Demo

Quality Control Technician

Cynet Systems
Summit, NJ Contractor
POSTED ON 2/28/2025
AVAILABLE BEFORE 3/27/2025
Job Description:

Pay Range: $34hr - 37hr

Responsibilities:
  • Perform testing of in-process, final product, and stability samples.
  • Utilize scientific principles to assist in analytical testing methods and the proper use of laboratory equipment.
  • Anticipate and troubleshoot problems.
  • Recommend corrective actions and participate in the development of best practices.
  • Understanding of regulatory guidelines and can independently develop, write and execute methods, protocols, reports and other related documents.
  • Complete all work in a timely manner.
  • Work and communicate effectively within the team to ensure timelines are met.
  • Perform peer review of testing data.
  • Review all data in accordance with applicable procedures and cGMP requirements.
  • Apply technical knowledge and abilities to ensure all testing is performed in a compliant manner.
  • Complete all review in accordance with required release timelines.
  • Communicate effectively with peers, and demonstrate teamwork, with regards to results of review and corrections required.
  • Train new analysts to general job duties.
  • Complete necessary training to become a qualified trainer.
  • Perform training effectively.
  • Document training per procedural and cGMP requirements.
  • Support document revision, project, CAPA, and investigation/deviation related tasks.
  • Perform assigned tasks within a CAPA, deviation, or project.
  • Draft and review technical documents, such as SOPs and protocols/reports.
  • Communicate effectively with management regarding task completion, roadblocks, and needs.
  • Demonstrate initiative, courage, and continuous improvement throughout investigation/corrective action lifecycles.
  • Performs other tasks as assigned.
Working Conditions:
  • The incumbent should be able to distinguish colors and possess correctable vision to 20/20, annual eye exam is required.
  • The incumbent must analyze numerical values on a daily basis.
  • The incumbent will be working a laboratory setting up to six hours per day.
  • The incumbent will be working around biohazardous materials, including chemical agents, up to six hours per day.
  • This job description is intended to describe the general nature and level of work being performed by the person assigned to this position.
  • The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job.
  • This job description does not state or imply that the above are the only duties and responsibilities assigned to this position.
  • There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job.
  • Employees holding this position will be required to perform any other job-related duties as requested by management.
  • Lab w/o blood & animal.
  • Position Handles Hazardous Materials.
Education:
  • Bachelor’s degree required, preferably in Science.
  • 2-4 years of relevant work experience, preferably in a regulated environment.
  • An equivalent combination of education and experience may substitute.
Experience:
  • Hands-on experience with various bioanalytical techniques including ELISA, qPCR and FACS.
  • Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements.
  • Technical writing skills.
  • Problem-solving ability/mentality, technically adept and logical.
  • Ability to represent the interests of the group on cross-functional teams.
  • Ability to set priorities of the group and manage timelines.
  • Ability to work with management locally and globally.
  • Ability to communicate effectively with peers, department management and cross-functional peers.

Salary : $34

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