Quality Control Analyst II

Quality Control Analyst Role Overview

Join an innovative organization dedicated to maintaining the highest standards of quality and precision within the pharmaceutical and biotech industries. This role will provide an opportunity to contribute significantly to quality control operations from development through commercialization.

Key Responsibilities

• Conduct routine and complex analytical assays to support raw materials, in-process samples, product release, and stability studies.
• Maintain training records, adhere to testing schedules, and ensure the timely completion of assignments.
• Assist in maintaining laboratory equipment, inventory, and preparation of reagents and samples.
• Submit data promptly and review to ensure accuracy and availability.
• Perform operational tasks such as raw material sampling, environmental monitoring, and product testing.
• Update controlled documents including SOPs, work instructions, and test methods for continuous improvement.
• Adhere to internal policies and regulatory standards (e.g., GMP, GLP, ICH guidelines).
• Collaborate with cross-functional teams to support seamless quality control operations.
• Participate in ongoing training to enhance expertise in QC techniques and regulatory compliance.
• Support inspection readiness activities and assist during audits and inspections.
• Contribute to continuous improvement initiatives to enhance laboratory efficiency.
• Work closely with departments such as Manufacturing, Materials Management, and Quality Assurance to align with business goals.

Qualifications

• A degree in chemistry, biology, biochemistry, or a related scientific field (Associate's Degree or Biotech Certificate considered).
• Experience in a regulated laboratory setting, preferably in Quality Control within the pharmaceutical or biotech industry.
• Proficiency in data analysis is preferred.
• Strong attention to detail and the ability to adapt to shifting priorities.
• Effective communication and teamwork skills in a collaborative environment.
• Familiarity with LIMS, Excel, Word, and PowerPoint is advantageous.

Compensation

Competitive hourly rate ranging from $30 to $45.

This is an exciting opportunity to be part of a forward-thinking organization in the life sciences sector, committed to excellence and continuous improvement. Engage in a role that prioritizes quality, teamwork, and regulatory compliance.