PART_TIME

FEED

UNKNOWN

Knowledge of child development, current health issues, developmentally age appropriate health risk factors, mental health issues, chronic and acute health conditions, current health practice, legislative issues, current laws associated with student educational placement, infection control, universal health precautions and personal hygiene. Excellent knowledge of nursing assessment and nursing diagnosis, pediatric health issues including care of technology dependent students, nursing principles, interventions and techniques and their relation to medical practices and promote quality assurance in nursing practice.

CAPS Collaborative

Substitute Registered Nurse

Talent Acquisition

Required knowledge or experience with: 5 years of experience with following, drafting, reviewing SOP's; 5 years of experience within cGMP environment, including the ability to clean room gown; 5 years of experience with Detail cGMPs and organizational FDA/industry expectations; 5 years of experience with facility and utility qualification requirements in compliance with associated regulations; 3 years of experience with data integrity and 21CFR Part 11 regulations and application in both GMP manufacturing and analytical laboratories; 3 years of experience working on projects of moderate to high complexity in regards to compliance of processes and product within facilities, equipment manufacturing and support areas; 3 years of experience with cGMP equipment including, for example, isolators and aseptic filling machines, autoclaves, bioreactors, chromatography and TFF skids, analytical instruments; and. DUTIES: Perform validation activities that include drafting, executing, reviewing, and approving quality documentation (User Requirement Specifications (URS), Commissioning protocols, IOQs, PQs, Re-qualifications, Periodic Reviews, Final Reports, Validation project plans, Investigations, and Risk Assessments) for clinical and commercial drug substance manufacturing of cell and gene therapy products.

YEAR

Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science. Our mission is to enable our customers to make the world healthier, cleaner and safer. With revenues of nearly $11 billion, we have approximately 37,000 employees and serve customers within pharmaceutical and biotech companies, hospitals and clinical diagnostic labs, universities, research institutions and government agencies, as well as in environmental and process control industries. We create value for our key stakeholders through two premier brands, Thermo Scientific and Fisher Scientific, which offer a unique combination of continuous technology development and the most convenient purchasing options. Our products and services help accelerate the pace of scientific discovery, and solve analytical challenges ranging from complex research to routine testing to field applications. All of our employees share a common set of values - Integrity, Intensity, Innovation and Involvement. Our ability to grow year after year is driven by our ability to attract, develop and retain world-class people who will thrive in our environment and share in our desire to improve mankind by enabling our customers to make the world healthier, cleaner and safer. If you share in our values and if you're looking for an employer who is strongly committed to developing talent and rewarding achievement, come grow with us at Thermo Fisher Scientific. Thermo Fisher Scientific is an Equal Employment Opportunity and Affirmative Action employer.

Thermo Fisher Scientific Inc

Engineer III, Validation

FULL_TIME

Registered Nurse

Registered School Nurse

At the project task level, the specialist participates in the development of functional specifications, proactively acts upon work assignments as required, delivers projects on agreed upon time schedule within allocated resources, ensures the accuracy of application systems documentation, and assists in providing end user training and support of developed applications. The Principal Application Specialist participates extensively (via committee membership or individual interviewing) in the needs assessment and system requirement process of applications development and is responsible for the assurance of quality control and risk management procedures during the life cycle application development process.

We are a $125 Million, NMSDC-certified Minority & Woman owned Workforce Solutions Company headquartered in the DC metro area with presence across US with global presence - Canada, Mexico, India, UK, Malaysia, Indonasia, Hongkong, Singapore, UAE. We are specialized in providing Workforce Solutions, SOW project delivery, Engineering Solutions, Creative Services. We currently support 100+ Fortune companies globally and across multiple industry segments. We are currently supporting several massive programs across industry segment nationally/globally (Intel, Ally, AMD, QUALCOMM, Morgan Stanley, Kraft/ Mondelez, MNP, Amdocs, Dell, SanDisk, Medtronic, Becton Dickinson, GE, Lockheed Martin, UTC, L-3 Communications, Caterpillar, BMW, Mercedes Benz, National Grid, Dominion, Energy Future Holdings, PSEG, 3M, Fidelity, Aetna, Humana, Johnson & Johnson, Pfizer, Merck etc). 
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender, identity, national origin, disability, or protected veteran status.

