Energy Jobline ZR
QC Manager - Simply Biotech
Are you looking for a new career opportunity with an exciting biotech company? In this role, you are responsible for the duties listed below. Immediate opening for QC Manager in Anaheim, CA who possess: Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, or a related technical field. (Must be able to pass education verification) Minimum 57 years of progressive experience in Quality Assurance/Quality Control, with at least 3 years in a managerial role. Experience in a cGMP?compliant environment; personal care, cosmetics, or OTC manufacturing experience strongly preferred. Deep understanding of FDA regulations (21 CFR 210/211), ISO 22716 (GMP for cosmetics), and related quality standards.
Email resumes to dandriacchi@talentzok.com or call 858.633.2357. Full Description
The QA/QC Manager is responsible for overseeing the Quality Assurance and Quality Control functions across all manufacturing activities. This role ensures that products meet internal specifications, customer requirements, and regulatory standards. The QA/QC Manager will lead the implementation and continuous improvement of the Quality Management System (QMS), supervise quality staff, and serve as the primary contact for audits and compliance issues. Responsibilities Lead the QA and QC teams, including training, development, and performance management. Develop, implement, and maintain a robust Quality Management System in compliance with GMP, FDA, ISO 22716, and customer standards. Oversee all quality-related activities, including raw material testing, in-process checks, customer component AQL, finished goods inspection, and batch record review. Investigate and resolve quality issues including non-conformances, deviations, customer complaints, CAPAs, and root cause analyses. Ensure timely review and approval of production and laboratory documentation to support product release. Manage internal audits, coordinate external audits (including customer and regulatory), and ensure timely resolution of findings. Partner with R&D, Regulatory, Production, and Supply Chain to support product development, scale-up, and commercialization. Maintain and report quality metrics (KPIs) and drive continuous improvement initiatives. Ensure calibration and maintenance of lab equipment and oversee environmental monitoring and cleaning validation, if applicable. Stay current with changes in regulatory requirements and ensure company compliance.
Qualifications
Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, or a related technical field. Minimum 57 years of progressive experience in Quality Assurance/Quality Control, with at least 3 years in a managerial role. Experience in a cGMP-compliant environment; personal care, cosmetics, or OTC manufacturing experience strongly preferred. Deep understanding of FDA regulations (21 CFR 210/211), ISO 22716 (GMP for cosmetics), and related quality standards. Strong leadership, problem?solving, and communication skills. Experience with QMS platforms, LIMS, and document control systems. Ability to manage multiple priorities and thrive in a fast?paced, deadline?driven environment.
Salary Range: $100k-120k/yr For immediate and confidential consideration, please email your resume to dandriacchi@talentzok.com or call 858.633.2357. More information can be found at www.simplybiotech.com Company Description: Simply Biotech was founded in 2008 and has been repeatedly recognized as one of San Diego Countys fastest growing businesses. In 2022, we were named Business Journals Best Places to Work. Even as our competitors are scaling back and laying off staff, Simply Biotech is expanding to new markets and hiring additional staff in existing offices. If you are interested in applying for this job please press the Apply Button and follow the application process. Energy Jobline wishes you the very best of luck in your next career move. #J-18808-Ljbffr
Are you looking for a new career opportunity with an exciting biotech company? In this role, you are responsible for the duties listed below. Immediate opening for QC Manager in Anaheim, CA who possess: Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, or a related technical field. (Must be able to pass education verification) Minimum 57 years of progressive experience in Quality Assurance/Quality Control, with at least 3 years in a managerial role. Experience in a cGMP?compliant environment; personal care, cosmetics, or OTC manufacturing experience strongly preferred. Deep understanding of FDA regulations (21 CFR 210/211), ISO 22716 (GMP for cosmetics), and related quality standards.
Email resumes to dandriacchi@talentzok.com or call 858.633.2357. Full Description
The QA/QC Manager is responsible for overseeing the Quality Assurance and Quality Control functions across all manufacturing activities. This role ensures that products meet internal specifications, customer requirements, and regulatory standards. The QA/QC Manager will lead the implementation and continuous improvement of the Quality Management System (QMS), supervise quality staff, and serve as the primary contact for audits and compliance issues. Responsibilities Lead the QA and QC teams, including training, development, and performance management. Develop, implement, and maintain a robust Quality Management System in compliance with GMP, FDA, ISO 22716, and customer standards. Oversee all quality-related activities, including raw material testing, in-process checks, customer component AQL, finished goods inspection, and batch record review. Investigate and resolve quality issues including non-conformances, deviations, customer complaints, CAPAs, and root cause analyses. Ensure timely review and approval of production and laboratory documentation to support product release. Manage internal audits, coordinate external audits (including customer and regulatory), and ensure timely resolution of findings. Partner with R&D, Regulatory, Production, and Supply Chain to support product development, scale-up, and commercialization. Maintain and report quality metrics (KPIs) and drive continuous improvement initiatives. Ensure calibration and maintenance of lab equipment and oversee environmental monitoring and cleaning validation, if applicable. Stay current with changes in regulatory requirements and ensure company compliance.
Qualifications
Bachelor's degree in Chemistry, Biology, Pharmaceutical Sciences, or a related technical field. Minimum 57 years of progressive experience in Quality Assurance/Quality Control, with at least 3 years in a managerial role. Experience in a cGMP-compliant environment; personal care, cosmetics, or OTC manufacturing experience strongly preferred. Deep understanding of FDA regulations (21 CFR 210/211), ISO 22716 (GMP for cosmetics), and related quality standards. Strong leadership, problem?solving, and communication skills. Experience with QMS platforms, LIMS, and document control systems. Ability to manage multiple priorities and thrive in a fast?paced, deadline?driven environment.
Salary Range: $100k-120k/yr For immediate and confidential consideration, please email your resume to dandriacchi@talentzok.com or call 858.633.2357. More information can be found at www.simplybiotech.com Company Description: Simply Biotech was founded in 2008 and has been repeatedly recognized as one of San Diego Countys fastest growing businesses. In 2022, we were named Business Journals Best Places to Work. Even as our competitors are scaling back and laying off staff, Simply Biotech is expanding to new markets and hiring additional staff in existing offices. If you are interested in applying for this job please press the Apply Button and follow the application process. Energy Jobline wishes you the very best of luck in your next career move. #J-18808-Ljbffr