Penray
Overview
PLZ is committed to product stewardship and innovation, strong ethical standards, sustainable operations and most importantly, the development of our people. Whether at our manufacturing facilities or corporate headquarters, PLZ prioritizes health and safety, and offers you the support you need to create the career you want, through engagement, equity and inclusion, and opportunity. From household cleaning solutions to personal care products, and food to automotive lubricants, PLZ produces more than 2,500 different aerosol and liquid products in our facilities across the continent. We know that being the partner of choice for our clients starts with being the partner of choice for our employees. Learn more at
www.plzcorp.com/careers or visit
https://youtu.be/XYNIFpLQIJY Key Responsibilities
The Quality Manager will have responsibility for the daily oversight of the analytical laboratory, all inspection and testing activities in the lab and online. This position is responsible for FDA, ISO 22716, and customer compliance. Develops, implements, communicates, and maintains the quality system and operating standards. Ensured full compliance with all applicable legal regulations and Food and Drug Administration (FDA), allergens, etc. Lead all third-party and regulatory audits close all the non-conformances and submit the CAPA report within the designated time frame. The Quality Manager has the responsibility and authority to approve or reject raw material, packaging material, bulk product, in-process material, labeling and Finished products and OTC drug products. Lead and develop a team of QC analysts and QA technicians, providing mentorship, training, and support to ensure efficient and effective lab operations. Qualifications
Must have a minimum of 3 years’ experience in a pharmaceutical GMP environment. Must have a bachelor’s degree in engineering, chemistry, biology, or related science with extensive experience with quality assurance, quality control, and regulatory compliance in a leadership capacity (5+ years experience) Substantial direct job-related experience in the OTC drug/personal care industry working with ISO 22716, FDA, CFIA, and Health Canada regulations. Expert knowledge MoCRa, ISO Standards, and FDA / Health Canada regulatory requirements applicable to FDA-regulated products. Excellent communication, facilitation, presentation, and technical writing skills. Benefits
Medical, Dental & Vision benefits. Company paid Life and Short-Term disability. Voluntary benefits including additional life, disability, and hospital/accident insurance. 401k & company provided match. Paid Time Off Bonus incentive programs (Note, bonuses are subject to the rules governing the program, whereby an award, if any, depends on various factors, including, without limitation, individual and organizational performance.) All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability, protected veteran status or other protected status. EEOE/M/F/Vet/Disabled. All your information will be kept confidential according to EEO guidelines. Equal Opportunity Employer. This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
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PLZ is committed to product stewardship and innovation, strong ethical standards, sustainable operations and most importantly, the development of our people. Whether at our manufacturing facilities or corporate headquarters, PLZ prioritizes health and safety, and offers you the support you need to create the career you want, through engagement, equity and inclusion, and opportunity. From household cleaning solutions to personal care products, and food to automotive lubricants, PLZ produces more than 2,500 different aerosol and liquid products in our facilities across the continent. We know that being the partner of choice for our clients starts with being the partner of choice for our employees. Learn more at
www.plzcorp.com/careers or visit
https://youtu.be/XYNIFpLQIJY Key Responsibilities
The Quality Manager will have responsibility for the daily oversight of the analytical laboratory, all inspection and testing activities in the lab and online. This position is responsible for FDA, ISO 22716, and customer compliance. Develops, implements, communicates, and maintains the quality system and operating standards. Ensured full compliance with all applicable legal regulations and Food and Drug Administration (FDA), allergens, etc. Lead all third-party and regulatory audits close all the non-conformances and submit the CAPA report within the designated time frame. The Quality Manager has the responsibility and authority to approve or reject raw material, packaging material, bulk product, in-process material, labeling and Finished products and OTC drug products. Lead and develop a team of QC analysts and QA technicians, providing mentorship, training, and support to ensure efficient and effective lab operations. Qualifications
Must have a minimum of 3 years’ experience in a pharmaceutical GMP environment. Must have a bachelor’s degree in engineering, chemistry, biology, or related science with extensive experience with quality assurance, quality control, and regulatory compliance in a leadership capacity (5+ years experience) Substantial direct job-related experience in the OTC drug/personal care industry working with ISO 22716, FDA, CFIA, and Health Canada regulations. Expert knowledge MoCRa, ISO Standards, and FDA / Health Canada regulatory requirements applicable to FDA-regulated products. Excellent communication, facilitation, presentation, and technical writing skills. Benefits
Medical, Dental & Vision benefits. Company paid Life and Short-Term disability. Voluntary benefits including additional life, disability, and hospital/accident insurance. 401k & company provided match. Paid Time Off Bonus incentive programs (Note, bonuses are subject to the rules governing the program, whereby an award, if any, depends on various factors, including, without limitation, individual and organizational performance.) All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability, protected veteran status or other protected status. EEOE/M/F/Vet/Disabled. All your information will be kept confidential according to EEO guidelines. Equal Opportunity Employer. This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
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