Quality Control Laboratory Analyst

Description

Make an Impact. Support Quality. Be Part of Something Meaningful.

At Halocarbon, we specialize in high-performance fluorochemistry, developing and manufacturing specialty chemical and pharmaceutical products that support critical applications across a variety of industries. Our work combines technical expertise, innovation, and a commitment to quality, safety, and continuous improvement.

We're seeking a detail-oriented QC Laboratory Analyst to join our Quality Control team at our North Augusta manufacturing facility.

This is a great opportunity for someone who enjoys hands-on laboratory work, problem-solving, and being part of a team that takes pride in delivering accurate, reliable results.

You'll play an important role in supporting our specialty chemical and pharmaceutical production processes by performing laboratory testing, maintaining analytical equipment, and ensuring our products meet established quality and regulatory standards.

Work Schedule: 12-hour rotating shifts, four days on/four days off, alternating between day and night shifts.

What You'll Do

Laboratory Testing & Analysis

• Perform analytical testing on a variety of specialty chemical and pharmaceutical products using established laboratory methods and instrumentation, including Gas Chromatography (GC).
• Prepare and set up laboratory equipment, apparatus, reagents, and solutions for testing.
• Review, interpret, and accurately document analytical results in accordance with established procedures.
• Prioritize laboratory testing and analysis based on production needs, supervisory direction, and team priorities.
• Troubleshoot analytical equipment issues and perform routine calibrations and preventative maintenance.

Quality & Regulatory Compliance

• Follow current Good Manufacturing Practices (cGMP), Halocarbon's Quality Management System (QMS), and applicable regulatory requirements.
• Read, interpret, and apply applicable regulations, industry guidelines, and established procedures within pharmaceutical and specialty chemical quality management systems.
• Maintain accurate and complete laboratory documentation, including logbooks, data sheets, and test records.
• Apply established quality standards, procedures, and customer requirements to daily laboratory activities.
• Demonstrate quality stewardship through compliance with Halocarbon policies, management systems, procedures, and training requirements.
• Support consistent laboratory practices that contribute to product quality, regulatory compliance, and continuous improvement.

Laboratory Safety & Operations

• Follow laboratory safety procedures, the Chemical Hygiene Plan, and applicable OSHA requirements, including 29 CFR 1910.1450.
• Safely handle hazardous chemicals and use required personal protective equipment (PPE).
• Maintain clean, organized, and properly equipped laboratory work areas.
• Maintain the laboratory inventory system and support the laboratory reagents and solutions program.
• Promptly report all accidents, incidents, equipment concerns, and potential safety hazards.
• Demonstrate safe work practices and contribute to a positive safety culture.

Collaboration & Team Support

• Partner with Quality, Production, and other departments to support manufacturing operations and testing priorities.
• Communicate clearly and effectively regarding test results, laboratory activities, and potential issues.
• Participate in required training, team activities, and continuous improvement initiatives.
• Demonstrate Halocarbon's Core Values of Caring, Curiosity, Collaboration, and Competitive Spirit through daily actions and teamwork.
• Work independently and proactively while following QC leadership direction and established procedures.

Requirements

What We're Looking For:

We're interested in candidates who bring strong attention to detail, analytical thinking, and a commitment to quality, safety, and teamwork.

Education & Experience

• Bachelor's degree in science (e.g., biology or chemistry) is preferred.
• High School Diploma with relevant work experience will be considered.
• cGMP and/or quality system knowledge is desired.
• General math aptitude is required.

Skills & Qualifications

• Good written and verbal communication abilities.
• Good analytical abilities to review and interpret information.
• Exceptional attention to detail with high standards of excellence.
• Adaptable and reacts positively to change.
• Strong organization and time management skills.
• Able to work overtime as needed to accomplish goals.
• Experience with computer software (Word, Outlook, Excel, Access, and PowerPoint).
• Excellent organizational skills with a strong work ethic and continuous improvement mentality.
• Strong self-awareness with a steady personality, adaptable and reacts positively in a dynamic environment.
• Ability to work autonomously and proactively with supervisory direction.

What Makes You Successful Here

• A strong commitment to safety, quality, and doing things right.
• Exceptional attention to detail and accuracy in laboratory testing and documentation.
• A curious, analytical mindset with the ability to troubleshoot and solve problems.
• Strong organizational skills and the ability to manage changing priorities.
• A positive, adaptable attitude and willingness to learn.
• A collaborative approach and ability to communicate effectively across teams.
• A strong work ethic, self-awareness, and commitment to continuous improvement.

Safety/Essential Functions

• Must be capable of lifting containers weighing up to 50 pounds.
• Must be able to evacuate the plant, reporting to appropriate assigned muster point, in the event of an emergency or drill.
• Must be able to work in an environment where chemical odors may exist at permissible threshold limits of exposure.
• Must be able to climb and descend stairs and ladders.
• Must be able to use all available or assigned personal protective equipment and tools.
• Must be able to safely handle hazardous chemicals on a regular basis.

Let's Create Your Next Breakthrough®*Applicants must be authorized to work in the United States without current or future employer sponsorship