QC Scientist I

QC Scientist I Location: Greenville, NC Pay Rate: $ 27.00/hour Schedule: Monday-Friday, 8:00 AM-5:00 PM Work Arrangement: 100% Onsite Employment Type: Full-Time Position Summary We are seeking a QC Scientist I to support quality control testing that helps ensure the safety, quality, and efficacy of pharmaceutical products. This role performs chemical, physical, microbiological, and bioanalytical testing in support of pharmaceutical manufacturing operations. Working in a regulated GMP environment, you will test raw materials, in-process samples, finished products, and stability samples while using laboratory equipment and following established quality and safety procedures. This is an excellent opportunity for a recent Bachelor's degree graduate in Chemistry, Biology, Biochemistry, or a related scientific field to build hands-on experience in pharmaceutical quality control. Key Responsibilities Perform microbiological and bioanalytical testing to support product release and quality decisions. Perform testing including: Sterility testing Bacterial testing Endotoxin testing Particulate matter testing Membrane filtration Total Organic Carbon (TOC) Conductivity Generate accurate and reliable analytical data. Document testing procedures, observations, and results in laboratory notebooks, databases, and applicable systems in accordance with cGMP requirements. Compare laboratory results against established specifications and assist QA and management in determining whether testing repetition or an Out-of-Specification (OOS) investigation is required. Maintain laboratory equipment and ensure work areas remain clean, organized, and safe. Report equipment, laboratory, or testing issues to appropriate supervisors. Complete assigned testing activities accurately and within established timelines. Collaborate with Quality, Manufacturing, and other cross-functional teams to solve problems, improve efficiency, reduce costs, and enhance quality. Follow all applicable safety guidelines, Standard Operating Procedures (SOPs), Good Manufacturing Practices (GMP), and Good Laboratory Practices (GLP). Maintain all required compliance and training qualifications. Qualifications Bachelor's degree required; no prior professional experience required. Preferred fields of study include: Chemistry Biology Biochemistry Related scientific disciplines Experience with microbiological identification, testing, environmental monitoring, or aseptic techniques is preferred. Knowledge of GMP regulations, documentation practices, and pharmaceutical quality standards is preferred. Strong attention to detail and commitment to data integrity. Ability to follow detailed procedures and established laboratory protocols. Strong problem-solving skills and logical approach to scientific challenges. Proficient computer skills, including Microsoft Office and laboratory information systems. Strong written and verbal communication skills. Ability to work independently and collaboratively in a dynamic laboratory environment. Pharmaceutical or other regulated-industry experience is preferred but not required. Schedule & On-Call Requirements Regular Schedule: Monday-Friday, 8:00 AM-5:00 PM The position may require occasional: On-call coverage approximately once every 5-6 weeks Weekend work during assigned on-call periods Holiday coverage, with employees expected to cover at least one holiday per year Other shifts as business and manufacturing needs require Physical & Work Environment This is a fully onsite position in Greenville, NC. The role requires the ability to: Stand and walk for extended periods. Periodically stoop, kneel, crouch, and reach. Lift, carry, and move materials generally weighing 10-35 pounds , with some activities potentially requiring lifting up to 50 pounds . Perform repetitive hand and finger movements, including typing and laboratory tasks. Operate laboratory equipment and read computer monitors and written materials for extended periods. Work safely in cleanroom and controlled laboratory environments. Maintain manual dexterity and visual acuity necessary for laboratory testing. Required PPE Depending on the work area and assigned activities, required PPE may include: Safety glasses Safety shoes Lab coat Nitrile or similar gloves Safety apron Organic respirator when required Compensation $27.00 per hour This is a hands-on opportunity to develop experience in pharmaceutical quality control, microbiological testing, GMP compliance, laboratory operations, and product release testing while contributing to products that support patient health. Pay Details: $27.00 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled Military connected talent encouraged to apply To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: The California Fair Chance Act Los Angeles City Fair Chance Ordinance Los Angeles County Fair Chance Ordinance for Employers San Francisco Fair Chance Ordinance Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Adecco US, Inc.