in quality or manufacturing engineering with process and CSV validation; or an advanced degree with equivalent experience...Position Summary: We are looking for a skilled and driven Quality Engineer / Process Engineer to develop, implement...
validation [PV: characterization, OQ, PQ] (not cleaning process) and equipment qualification [CSV: URS, FAT, IQ, OQ, PQ, TMV...QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry...
validation [PV: characterization, OQ, PQ] (not cleaning process) and equipment qualification [CSV: URS, FAT, IQ, OQ, PQ, TMV...QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry...
). Project Management skills. Shift: Administrative, and according to business needs. Experience in: CQV Validation Expert... & Cleaning Specialist (SME): CIP and SIP processes GMP Document Controller: Validation Protocols (IQ/OQ/PQ), Risk Assessments...
validation [PV: characterization, OQ, PQ] (not cleaning process) and equipment qualification [CSV: URS, FAT, IQ, OQ, PQ, TMV...QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry...
validation [PV: characterization, OQ, PQ] (not cleaning process) and equipment qualification [CSV: URS, FAT, IQ, OQ, PQ, TMV...QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry...
validation [PV: characterization, OQ, PQ] (not cleaning process) and equipment qualification [CSV: URS, FAT, IQ, OQ, PQ, TMV...QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry...
validation [PV: characterization, OQ, PQ] (not cleaning process) and equipment qualification [CSV: URS, FAT, IQ, OQ, PQ, TMV...QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry...
). Project Management skills. Shift: Administrative, and according to business needs. Experience in: CQV Validation Expert... & Cleaning Specialist (SME): CIP and SIP processes GMP Document Controller: Validation Protocols (IQ/OQ/PQ), Risk Assessments...
. Minimum of 4 years of relevant experience in quality or manufacturing engineering with process and CSV validation... and driven Quality Engineer to develop, implement, and maintain quality standards and procedures across the manufacturing process...
and sustaining engineering support in a manufacturing area. Recommends and implements equipment and process modifications to meet... quality standards and improve production efficiencies, manufacturing techniques as well as production yields for existing...
and sustaining engineering support in a manufacturing area. Recommends and implements equipment and process modifications to meet... quality standards and improve production efficiencies, manufacturing techniques as well as production yields for existing...
systems quality assurance, including consulting‑level technical proficiency. Experience with validation of GxP applications...Career Category Quality Job Description Join Amgen’s Mission of Serving Patients At Amgen, if you feel...
, process validation, procedures, training, and new product introductions. Apply process, operational, scientific expertise.../system Root Cause Analysis investigations and support trend evaluations. Process Validation Assist with generation...
solutions that meets the needs and goals of the company and its customers/users. Leverages platform process expertise to assess... and prioritize integration requirements. Test the quality of a product and its ability to perform a task or solve a problems...
) Job Description: Support the execution of manufacturing/quality systems such as non-conformances, process validation, procedures, training... Cause Analysis investigations and support trend evaluations. Process Validation Assist with generation of process...
on engineering, regulatory, compliance, calibration, quality, microbial/environmental, technical cleaning, validation, electrical..., industry standards, regulatory standards and FDA standards. FUNCTIONS 1. Evaluate and determine if utility systems, process...
engineering support in a manufacturing area. Recommends and implements equipment and process modifications to meet quality...) 2+ years in experience in Process Validation and / Computer System Validations Knowledge in Medical Devices...
with cross-functional teams to troubleshoot issues, support batch execution, implement process improvements, and maintain quality... in collaboration with Quality and Engineering. Participate in continuous improvement initiatives to enhance process robustness...
engineering support in a manufacturing area. Recommends and implements equipment and process modifications to meet quality...) 2+ years in experience in Process Validation and / Computer System Validations Knowledge in Medical Devices...