Quality Control Technician - Night Shift

at  Diversey Inc

Solenis is a leading global producer of specialty chemicals focused on delivering sustainable solutions for water-intensive industries, including consumer, industrial, institutional, food and beverage, and pool and spa water markets. Owned by Platinum Equity, the company’s product portfolio includes a broad array of water treatment chemistries, process aids, functional additives, and cleaners and disinfectants, as well as state-of-the-art monitoring and control systems. These technologies are used by customers to improve operational efficiencies, enhance product quality, protect plant assets, minimize environmental impact, and create cleaner and safer environments.
Headquartered in Wilmington, Delaware, the company has 69 manufacturing facilities strategically located around the globe and employs a team of over 16,100 professionals in 130 countries across six continents. Solenis is a 2024 US Best Managed Company, recognized fouryears in a row. For more information about Solenis, please visit
www.solenis.com
.
Position Summary:
Reporting to the Quality Assurance Manager, this position is responsible to provide technical support regarding the chemistry of products, adherence to quality specifications, regulatory and environmental compliance. Perform chemical testing and analysis and provide batch adjustments as necessary. Tabulate and summarize a variety of data. Must actively participate and comply with our Health and Environmental program including training initiatives and following all policies and procedures. This position works in a team environment and is required to assist others as necessary.

Responsibilities:

• Employ safe work habits and complies with all applicable Diversey safety requirements.
• Works closely with Corporate Quality Assurance, Plant Management, Production Teams, and QA Technicians at other plant sites.
• Provide daily production support which includes wet chemistry, analysis and technical support.
• Ensure products are produced according to Bill of Material (BOM).
• Calculate and provide adjustments to products as required.
• Direct and/or perform special laboratory analysis varying from CODs/BODs, enzymes, and products in any stage of the manufacturing process.
• Sample, test and release critical raw materials controlled under GMP regulations.
• Operate/Maintain laboratory instrumentation.
• Coordinate microbiological testing and the auditing and release of personal care products.
• Conduct audits and summarize data for management review.
• Provide support to the plant with regard to waste minimization, environmental compliance, regulatory compliance, and timely dispositions of returns, discrepant product and materials.
• Train and assist Plant Personnel in the use and standardization of laboratory equipment and procedures in their departments.
• Train new lab personal in procedures, product analysis and instrumentation use and maintenance.
• Ensure that present and new manufacturing and packaging BOM, components and labels are maintained concurrently with product specifications.
• Maximize batch making efficiency by continuously improving and implementing BOM revisions.
• Utilize SPC methods in Data Collection, Root Cause Analysis, Corrective/Prevention action effectiveness, and Cost Saving/Avoidance Analysis
• Support with the compliance and maintenance of GMP and ISO 9001/ISO 14001 documentation.
• Perform GMP and ISO 9001& ISO 14001 audits as scheduled.
• Communicate with R&D and Regulatory Department for process improvements as well as adjustments which are out of compliance for both the mixing area(products) and packaged goods.
• Review, inspect and authorize the release of DIN products (GMP) as well as perform routine stability testing on Plant manufactured goods and imported DIN products.
• Performs audits as required ie) BBS, Gemba, Finished Product.
• Participate in continuous improvement activities such as 5 Why investigations, Kaizen, TPM.
• Ability to change shifts to cover vacation and needs of the business.
• Other duties as assigned.

Required Qualifications:

• Minimum Education Required: Bachelor’s in Chemistry or related science with minor in Chemistry OR college equivalent education in chemistry.
• 1+ years of experience in a Quality Control environment within a GMP regulated facility.
• Experience with IR, UV/VIS, HPLC, and GC instruments.
• Working knowledge of computer applications such as email, MS office, SAP (a plus).

Other Qualifications:

• Organizational Skills: Ability to work in a paced environment, multitask, to take and follow directions.
• Self-Starter- takes initiative.
• Adaptability: Adhere to changing priorities and deadlines. Can effectively cope with change; can shift gears comfortably.
• Safety Focused: Dedicated to the health and safety of yourself and your colleagues. Maintaining a safe and respectful work environment.
• Professional Communication Skills: Must communicate well with Solenis employees, visitors, vendors and customers.
• Problem Solving: Analysis, problem solving and creativity.
• Attention to Detail: Must be able to complete accurate data and develop accurate written materials.
• Teamwork: respectful, team player, collaborative.
• Ability to work overtime, evenings and weekends where necessary.

We understand that candidates will not meet every single desired qualification. If your experience looks a little different from what we’ve identified and you think you can bring value to the role, we’d love to learn more about you.
At Solenis, we understand that our greatest asset is our people. That is why we offer competitive compensation, comprehensive benefits which include medical, dental, vision & 401K, and numerous opportunities for professional growth and development. So, if you are interested in working for a world-class company and enjoy solving complex challenges, whether in the lab or the field, consider joining our team.
Solenis is proud to be an Equal Opportunity Affirmative Action Employer, including Minorities / Women/ Veterans / Disabled. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability

• Employ safe work habits and complies with all applicable Diversey safety requirements.
• Works closely with Corporate Quality Assurance, Plant Management, Production Teams, and QA Technicians at other plant sites.
• Provide daily production support which includes wet chemistry, analysis and technical support.
• Ensure products are produced according to Bill of Material (BOM).
• Calculate and provide adjustments to products as required.
• Direct and/or perform special laboratory analysis varying from CODs/BODs, enzymes, and products in any stage of the manufacturing process.
• Sample, test and release critical raw materials controlled under GMP regulations.
• Operate/Maintain laboratory instrumentation.
• Coordinate microbiological testing and the auditing and release of personal care products.
• Conduct audits and summarize data for management review.
• Provide support to the plant with regard to waste minimization, environmental compliance, regulatory compliance, and timely dispositions of returns, discrepant product and materials.
• Train and assist Plant Personnel in the use and standardization of laboratory equipment and procedures in their departments.
• Train new lab personal in procedures, product analysis and instrumentation use and maintenance.
• Ensure that present and new manufacturing and packaging BOM, components and labels are maintained concurrently with product specifications.
• Maximize batch making efficiency by continuously improving and implementing BOM revisions.
• Utilize SPC methods in Data Collection, Root Cause Analysis, Corrective/Prevention action effectiveness, and Cost Saving/Avoidance Analysis
• Support with the compliance and maintenance of GMP and ISO 9001/ISO 14001 documentation.
• Perform GMP and ISO 9001& ISO 14001 audits as scheduled.
• Communicate with R&D and Regulatory Department for process improvements as well as adjustments which are out of compliance for both the mixing area(products) and packaged goods.
• Review, inspect and authorize the release of DIN products (GMP) as well as perform routine stability testing on Plant manufactured goods and imported DIN products.
• Performs audits as required ie) BBS, Gemba, Finished Product.
• Participate in continuous improvement activities such as 5 Why investigations, Kaizen, TPM.
• Ability to change shifts to cover vacation and needs of the business.
• Other duties as assigned