Quality Assurance Specialist
Job Description
Shift: Day Shift - Mon-Thur 06:00a - 04:30p
Job Type: Full-time
Salary: $12.00 to $15.00 /hour
Job Type: Full-time
Summary:
Performs quality inspections, audits and testing during the manufacturing processes. Provides support to the various other quality areas, such as document control, calibration and other related areas as assigned.
Responsibilities
Primary
Responsibilities:
Performs quality control audits of manufacturing processes
Inspects materials, parts and products at different stages of production
Records observations and may make recommendations for improving
processes
Performs burst testing on stick pack and other products as assigned
Conducts line clearances and verifies accuracy of batch records, MMRs
and etc.
Reviews batch records and approves them for product release
Conducts failure mode investigations relating to product
nonconformance
Other duties as assigned
Qualifications
A high school diploma or GED is required with 1-3 years of related experience.
Knowledge and experience with applicable FDA cGMPs required.
Excellent communication and organizational skills.
Basic computer skills, experience with Microsoft Word, and Excel required.
Ability to conduct basic mathematical computations such as addition, subtraction and calculating percentages.
Ability to read and interpret procedures and documents, safety rules, and operating and maintenance instructions. Must be able to write corrective action reports, deviations and other quality documents.
Ability to calculate figures and amounts such as proportions, percentages and volume.
Ability to apply common sense understanding to carry out instructions furnished in written, oral, or diagram form. Must be able to identify and respond to non-conformances in the manufacturing processes.Estimated Salary: $20 to $28 per hour based on qualifications.
Shift: Day Shift - Mon-Thur 06:00a - 04:30p
Job Type: Full-time
Salary: $12.00 to $15.00 /hour
Job Type: Full-time
Summary:
Performs quality inspections, audits and testing during the manufacturing processes. Provides support to the various other quality areas, such as document control, calibration and other related areas as assigned.
Responsibilities
Primary
Responsibilities:
Performs quality control audits of manufacturing processes
Inspects materials, parts and products at different stages of production
Records observations and may make recommendations for improving
processes
Performs burst testing on stick pack and other products as assigned
Conducts line clearances and verifies accuracy of batch records, MMRs
and etc.
Reviews batch records and approves them for product release
Conducts failure mode investigations relating to product
nonconformance
Other duties as assigned
Qualifications
A high school diploma or GED is required with 1-3 years of related experience.
Knowledge and experience with applicable FDA cGMPs required.
Excellent communication and organizational skills.
Basic computer skills, experience with Microsoft Word, and Excel required.
Ability to conduct basic mathematical computations such as addition, subtraction and calculating percentages.
Ability to read and interpret procedures and documents, safety rules, and operating and maintenance instructions. Must be able to write corrective action reports, deviations and other quality documents.
Ability to calculate figures and amounts such as proportions, percentages and volume.
Ability to apply common sense understanding to carry out instructions furnished in written, oral, or diagram form. Must be able to identify and respond to non-conformances in the manufacturing processes.Estimated Salary: $20 to $28 per hour based on qualifications.
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