Manufacturing Technician III - Accellix

bioMerieux Inc.; Lombard (IL); On-site; USD 37,195 - 53,726; Full time

Benefits offered by this job

Medical, dental, vision plans

Life Insurance

Disability Insurance

Retirement plan

Adoption assistance

Wellness programs

Employee Assistance Program

Commuter benefits

Voluntary benefits

Discount programs

Parental leaves

Job summary

bioMerieux Inc. in Illinois is seeking a Manufacturing Technician III - Accellix to prepare, formulate, and manufacture reagents for the Accellix product line in a GMP-regulated environment.

You will perform precision production activities to ensure product quality and accurate documentation. Responsibilities include following approved procedures, monitoring processes, line clearance, and applying continuous improvement initiatives while maintaining safety and compliance.

Qualifications

• Requires high school diploma or equivalent; 4+ years in regulated manufacturing or biotech.
• Experience with precision liquid handling equipment and following detailed procedures.
• Ability to maintain accurate documentation and work in GMP-regulated environments.

Responsibilities

• Prepare and formulate reagents and antibody mixtures per procedures.
• Perform precision liquid handling and verify materials and traceability.
• Maintain process controls, line clearance, and equipment readiness.

Skills

Precision liquid handling

Documentation

Quality compliance

Attention to detail

Teamwork

Microsoft Excel

Microsoft Outlook

Microsoft Teams

Microsoft Word

Education

High School Diploma

Associate degree or technical certification

Tools

Micropipettes

Repeat dispensers

Job description

The Manufacturing Technician III - Accellix is responsible for preparing, formulating, and manufacturing reagents and consumables used in the Accellix product line. This role performs precision production activities that directly impact product quality, assay performance, and customer outcomes. The position works within a GMP-regulated environment and ensures all manufacturing activities are completed safely, accurately, and in compliance with quality standards.

Key Responsibilities

• Prepare and formulate reagents, solutions, and antibody mixtures according to approved procedures.
• Perform precision liquid handling using micropipettes and other dispensing equipment.
• Verify materials, lot numbers, concentrations, and traceability before use.
• Execute manufacturing processes while maintaining strict process controls and tolerances.
• Perform line clearance and verify equipment readiness before production activities.
• Handle biological materials and reagents according to established environmental and storage requirements.
• Monitor manufacturing processes and identify quality, process, or material issues.
• Perform inspections of materials and finished components to ensure quality standards are met.
• Support in-process testing and quality control activities.
• Maintain accurate production records and documentation.
• Participate in investigations, corrective actions, and continuous improvement initiatives.
• Follow GMP, GDP, safety, and quality requirements at all times.
• Perform other duties as assigned.

Qualifications

Required

• High School Diploma, GED, or equivalent.
• 4+ years of experience in manufacturing, laboratory, biotechnology, pharmaceutical, diagnostics, or a related regulated environment; including:
  • experience using precision liquid handling equipment such as micropipettes or repeat dispensers.
  • experience following detailed procedures and maintaining accurate documentation.

Preferred

• Associate degree or technical certification in Biotechnology, Biology, Chemistry, or a related field.
• Experience in laboratory-based or precision manufacturing environments.
• Experience working in GMP-regulated manufacturing.

Skills & Abilities

• Strong attention to detail and commitment to quality.
• Ability to follow detailed procedures and work instructions.
• Knowledge of reagent handling, traceability, and controlled manufacturing processes.
• Strong troubleshooting and problem-solving skills.
• Ability to manage multiple priorities in a fast-paced environment.
• Effective communication and teamwork skills.
• Proficiency with Microsoft Outlook, Teams, Word, and Excel.
• Commitment to safety, compliance, and continuous improvement.

Working Conditions

• Ability to sit or stand for extended periods.
• Ability to wear required PPE for extended periods.
• Ability to lift and move up to 50 pounds.
• Manufacturing and laboratory environment requiring adherence to quality and safety standards.

The estimated salary range for this role based in Illinois is between $27.00 - $38.80. This role is eligible to receive a variable annual bonus based on company, team, and individual performance per bioMerieux's bonus program. This range may differ from ranges offered for similar positions elsewhere in the country given differences in cost of living. Actual compensation within this range is determined based on the successful candidate's experience and will be presented in writing at the time of the offer.

• A choice of medical (including prescription), dental, and vision plans providing nationwide coverage and telemedicine options
• Company-Provided Life and Accidental Death Insurance
• Short and Long-Term Disability Insurance
• Retirement Plan including a generous non-discretionary employer contribution and employer match.
• Adoption Assistance
• Wellness Programs
• Employee Assistance Program
• Commuter Benefits
• Various voluntary benefit offerings
• Discount programs
• Parental leaves

BioMerieux Inc. and its affiliates are Equal Opportunity/Affirmative Action Employers. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information. Please be advised that the receipt of satisfactory responses to reference requests and the provision of satisfactory proof of an applicant's identity and legal authorization to work in the United States are required of all new hires. Any misrepresentation, falsification, or material omission may result in the failure to receive an offer, the retraction of an offer, or if already hired, dismissal. If you are a qualified individual with a disability, you may request a reasonable accommodation in BioMerieux's or its affiliates' application process by contacting us via telephone at [phone], by email at [emailprotected], or by dialing 711 for access to Telecommunications Relay Services (TRS).