Lancesoft

Principal Application Specialist

HaleyMarketing

Collaborate with Project Managers (PM’s) to analyze customer ECN’s and ensure effective implementation to the production floor through proper use of the Engineering Change Order (ECO) process, including reviewing and communicating impacts of any changes (e.g., financial, inventory, WIP, open supplier orders, etc.), as it pertains to Quality. Collaborate with all internal groups and customers to help determine root cause of customer issues, Complaints, and CAPAs using various techniques including but not limited to Reenactment, PFMEA, Control Plans, Five Whys, Ishikawa (fishbone) Diagrams, Pareto Analysis, etc.

All Coghlin Companies

CT - 5134 Product Engineer II

ea_via_bold

ADAPTED_NOW

OTHER

Documentation and Record-Keeping : Maintain accurate and detailed records of the infusion process, including patient assessments, IV access site monitoring, medications administered, and patient responses. Collaboration with Healthcare Team : Collaborate with physicians, pharmacists, and other healthcare professionals to develop and adjust infusion therapy plans, ensuring that patient needs are met.

Magnet Medical

Travel Nurse RN - Infusion - $2,271 per week in Newton Lower Falls, MA

TravelNurseSource.com

Quality Inspector Location: Plainville, MA Compensation: $25.00 – $32.00 per hour Job Type: Full-time About the Role We are looking for a reliable Quality Assurance Professional to ensure that all external and internal requirements are met before our product reaches our customers. Quality Monitoring: Monitor all operations that affect quality and assure the reliability and consistency of production by checking processes and final output.

Butler Recruitment Group LLC

Quality Inspector

LogicMelon

About Prilenia Prilenia Therapeutics, a clinical-stage biotechnology company focused on the urgent mission of developing novel therapeutics to slow the progression of neurodegenerative diseases and neurodevelopmental disorders, is looking for a Director/Senior Director, GCP Quality Assurance Lead, to support programs in both Huntington’s Disease and ALS. The ideal candidate is both a hands-on quality practitioner and a strategic partner to Clinical Development, Regulatory Affairs, Drug Safety, and Biostatistics, combining deep GCP/GvP/GLP expertise with the executive presence to influence cross-functional teams and senior leadership.

Prilenia

Director / Senior Director, GCP Quality Assurance Lead (US/IL/EU)

This position is responsible for managing complex revenue transactions, reviewing customer contracts, performing technical accounting analyses, supporting month-end and quarter-end close activities, and partnering with cross-functional teams to ensure compliance with accounting policies and business objectives. The Lead Financial Analyst - FP&A for the Surgical Division serves as a strategic finance partner to the Commercial organization, supporting Sales and Marketing leadership with advanced financial analysis.

Hologic Inc

Senior Revenue Accountant

As one of the fastest-growing, diversified surgical ophthalmic businesses in the world, our purpose-built portfolio of trusted brands includes: Beaver (Knives and Blades), Visitec (Cannulas), Malosa (Single-Use Instruments), Vitreq (Vitreoretinal Surgical Products) and PhysIOL (Premium IOLs), and spans more than 90 countries. We've set our sights on touching the lives of millions of patients affected by conditions such as cataracts, refractive error, glaucoma, retinal disease, and dry eye.

Beaver-Visitec International Inc

Senior Design Quality Assurance Engineer

Since 2011, KKR portfolio companies have awarded billions of dollars of total equity value to over 60,000 non-senior management employees, demonstrating how broad-based engagement and alignment can create business value while driving greater financial inclusion. We are building precision technology that operates in the harshest environments on earth—on submarines deep below the surface, on ships safeguarding freedom at sea, and in missions where failure is not an option.

Circor Careers

Quality Tech Compliance

The Quality Technician performs quality audits of the facility and production processes, supports work order management, and assists with microbiological preparation, testing, and release of samples. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

HOUR

Actalent Inc

Quality Technician

The Associate Director serves as a key member of the Operations leadership team and partners closely with Quality, Engineering, Supply Chain, Regulatory, and Product Development functions to drive operational excellence, maintain inspection readiness, and support company growth objectives. The Associate Director, Manufacturing is responsible for the leadership, strategic planning, and operational execution of manufacturing activities supporting the production of GMP-regulated combination products.

