QC Inspector Salary at Memry Corp BETA

Job Description Job Description Entry Level - Quality Control Analyst I - 1st Shift 6 Months (Possibility of Extension) Pearl River, NY Shift: M-F 9-5PM. Fully onsite position Local candidates only Free parking onsite Fully onsite Reliable transportation Extension is possible, however TBD Required: Soft Skills: Strong work ethic, self-starter, critical thinking Technical Skills: Aseptic Technique (nice to have) Job Description The QC Micro team in Pearl River is a diverse group of individuals, with varying degrees of experience, who are Quality-orientated and can continuously deliver high-quality results while remaining compliant with the changing regulations associated with the pharmaceutical industry. We are singularly focused on delivering the safest product to our end-user (the patient) in an efficient and compliant manner. This is a dynamic and flexible group, capable of switching gears, at a moment’s notices. Job Responsibilities • Bioburden/ Microbial Enumeration, Endotoxin, Mic

Job Description Job Description Job Title Quality Control Analyst Department Reports To FLSA Status EEO Category Job Class Last Modified 900 Director – Quality Exempt Tech Indiv Con. 03.20.2025 Job Summary Ensure consistent quality of our production output. Conduct laboratory tests on incoming raw materials, in-process production samples, and final products before distribution. Essential Functions / General Accountabilities Perform daily analysis of incoming raw materials, blends, and reevaluations. Perform qualitative organoleptic evaluations of material. Analysis techniques include Specific Gravity, Refractive Index, Optical Rotation, LAB Color, Gas Chromatography, and GCMS. Interpret complex GC analysis of essential oils. Assist in the investigation of root causes of internal and external non-conformances. Aid in the implementation of corrective and preventative actions. Maintain all lab equipment including daily calibrations. Modify, improve, and validate analytical procedures to m

As a Quality Assurance Engineering Intern, you will assist in ensuring product quality through inspection, measurement, and process evaluation. You will work closely with experienced quality engineers and production teams to support continuous improvement initiatives. This internship is ideal for students with strong attention to detail and an interest in quality systems in a manufacturing environment. Key Responsibilities: Conduct inspections of molded and assembled components using precision measuring tools (calipers, micrometers, height gauges, etc.). Interpret and analyze blueprints, technical drawings, and specifications to ensure compliance with quality standards. Assist in performing First Article Inspections (FAI) and process capability studies. Support root cause analysis and corrective action implementation for quality issues. Document inspection results and maintain quality records per company procedures. Assist in developing and updating Standard Operating Procedures (SOPs)

Pharmaceutical Quality Control Supervisor Danbury, CT$85,000 to $100,000 + Full Benefits + Paid Relocation Job SummaryDevelops, implements and maintains the activities of quality control systems. Oversees methods and procedures for inspecting, testing and evaluating the precision, accuracy and reliability of company products. Contributes information to help develop budgets. Makes recommendations for corrective action necessary to assure conformity with quality specifications. Assures finished products conform to government and company standards and satisfies GMP regulations. Essential duties and key job responsibilities and essential functions. Provide general or direct supervision to exempt employees and/or skilled nonexempt employees Act as advisor to unit or sub-units, becomes actively involved as required to meet schedules or resolve problems Provides supervision on the floor enforcing compliance data integrity, SOPs, specifications, methods, USP, and cGMP through real time verific

Job Description Job Description Job Description:We are looking for an energetic, self-driven, quality assurance associate to become part of our Quality team. This hands-on position will be responsible for day-to-day production inspections, as well as being an integral part of continuous improvement and assuring quality standards are maintained in-line with ISO 9001 guidelines. This job is located in Guilford, CT. PRINCIPAL DUTIES AND RESPONSIBILITIES (but not limited to) · Real-time inspection of products, processes and systems. · Review/ Approval of process paperwork for critical customer/production processes. · Aid in administration and execution of facility quality programs, (i.e., Training, Corrective Action, Continuous Improvement, Lean, Non-Conformance, etc.). · Daily auditing of departmental processes and paperwork according to QA procedures.. · Create reports / analysis as necessary / required. · Perform tasks in accordance to all GSC safety rules and regulations... · Performs

Job Description Job Description Quality Control Technician Westport Precision, founded in 1979, has grown from a small shop to one of New England’s largest precision sheet metal fabrication companies. Our new state-of-the-art facility allows us to provide our employees with an up-to-date, clean work environment and modern equipment. Choose Westport Precision. Let’s Build Your Success Story: Development Opportunities – We will connect you with opportunities to advance. Dedicated Support – We will support you every step of the way. Career Advancement – As we build your work experience and develop your skills, we will help you turn that hard work into your next great opportunity. How this job will fit your life: Hours – 7:00 AM to 3:30 PM Days – Monday through Friday (No Weekends!!) Pay – TBD What you can expect each day: Conduct thorough checks on products to see if they meet company guidelines and safety standards. Reject unacceptable products and initiate corrective action. Monitor man

Overview Alliant operates on the forward edge of innovation in data-driven marketing, helping brands target consumer audiences effectively in digital and traditional advertising channels. We are looking for a hands-on IT Quality Assurance Specialist who will grow Alliant’s manual and automated software testing capabilities. This position will have overall ownership of the testing process and take responsibility for driving quality assurance throughout the software development lifecycle. The QA specialist will prepare and implement test plans, champion automation in testing, drive the resolution of defects, and document test outcomes. This role will also orchestrate test execution in a hybrid environment having both on-premises and cloud-based components. The ideal candidate is at home in a dynamic environment, exhibits a detail-oriented mindset, performs thoughtful problem-solving, fosters enthusiasm and motivates colleagues. Principal Responsibilities Work closely with project teams a

Key Responsibilities: Conduct research on applicable mandatory and voluntary safety standards to ensure product compliance. Develop and implement product safety and performance requirements to maintain quality benchmarks. Perform risk analysis to identify potential safety concerns and ensure mitigation strategies. Coordinate third-party testing to verify product safety and regulatory compliance. Analyze consumer complaint trends, conduct root cause investigations, and implement corrective actions. Oversee Supplier Quality Management Systems Audits to ensure vendors meet quality expectations and are current on all audits. Attend annual JPMA/CPSC meetings to stay updated on industry regulations and best practices. Ensure that all tests and procedures are properly understood, executed, and evaluated, implementing modifications when necessary. Monitor product performance by gathering relevant data and generating statistical reports for quality assessment. Qualifications & Requirements: 5+