What are the responsibilities and job description for the Quality Control Associate position at Cynet Systems?
We are looking for Quality Control Associate for our client in Tucson, AZ
Job Title: Quality Control Associate
Job Location: Tucson, AZ
Job Type: Contract
Job Overview:
Requirement/Must Have:
- 1 years work experience, preferably in regulated industry with High School Diploma.
- 3 years work experience with an Associate s Degree.
- Less than 1 year work experience, entry level with a Bachelor's Degree.
Responsibilities:
- Perform inspection and testing of raw materials, in-process materials and finished goods in a compliant manner.
- Document test results, complete batch records, document observations and generate reports for qualification testing.
- Conduct data analysis of raw material, in-process and finished goods test results.
- Responsible for generating compliant QC documentation as part of the Device History Record required for releasing items into inventory from the raw material to the in-process finished goods.
- Maintain records and QC lab environment to comply with cGMP, OP and regulatory requirements.
- Perform routine maintenance of laboratory equipment outlined by operating procedures.
- May assist in coordinating vendor activities for user maintained laboratory equipment.
- Perform regular laboratory and manufacturing environmental monitoring testing.
- Perform lab supply ordering and inventory management in order to support the QC laboratory and adherence to inventory control processes.
- Foster and follow an established safety culture, environmental guidelines and procedures for all work performed.
- Formulate reagents with high complexity for material testing process.
- Act as QC representative in transferring processes from development to QC.
- May assist in testing raw materials for reliability and stability.
- May assist in process monitoring and trending.
- May assist in collecting, interpreting and communicating process metrics for recommended improvements.
- Assist in performing, reviewing and/or generating validations for QC processes and laboratory equipment.
- Assist in the development and implementation of testing processes.
- Assist in reagent manufacturing activities unrelated to QC activities.
Nice to Have:
- Experience with handling corrosive and biohazardous reagents.
- Experience working in GLP, cGMP or ISO regulated environments.
- Experience with 6S and Lean techniques.
Skills:
- Excellent oral and written communication skills demonstrated by communicating with other functions and management regarding resolving testing, investigations and theory.
- Strong data-analysis skills, with clear demonstrated understanding of analytical, troubleshooting and problem solving skills.
- Hands-on experience in a laboratory.
- Accurate and precise manual pipetting and measuring techniques.
- Demonstrated attention to detail and strong organizational skills.
- Ability to utilize Google suite and computer programs.
- Proven ability to meet deadlines.
- Demonstrated ability to work effectively in a team environment.
- Ability to work in department and/or cross functional meetings and projects.
- Proficient ability to perform a wide range of moderate and high complexity laboratory techniques and their application.
Qualification And Education:
- High School Diploma.
- Associates or Bachelor s Degree in Science or Life Science discipline.