Quality Control Analyst I performs various scientific analyses to evaluate the quality of raw materials, in-process materials, and finished goods and ensure compliance with established standards. Conducts and validates various biological and chemical quality control (QC) assays. Being a Quality Control Analyst I compiles, interprets, and documents statistical data from testing processes to either confirm compliance with established quality standards or identify deviations. May be responsible for establishing specifications for conducting assays and writing standard operating procedures. Additionally, Quality Control Analyst I typically requires a bachelor’s degree. Typically reports to a supervisor or manager. The Quality Control Analyst I work is closely managed. Works on projects/matters of limited complexity in a support role. To be a Quality Control Analyst I typically requires 0-2 years of related experience.
Quality Control Analyst Job Description Template
Our company is looking for a Quality Control Analyst to join our team.
Responsibilities:
- Lead trainer for respective area;
- Management of Master Data. Examples include: – create/ modify tests, products, sample groups templates, specifications, methods, materials, etc;
- execute Warren training development and deployment for LIMS;
- Has risk and issue ownership;
- Change Management and Training Lead for global/international LabWare (Environmental Monitoring and LIMS) implementation;
- Perform testing and inspection in accordance with SOP’s;
- Lab general duties including cleaning, glassware, washing etc;
- Demonstrate proficiency in a task by completing On the Job Training;
- Support and lead projects – such as method transfers, new instruments, method qualifications;
- Work towards accomplishment of Site Goals;
- Maintain on-time completion of all training requirements;
- Participate in department initiatives to support continuous improvement;
- Analyzes In-Process, Lot Release and Stability samples;
- Conduct Safety and weekly compliance walkthroughs;
- Reviews analytical results.
Requirements:
- Use of Microsoft Suites (Word, Excel, Powerpoint);
- Use of Laboratory computer systems;
- Relate to others in a team setting;
- Direct, control and plan tasks/projects;
- Must have expert GMP, Quality, and in-depth risk management knowledge;
- Potential previous use of GMP Quality Systems such as: TrackWise, Laboratory Information Management Systems (LIMS);
- Experience using a PIT;
- Displays commitment to quality and performs job functions to the best of your ability;
- Perform assigned, complex and/or varied tasks. Make basic quality decisions independently;
- Experience with packaging/component inspection or packaging engineering;
- Solid ability to speak publicly;
- Works entire assigned shift, including arriving on time;
- Excellent PC skills and proficiency with Microsoft applications including Excel;
- Experience with databases, VBA, Access, SQL;
- Strong communication skills, both written and verbal.