Fda Regulations Jobs in Hartville

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 More...

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 More...

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 More...

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 More...

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 More...

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 More...

Our clients contribution to healthcare is offering a range of diagnostic solutions clinical data management tools and process management expertise. Their goal is to provide solutions improving healthcare around the globe. They are part of a team of life science companies who are deve More...

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 More...

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 More...

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 More...

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 More...

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 More...

Quality Management ISO 13485 Medical Device Regulatory Standards Quality Compliance CAPA / NC Windchill PLM system Quality Engineer A minimum with 5 years of related experience Quality Management in Medical Device Industry Knowledge of Medical procedure and corresponding Medical Equi More...

Title: IT Project Manager Location: Remote mostly but then come onsite once a month for Institute week (2nd week a month) must be local; One Kendall Square Building 600 3RD FL Cambridge MA 02139 Duration: through the end of the year Start: ASAP Visa: USC GC Important Skills Tech More...

Description: Accepting candidates in Charlotte NC in addition to Orlando FL Position Overview As a member of the Client Energy customs team the individual will provide guidance relating to US Customs processes as well as facilitate transactional support for US imports and exports. More...

Regulatory Operations Consultant Thousand Oaks CA Day 1 Onsite Contract TCS (Tata Consultancy Services) Job Description: Ability to learn complex data standards/requirements coming from regulatory authorities like EMA and FDA. Knowledge of EMA IDMP guidelines including EMA SPOR. More...

$2 Billion national foods manufacturer that has been in business for 102 years has a need for Production Supervisor They have 6 facilities worldwide and this is the largest operation Our client offers fantastic benefits stability growth and a great team atmosphere. This job is open d More...

Description: Pay rate $$$ Daytime hours Job Description Summary This position is responsible for conducting routine inspection and analysis of incoming service material and quality reviews of domestic and international service records by identifying conflicts dependencies and risk More...

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 More...

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 More...