excellent interpersonal skills with the ability to cooperate with others in a high-performance setting.
4. Strong mathematical and organizational skills.
5. English communication skills, both written and verbal.
6. Must possess honesty and integrity, commitment to the highest legal and ethical standards
7. Ability to treat every person with courtesy and respect
8. Demonstrate ownership and accountability to production schedule without compromising product quality
9. Desire to work with others and share best practices with colleagues on their shift and on other shifts
10. Knowledge of fundamental cGMP and regulatory principles

Physical Requirements:

1. The Production Associate position requires the ability to
   1. Routinely lift up to 50 pounds
   2. Stand for periods lasting up to 6 hours of an 8-hour shift
   3. Properly gown for entry into the controlled manufacturing area

Work Experience and Education Requirements:

• A High School Diploma or GED