
Job Overview
Compensation
Hourly
Range $16.00 - $20.50
Work Schedule
Standard Hours
Benefits
Health Insurance
Paid Time Off
Retirement Plan
Disability insurance
Life insurance
Employee assistance program
Career Development
Job Description
About the Company:
The hiring establishment is a reputable pharmaceutical manufacturing company located in Clayton, North Carolina. This company specializes in the production of active pharmaceutical ingredients (API) and filled pharmaceutical products. The firm operates with a commitment to compliance with current Good Manufacturing Practices (cGMP) and is known for maintaining rigorous quality standards within all aspects of its operations. With a focus on innovation and quality, this company supports the advancement of medical science through the production of safe and effective pharmaceutical products. The company's facilities are equipped with state-of-the-art laboratory and manufacturing technologies that allow it to meet stringent industry and regulatory requirements. It employs a team of highly motivated professionals who work collaboratively to ensure that products meet specifications and adhere to industry best practices.
About the Role: The position of Quality Control Technician is a critical role offered as a 12-month contract, requiring the candidate to work on-site in Clayton, North Carolina. The technician will perform and review detailed analyses of in-process, release, and stability samples of both active pharmaceutical ingredients and filled products. The role demands strict adherence to cGMP, site-specific policies, and corporate procedures, ensuring that all laboratory data generated are accurate, scientifically sound, and compliant with regulatory standards. This role supports the transfer of technology and processes aligned with project plans and timelines, which is essential to maintaining production efficiency and product quality.
The technician will be responsible for preparing microbiological media and overseeing the washing and sterilization of equipment and media using autoclaves. They will read and interpret environmental monitoring samples and perform bioburden testing of utility samples through membrane filtration methods. Furthermore, the technician must ensure environmental compliance and support overall Good Manufacturing Practice within the laboratory. The role involves maintaining proficiency in testing methods, delivering timely laboratory results, supporting investigations, and deviation reporting. Strong attention to safety and environmental requirements will be critical to successfully perform the duties assigned.
This position suits professionals with an associate's degree in science or a related field, though a bachelor's degree is preferred. Experience in clinical or industrial pharmaceutical laboratory settings is highly desirable. Candidates should demonstrate skills in routine testing, troubleshooting laboratory equipment, and possess knowledge of GMP and laboratory techniques. The role is physically demanding, requiring the ability to move equipment or supplies weighing up to 33 pounds, perform precise manual tasks, and maintain stationary positions both sitting and standing for extended periods. The position also requires occasional work at elevated heights and around odorous or hazardous materials.
In summary, the Quality Control Technician role is vital in assuring the quality and safety of pharmaceutical products by executing precise laboratory testing, supporting technological processes, and ensuring regulatory compliance in a fast-paced and safety-conscious environment. The 12-month contract position offers an opportunity to be part of a dedicated team within a respected pharmaceutical company operating under high-quality standards in Clayton, NC.
About the Role: The position of Quality Control Technician is a critical role offered as a 12-month contract, requiring the candidate to work on-site in Clayton, North Carolina. The technician will perform and review detailed analyses of in-process, release, and stability samples of both active pharmaceutical ingredients and filled products. The role demands strict adherence to cGMP, site-specific policies, and corporate procedures, ensuring that all laboratory data generated are accurate, scientifically sound, and compliant with regulatory standards. This role supports the transfer of technology and processes aligned with project plans and timelines, which is essential to maintaining production efficiency and product quality.
The technician will be responsible for preparing microbiological media and overseeing the washing and sterilization of equipment and media using autoclaves. They will read and interpret environmental monitoring samples and perform bioburden testing of utility samples through membrane filtration methods. Furthermore, the technician must ensure environmental compliance and support overall Good Manufacturing Practice within the laboratory. The role involves maintaining proficiency in testing methods, delivering timely laboratory results, supporting investigations, and deviation reporting. Strong attention to safety and environmental requirements will be critical to successfully perform the duties assigned.
This position suits professionals with an associate's degree in science or a related field, though a bachelor's degree is preferred. Experience in clinical or industrial pharmaceutical laboratory settings is highly desirable. Candidates should demonstrate skills in routine testing, troubleshooting laboratory equipment, and possess knowledge of GMP and laboratory techniques. The role is physically demanding, requiring the ability to move equipment or supplies weighing up to 33 pounds, perform precise manual tasks, and maintain stationary positions both sitting and standing for extended periods. The position also requires occasional work at elevated heights and around odorous or hazardous materials.
In summary, the Quality Control Technician role is vital in assuring the quality and safety of pharmaceutical products by executing precise laboratory testing, supporting technological processes, and ensuring regulatory compliance in a fast-paced and safety-conscious environment. The 12-month contract position offers an opportunity to be part of a dedicated team within a respected pharmaceutical company operating under high-quality standards in Clayton, NC.
Job Requirements
- Preparation of microbiological media
- Washing and sterilization of equipment and media using autoclaves
- Reading and interpretation of environmental monitoring samples
- Bioburden testing of utilities samples via membrane filtration
- Ensure accuracy and scientific soundness of laboratory data
- Ensure environmental compliance
- Support and ensure GMP laboratory compliance
- Maintain testing proficiency for methods
- Ensure timeliness of laboratory results and investigations
- Perform analysis of samples and support deviations
- Follow all safety and environmental requirements in the performance of duties
- Other accountabilities as assigned
Job Qualifications
- Associate's degree in science or relevant field of study from an accredited university required
- Bachelor's degree in science or relevant field of study from an accredited university preferred
- One year of work experience in a clinical or industrial pharmaceutical laboratory preferred
- Ability to author scientific and technical reports is a plus
- Able to perform routine testing per SOP and GMP standards preferred
- Basic troubleshooting skills for laboratory equipment is a plus
- Knowledge of GMP and laboratory techniques is a plus
- Demonstrated attention to detail required
- Strong verbal and written communication skills preferred
- Skills or knowledge in chemistry analysis such as HPLC, UPLC, GC, TOC, AA, UV, pH, KF
- Skills or knowledge in microbiology analysis including isolator, sterility, bacterial endotoxin testing, growth promotion, microbial identification, ELISA, bioburden
- Skills or knowledge in raw materials analysis including compendial testing, FTIR, NIR, titration, UVVis
Job Duties
- Preparation of microbiological media
- Washing and sterilization of equipment and media using autoclaves
- Reading and interpretation of environmental monitoring samples
- Bioburden testing of utilities samples via membrane filtration
- Ensure accuracy and scientific soundness of laboratory data
- Ensure environmental compliance
- Support and ensure GMP laboratory compliance
Job Criteria
Experience
Entry Level (1-2 years)
Job Location
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