Chemical Operator Salary at Nft Inc BETA

About Us Competition Headwear is a leading manufacturer of 100% American-made baseball caps, located right here in Denver, Colorado. With a commitment to high quality craftsmanship and American values, we design, manufacture, and deliver premium headwear for businesses, customers, and organizations nationwide. Competition Headwear is a family-owned business and has been for over 30 years. When you join us you will be joining a team that cares about the work we do and each employee feels like an owner. Your Job As the Production Supervisor, you will be responsible for helping drive production output, meeting our goals and targets and helping increase manufacturing efficiency dramatically. You will report and work closely with the leadership team (President & VPs) and help manage an embroidery and sewing department of ~30 people. This role requires exceptional communication skills - ideally in both English and Spanish, a deep understanding of manufacturing processes including embroidery

Position: QC Microbiologist / QC Chemist Location: Denver, CO (Onsite) Duration: 2-3 months (Contract) Sponsorship: Unavailable Key Responsibilities: Perform Microbial Identification (Microbial ID) tests using validated test methods and procedures. Ensure compliance with Good Laboratory Practices (GLP) and regulatory standards. Conduct method transfer, particularly for potency methods, if assigned as a QC Chemist. Accurately document results and maintain laboratory records. Collaborate with cross-functional teams to ensure high-quality lab operations. Troubleshoot and resolve technical issues related to microbial or chemical testing. Required Qualifications: ✔ Strong lab experience with hands-on work in a QC environment. ✔ Knowledge of GLP and experience following test methods and procedures. ✔ Ability to work independently and within a team setting. ✔ Experience in Test Method Development is a plus but not required. Work Conditions: Must be available to work onsite in Denver, CO for t

Chemical Operator - Production Mead, CO Full Time Production Entry Level Share (https://boulderscientificcompany.applytojob.com/app/share/ULDfWPKEcw) Earning potential of $29.00 per hour; 1st year earning potential $66,500 with bonus at target and 2nd year potential $72,000 with bonus at target The Production Operator follows established procedures to manufacture chemical intermediates and finished products. The Operator follows procedures that are set forth in the form of batch records and work instructions. This person completes a variety of duties: in addition to operating chemical processes, the employee may perform setup, cleaning of equipment, waste disposal, emergency response, warehouse activities, maintenance, and clean-up activities needed to facilitate general operations and regulatory compliance. Operators are given extensive safety and Operator-specific training before they are assigned process work. After the initial training period, Production employees work 12-hour shif

Supervisor – Denver, CO General Shale Brick, Inc., a leading manufacturer of brick and masonry materials, is seeking a Supervisor for our production facility in Denver, CO. The successful candidate will manage the departmental operations within a highly automated manufacturing environment. Responsibilities will include: Motivating and directing employees to ensure compliance with production and quality goals, safety policies, and company rules. Coordinating maintenance repair work and ensuring equipment is kept in proper working condition. Using problem-solving and critical thinking techniques to improve process and safety issues. Organizing production schedules to ensure the maximum utilization of equipment and personnel. Production inventory accuracy, periodic physical counts, and adjustment requests. Preferred Qualifications: Excellent communication skills, computer literacy, and mechanical aptitude. Experience with Programmable Logic Controllers (PLCs) and robotics is a plus. The d

This position is responsible for establishing, implementing, and maintaining the QC and Regulatory systems, including: Performing routine quality control functions which require application of standard techniques, procedures, and criteria. Reporting and correlating data, recognizing discrepancies in results and following operations through a series of related, detailed steps or processes. Amending and keeping accurate quality and regulatory documentation records. Essential Duties/Responsibilities Review and approve product carton renderings, codes, descriptions, and labels. Create and update product labeling. Manufacturing Quality Support for all shifts. Audit incoming finished goods and compare to set quality data. Investigate known or reported quality issues and report discrepancies to Quality and Regulatory Manager. Support packaging department and warehouses in Quality areas. Conduct product inspections and testing. Assist with new product reviews. Preserve Quality Control Site Dat

Overview: Job Summary Perform the approval for return to service after maintenance or modifications of an aircraft/engine/article in accordance with regulations, to include completion of FAA Forms 8130-3 and 337s when required along with logbook entries. Ensure aircraft or any component returned to service meet type design or properly altered state and in condition for safe flight. Ensure aircraft airworthiness by maintaining safety conditions conforming to standards set by the FAA and company policy. Verify all inspections performed comply with Manufacturers Instructions for Continued Airworthiness and Air Methods Repair Station Manual. Essential Functions and Responsibilities include the following: Perform work order opening and closing tasks, preliminary inspections, hidden-damage inspections, statement of work review, and final inspections on civil aviation articles in accordance with the current maintenance data. Enters the return to service / airworthiness release authorization i

Job Title: QUALITY ASSURANCE SPECIALIST Medical Device manufacturer is seeking a Quality Assurance Specialist to join their growing team! Tasks will include supporting key quality assurance processes throughout the quality team and diverse departments. Ideal candidate will have experience working through SOPs, understand FDA regulations and are strong in quality documentation. Company is seeking individual's with strong time management skills, Hands on abilities and excitement for industry! Qualifications: - 3-5+ year's Experience within Quality Specialist/Quality Assurance Roles - Experience Working in Electro-Mechanical Industry or High Tolerance - Background Managing Complaints - Writing, Creating Complaints, Tracking, etc - Experience Working with CAPA's/NCRs - Skilled in Technical Writing (Creating SOPs) - Documentation Experience Top Skills Desired: Quality assurance and ISO 13485 If Interested in Learning More - Please Apply! Top Skills Details: Quality assurance, medical device

Integrated DNA Technologies (IDT) is the leading manufacturer of custom oligonucleotides and proprietary technologies for genomics applications. Our work is complex and cutting-edge, and our team members are curious, creative thinkers who understand that good data drives smart decisions. At IDT, we realize that although science may be uniform, people are unique. We promote a culture where engaged people are motivated and have opportunities to achieve their full potential, as part of one global team. IDT is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health. This position is part of the Quality Assurance Team located in Boulder, Colorado and will be on-site. At IDT, we are one global team. We celebrate our differences, engage in healthy debate, and are inclusive. Together, we accomplish great things! In this role, you will have the opportunity to: + Maintains records and proce