QC Chemist I

Greenfield Global • Brookfield, CT

17h • Onsite

About The Position

Greenfield is looking for an QC Chemist I to join our growing team. The Brookfield site is a critical manufacturing facility for specialty chemical ingredients for pharmaceutical excipients, food flavors, beverages, and industrial alcohol blends. The entry-level position entails performing routine lab analysis, data entry, and ensuring the maintenance of lab equipment. As a team member, you will contribute to the overall success of the laboratory by conducting various analytical tests, documenting results, and maintaining a safe and organized work environment.

Requirements

• Bachelor's degree in chemistry, biochemistry, or related fields.
• A solid foundation in analytical chemistry is preferred.
• Previous experience working in an analytical laboratory setting, with proficiency in operating and maintaining analytical instruments such as GC and UV-Vis spectroscopy.
• Experience with other relevant techniques is a plus.
• Knowledge of Good Manufacturing Practices (GMPs) and regulatory guidelines is preferred, particularly in laboratory operations.
• Strong attention to detail and accuracy, ensuring meticulous documentation and adherence to established protocols.
• Excellent problem-solving and troubleshooting skills, with the ability to identify and address issues promptly.
• Effective communication skills, both written and verbal, allowing for clear and concise reporting and collaboration with team members.
• Ability to work independently with minimal supervision while being a proactive and reliable team player.

Responsibilities

• Conduct routine and non-routine analyses of raw materials, in-process samples, final products, and stability samples for product release. This involves following established testing procedures accurately and efficiently.
• Utilize various analytical testing techniques such as Gas Chromatography (GC), UV-Visible spectroscopy, titrations, and other relevant methods.
• Perform required performance verifications (PV's) on all applicable instrumentation.
• Be observant of all laboratory equipment and instrumentation calibration requirements, assuring instruments are properly calibrated, maintained, and operated in accordance with Standard Operating Procedures (SOPs).
• Maintain accurate and timely documentation of all analytical testing processes and outcomes. Prepare and review data. Ensure that results are recorded and archived appropriately in compliance with regulatory requirements.
• Assist in developing and writing departmental procedures, work instructions, test methods, and SOP (Standard Operating Procedure).
• Assist in the investigation and troubleshoot any analytical testing issues that may arise, collaborating with team members to identify and address potential root causes. Communicate findings effectively and propose potential solutions or corrective actions as needed.
• Uphold a clean, safe, and organized laboratory environment in compliance with current Good Manufacturing Practices (cGMP) guidelines and regulations. Follow established safety protocols and focus on cleanliness and orderliness to ensure a productive and hazard-free workspace.
• Participate in company safety and other training programs.
• Maintain effective communication relationships bot within function and across functions withing the organization.
• Develop basic competency in ERP system.

Benefits

• Comprehensive health and dental benefits
• Income protection: short- and long-term disability coverage, life insurance, paid personal sick time
• Vacation time exceeding industry standards
• Company funded retirement savings program with individual contribution opportunities

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level