Senior Principal Scientist Salary at Merlin Development Inc BETA

Job Description Job Description This is a hybrid position where the majority of your time would be spent working in the quality department inspecting parts and filling out quality control documentation. The other part of your time would be spent learning how to perform tests and analyze chemistry in the chemistry laboratory under the guidance of a full-time chemist. The intention would be to assist our chemist part of your day on a daily basis and to fill in for the chemist when the chemist is absent. Job Duties · Inspect finished parts visually and for thickness according to customer and specification requirements. · Work with unracking department to evaluate the quality of parts coming off the plating line. · Work with packing department to evaluate the quality of parts being packaged to ship. · Work closely with plating department to inspect parts in-process and to communicate key information pertaining to quality. · Ensure that work order shop travelers are filled out completely an

Anodizing Chemist - Fridley, MN The Anodizing Chemist oversees all operations of the Anodizing Lab. This position supports manufacturing and quality teams by driving continuous process improvements and researching new processes/finishes for the chemical and mechanical finishing lines, aligning with the company's core strengths and objectives. Additionally, this role leads Environmental Health & Safety (EH&S) initiatives to enhance workplace conditions for employees and ensure compliance. Responsibilities: Carries out research on finishes and processes, undertaking departmental research and development tasks as directed by the Director of Engineering & Technical Services. Assist manufacturing to troubleshoot anodizing and other manufacturing problems. Under the direction of the Manager, Responsible for managing the analysis and upkeep of the production line's chemical processes. The testing encompasses cleaners, rinses, etching, brightening, anodizing, and sealing tanks. Make necessary

Job Description Job Description · 100% Onsite Role will ensure integrity of study data by entering, reviewing, modifying, reconciling, and organizing data Testing and verification of clinical data management systems · Discrepancy management (creating, routing, and resolving) Comply with FDA regulations · Develop and maintain positive and trusting relationships with all levels of employees and customers · Continuous Improvement mindset · Will identify potential issues, this is very repetitive work · Will require long periods of sitting or standing in the office Data will be studied and analyzed in Excel format so knowledge of pivot tables, search functions, and x-lookups are required at an intermediate level · Nice to have - Medical Device experience Will need to have a minimum of 2 years of experience: comparable or closely related clinical research environment; HM is not opposed to 1 year of experience if all of the other requirements are met · Education: H. S. Diploma or GED is requi

Duration: 12+ Month W2 Contract (C2C not available) Onsite in Plymouth, MN We are looking for a detail-oriented individual to perform tests on medical devices (e.g., heart catheters) in a hands-on, onsite role. The position involves executing a variety of tests (mechanical, electrical, conditioning, length, OD, and visual) under written and verbal instructions. Key Responsibilities: Conduct simple to complex tests on medical devices. Follow written and verbal instructions accurately. 85% of the time spent in the lab and 15% spent at a desk. Collaborate with engineers to communicate findings, problems, and solutions. Adhere to safety guidelines and use appropriate safety equipment. Required Experience and Skills: Familiarity with medical device testing (or related product-building experience). Experience with R&D or working with test methods. Strong attention to detail, documentation skills, and ability to follow good documentation practices. Proficiency in time management, task priorit

Clinical Studies Support Coordinator II (24 month contract // Minneapolis, MN): HM's Top 3: Proficiency in MS Office applications (Excel, PPT, Word, web-based applications) Clinical research, academic research, or clinical care experience preferred. Experience with GCP, regulatory and/or compliance guidelines for clinical trials (nice to have). Education Required: Bachelor’s degree with 0 years of clinical research experience. Years’ Experience Required: 0 years of Clinical Research Experience Required Duties: Supports clinical studies by executing and maintaining one or more of the following areas: Data coordination: actively participates in the development and testing of case report forms, study reports, and study databases based on protocol requirements. Ensures timely and quality completion of data forms; verifies study data; and generates, manages, and resolves data discrepancies. May process compensation & identify and resolve compensation discrepancies. Document coordination - c

Primary Duties Provide a summary describing the major role, responsibility, and purpose of the job. Summarize key areas of accountability and budget responsibility, if applicable. Execute routine in-process, drug substance, and stability test methods. Use a variety of laboratory instrumentation and computer systems to collect and record data (such as LIMS, SoftmaxPro, Charles River Endoscan, MODA, and Empower). Maintain lab operations (including cleaning, ordering of supplies, reagent preparation, stocking, waste disposal). Responsibilities: Job Function and Description Describe the essential daily job functions. Demonstrate a functional understanding of a laboratory setting and Standard Operating Procedures (SOP’s). Work within laboratory environment for extended periods of time, conducting facility monitoring (i.e., Environmental Monitoring and Critical Utility Monitoring) and product tests, reviewing data, maintaining laboratory materials and instruments and other laboratory functio

Position: Lab Technician Type: Contract-to-Perm Worksite Location: Minneapolis, MN (On-Site, 5 Days a Week) Job Duration: 6 Months, Contract-To-Hire Pay Rate: $22 - $25 / Hourly JOB RESPONSIBILITIES • Ownership of technical service requests, including documenting work, providing status updates, and communicating with requestors. • Execution of application/laboratory test plans for material and process characterizations and root cause analysis. • Management of laboratory equipment, products, and supplies, including preventative maintenance and shipment of materials. • Support for quality and cost savings initiatives. • Practice of safe work habits and compliance with all safety, health, and environmental regulations. REQUIRED SKILLS AND EXPERIENCE • Junior college or science-related courses. • Good hands-on skills. • Strong communication and teamwork skills. • Attention to detail and strong problem-solving abilities. • Ability to perform routine and non-routine tests and analyses accura

Please note this job description is not designed to cover or contain a comprehensive listing of duties that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice. ABM offers a comprehensive benefits package including health insurance (medical, dental and vision), 401(k) plan with immediate vesting, short and long-term disability, PTO, paid holidays and more. ABM values the rich diversity of its workforce. We strive to foster a work environment of respect and engagement that harnesses our workforce’s diversity to our common goal of providing prompt and superior client service. ABM is an EOE/AA (M/F/Vet/Disability/Gender Identity/Sexual Orientation)and is committed to working with and providing reasonable accommodation to individuals with disabilities. If you have a disability and need assistance in completing the employment application, please call 888-328-8606. We will provide you with assistance and make a dete