Associate at Bryllan LLC in Brighton, MI

📌 Brighton 🏷️ Other 🕑 2021-07-24
View Application

You will be redirected to Bryllan LLC's preferred application process.

Pharmaceutical - Inspection, Labeling, and Packaging Associate

Bryllan is hiring an Inspection, Labeling, and Packaging Associate to execute various operations of pharmaceutical manufacturing at the Brighton facility. The duties of the Inspection, Labeling, and Packaging Associate cover several aspects of production, including but not limited to: Inspection, Labeling, Packaging, and Cleaning/Disinfection of the Controlled Production Area. The Inspection, Labeling, and Packaging Associate ensures a clean, safe workplace and quality production of drug product adhering to current Good Manufacturing Practices (GMP's).A Inspection, Labeling, and Packaging Associate is a member of the Operations team, responsible for the safe, efficient, and routine manufacturing of drug product.
Essential Duties and

Responsibilities

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

Responsibilities

Verify identity and quantity of components/materials for use in manufacturing. Record GMP data on controlled documentation accurately, precisely, contemporaneously. Transport hazardous and non-hazardous materials into/out of manufacturing area. Wash, sanitize, and utilize material carts / bins / totes. Complete and maintain training records within expected timelines. Identify and help implement process, procedure, safety improvements. Seek value-added tasks during unplanned downtime. Behavioral Expectations: Strong work ethic and ability to accomplish tasks without supervision. Excellent interpersonal skills with the ability to cooperate with others in a high-performance setting. Strong mathematical and organizational skills. English communication skills, both written and verbal. Must possess honesty and integrity, commitment to the highest legal and ethical standards.
Ability to treat every person with courtesy and respect.
Demonstrate ownership and accountability to production schedule without compromising product quality.
Desire to work with others and share best practices with colleagues on their shift and on other shifts.
Knowledge of fundamental cGMP and regulatory principles.
Physical

Requirements

The Inspection, Labeling, and Packaging Associate position requires the ability to Routinely lift up to 50 pounds.
Stand for periods lasting up to 6 hours of an 8-hour shift Properly gown for entry into the controlled manufacturing area.
Work

Experience

&

Education

RequirementsAn Associate's Degree and/or 2-3 years of equivalent industry experience

View Application

You will be redirected to Bryllan LLC's preferred application process.

You will be redirected to Bryllan LLC's preferred application process.

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