Associate Scientist, Quality Control

ZipRecruiter; Worcester; On-site; GBP 30,000 - 50,000; Full time

Job summary

An established industry player is seeking an Associate QC Scientist to join their dynamic team. In this pivotal role, you will perform laboratory testing within a GMP environment, ensuring the quality and safety of products. Your responsibilities will include analyzing test data, maintaining compliance with GMP standards, and supporting laboratory investigations. This position offers a unique opportunity to contribute to innovative solutions that address serious health issues. If you are passionate about science and quality control, this role is perfect for you.

Qualifications

• 2+ years of GMP and QC experience in laboratory settings.
• Knowledge of various laboratory techniques and data analysis.

Responsibilities

• Perform laboratory testing in a GMP environment for product release.
• Maintain GMP standards and support lab investigations.

Skills

GMP Experience

QC Techniques

Data Analysis

Education

BA/BS in Chemistry

BA/BS in Biochemistry

BA/BS in Biology

Tools

IR Spectroscopy

FTIR

UV-Vis Spectroscopy

SoloVPE

Truscan

Job description

Job Description

Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn, and TikTok.

Job Overview

Purpose:

The Associate QC Scientist performs laboratory testing within a GMP environment supporting raw materials, in-process, final bulk products, stability, or validation. Responsibilities include analyzing test data, writing procedures with guidance, managing time efficiently, trending data, and assisting in lab investigations.

Key Responsibilities

1. Perform test methods to support product/material release.
2. Maintain a safe work environment in accordance with procedural requirements.
3. Implement and maintain GMP standards for laboratory records, procedures, and systems.
4. Perform various laboratory techniques as trained.
5. Complete assigned tasks responsibly and foster a positive team environment.
6. Revise procedures as needed and support departmental functions.
7. Maintain trend reports supporting departmental performance.
8. Support laboratory investigations.

Qualifications

• BA/BS in Chemistry, Biochemistry, Medical Technology, Biology, or related science.
• 2+ years of GMP and QC experience, with knowledge of techniques like IR, FTIR, UV-vis, SoloVPE, Truscan.
• Maintain necessary certifications for job tasks.

Additional Information

Details about pay range, benefits, and equal opportunity employment are provided, emphasizing compliance with legal requirements and company policies.