EyePoint Inc

Associate Director, Manufacturing Operations

You will direct the work of a team of QA Reviewers, own the QA relationship with internal operational leaders and vendor partners (including AHS off-shore coding teams), review escalated charts yourself or facilitate further escalation, and turn findings into education and process changes that raise coding accuracy across the department. The actual base salary offered will depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job.

Devoted Health Services

Coding Quality Assurance Manager

You'll contribute to the success of our program by safely and efficiently performing chemical, biochemical, and bacteriological tests using laboratory equipment and materials to evaluate conclusions and solutions to complex challenges that may arise in the municipal facilities. One year of experience with knowledge of the concepts of chemistry, biology, and related experiences; procedures and materials used in chemical, biochemical, and bacteriological testing; laboratory safety; and equipment and material care and maintenance.

Solvenow

Lab analyst

The applicable full salary ranges for this position, by specific state, are listed below: New York City Metro Area: $186,900.00 - $307,800.00 Non-Metro New York state & Washington state: $166,300.00 - $274,100.00 * For quota-based sales roles on Cisco’s sales plan, the ranges provided in this posting include base pay and sales target incentive compensation combined. Comprised of experienced QA engineers and automation specialists with expertise in cybersecurity, AI-driven testing, and software validation, the team operates in a highly collaborative and technically focused environment.

Cisco

Software Quality Engineering Manager

Employee may be occasionally exposed to wet and/or humid conditions, fumes or airborne particles, toxic or caustic chemicals, extreme cold, extreme heat, and risk of electrical shock. EDUCATION: Bachelor's Degree required, preferably in Science, Engineering, Quality Management, Technical, or Healthcare related field; Advanced Degree desirable.

Fresenius Medical Care North America is a wholly owned subsidiary of Fresenius Medical Care AG & Co. KGaA, located in Bad Homburg, Germany. Through our dialysis services entity, Fresenius Medical Services, we operate more than 2,100 outpatient dialysis clinics in the U.S. Our Renal Therapies Group is responsible for the manufacture and distribution of a variety of dialysis products and equipment, including dialysis machines, dialyzers and other dialysis-related supplies. 

Fresenius Medical Care

Sr QMSR Manager

Quality Control TechnicianLocation: Marlboro, MARole SummaryWe are seeking a Senior Quality Control Technician with experience in optical or precision component manufacturing to support inspection, documentation review, and day-to-day quality activities in a high-mix manufacturing environment. Role requires the ability to transition between multiple process steps and products within a single shiftRole includes handling and use of chemicals, including the use of proper protective equipment.

Headwall Photonics Inc.

Senior Quality Assurance Technician

This position is responsible for performing the following tasks as assigned while receiving strategic supervision with assignments: Technically leads small to medium sized projects including one or more subsystem ownership while managing short & long term deliverables to meet project milestones. R&D Manager/ R&D Manager Organizational Relationships: Works with Divisional personnel and cross-functional personnel including R&D, Regulatory, Marketing, PMQA, Manufacturing Engineering, and Quality Engineering.

Sales Associate Jobs in Minnetonka, MN

Substitute Registered Nurse CAPS Collaborative

Engineer III, Validation Thermo Fisher Scientific Inc

Registered Nurse CAPS Collaborative

Registered School Nurse CAPS Collaborative

Principal Application Specialist Lancesoft

CT - 5134 Product Engineer II All Coghlin Companies

Travel Nurse RN - Infusion - $2,271 per week in Newton Lower Falls, MA Magnet Medical

Quality Inspector Butler Recruitment Group LLC

Director / Senior Director, GCP Quality Assurance Lead (US/IL/EU) Prilenia

Senior Revenue Accountant Hologic Inc

Senior Design Quality Assurance Engineer Beaver-Visitec International Inc

Quality Tech Compliance Circor Careers

Quality Technician Actalent Inc

Associate Director, Manufacturing Operations EyePoint Inc

Coding Quality Assurance Manager Devoted Health Services

Lab analyst Solvenow

Software Quality Engineering Manager Cisco

Sr QMSR Manager Fresenius Medical Care

Senior Quality Assurance Technician Headwall Photonics Inc.

R&D Engineer 3 Hologic Inc

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