Associate Scientist, Quality Control (2nd shift, Sun-Wed, 4pm-2:30am)

BioSpace; Worcester (MA); On-site; USD 60,000 - 90,000; Full time

Job summary

An established industry player is seeking an Associate Scientist in Quality Control to join their dynamic team. This role involves performing laboratory testing in a fast-paced GMP environment, ensuring the quality of raw materials and products. The successful candidate will analyze test data, write procedures, and support departmental performance through investigations and trend reports. If you have a passion for science and quality assurance, this opportunity is perfect for you to make a significant impact in the field of healthcare.

Qualifications

• 2+ years of relevant work experience in a GMP environment.
• Ability to analyze test data and write procedures.

Responsibilities

• Perform laboratory testing to support product/material release.
• Maintain GMP standards and a safe work environment.

Skills

Laboratory Testing

Data Analysis

GMP Standards

Collaboration

Education

Bachelor's Degree in Chemistry

Bachelor's Degree in Biochemistry

Bachelor's Degree in Medical Technology

Bachelor's Degree in Biology

Job description

Associate Scientist, Quality Control (2nd shift, Sun-Wed, 4pm-2:30am)

Join to apply for the Associate Scientist, Quality Control (2nd shift, Sun-Wed, 4pm-2:30am) role at BioSpace.

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, along with 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 Description
The Associate QC Scientist performs laboratory testing within a fast-paced GMP environment supporting raw materials, in-process product, final bulk product, stability, and validation. Analyzes test data, evaluates results, writes procedures with guidance, and assists in trending data and lab investigations. The work schedule is Sunday through Wednesday, 4:00pm to 2:30am.

Responsibilities

• Performs test methods as written to support product/material release.
• Maintains a safe work environment in accordance with procedural requirements.
• Implements and maintains GMP standards for laboratory records, procedures, and systems.
• Performs various laboratory techniques as trained.
• Completes assigned tasks responsibly and collaborates positively with team members.
• Revises procedures as necessary and supports departmental performance through trend reports and investigations.

Qualifications

• BA/BS in Chemistry, Biochemistry, Medical Technology, Biology, or a related science field.
• 2+ years of relevant work experience.
• Maintains necessary certifications for assigned tasks.