Lead Vaccine Manufacturing Technician

Boehringer Ingelheim Pharmaceuticals, Inc.; Athens (GA); Vor Ort; USD 28.000 - 39.000; Vollzeit

Zusammenfassung

Boehringer Ingelheim Pharmaceuticals, Inc. in Georgia is seeking a Technician IV to manufacture animal health vaccine active ingredients in an aseptic clean room following defined procedures and USDA regulations. The role emphasizes teamwork, problem solving, adherence to cGMP, and continuous improvement through coaching and training while handling documentation and site projects.

Strong communication and organizational skills are required. The scheduled shift is 6:45am–5:15pm (10 hours).

Qualifikationen

• High School Diploma or equivalent.
• Preferred Biology Degree or related field with 3+ years laboratory or manufacturing experience.
• Strong math, problem solving, and documentation skills.
• Proficient with Microsoft Office and basic data handling.
• Excellent oral and written communication and teamwork.

Aufgaben

• Prepare vaccine components in aseptic clean room using virus/bacterial and cell culture techniques per USDA regulations.
• Ensure SOP compliance and train/new employees on required skills.
• Review in-process documentation for accuracy and compliance; maintain technical data and support documentation.
• Initiate/root cause analysis and implement corrective and preventative actions; escalate production flow disturbances.
• Demonstrate commitment to EHS (Environment, Health, and Safety) programs and initiatives.
• Participate in site projects and change control management.

Kenntnisse

Basic math

MS Office

Communication

Teamwork

Problem solving

Leadership

Time management

Attention to detail

Aseptic technique

Lean manufacturing

Ausbildung

High School Diploma or equivalent

Biology degree (preferred)

Jobbeschreibung

Boehringer Ingelheim Pharmaceuticals, Inc. in Georgia is seeking a Technician IV to manufacture animal health vaccine active ingredients in an aseptic clean room following defined procedures and USDA regulations. The role emphasizes teamwork, problem solving, adherence to cGMP, and continuous improvement through coaching and training while handling documentation and site projects.

Strong communication and organizational skills are required. The scheduled shift is 6:45am–5:15pm (10 hours).