Onsite Night-Shift Filling & Inspection Associate

Boehringer Ingelheim GmbH; Fremont, Northern (CA, KY); Hybrid; USD 75,000 - 122,000; Full time

Benefits offered by this job

Discretionary bonus

Relocation assistance

Job summary

Böhringer Ingelheim GmbH in Fremont, CA, seeks a Sr Manufacturing Associate for Filling and Visual Inspection on onsite night shift (Sunday–Thursday, 10pm–6:30am). The role executes unit operations in a multi-product facility and coordinates with management and other teams to maintain compliant, efficient production.

The position requires GMP/cGMP experience, strong documentation and teamwork skills, and the ability to operate in a high-precision manufacturing environment.

Qualifications

• GMP-regulated industry experience (2+ years).
• Strong written and verbal communication.
• Ability to work with computer-based systems.
• Ability to read and understand SOPs and document work in a written format applying cGMP standards.
• Detail-oriented in a complex technical setup with a Quality mindset.
• Able to work as part of a high performing team and adapt schedules.

Responsibilities

• Perform basic Filling or Visual Inspection operations.
• Execute low-to-moderate complexity continuous improvement projects.
• Coordinate shift change information between departments.
• Stock consumables and discard expired reagents; report anomalies.
• Maintain production areas per 5S standards.
• Document work per cGMP using batch records, logbooks, or SOP attachments.
• Identify and correct problems in real time; support quality investigations.

Skills

GMP experience

cGMP

Documentation

Attention to detail

Verbal communication

Team collaboration

Education

Associate degree

Bachelor's degree

Biotechnology training

Tools

MAXIMO

LIMS

BioMES

Job description

Böhringer Ingelheim GmbH in Fremont, CA, seeks a Sr Manufacturing Associate for Filling and Visual Inspection on onsite night shift (Sunday–Thursday, 10pm–6:30am). The role executes unit operations in a multi-product facility and coordinates with management and other teams to maintain compliant, efficient production.

The position requires GMP/cGMP experience, strong documentation and teamwork skills, and the ability to operate in a high-precision manufacturing environment.