SQC Inspector 1
2.
3 Bristol, TN Bristol, TN Estimated:
$38.
3K - $48.
4K a year Estimated:
$38.
3K - $48.
4K a year Position with training in statistical sampling and inspection of incoming materials, packaged products and processes for conformance to approved written specifications, SOP's, cGMPs, and FDA regulations.
Requires physical testing training.
Is able to perform sampling and inspection with minimal supervision.
Essential Duties and Responsibilites Performs manufacturing room inspections, in-process checks, cleaning verifications and raw material verifications for all drug products and manufacturing operations.
Performs in-process inspections, labeling verifications, line clearances, and cleaning verifications on all packaging operations.
Reports any problems found during inspections to Quality Assurance management.
Follows cGMP documentation practices in manufacturing and packaging records.
Reviews manufacturing and packaging batch records.
Understands and recognizes product status such as Approved, Hold, Rejected, etc.
Understands and follows current Good Manufacturing Practice regulations.
Understands and utilizes ANSI sampling plans.
Recognizes and reports problems and adverse quality events to quality management.
Other job duties as assigned.
Education /
Experience:
HS/GED 3 years or more related experience and/or successful completion of a job-specific training program or equivalent combination of education and experience.
Knowledge Necessary to Perform the Job:
Knowledge of 21 CFR Parts 210 and 211.
Knowledge of all applicable quality, manufacturing, packaging, and multi departmental SOP's in order to perform duties.
To apply, send resume and salary requirements to:
email protected .
Estimated Salary: $20 to $28 per hour based on qualifications.
3 Bristol, TN Bristol, TN Estimated:
$38.
3K - $48.
4K a year Estimated:
$38.
3K - $48.
4K a year Position with training in statistical sampling and inspection of incoming materials, packaged products and processes for conformance to approved written specifications, SOP's, cGMPs, and FDA regulations.
Requires physical testing training.
Is able to perform sampling and inspection with minimal supervision.
Essential Duties and Responsibilites Performs manufacturing room inspections, in-process checks, cleaning verifications and raw material verifications for all drug products and manufacturing operations.
Performs in-process inspections, labeling verifications, line clearances, and cleaning verifications on all packaging operations.
Reports any problems found during inspections to Quality Assurance management.
Follows cGMP documentation practices in manufacturing and packaging records.
Reviews manufacturing and packaging batch records.
Understands and recognizes product status such as Approved, Hold, Rejected, etc.
Understands and follows current Good Manufacturing Practice regulations.
Understands and utilizes ANSI sampling plans.
Recognizes and reports problems and adverse quality events to quality management.
Other job duties as assigned.
Education /
Experience:
HS/GED 3 years or more related experience and/or successful completion of a job-specific training program or equivalent combination of education and experience.
Knowledge Necessary to Perform the Job:
Knowledge of 21 CFR Parts 210 and 211.
Knowledge of all applicable quality, manufacturing, packaging, and multi departmental SOP's in order to perform duties.
To apply, send resume and salary requirements to:
email protected .
Estimated Salary: $20 to $28 per hour based on qualifications.
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