Associate Scientist, Bio QC 1st shift Mon-Fri

Boehringer Ingelheim; Saint Joseph (MO); On-site; USD 65,000 - 85,000; Full time

Job summary

A leading company in the pharmaceutical industry is seeking an Associate Scientist for their Bio QC team. In this role, you will perform various bio-analytical tests on raw materials and finished products, ensuring compliance with stringent regulatory guidelines. Ideal candidates will demonstrate industrial experience and a solid educational background in a scientific discipline, emphasizing teamwork and effective communication.

Qualifications

• 5+ years of relevant Bio QC testing or related experience in a cGMP environment preferred.
• Knowledge of bio-analytical methods for bio QC tests.
• Documents results clearly and accurately.

Responsibilities

• Performs routine testing and prepares reagents/materials.
• Calculates test results and communicates status/concerns.
• Trains others on methods and procedures.

Skills

Scientific principles

Communication

Teamwork

Education

High school degree or GED

Associate's degree in relevant scientific discipline

Bachelor's degree in relevant scientific discipline

Tools

Word

Excel

QM software (SAP)

MRP inventory software

Document Management System

Job description

Join to apply for the Associate Scientist, Bio QC 1st shift Mon-Fri role at Boehringer Ingelheim

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. A Bachelor's degree with one or more (1+) years of Bio QC testing experience in a cGMP or similar 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.

Why Boehringer Ingelheim? With us, you can develop your own path in a company that values our differences as strengths and aims to make a difference in healthcare. We prioritize your development, support a healthy work environment, and invest in your wellbeing. Join us to help transform lives for generations.

Visit https://www.boehringer-ingelheim.com

Seniority level

• Associate

Employment type

• Full-time

Job function

• Research, Analyst, and Information Technology

Industries

• Pharmaceutical Manufacturing