Job Title-Quality Technician 3
Shift 1st shift position 8 am to 4:30 pm
Duration- 12 months contract with high possibility of extension.
Location-NewarkDE.19702
Position Overview:
Required Skills:
1. Strong attention to detail
2. Ability to work independently
3. Proficiency in troubleshooting analytical instruments and resolving issues with chemistry assays
4. Adherence to good documentation practices
5. Collaborative and team-oriented mindset
Preferred Qualifications:
Experience handling biohazardous materials
Quality control laboratory experience particularly in release testing
Familiarity with operating Dimension instruments
Educational Requirements:
Bachelors degree in Chemistry Biology Biochemistry or a related field
Alternatively a 2-year or Associates degree with relevant experience will be considered
Position Overview /Responsibilities
The technician will be responsible for activities related to manufacturing testing within the Quality Control Organization. Functions and responsibilities may include and are not limited to:
Completes analytical related testing/processes on analytical instruments such as Titrator Karl Fisher UV-VIS Spectrophotometer and pH meter.
Completes manufacturing related testing/processes on Diagnostic equipment and analyzers such as Dimension DM Vista SCS Stratus ADVIA Centaur and Atellica analyzers.
Performs complex quantitative and qualitative analysis such as sampling testing and measuring using analytical instruments and diagnostic analyzers.
Compiles analyzes and interprets large sets of test data.
Performs complex analysis of data and calculations in excel or LIMS which includes graphs and charts.
Performs periodic inspections of equipment and preventative maintenance work.
Maintains instrument logs.
Ability to follow protocol and set schedule.
Performs troubleshooting on issues that may arise during testing process.
Might be required to participate on cross functional teams as needed (scientists engineers and management).
Potential to work independently on projects which includes defining tasks setting priorities and driving to completion.
Flexible to work overtime and/or irregular work hours as needed.
Knowledge of QSRs and ISO standards.
May require participation in new product development production support and/or reference materials.
Knowledge/Skills and Experience
Knowledge and skills of a technical or specialty area with 3-5 years of experience including but not limited to the following:
Understands the quality management system and ensures that their area complies with FDA QSR ISO and IVDD standards.
Familiarity with GMP GLP and GDP processes
Mathematical skills: concentration calculations and statistical analysis.
Computer skills: customary MS Office programs SAP LIMS and/or Clinical testing software.
Laboratory skills: Operation Maintenance and Troubleshooting of analytical instruments and chemistry assays.
Knowledge and experience with analytical instruments and testing methodologies are a must.
Demonstrates ability to work independently and on a team.
Must be able to multi-task and prioritize daily work.
Strong communication and interpersonal skills.
Knowledge and experience in handling bio-hazard materials.