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Quality Control Analyst - Contract - Minneapolis, MN

Ensure quality, drive compliance-join us as a QC Analyst and keep standards at their peak.

ºÚÁÏ´«ËÍÃÅ is seeking a Quality Control Analyst for a contract position located in The US. This position requires a proactive individual with strong analytical skills and the ability to work collaboratively in a fast-paced environment.

Primary Responsibilities:

The successful candidate will be responsible for performing routine and specialized quality control testing, maintaining laboratory operations, and ensuring compliance with regulatory standards.

Skills & Requirements:

• Degree in Life Sciences with relevant laboratory coursework.
• Experience in a regulated environment is preferred.
• Proficiency with laboratory instrumentation and software systems.
• Strong understanding of cGMP manufacturing and laboratory safety procedures.
• Effective communication and teamwork skills.
• Knowledge of QC analytical techniques (e.g., HPLC, UPLC, pH, TOC), bioassays (e.g., ELISAs, cell-based assays), and microbiological methods (e.g., endotoxin, bioburden, environmental monitoring).
• Ability to work independently and solve moderately complex problems.
• Physical ability to perform laboratory tasks, including lifting materials up to 30 pounds and working in cleanroom environments.
• Willingness to travel occasionally and participate in on-call rotations if needed.

The Quality Control Analyst's responsibilities will be:

• Perform and review routine in-process drug substance and stability test methods.
• Operate laboratory instruments and systems such as LIMS, SoftmaxPro, Charles River Endoscan, MODA, and Empower.
• Conduct facility monitoring, including Environmental Monitoring and Critical Utilities, as well as product testing.
• Maintain laboratory operations, including cleaning, supply ordering, reagent preparation, stocking, and waste disposal.
• Author and manage quality system events, including laboratory investigations, deviations, CAPAs, and change controls.
• Ensure data integrity and compliance with SOPs, specifications, and cGMP regulations.
• Train new team members on standard procedures and practices.
• Perform equipment maintenance and calibrations as required.
• Participate in cross-functional teams and contribute to problem-solving and decision-making processes.
• Draft and revise SOPs and initiate procedural changes.
• Complete mandatory training and adhere to safety protocols.

If you are having difficulty in applying or if you have any questions, please contact Anderson Maldonado at a.maldonado@proclinical.com

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

ºÚÁÏ´«ËÍÃÅ is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. ºÚÁÏ´«ËÍÃÅ is acting as an Employment Agency in relation to this vacancy.

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