Quality Control Analyst I

Immediate need for a talented Quality Control Analyst I. This is a 03+ Months contract with possible extension opportunity with long-term potential and is located in St. Paul, MN (Onsite). Please review the job description below and contact me ASAP if you are interested.
 
Job ID:25-64957
 
Pay Range: $23 - $24/hour.  Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location).
 
Key Responsibilities:

• Conduct biological, chemical, and physical analyses on pharmaceutical products (biologics and drugs) and medical devices throughout the manufacturing process, from raw materials to finished goods, Includes participation in environmental monitoring programs.
• Essential Duties and Responsibilities:
• Perform critical testing on raw materials, in-process samples, final products, and environmental monitoring samples.
• Operate laboratory instrumentation and computer systems (e.g., LIMS) to collect and record data.
• Execute precise analytical assays with a strong understanding of biology and chemistry principles.
• Complete all testing, including special project/protocol testing, in a timely manner.
• Ensure data integrity and compliance with SOPs, FDA, GLP, QSR, and cGMP regulations.
• Write and review exception documents.
• Participate in cross-functional teams to improve production efficiency, quality, and cost-effectiveness.
• Conduct laboratory and manufacturing audits as required.
• Review and update plant SOPs as needed.
• Perform equipment maintenance and calibrations (if required).
• Additional duties as assigned.

Key Requirements and Technology Experience:

• Key Skills:Proficiency in conducting biological, chemical, and physical analyses.
• Strong understanding of lab instrumentation (e.g., LIMS, analytical equipment).
• Ability to perform precise assays while adhering to SOPs, cGMP, and FDA regulations.
• Ability to multitask efficiently and meet deadlines.
• Proficient in computer systems and data entry.
• Detail-oriented with strong reading comprehension.
• Basic understanding of laboratory instrumentation.
• Effective communication with supervisors and peers.
• Fluency in English (reading, writing, and verbal).
• Ability to navigate PC-based systems for training, performance management, and self-service.
• Strong interpersonal skills and ability to work in a team environment.
• Knowledge of cGMP manufacturing and laboratory safety procedures.
• Familiarity with lab and production equipment (autoclaves, process tanks, incubators, CIP/SIP systems, etc.).
• Strong analytical and problem-solving skills.
• Personal Attributes:
• Integrity, work ethic, sound judgment, and intellectual honesty.
• Pragmatic, courageous, and results driven.
• Passion for innovation and continuous improvement.
• Uncompromising dedication to quality.
• Required: Bachelor’s degree in Chemistry, Biological Sciences, or related field with coursework in Analytical Chemistry or Laboratory Sciences.
• Experience: 0-2 years in a laboratory or pharmaceutical manufacturing setting.
• Certifications: Additional certifications may be required per state/federal regulations.

Our client is a leading Pharmaceutical Industry, and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration.
 
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