Planet Pharma
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https://www.propharmagroup.com
https://www.propharmagroup.com
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Target PR Range: 20-29/hr
*Depending on experience
Purpose:
Perform sampling, inspecting, and physical testing of incoming commodities per appropriate product specification in a laboratory
environment. Applies scientific knowledge to daily operations, data management, and problem solving. Understands and
follows documentation. Analyzes basic/simple data, evaluates results, forms conclusions, and recommends
process and/or document improvements. Recognizes deviation from normal operating procedures. Recognizes
and troubleshoots instrumentation and/or work order problems and routine operational issues.
Responsibilities:
Responsible for performing routine testing on incoming materials in accordance with approved specifications and procedures.
Disposition incoming material for use in manufacturing.
Maintains certification in assigned job responsibilities and completes training on-time.
Participates in complaint handling, failure investigations, and CAPA documentation.
Understands, implements, and maintains the quality policy and ensures compliance to site level policies and
procedures.
Develops knowledge of products and technologies. Interacts on a necessary basis with internal and external
support groups to perform core skills.
Participates in team activities and area metric tracking.
Responsible for supporting Operations efforts in meeting established production schedule.
Reports problems in a timely and accurate manner.
Seeks additional guidance or advice when problem is beyond scope of training or knowledge.
Qualifications:
High School Diploma required; Bachelor’s degree preferred.
Good understanding of basic math.
Good clerical skills is required.
4+ years of overall work experience
Computer skills proficiency including word processing, spreadsheets, instrumentation related and network systems.
Previous experience in Quality Assurance
2+ Experience in a manufacturing/finishing environment is desired.
Previous knowledge of GMP regulations and standards affecting pharmaceutical products is desired.
Have an understanding of material/product traceability and Device History Records
QA Specialist
Posted: 09/12/2023
2023-09-12
2024-08-25
Employment Type:
Contract
Job Category: Scientific
Job Number: 585412
Is job remote?: No
Country: United States
Job Description
Target PR Range: 20-29/hr
*Depending on experience
Purpose:
Perform sampling, inspecting, and physical testing of incoming commodities per appropriate product specification in a laboratory
environment. Applies scientific knowledge to daily operations, data management, and problem solving. Understands and
follows documentation. Analyzes basic/simple data, evaluates results, forms conclusions, and recommends
process and/or document improvements. Recognizes deviation from normal operating procedures. Recognizes
and troubleshoots instrumentation and/or work order problems and routine operational issues.
Responsibilities:
Responsible for performing routine testing on incoming materials in accordance with approved specifications and procedures.
Disposition incoming material for use in manufacturing.
Maintains certification in assigned job responsibilities and completes training on-time.
Participates in complaint handling, failure investigations, and CAPA documentation.
Understands, implements, and maintains the quality policy and ensures compliance to site level policies and
procedures.
Develops knowledge of products and technologies. Interacts on a necessary basis with internal and external
support groups to perform core skills.
Participates in team activities and area metric tracking.
Responsible for supporting Operations efforts in meeting established production schedule.
Reports problems in a timely and accurate manner.
Seeks additional guidance or advice when problem is beyond scope of training or knowledge.
Qualifications:
High School Diploma required; Bachelor’s degree preferred.
Good understanding of basic math.
Good clerical skills is required.
4+ years of overall work experience
Computer skills proficiency including word processing, spreadsheets, instrumentation related and network systems.
Previous experience in Quality Assurance
2+ Experience in a manufacturing/finishing environment is desired.
Previous knowledge of GMP regulations and standards affecting pharmaceutical products is desired.
Have an understanding of material/product traceability and Device History Records
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