Production Associate Shift Premiums Available (ALL SHIFTS AVAILABLE)

Bryllan LLC; Brighton (MI); On-site; USD 24,796 - 33,062; Full time

Job summary

Biovire is seeking a Production Associate to execute pharmaceutical manufacturing operations at the Brighton facility. The role emphasizes adherence to MBRs/SOPs, accurate documentation, and strict aseptic technique within a cGMP environment.

Responsibilities include verifying components, recording GMP data, handling materials, and maintaining training records; candidates should have an associate degree or relevant experience and a high school diploma or GED.

Qualifications

• Associate's Degree and/or 2–3 years of relevant industry experience preferred.
• High School Diploma or GED required.
• Background check will be completed.

Responsibilities

• Follow issued MBRs and SOPs for manufacturing processes.
• Accurately complete production documentation during operations.
• Perform visual inspection of finished product per SOPs.
• Maintain safety and compliance with cGMP and procedures.
• Uphold quality standards and best practices throughout production.
• Maintain clean CPA area and proper aseptic technique.
• Keep work area organized and stocked with materials.
• Perform additional duties as assigned.

Skills

Attention to detail

Team collaboration

English communication

Mathematical skills

Organizational skills

Education

Associate's Degree

High School Diploma or GED

Job description

General Description

Biovire is hiring a Production Associate to execute various operations of pharmaceutical manufacturing at the Brighton facility.

Duties And Responsibilities

A Production Associate is a member of the Production 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.
• Follow SOP's to complete visual inspection of finished product (with the aid glasses or contact lenses as applicable).
• 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.
• Demonstrate general knowledge and consistent practice of good aseptic technique.
• 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.
• Ability to understand abstract concepts, such as sterility, contamination, etc.
• 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 Production 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
• Pass annual vision tests (including color blindness) with or without the aid of glasses and/or contact lenses due to completing routine visual inspection of finished product as an essential job function

Work Experience And Education Requirements

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

High School Diploma or GED Required

Employment at Biovire is contingent upon a successful Background check.