This is an excellent opportunity for a laboratory professional who enjoys hands-on analytical work and wants to grow within a collaborative, science-driven environment focused on quality, continuous improvement, and operational excellence.

The level of Analyst I or Analyst II will be determined based on the candidate’s education, laboratory experience, technical skills, and demonstrated level of independence.

Benefits include, but are not limited to:

• Up to 4 weeks of paid time off.
• Paid holidays.
• Medical, dental, vision, and prescription coverage (employees & eligible dependents).
• 401(k) retirement plan with employer match.
• Opportunities for professional growth and continued learning.
• Stable, full-time employment.

The Analyst will perform testing in accordance with current Good Manufacturing Practices (cGMP), Good Laboratory Practices (cGLP), Standard Operating Procedures (SOPs), validated test methods, and established laboratory procedures.

The position requires strong attention to detail, sound analytical judgment, accurate documentation, and the ability to identify and communicate laboratory or analytical issues that may affect product quality, compliance, or laboratory operations.

· Perform analytical testing of bioanalytical specimens, including blood, urine, and tissue samples.

· Analyze production and research samples using laboratory instrumentation and established analytical techniques.

· Operate, maintain, calibrate, and troubleshoot laboratory equipment and analytical instrumentation.

· Execute analytical methods in accordance with approved Test Methods (TSMs), SOPs, protocols, and validated procedures.

· Accurately document analytical activities, observations, calculations, results, and equipment use in accordance with applicable requirements.

· Review analytical data for accuracy, completeness, and compliance with established acceptance criteria.

· Identify, investigate, and communicate analytical, equipment, or procedural issues that may affect product identity, strength, quality, purity, compliance, or laboratory efficiency.

· Assist with laboratory equipment qualification, validation, calibration, and maintenance activities.

· Support laboratory investigations, deviations, out-of-specification/out-of-trend investigations, and corrective and preventive actions, as applicable to the position level.

· Assist in the preparation, revision, review, and maintenance of test methods, SOPs, protocols, reports, and other quality documentation.

· Support Research & Development projects and analytical laboratory investigations.

· Maintain laboratory inventory, Safety Data Sheets (SDS), and assist with purchasing laboratory supplies.

· Complete required training and maintain current training records.

· Participate in continuous improvement initiatives designed to improve laboratory efficiency, quality, compliance, and reliability.

· Communicate effectively with Quality Assurance, Quality Control, Manufacturing, Research & Development, and other departments as required.

· Perform other duties as assigned.

Quality Control Analyst I is an early-career laboratory professional who performs routine analytical testing under established procedures and appropriate supervision.

· Bachelor's degree in Chemistry, Biology, Biochemistry, Pharmaceutical Sciences, or another related scientific discipline preferred.

· One (1) year of relevant laboratory experience preferred.

· Laboratory experience in a pharmaceutical, biotechnology, medical device, academic, research, or other scientific environment will be considered.

· Equivalent combinations of education and relevant laboratory experience will be considered.

Quality Control Analyst II is an experienced laboratory professional capable of performing analytical testing with greater independence and technical judgment.

· Bachelor's degree in Chemistry, Biology, Biochemistry, Pharmaceutical Sciences, or another related scientific discipline preferred.

· Two (2) to three (3) or more years of progressively responsible laboratory experience preferred.

· Experience in a regulated pharmaceutical, biotechnology, medical device, or other GMP environment strongly preferred.

· Demonstrated experience with analytical laboratory instrumentation and laboratory testing.

· Experience with laboratory investigations, equipment qualification/validation, analytical method validation, or related quality activities is a plus.

· Equivalent combinations of education and relevant laboratory experience will be considered.

· Working knowledge of cGMP and cGLP requirements.

· Strong analytical, critical-thinking, and problem-solving skills.

· Experience operating and troubleshooting analytical laboratory instrumentation.

· Strong attention to detail and commitment to data accuracy and integrity.

· Ability to recognize and communicate laboratory, analytical, equipment, or quality issues.

· Ability to read, interpret, and follow technical documents, SOPs, test methods, protocols, and laboratory procedures.

· Strong written and verbal communication skills.

· Proficiency with Microsoft Office applications.

· Ability to work independently while collaborating effectively with a cross-functional team.

· Ability to manage multiple priorities in a laboratory environment.

· Commitment to safety, quality, compliance, accuracy, and continuous improvement. 

· Ability to occasionally lift up to 20 pounds.

· Ability to stand, sit, walk, bend, reach, and perform routine laboratory activities as required.

· Ability to work safely in a laboratory environment and wear required personal protective equipment (PPE).

The Company is committed to providing reasonable accommodations to qualified individuals with disabilities to enable them to perform the essential functions of the position. 

· Night Shift 

· Consistent weekday schedule.

· Specific schedule and hours may vary and are subject to change based on business needs.

· $25.00-$28.00 per hour, based on qualifications and experience.

· Stable, full-time opportunity.

· Growth potential within Quality Control and pharmaceutical manufacturing.

Join a team where your scientific knowledge and laboratory expertise contribute directly to quality, compliance, product integrity, and continuous improvement.