Manufacturing Technician I

Medix Biochemica•Weston, FL

57d•Onsite

About The Position

Bioresource Technology, Inc. (BRT), a Medix Biochemica company in Weston, Florida, is seeking a Manufacturing Technician II to support daily manufacturing and production operations in a regulated life sciences environment. The position performs manufacturing activities, supports equipment setup and operation, maintains accurate production documentation, and follows applicable quality, safety, and regulatory standards. The posting describes the role as an experienced technician who can work independently on routine manufacturing processes and assist with troubleshooting, training, and continuous improvement initiatives.

Requirements

High school diploma or equivalent required.
Associate degree in Biotechnology, Biology, Chemistry, Manufacturing Technology, or a related scientific or technical field preferred.
Minimum of 2–4 years of manufacturing or production experience in biotechnology, medical device, pharmaceutical, diagnostics, or a related regulated industry preferred.
Experience in GMP, ISO, FDA-regulated, or quality-controlled environments strongly preferred.
Understanding of manufacturing operations, production workflows, and documentation.
Ability to follow detailed procedures and maintain accurate documentation.
Strong attention to detail and organizational skills.
Ability to identify and appropriately escalate operational issues.
Strong communication and teamwork skills.
Ability to work independently with limited supervision.
Proficiency with Microsoft Office and basic computer systems.
Ability to stand, walk, bend, and regularly lift up to 40 pounds.
Ability to work in laboratory and manufacturing environments and wear required PPE, including gloves, lab coats, hair coverings, and safety equipment as required.

Nice To Haves

Associate degree in Biotechnology, Biology, Chemistry, Manufacturing Technology, or a related scientific or technical field.
Two to four years of manufacturing or production experience in biotechnology, medical device, pharmaceutical, diagnostics, or a related regulated industry.
Experience in GMP, ISO, FDA-regulated, or quality-controlled environments.
Basic mechanical aptitude and troubleshooting ability.
Comfort working with laboratory and manufacturing equipment.

Responsibilities

Perform manufacturing, processing, and production activities according to approved procedures, batch records, and work instructions.
Prepare materials, reagents, buffers, and equipment for manufacturing activities.
Operate, clean, sanitize, and maintain manufacturing equipment and work areas.
Complete inventory and quality documentation accurately in compliance with GMP/ISO requirements.
Document manufacturing activities contemporaneously and accurately in accordance with GMP/ISO requirements.
Promptly escalate deviations, atypical observations, equipment concerns, and documentation discrepancies to the supervisor.
Assist with troubleshooting operational and process-related issues to minimize downtime and maintain productivity.
Support inventory handling, labeling, storage, and cycle counts.
Participate in equipment calibration, preventative maintenance coordination, and process verification activities.
Follow applicable safety, environmental, and quality procedures and requirements.
Support internal audits, inspections, and continuous improvement initiatives.
Train and assist Manufacturing Technician I employees as needed in a non-supervisory capacity.
Collaborate with Quality, Supply Chain, Operations, and R&D teams.
Maintain a clean, organized, and inspection-ready manufacturing environment.
Perform additional duties as assigned based on business needs.