US_Associate Scientist, Bio QC

Boehringer Ingelheim GmbH

Saint Joseph (MO)

On-site

USD 60,000 - 90,000

Full time

2 days ago
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Job summary

Boehringer Ingelheim is seeking an Associate Scientist, Bio QC to perform a range of bio-analytical tests on raw materials, in-process, release, and stability samples in a cGMP setting.

The role requires strong organizational skills, clear communication, and the ability to train others while maintaining compliant documentation and QA procedures. Eligibility to work in the U.S. is required.

Qualifications

  • Requires science background and relevant Bio QC testing experience in a cGMP environment.
  • Experience with data management and compliant documentation practices.
  • Proficiency with Word/Excel and QA software used for data handling.

Responsibilities

  • Performs routine Bio QC testing on materials and samples.
  • Maintains reagents, supplies, and calibrated equipment.
  • Prepares reagents and materials and calculates results.
  • Communicates test status and concerns to supervisors.
  • Reviews results and test sheets; revises SOPs as needed.
  • Trains others on methods and procedures.

Skills

Bio QC testing
cGMP compliance
Data management
Communication

Education

High school diploma or GED
Associate's degree in relevant science
Bachelor's degree in science

Tools

SAP
MRP software
Document Management System

Job description

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 several 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.

The Associate Scientist, Bio QC performs bio-analytical methods (immunological, in vivo, microbiological, molecular biological, or virological) for various Bio QC tests on raw materials, in-process, release or stability samples in compliance with 9CFR, EU and VICH regulatory guidelines, Outlines of Production and Special Outlines. This role initiates, executes and completes assays as per validated procedures and within Quality and Compliance guidelines and communicates testing results, compliance and/or scheduling issues to supervisors.

Duties & Responsibilities
  • Performs routine testing using a portion of the existing laboratory assays.
  • Maintains laboratory reagents, supplies and calibrated equipment.
  • Prepares reagents and materials.
  • Calculates test results.
  • Communicates schedule, test status and concerns.
  • Reviews and approves results and test sheets.
  • Revises a Pre-existing Standard Methods and SOPs.
  • Trains others on methods & procedures.
Requirements
  • High school degree or GED with a minimum of five (5) years of relevant Bio QC testing or relevant experience in a cGMP or similar environment.

OR

  • Associate's degree in relevant scientific discipline and a minimum of two (2) years of Bio QC testing or relevant experience in a cGMP or similar environment.

OR

  • Bachelor's degree in relevant scientific discipline with or without additional Bio QC testing experience.
  • Bachelor's degree in a scientific discipline with one-plus (1+) years of Bio QC testing experience in a cGMP or similar manufacturing environment is preferred.
  • Knowledge of basic scientific principles and techniques.
  • Ability to effectively communicate in a clear, concise and appropriate manner.
  • Documents results and data clearly and accurately.
  • Effectively interacts with co-workers and others as needed.
  • Demonstrates teamwork within own group and other internal groups.
  • Use of Word and Excel, QM software for data management (SAP), MRP inventory software, and Document Management System)

Eligibility Requirements:

  • Must be legally authorized to work in the United States without restriction.
  • Must be willing to take a drug test and post-offer physical (if required).
  • Must be 18 years of age or older.
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