- ThermoFisher Scientific (Cincinnati, OH)
- …Conditions** Office **Job Description** Investigates and observes Operations and Quality Operations departments to assure that FDA current Good Manufacturing ... the Code of Federal Regulations. Assists the Operations and Quality Operations departments in satisfying all FDA and DEA...of management + Assist on functional area GEMBAs and GMP inspections of facilities to assure compliance with the… more
- Novo Nordisk (Clayton, NC)
- …+ Minimum of three (3) years progressively responsible experience in material management &/or GMP quality , required + Experience in one or more of the following ... At Novo Nordisk, we are helping to improve the quality of life for millions of people worldwide. For...+ API & raw materials a plus + Regulations GMP &/or ISO a plus + Pharmaceutical or other… more
- ThermoFisher Scientific (Middleton, WI)
- …lab coat, ear plugs etc.) **Job Description** Job Description Scientist - Inhalation Specialist II , Clinical Lab Scientist Middleton, Wisconsin, United States of ... (Mon-Fri) **Environmental Conditions** Adherence to all Good Manufacturing Practices ( GMP ) Safety Standards, Some degree of PPE (Personal Protective Equipment)… more
- Catalent Pharma Solutions (Harmans, MD)
- ** Specialist II , MTO** **Summary:** _Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, ... products including AAV and other viral vector-based therapies and vaccines._ The ** Specialist II , MTO** will provide support to Manufacturing Associates to… more
- Actalent (Baltimore, MD)
- Job Title: Quality Assurance Specialist IIJob Description The Quality Assurance Specialist II is responsible for maintaining quality assurance ... sustainability initiatives, and other special projects. Essential Skills + GMP + Quality assurance + ISO standards...and airborne particles, with a moderate noise level. The Quality Assurance Specialist II will… more
- Fujifilm (College Station, TX)
- **Position Overview** The Quality Assurance - Compliance Specialist II - Audit and Inspectionwill support all associated responsibilities in compliance with ... FUJIFILM Diosynth Biotechnologies quality policies and site SOPs to ensure regulatory compliance....Quality Culture' by coaching in the application of GMP Principles including the underlying rational of those principles.… more
- Fujifilm (College Station, TX)
- …to passionately support delivery and embedding of the Data Integrity projects at FDBT. The Quality Assurance (QA) Specialist II for Data Integrity will be ... to instill a ' Quality Culture' by coaching in the application of GMP Principles including the underlying rational of those principles. + Act as an ambassador… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Description** **Role and Responsibilities:** + Interact with contract manufacturers to resolve quality issues with minimal supervision + Performs a wide variety of ... requirements. + Participates in developing Standard Operating Procedures (SOPs) to ensure quality objectives are met. + Maintains routine programs and processes to… more
- Abbott (St. Paul, MN)
- …of structural heart disease. **The Opportunity** We are recruiting for a **Regulatory Affairs Specialist II ** to join our team on-site in St. Paul, MN.As an ... Our business purpose is to restore health and improve quality of life through the design and provision of...individual contributor, the function of a Regulatory Affairs Specialist II is to provide support for… more
- Fujifilm (College Station, TX)
- …of technical training for the Manufacturing organization. Also, the Manufacturing Training Specialist II will prepare training, design documents, and manage ... needed. + Schedule training sessions for manufacturing teams. **30% GMP Compliance** + Use various electronic tools to provide...to identify the level of training needed. + Perform quality review of training materials, as needed. + Perform… more
- Fujifilm (College Station, TX)
- **Position Overview** Under general supervision, the Materials Specialist II is responsible for the accurate receiving, ordering, shipping, general warehousing, ... and internal distribution of cGMP (current Good Manufacturing Practices) and non- GMP materials in support of company operations. **Company Overview** The work we do… more
- Eurofins (Lancaster, PA)
- …origin, traceability and purity of biological substances and products. + Applies GMP /GLP in all areas of responsibility, as appropriate + Applies the highest ... quality standard in all areas of responsibility + Demonstrates.... Regular attendance and punctuality + Applies the highest quality standard in all areas of responsibility + Demonstrates… more
- ThermoFisher Scientific (Millersburg, PA)
- …Shift (Days) **Environmental Conditions** Adherence to all Good Manufacturing Practices ( GMP ) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail ... HS Diploma/GED Preferred: Associates Degree **Experience:** + 2+ years of quality management system experience. + Experience working in a team environment… more
- Abbott (Scarborough, ME)
- …emergency departments, physician offices and clinics. We have an opportunity for **Production Specialist II ** based in **Scarborough, ME.** In this role, you ... routine work in all production areas with limited supervision + Ensures quality of product using standard operating procedures, templates, training and supervision,… more
- ThermoFisher Scientific (Richmond, VA)
- …Shift (Days) **Environmental Conditions** Adherence to all Good Manufacturing Practices ( GMP ) Safety Standards, Some degree of PPE (Personal Protective Equipment) ... digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities… more
- Catalent Pharma Solutions (Harmans, MD)
- …tradition of quality and service. Catalent provides process development and GMP manufacturing services for Phase I/ II clinical trials to industry leaders ... the Head of Facilities & Engineering. The role of Specialist is to provide regulatory guidance and GMP...required (Engineering preferred): + Minimum one (1) year of GMP quality system experience in pharmaceutical or… more
- ManpowerGroup (Millsboro, DE)
- …of the largest Pharmaceutical companies in USA is looking for Regulatory Operations Specialist - II (Associate) at Millsboro, DE **Job Title:** Regulatory ... Operations Specialist - II (Associate) **Location:** Millsboro, DE...labeling content** review **as per FDA guideline** . * ** Quality check** of **labeling** content errors. * **Label artwork**… more
- University of Pennsylvania (Philadelphia, PA)
- …and wellness programs and resources, and much more. Posted Job Title Quality Assurance Specialist (Regulatory) CVPF(Center for Cellular Immunotherapy) Job ... Profile Title Research Coordinator Senior Job Description Summary The Quality Assurance Specialist will work within the Clinical Cell and Vaccine Production… more
- Ascensia Diabetes Care (Portsmouth, NH)
- …solutions that simplify and improve their lives. We use our innovation and specialist expertise in diabetes to develop high quality solutions and tools ... Ascensia Diabetes Care is a global specialist diabetes care company, dedicated to helping people...machines, monitoring their operations, and ensuring that products meet quality standards. Location: Porstmouth, NH What you will be… more
- Iowa State University (Ames, IA)
- …This position will be classified as an Agriculture and Natural Resources Extension Specialist II . The Farm, Food and Enterprise development team supports ... Position Title:Food Safety Extension Specialist Job Group:Professional & Scientific Required Minimum Qualifications:Bachelor's degree and 2 years of related… more