Quality Assurance Technician

Pay: $22-$25

Shift 3PM-11:30PM

Skills:

quality assurance, fda, audit, batch record, sap systems, qms, gmp, iso standards, documentation review, data entry, cgmp, sop, quality assurance documentation, Biochemistry, inspection, chemistry, biology, capa, batch record review, document control, quality control, food quality, statistics, root cause analysis, change management

Description:

• Inspects shipments, reconciles labels, reviews and releases finished product and other paperwork.
• Reviews and approves/rejects other various quality-related documents.
• Assists in planning, developing, and implementing quality assurance programs.
• Responds to customer requests, including but not limited to investigating complaints and

completing required paperwork for corrective and preventive actions and associated follow-up.

• Assists in changing and maintaining ISO and cGMP paperwork. Trains or oversees training.
• Ensures the quality requirements of all departments are being followed and are accurately

documented.

• Interprets, understands and manages a variety of technical information.
• Prepares routine, technical and special presentations/reports to staff and management as required.
• Prepares and compiles statistical analysis of quality assurance data.
• Oversees the writing and maintaining of owner’s process manuals.
• May coordinate and perform quality assurance system internal audits, investigate non-conformances and determine root cause

analyses.

• Reviews the current policies determining and documenting any areas that may need quality improvements.
• This role is in the lab but not doing benchtop testing. They will be in front of a computer most of the day.
• Will compile lab results
• Will make sure lab results are within specifications
• Will make sure testing, materials, and, results are within compliance.
• will work with QC department as well as pilot plant
• Perform other duties as assigned

Top Skills Details:

quality assurance,fda,audit,batch record,sap systems,qms,gmp,iso standards,documentation review,data entry,cgmp,sop,quality assurance documentation

Additional Skills & Qualifications:

• High school diploma required; Bachelor’s Degree (Science, engineering, or business) preferred
• 1-4+ years applicable experience
• Must have previous GMP experience
• 2nd Shift - 3pm-11:30pm

Experience Level:

Intermediate Level

About Actalent:

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.