Junior (1 to 2 years), Mid-level (3 to 4 years)Experience Level
Full TimeJob Type
UnknownVisa
Consumer Goods, ManufacturingIndustries
Requirements
2-year degree (or more) in a Science Field, or commensurate experience of 5 years in a QC lab or GMP manufacturing operations
Computer literacy sufficient to use standard software (MS Office) and learn specific software and instrumentation
Experience and knowledge of basic laboratory operations such as weighing, titrating, and preparing volumetric solutions
Ability to interpret analytical and microbiological methods
Responsibilities
Collect, label, analyze, and record results for raw materials, intermediate products, finished goods, packaging materials, and other samples
Perform tracking, trend analysis, and other QC-related responsibilities as directed by laboratory systems
Write control documents like Standard Operating Procedures (SOPs)
Deliver training, perform system health assessments, carry out “on the floor” coaching, and facilitate or participate in quality system failure investigations
Maintain cGMP principles and Good Documentation practices
Perform raw material, finished goods, intermediate, and development sample analysis according to standard analytical procedures
Conduct routine instrument maintenance and calibration during analytical work
Conduct limited instrument troubleshooting and problem diagnosis
Use discernment to assess accuracy and reliability of analytical results, observe and identify problems, and report to supervisor
Conduct analytical method development work under direct supervision and mentorship
Sample and label materials according to written procedures or instructions, and inspect appearance of raw materials during unloading as needed
Coordinate work with Production Lead on night and weekend shifts for appropriate prioritization