وظيفة في Fda Regulations في Houston

No Sponsorship is available now or in the Future. The Quality Assurance Manager will be responsible for managing the quality management system and ensuring regulatory compliance for the companys products processes and services. RESPONSIBILITIES: Oversee the companys adherence to dome المزيد...

Our direct client is looking for a QA Analyst in Massachusetts(Onsite). Job Title: QA Analyst Location: Tyngsborough MA Type: Full Time W2 SUMMARY: The Quality Assurance Manager will be responsible for managing the quality management system and ensuring regulatory compliance for the المزيد...

POSITION Project Coordinator LOCATION Remote DURATION Long Term INTERVIEW TYPE Video REQUIRED SKILLS Must have Pharma/FDA regulations experience Strong MS project MUST HAVE MS PROJECT work within the PMO support resource management The role المزيد...

Job Description: Position Overview: As a Senior MES PASX MBR Modeler you will play a critical role in the design implementation and maintenance of our MBR using Werum PASX V2/V3. You will ensure compliance with industry standards and regulations while optimizing production processes. المزيد...

Job description Job Title: Junior Quality Control Chemist Job Summary: The Quality Control Chemist plays a crucial role in ensuring the quality and safety of products in various industries including pharmaceuticals cosmetics food and beverages and manufacturing. The primary resp المزيد...

We are seeking a highly skilled and experienced Senior iOS App Developer with a proven track record of 8 to 10 years in iOS app development and a strong background in Bluetooth Low Energy (BLE) technology. The ideal candidate will bring expertise in developing innovative and userce المزيد...

Salary Expectations: Annual: $65000 BR000 ***We will do a Sign on Bonus*** Discussed at time of Interview18% Perm Placement FeeThe Lead Mammography technician performs and supervises mammography exams in accordance with ACR guidelines manages ACR and MQSA QA testing and maintains Q المزيد...

Salary Expectations: Annual: xx65000 xx95000 ***We will do a Sign on Bonus*** Discussed at time of Interview18% Perm Placement FeeThe Lead Mammography technician performs and supervises mammography exams in accordance with ACR guidelines manages ACR and MQSA QA testing and maintain المزيد...

Minimum of 5 years experience as a Computer System Validation Consultant in a regulated environment (preferably Pharma) and must have played a lead role (able to work independently with minimal guidance). Worked in a Pharmaceutical company as QA/QC within the Sales and Marketing المزيد...

Principal Specialist Validation Athens GA Full time Description As an employee of Boehringer Ingelheim you will actively contribute to the discovery development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees المزيد...

Description: Work day/hours: 40 hours M F day shift Pay rate: $40/hour Hybrid (at least 3 days onsite) ***LOCALS ONLY please do not submit anyone that is not local to San Jose*** **HM is looking for serious candidates that are committed to attending interviews and accepting the j المزيد...

Project Manager Medical Device Experience Irvine CA or Danvers MA Onsite Hire Fulltime Hire Job Skills and Responsibilities: Project Management Professional (PMP) certification is required Must possess knowledge of theoretical and practical fundamentals and experimental en المزيد...

The Animal Facility Compliance Manager is responsible for ensuring the smooth operation and adherence to regulatory standards at our In Vivo Primate Quarantine and Breeding Facility. This role involves SOP management quality control inspections regulatory agency interactions IACUC ove المزيد...

Duluth GA or St Joseph MO Contract Duration: 1236 months Rate: Negotiable Responsibilities: Excellent employment opportunity for a Vet Tech Services Specialist in the Duluth GA or St Joseph MO areas. Hours will be 96 EST / 85 CST. 40 hours/week. Our roles are not considered fully re المزيد...

Job Description: Position Summary:The Technical Writer II is responsible for supporting the Quality Assurance and Regulatory Affairs teams by creating revising and maintaining documentation related to IVDR submissions. This role works crossfunctionally with Manufacturing Operations an المزيد...

Job Description: Position Summary:The Technical Writer II is responsible for supporting the Quality Assurance and Regulatory Affairs teams by creating revising and maintaining documentation related to IVDR submissions. This role works crossfunctionally with Manufacturing Operations an المزيد...

Project Manager A minimum of Technical/Engineering Degree with 10 years of related experience Medical Device Product Management domain. Project Management Professional (PMP) certification is required Must possess knowledge of theoretical and practical fundamentals and experimental المزيد...

Job Description: The main function of a Global Trade Compliance Manager is to assess and lead actions required to ensure the compliance of the organization its Vendors and entities with all government import export and trade compliance laws and regulations globally. Key Responsibil المزيد...

Overview: TekWissen Group is a workforce management provider throughout the USA and many other countries in the world. Our client is a passionate about improving and saving the lives of patients through high quality innovative medical devices and services. A leading global man المزيد...

Hello guys Sr. Solutions Architect Anywhere USA ( Remote ) 6month Contract to Hire Pay Range: $80.00 Salary Target: $ 1 7 0K $20 0K USC GC only Job Description: Our client is a fastgrowing Medical Device company looking to scale their software development team that b المزيد...