LanceSoft
Quality Engineer
LanceSoft, San Diego, California, United States, 92189
Quality Engineer
Pay: $50- $55/hr based on experience
100% onsite, 5 days a week
Job Summary: As directed by the Quality Engineering Leader, the Quality Engineer II is accountable for validation execution for manufacturing equipment and support in process validation or verification studies. Successful performance requires close work with quality management, operations, suppliers, and/or Client associates to assure compliance with all Client quality policies, procedures, and practices. Must demonstrate a working understanding of the ISO 13485 Quality Systems Regulations on Class I/II/III products. Preferred core experience in Quality Assurance, Quality Control, Validation (IQ, OQ, PQ), and Nonconformance management for regulated devices (i.e., Good Manufacturing Practices, ISO, FDA). Proven ability to develop solutions to a variety of problems of moderate scope and complexity, using policies and procedures for guidance.
Job Responsibilities: (Primary Duties, Roles, and/or Authorities)
Experience performing equipment and process validation studies such as writing and/or reviewing protocol, report, data analysis, and deviations for new, existing, and site relocation activities. Have a working knowledge of medical device or biological equipment maintenance from a Quality standpoint such as Preventive Maintenance, Calibration, and Out Of Tolerance activity support to the site and equipment owners. Author and execute installation, operational, and performance qualifications for analytical and manufacturing equipment. Execute validation and qualification of GMP equipment and functions throughout the manufacturing facility. Review and update FMEA or Risk documents as needed for validation activity for the site. Perform additional duties to ensure business continuity during the relocation of the manufacturing processes into a new area. Duties include but are not limited to execution of QA inspection to support dual operations, review, and approval of documents such as batch records to support finished product release. Education and Experience: BS in Biological Sciences, Chemistry, Bio-tech engineering, Bio-engineering, or related field. Minimum of 3-5 years of experience for QE II and 5-7 years for Sr. QE in Medical Device, Biotech, or Pharma Industry.
Knowledge and Skills:
Strong verbal and written communication skills; ability to write technical documents. Knowledge of quality system methodologies. Basic knowledge of Statistical Analysis (e.g., Minitab or Excel). Strong knowledge of Process Validation and equipment validation. Strong understanding and knowledge of ISO 9001, ISO 14971, and/or ISO 13485 (Design Control, Supplier Management, and Risk Management). Hands-on experience using Six Sigma methodology. SAP knowledge. Equipment management system such as BMRAM knowledge preferred. The ability to work in teams and independently with minimal supervision to obtain results as required. Must be self-motivated/directed, organized, detail-oriented, and have the ability to multi-task projects. Physical Demands: (if applicable) General physical requirements: ability to work in controlled environments. Ability to work with laboratory-grade equipment such as refrigerators, freezers, centrifuges, etc., during validation work.
Work Environment: (if applicable) Onsite model. Ability to be present in the manufacturing area as needed.
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Job Summary: As directed by the Quality Engineering Leader, the Quality Engineer II is accountable for validation execution for manufacturing equipment and support in process validation or verification studies. Successful performance requires close work with quality management, operations, suppliers, and/or Client associates to assure compliance with all Client quality policies, procedures, and practices. Must demonstrate a working understanding of the ISO 13485 Quality Systems Regulations on Class I/II/III products. Preferred core experience in Quality Assurance, Quality Control, Validation (IQ, OQ, PQ), and Nonconformance management for regulated devices (i.e., Good Manufacturing Practices, ISO, FDA). Proven ability to develop solutions to a variety of problems of moderate scope and complexity, using policies and procedures for guidance.
Job Responsibilities: (Primary Duties, Roles, and/or Authorities)
Experience performing equipment and process validation studies such as writing and/or reviewing protocol, report, data analysis, and deviations for new, existing, and site relocation activities. Have a working knowledge of medical device or biological equipment maintenance from a Quality standpoint such as Preventive Maintenance, Calibration, and Out Of Tolerance activity support to the site and equipment owners. Author and execute installation, operational, and performance qualifications for analytical and manufacturing equipment. Execute validation and qualification of GMP equipment and functions throughout the manufacturing facility. Review and update FMEA or Risk documents as needed for validation activity for the site. Perform additional duties to ensure business continuity during the relocation of the manufacturing processes into a new area. Duties include but are not limited to execution of QA inspection to support dual operations, review, and approval of documents such as batch records to support finished product release. Education and Experience: BS in Biological Sciences, Chemistry, Bio-tech engineering, Bio-engineering, or related field. Minimum of 3-5 years of experience for QE II and 5-7 years for Sr. QE in Medical Device, Biotech, or Pharma Industry.
Knowledge and Skills:
Strong verbal and written communication skills; ability to write technical documents. Knowledge of quality system methodologies. Basic knowledge of Statistical Analysis (e.g., Minitab or Excel). Strong knowledge of Process Validation and equipment validation. Strong understanding and knowledge of ISO 9001, ISO 14971, and/or ISO 13485 (Design Control, Supplier Management, and Risk Management). Hands-on experience using Six Sigma methodology. SAP knowledge. Equipment management system such as BMRAM knowledge preferred. The ability to work in teams and independently with minimal supervision to obtain results as required. Must be self-motivated/directed, organized, detail-oriented, and have the ability to multi-task projects. Physical Demands: (if applicable) General physical requirements: ability to work in controlled environments. Ability to work with laboratory-grade equipment such as refrigerators, freezers, centrifuges, etc., during validation work.
Work Environment: (if applicable) Onsite model. Ability to be present in the manufacturing area as needed.
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