Associate Scientist, Bio QC

Boehringer Ingelheim GmbH; Athens (GA); Hybrid; USD 65,000 - 90,000; Full time

Job summary

Boeehringer Ingelheim GmbH is seeking an Associate Scientist, Bio QC to perform bio-analytical testing across immunological, in vivo, microbiological, molecular, or virological assays in a cGMP environment. You will initiate, execute and complete assays, maintain reagents and equipment, and communicate results to supervisors while adhering to regulatory guidelines and quality standards.

Eligibility includes work authorization in the United States; strong documentation, teamwork, and data

Qualifications

• High school diploma or GED with 5 years of Bio QC testing in a cGMP or similar environment.
• Associate degree with 2 years Bio QC testing in a cGMP or similar environment.
• Bachelor's degree in relevant scientific discipline with 1+ year Bio QC testing in a cGMP or similar manufacturing environment is preferred.
• Knowledge of basic scientific principles and techniques.
• Ability to communicate clearly and document results accurately.

Responsibilities

• Perform routine testing using laboratory assays.
• Maintain reagents, supplies and calibrated equipment.
• Prepare reagents and materials.
• Calculate test results.
• Communicate schedule, test status and concerns to supervisors.
• Review and approve results and test sheets.
• Train others on methods and procedures.

Skills

Communication

Teamwork

Documentation

Data management

Laboratory techniques

Education

High school diploma or GED

Associate degree in relevant science

Bachelor's degree in relevant science

Tools

SAP QM software

MRP inventory software

Document Management System

Microsoft Word

Microsoft Excel

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).