CGMP/Finished Pharmaceuticals/Unapproved New Drug/Misbranded/Adulterated

FDA Supplement Manufacturing Inspections: ConsumerLab found that 49.1% of 800 dietary supplement manufacturing facilities inspected by the FDA in FY 2025 received letters indicating noncompliance with cGMPs. Learn which countries had the highest citation rates and how the results compare to prior years.

On August 10, 2026, Church &amp; Dwight Co., Inc. recalled certain lots of <em>Zicam Cold Remedy Medicated Nasal Swabs With Cooling Menthol &amp; Eucalyptus</em> because an FDA inspection of the contract manufacturer found deviations from current Good Manufacturing Practice (cGMPs).

This turnkey training solution for biomanufacturing covers topics including CGMPs, regulatory compliance, and more.

On March 12, 2025, Kabana Skin Care recalled four brands of organic and/or mineral sunscreen products due to unspecified &quot;deviations&quot; in Current Good Manufacturing Practices (cGMPs).

Learn why cGMPs are crucial for ensuring community safety, and how we are taking it one step further.

YouTube video by Ominouslionheart

Eli Lilly and Company seeks a Process Engineer (R2-R4) to support and continuously improve delivery devices, sub-assemblies, and components for packaging and manufacturing sites. Ensure compliance with current Good Manufacturing Practices (cGMPs), Health, Safety, and Environment (HSE) guidelines and regulations, company standards, and regulatory requirements. Develop, monitor, and provide technical oversight for control systems for process indicators to identify and address performance issues. Lead investigations concerning process and equipment safety incidents. Perform and summarize improvement opportunities in technical studies, reports, investigations, data analysis, and process modeling. Provide technical assessments of Original Equipment Manufacturer (OEM) technical proposals and make recommendations related to suitability. Support all aspects of tool and process qualification, including computer system validation. #LI-DNI Position requires a Bachelor's degree in Industrial Engineering, Mechanical Engineering, Chemical Engineering, or a closely related STEM field and 4 years of experience with process and equipment requirements in pharmaceutical manufacturing. In the alternative, employer will accept a Master's degree in Industrial Engineering, Mechanical Engineering, Chemical Engineering, or a closely related STEM field and 3 years of experience with process and equipment requirements in pharmaceutical manufacturing. Experience must include a minimum of: 3 years of experience with programming and debugging Programmable Logic Controllers (PLCs) and Human Machine Interfaces (HMIs); 3 years of experience with leading resolution of manufacturing-related issues, including deviations, data review, and supply chain coordination using Root Cause Analysis tools; 3 years of experience with computer-aided design tools; 3 years of experience with identifying and implementing process and product changes to improve manufacturing processes; and 3 years of experience with using DOE, Six Sigma, and statistical methods as applied to engineering studies and reports. Up to 25% domestic and international travel required. #LI-DNI To apply, please visit https://jobsearch.lilly.com/ and enter job requisition number R-107954 when prompted. Alternatively, please send your resume, cover letter, and a copy of the ad to: Eli Lilly and Company, Lilly Corporate Center, Drop Code 1093, Indianapolis, IN 46285. ----------------------------------------------------------------------------------- JOBS.NOW Note: To tap into these hidden job opportunities, it's crucial to adhere strictly to the application process outlined in each job ad. At JOBS.NOW, we ensure that every listing includes detailed employer instructions. Follow them precisely to be considered for these unique positions! The "Log Application" button simply allows you to log the application for your records - JOBS.NOW does not submit any applications to employers directly. Remember to still apply through the method indicated in the job ad (mail, email, or via link). Please note that JOBS.NOW is an independent website and does not post this listings on behalf of any employers nor do we receive any compensation for these listings. All listings are sourced via media or internet channels required by the PERM process.

Verista, Inc. seeks Validation Engineer 2 (Reports to: Fishers, IN) to independently understand client's quality standards, cGMPs & regulatory standards to support team in compliance of validation effort. Requirements: (i) BA in Mech. Eng. or related field or foreign degree equivalent & 5 yrs. exp. in position involving validation eng. or (ii) MS in Mech. Eng. or related field or foreign degree equivalent & 2 yrs. exp. in position involving validation eng. Reports to Verista, Inc. HQ in Fishers, IN. Telecommuting permissible from home office anywhere in U.S. Long term placement at unanticipated client sites in U.S. possible. Benefits summary: https://verista.com/careers/ Application Instructions: Resumes to: HR Team at HR@verista.com ----------------------------------------------------------------------------------- JOBS.NOW Note: To tap into these hidden job opportunities, it's crucial to adhere strictly to the application process outlined in each job ad. At JOBS.NOW, we ensure that every listing includes detailed employer instructions. Follow them precisely to be considered for these unique positions! The "Log Application" button simply allows you to log the application for your records - JOBS.NOW does not submit any applications to employers directly. Remember to still apply through the method indicated in the job ad (mail, email, or via link). Please note that JOBS.NOW is an independent website and does not post this listings on behalf of any employers nor do we receive any compensation for these listings. All listings are sourced via media or internet channels required by the PERM process.