- Novo Nordisk Inc. (West Lebanon, IN)
- …certify compliance with specifications and procedures Works closely with Manufacturing and Quality Control to resolve open issues resulting from record reviews, walk ... Qualifications Education and Certifications: Bachelor's Degree (or equivalent) required, a scientific discipline preferred Work Experience: A minimum of one (1) year… more
- Novo Nordisk Inc. (Durham, NC)
- …our employees to embark on life-changing careers, and the opportunity to help improve the quality of life for millions of people around the world. In NC, we operate ... with IT, metrology & other key stakeholders to ensure the right quality , cost & timely completion of all deliverables. Relationships Manager. Essential Functions… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- The QA Specialist II - Engineering/Validation is responsible for cGMP compliance ensuring all FDA regulations, internal procedures/specifications, and other ... communicating with the Engineering and Validation departments. Job Responsibilities Perform Quality review/approval of URS, FAT, SAT, IQ,OQ,PQ protocols and summary… more
- DivIHN Integration Inc (Scarborough, ME)
- …contact one of our Talent Specialist Rashi | 630 8471027 Title: Regulatory Specialist II Location: Scarborough, ME Duration: 7 months Start Time (AM/PM) : ... experience and/or 2 years relevant industrial experience typically with a quality , product-development/support, or scientific affairs function Skills: Knowledge… more
- DivIHN Integration Inc (Scarborough, ME)
- …of our Talent Specialists Sivanesan at 224 369 0756 Title: Regulatory Affairs Specialist II Location: Scarborough, ME Duration: 7 Months Description The position ... of Regulatory Affairs Specialist II is within our Infectious Disease...and/or 2 years relevant industrial experience typically with a quality , product-development/support, or scientific affairs function COMPETENCIES:… more
- DivIHN Integration Inc (Lake Forest, IL)
- …one of our Talent Specialist Rashi | 630 8471027 Title: Regulatory Affairs Specialist II - 3 Openings Location: Lake Forest, IL Duration: 12 Months ... Description The position of Regulatory Affairs Specialist II is within our Infectious Disease business unit. In this role you will prepare documentation for EU… more
- DivIHN Integration Inc (Santa Clara, CA)
- …one of our Talent Specialists Rashi at ### Divya at ### Title: Regulatory Specialist II Location: Santa Clara, CA Duration: 6 Months Description: Exempt/Non ... experience and/or 2 years relevant industrial experience typically with a quality , product-development/support, or scientific affairs function. Seeking candidate… more
- George Washington University (Washington, DC)
- …resource maintenance, poison prevention educational programs, clinical research projects, scientific manuscript preparation, quality assurance and data ... with The George Washington University Medical Center. In recognition of its high quality , the Center is accredited by the American Association of Poison Control… more
- Spectraforce Technologies Inc (Bridgewater, NJ)
- …Excel, PowerPoint) VEEVA experience is a plus Description: The CMC Regulatory Technical Writer II authors high quality Module 2 and 3 regulatory submissions for ... Job title: CMC Regulatory Technical Writer II Location: Bridgewater, NJ, Hybrid Duration: 1 year...can change at any time. 5 years experience with scientific background (BA/BS, MS or PhD) Must have experience… more
- Viva USA, Inc. (Mettawa, IL)
- …of site and division level policies and procedures. The position of Regulatory Affairs Specialist II is within our Infectious Disease business unit. In this role ... Title: Regulatory Specialist - Onsite Description: Years Experience: 2-5 years...and/or 2 years relevant industrial experience typically with a quality , product-development/support, or scientific affairs function Skills:… more
- Kelly Services (West Hills, CA)
- …West Hills, CA** **Pay Rate: $42.00** **Contract Length: 12 Months** **Job Description:** Quality Specialist II , Post Market Surveillance (PMS) and Stability ... capability along with MDR/Vigilance reporting. The Post Market Surveillance Specialist may also review and monitor data and document... may also review and monitor data and document quality , as requested by the manager. **Product Complaints:** +… more
- ThermoFisher Scientific (Middletown, VA)
- …Advancement Opportunities **Location/Division Specific Information** Middletown, VA Shift: Days The Quality Specialist II will monitor/address/track ... **Job Description** As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues… more
- ThermoFisher Scientific (Cranbury, NJ)
- …unit. **Discover Im** **pactful Work:** We are seeking a highly motivated and meticulous Quality Systems Specialist to join our team. The Quality Systems ... **Job Description** As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes...the Life Sciences Solutions Group (LSG). Reporting to the Quality Assurance Systems Manager for the Recombinant Proteins business… more
- ThermoFisher Scientific (San Diego, CA)
- **Job Description** **Job Purpose** **The STS Quality Specialist II will provide support for Document Control and Technical Writing; this position will ... support the Quality Management System for the Science and Technology Team...support through conducting Document Reviews and use practical laboratory scientific work experience and Technical Writing skills to revise… more
- ThermoFisher Scientific (Bridgewater, NJ)
- **Job Description** When you're part of Thermo Fisher Scientific , you'll do challenging work, and be part of a team that values performance, quality and ... make significant contributions to the world. **Position Summary** : The Procurement Specialist role will be implementing procurement and sourcing activities, as well… more
- ThermoFisher Scientific (Cambridge, MA)
- **Job Description** When you're part of the team at Thermo Fisher Scientific , you'll do important work. And you'll have the opportunity for continual growth and ... will you make an impact?** As a Customer Site Specialist , you'll be a part of the important work...procedures and adhere to company standards. Provide compliance and quality system management support to help ensure the LIS… more
- ThermoFisher Scientific (Middletown, VA)
- **Job Description** As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues ... and Involvement - working together to accelerate research, solve sophisticated scientific challenges, drive technological innovation, and support patients in need.… more
- ThermoFisher Scientific (Florence, SC)
- …class outsourcing capabilities. This position partners with the members in Quality , Operations, and Procurement to provide GMP Compliance expertise to customers, ... through establishment and maintenance of the site Supplier Quality Management (SQM) program. **A Day in the Life.** 1. Serve as Quality contact and lead on… more
- ThermoFisher Scientific (Manati, PR)
- **Job Description** When you're part of the team at Thermo Fisher Scientific , you'll do meaningful work, that makes a positive impact on a global scale. Join 120,000 ... departmental objectives. Carry out all duties within strict compliance to Patheon quality systems SOP's and Good Manufacturing Practice (GMP). Maintain workspace in… more
- ThermoFisher Scientific (Memphis, TN)
- **Job Description** When you're part of the team at Thermo Fisher Scientific , you'll do important work, like helping customers in finding cures for cancer, ... operating procedures. (SOP's) + Owns and supports others regarding Quality requirements to ensure adherence to SOPs. + Actively...or members of the business community At Thermo Fisher Scientific , each one of our 90,000 extraordinary minds has… more
