Pharmaceutical Lead Production Technician:
Bryllan LLC

1556319663
Bryllan LLC
Brighton Tennessee
Pharmaceutical
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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 a Lead Production Technician to execute various operations of pharmaceutical manufacturing at the Brighton facility. The duties of the Lead Production Technician cover all aspects of production, including but not limited to: Dispensing, Formulation, Aseptic Filling, and Packaging.

A Lead Production Technician 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 function through the safe use of equipment in compliance with established company and regulatory safety requirements.
* Ensure quality standards and best practices are followed throughout the manufacturing process.
* Maintain function understanding of cGMP's and the impact of deviation from controlled processes and/or procedures. Participate in investigations as needed.
* Perform equipment change-over, set-up, and cleaning for manufacturing processes.
* Maintain a clean, orderly work environment that remains stocked with materials and supplies.
* Troubleshoot basic mechanical operations/equipment in support of manufacturing until operations.
* Operate and navigate equipment functionally through routine interaction with a Human-Machine Interface (HMI) or Supervisory Control and Data Acquisition (SCADA) systems.
* Utilize manufacturing knowledge and experience to revise and improve procedures and processes.
* Perform batch documentation review during manufacturing operations.
* Review batch documentation during revisions or modifications.
* Represent production in meetings (project, scheduling, investigation review, etc.) as needed.
* Demonstrate general knowledge and consistent practice of good aseptic technique.
* Verify identity and quantity of components/material for use in manufacturing.
* Initiate and monitor equipment cycles (CIP, SIP, Decontamination, etc.)
* Transport hazardous and non-hazardous materials into/out of manufacturing area.
* Complete and maintain training records within expected timelines.
* Load and un-load materials into and out of rapid transfer ports, isolators.
* Perform other duties as required.

Specific Position Duties and Responsibilities:

* Coordinate technician resources to meet the production schedule
* Train/mentor less experience operators.
* Assist with activity prioritization when necessary
* Foster training of fellow technicians through activity demonstration and On the Job Training (OJT)
* Provide accurate production data and reproducible timelines in support of manufacturing metrics
* Provide decisive and critical problem-solving skills when unexpected events occur.

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.
* Basic computer skills (proficient in Microsoft Office applications).
* 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 curtesy 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.
* Strong knowledge of fundamental cGMP and regulatory principles.

Physical Requirements:

* 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 & Education Requirements:

Minimum of 6 years' experience in the pharmaceutical or related industry through a combination of education and work experience:

Bachelor of Science in Life Sciences or Engineering with 2 years' experience in Pharmaceutical or Medical Environments

Associates Degree with 2-4 years' experience in Pharmaceutical or Medical Environments

High School Diploma or GED with 5-6 years' experience in Pharmaceutical or Medical Environments