QC Analyst I- 3rd Shift Weekends (7 pm-7:30 am)

Greenville, SC, USA|

Job Overview

Compensation

Hourly

Range $22.00 - $29.50

Benefits

Medical insurance

Dental Insurance

Vision Insurance

short-term disability

long-term disability

401k with match

Paid Time Off

Job Description

Ortec has been a pioneering chemical manufacturing company since 1980, offering custom chemical solutions and personalized service that caters to the unique production needs of its customers. With three state-of-the-art plants and a dedicated workforce of over 300 employees, Ortec prides itself on its ability to deliver high-quality chemical products while maintaining a close-knit, customer-focused approach. The company strikes a balance between being large enough to fulfill extensive orders and flexible enough to provide personalized care, making it a trusted partner across various industries. Over the years, Ortec has expanded its services and capabilities but has never deviated from the core values that built its reputation: integrity, commitment, and teamwork.

Ortec views itself as more than just a workplace — it is a family of talented, big-hearted professionals working collaboratively to drive success for their clients and growth within their communities. The company culture emphasizes honoring commitments and acting with integrity at all times, which motivates employees to excel and deliver dependable results consistently. This ethos, combined with continuous investment in cutting-edge technologies and training, allows Ortec to remain a leader in the chemical manufacturing sector.

The position of QC Analyst I at Ortec plays a crucial role in upholding the company’s quality standards. This entry-level role involves performing comprehensive laboratory testing on raw materials, in-process components, and finished products to ensure they meet strict quality criteria. The QC Analyst I supports routine laboratory functions such as environmental monitoring, equipment calibrations and verifications, sampling, and analytical testing using sophisticated instrumentation including chromatography techniques. This role is vital to maintaining production quality and compliance with regulatory standards such as FDA, ISO, and USP.

The successful candidate will be part of a dynamic, hardworking lab team dedicated to accuracy, safety, and efficiency. Responsibilities include handling chemical tests using advanced instruments like pH meters, viscometers, FTIR, UV-VIS, TOC analyzers, and chromatographs. The position requires solid organizational skills for keeping detailed records and preparing analytical reports in compliance with good manufacturing practices (GMP). Troubleshooting minor equipment issues and supporting audit readiness initiatives further contribute to the essential scope of this position. Ortec offers a stimulating laboratory environment outfitted with ventilated, temperature-controlled facilities designed for optimal testing conditions.

Committed to employee well-being, Ortec provides an excellent benefits package that includes medical, dental, and vision insurance, company-paid disability coverage, a 401k retirement plan with matching contributions, and various incentive programs such as attendance bonuses and anniversary awards. This rewarding role not only offers career growth opportunities but also enables employees to be part of a caring organization that values each person’s contribution. At Ortec, you are recognized as a unique individual, not just a number, fostering a positive and inclusive atmosphere where teamwork and respect drive success.

Job Requirements

Associates degree or higher in Chemistry or related field
1-5 years of laboratory experience preferably including chromatography
knowledge of analytical instrumentation
experience working in regulated environments such as ISO or FDA preferred
proficiency with Microsoft Office and laboratory software
excellent communication and documentation skills
ability to follow SOPs and safety guidelines
ability to maintain a clean and organized laboratory environment

Job Qualifications

Associates degree with 5+ years of laboratory experience (chromatography experience preferred)
Bachelor’s degree in Chemistry or related field with 1-2 years of experience
knowledge of analytical instrumentation (pH, viscosity, FTIR, UV-VIS, etc.)
experience working in an ISO or FDA-regulated environment preferred
excellent communication skills, including the ability to speak clearly, listen and gain clarification, respond well to questions, and write clearly and informatively
experience with Microsoft Office, LIMS, Empower, and other software
familiarity with USP interpretation and testing
understanding of FDA and ISO regulations and requirements

Job Duties

Perform chemical testing using analytical instrumentation and wet bench techniques including pH, viscometers, FTIR, UV-VIS, TOC, gas chromatography, and liquid chromatography
perform minor troubleshooting of testing and instrumentation as necessary and writing of minor laboratory investigations
assist in completing all laboratory investigations, including OOS investigations, as required by management
sampling of raw materials for QC lab testing, as well as performing the required testing for raw material release
sampling and performing analysis for site environmental monitoring
perform routine maintenance, calibrations, and verifications of QC laboratory equipment
maintain accurate lab notebooks and complete all related analytical reports, write summaries, and keep proper documentation in compliance with SOPs