Specialist, Technical Production M-F 8:00pm -4:30am

Boehringer Ingelheim GmbH; Spring Valley Estates (GA); On-site; USD 65,000 - 90,000; Full time

Job summary

Boehringer Ingelheim seeks a Specialist for Technical Production on a night shift (M–F, 8:00pm–4:30am) to support continuous vaccine manufacturing. You will coordinate with groups, lead preparation of active ingredients and components, and help ensure quality, compliance and safety.

The role requires GMP/USDA knowledge, aseptic technique, and strong documentation skills, with a focus on training, process improvement, and cross-functional collaboration.

Qualifications

• High School Diploma plus 3–5 years in related field.
• Biology or Science degree preferred with 3–4 years in related field.
• Solid math, writing and documentation skills.
• Experience with GMP/USDA vaccine manufacturing environment is a plus.

Responsibilities

• Plan, execute and evaluate production protocols/experiments for new product transfers and productivity improvements.
• Oversee training and qualification of team members.
• Review in-process documentation for accuracy and regulatory compliance.
• Initiate root-cause analyses and implement corrective actions; escalate production disturbances.
• Demonstrate commitment to EHS programs and initiatives.
• Provide feedback on individual and team performance in Production.
• Support site projects and initiatives.

Skills

Math skills

Technical writing

Equipment troubleshooting

MS Office / databases

Oral & written communication

Organization & time management

Clean room aseptic technique

GMP & USDA knowledge

Education

High School Diploma

Biology or Science degree

Tools

MS Office

Job description

Specialist, Technical Production M-F 8:00pm -4:30am

Description

To perform support/process duties associated with the continuous manufacture of Boehringer Ingelheim vaccines, will perform and coordinate with other groups and lead the activities associated with the preparation of active ingredient vaccine and components(cells and medias)requirements.As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.

Duties & Responsibilities

• Plans, executes and evaluate outcomes of Production protocols/experiments for new product transfers and productivity improvements. Full participation of direct and indirect tasks as required.
• Oversee and ensure training and qualification of team members.
• Review in process documentation for accuracy and compliance in a timely manner; maintenance of technical data sheets and support documentation.
• Initiate and facilitate root cause analysis and implement corrective and preventative actions to address problems; escalation of production flow disturbances to Team or Group Leader.
• Demonstrate a visible and tangible commitment to EHS (Environment, Health, and Safety) programs and initiatives.
• Provide feedback of individual and team performance in Production.
• Participate and provide support to site projects and initiatives.

Requirements

• High School Diploma or equivalent plus minimum three-five (3-5) years in related field.
• Preferred Biology Degree or Science Degree or in a related field from an accredited institution, plus three-four (3-4) years of experience in related field.
• Basic math skills.
• Technical writing and equipment/automation trouble shooting skills.
• Proficient with Microsoft Office and other database software systems.
• Excellent oral and written communication skills.
• Demonstrated, strong organizational and time management skills with exceptional attention to detail.
• Clean room and aseptic technique knowledge.
• Working knowledge of GMP and USDA requirements for Vaccine Manufacturing.