Associate I, Quality Control

Sentry BioPharma Services Inc; Edinburgh (IN); On-site; USD 42,000 - 60,000; Full time

Job summary

Sentry BioPharma Services is seeking a Quality Control Associate to ensure the quality and safety of pharmaceutical materials in a collaborative laboratory environment dedicated to high standards in testing and analysis.

Responsibilities include sample handling, aliquoting, equipment setup and calibration, analytical testing, and meticulous data recording, with emphasis on GLP and SOPs. Join a team focused on innovation and career growth in the pharmaceutical industry.

Qualifications

• Bachelor's degree in Chemistry, Biology, or pharmaceutical sciences
• Experience in analytical laboratory settings
• Knowledge of GLP and safety protocols
• Strong documentation and record-keeping
• Ability to follow SOPs and regulatory guidelines

Responsibilities

• Receive, label, and store samples with proper documentation.
• Set up, calibrate, and troubleshoot lab equipment.
• Conduct analytical tests and record results.
• Maintain a clean, compliant lab environment.
• Support other lab functions as needed.

Skills

Quality control

GLP knowledge

Equipment operation

Documentation

Team collaboration

SOP compliance

Education

Bachelor's degree in Chemistry/Biology/Pharmaceutical Sciences

Tools

Pipettes

Balances

Analytical instruments

Job description

Description

Join our dynamic team at Sentry BioPharma Services as a Quality Control Associate, where you will play a vital role in ensuring the quality and safety of pharmaceutical materials. This position offers an excellent opportunity to contribute to a collaborative and innovative laboratory environment dedicated to maintaining the highest standards in pharmaceutical testing and analysis.

Key Responsibilities

• Receive, label, and safely store samples to be tested, ensuring proper documentation and handling.
• Perform aliquoting from bulk containers to obtain precise test samples.
• Organize and store samples in compliance with safety protocols and regulatory requirements to protect personnel and sample integrity.
• Prepare samples prior to testing, including proper labeling and handling.
• Set up, calibrate, and troubleshoot laboratory equipment to ensure accurate and reliable testing results.
• Prepare laboratory equipment and materials for upcoming analyses.
• Conduct analytical tests on pharmaceutical materials, recording and analyzing results accurately.
• Record test data meticulously and report findings in accordance with company and regulatory standards.
• Maintain a clean, organized, and compliant laboratory environment.
• Support other laboratory functions as needed to ensure smooth operations.

Skills and Qualifications

• Prior experience in a quality control laboratory, preferably within the pharmaceutical industry.
• Knowledge of laboratory safety protocols and good laboratory practices (GLP).
• Proficiency in operating laboratory equipment such as pipettes, balances, and analytical instruments.
• Strong attention to detail and excellent organizational skills.
• Ability to troubleshoot and resolve equipment issues efficiently.
• Good documentation and record-keeping skills.
• Effective communication skills and ability to work collaboratively within a team.
• Ability to follow standard operating procedures (SOPs) and regulatory guidelines.

At Sentry BioPharma Services, we foster a culture of innovation, continuous learning, and growth. We are committed to providing a supportive environment where our team members can develop their skills and advance their careers while contributing to meaningful work in the pharmaceutical industry. We offer competitive benefits and opportunities for professional development to help you succeed.

Requirements

• Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, or a related field.
• Preferred experience working in an analytical laboratory. Experience with pharmaceutical analyses, and/or analysis of large molecules, a plus.