Gamp Jobs in Salon-de-Provence

About the Job Oleson specialises in delivering highquality talent and solutions that enhance the capabilities and operational excellence of our global customers. We are focused on matching the dynamic needs of Data Centre and Life Science clients with skilled professionals thereby d More...

The CSV Consultant will develop and maintain comprehensive validation plans, prepare validation documentation including user requirements and test scripts, conduct and oversee installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ) tests, an More...

Job Title: CSV Lead Location: Raritan NJ Onsite Duration / Term: 6 months Contract Job Description: Validating ERP to AWS Data migration process and Validating Data migration project Experience in the Pharmaceutical biotechnology or medical device industry 5 years experienc More...

Perform project electrical and pneumatics hardware and PLC/HMI software design including test and validation activities on equipment and systems in accordance with applicable regulatory standards and to cGMP and GAMP 5 guidelines for the pharmaceutical industry. Liaise with associa More...

Overview: Tekwissen Group is a workforce management provider throughout the USA and many other countries in the world. This client is a German multinational Pharmaceutical and biotechnology company and one of the largest pharmaceutical companies in the world headquartered in More...

Job:Commissioning Engineer Location:Bangalore Experience:58 Years Job Description: Experience in executing precommissioning activities like walkdown mechanical completion partial statup of a distribution system etc Should have experience in clean utility qualificatio More...

Please share your resumes at Job Role: Validation Engineer Contract: W2 Location: Newark CA Position Overview/Responsibilities: Ensure quality and compliance with established procedures and standards. Generate review and approve baselevel documents such as the Valid More...

Using initiative and a self-driven approach to identify and deliver continuous improvement opportunities, the lead will be encouraged to: Ensure that all IT systems used by sites remain compliant throughout their lifecycle, with the relevant compliance policies, standards and More...

Job:CQV Senior Engineer Location:Bangalore Experience: 10 Years Job Description: Thrives in a fastpaced environment with many concurrent tasks. Support onsite and offsite activities such as: FATs SATs IOQ and PQ Executions and System Walkdowns. Hands on experience More...

Job:CQV Package lead Location:Bangalore Experience:1015 Years Job Description: Project management skills regarding C&Q facilitating board meetings to review status timelines quality challenges generating reports for steering group understanding to evaluate risk and More...

CK Group are recruiting for an experienced Senior Validation Specialist to join a growing Cell Therapy CDMO to be based at their site in Cambridge, on a permanent basis. This role will be fully onsite. The Role: Reporting to the Validation Manager, you will support multiple p More...

Hi Hope you are doing well! Please find the below job description & please share your updated resume. Role: CSV Lead Location: Raritan NJ Hybrid(23 days a week onsite) Duration: Long term Job description: Experience Validating ERP to AWS Data migration process and Validating Data More...

About Company: Our Company is a global technology consulting and digital solutions company that enables enterprises to reimagine business models and accelerate innovation through digital technologies. Powered by more than 84000 entrepreneurial professionals across more than 30 countri More...

Accountabilities: As a Senior IT Quality Manager, you will use your pharmaceutical regulatory compliance experience and intelligence to support and deliver an integrated IT QM strategy. You will be responsible for understanding and applying regulatory compliance policies and st More...

Hi Hope you are doing well! Please find the below job description & please share your updated resume. Role: Validation specialist Location: Raritan NJ Hybrid Duration: Long term Job Details: 10 years experience in Computer System Validation or Quality management or Business Analys More...

The ideal candidate must have knowledge of Design implementation and commissioning of S7 based Control Systems and/or Siemens TIA related software engineering activities for a variety of industrial control system applications predominately in the Life Science industry. The candidate s More...

Job Title:Sr. DeltaV Engineer Location:Onsite Muskegon MI Duration:9Months Years of Experience:12.00 Years of Experience No OT Standard Laptop BGV Initiated Must Haves: Strong Process Automation project & commissioning experience with the DeltaV platform in a Pharma/Biotech env More...

The Automation Engineer will provide day-to-day engineering support for on-going DeltaV, PLC, Allen Bradley manufacturing systems. Responsibilities:Provide quality automation support in the ongoing day to day maintenance and update of existing DeltaV system.Anticipate, recommend, and More...

Title Sr. DeltaV Engineer Location Muskegon MI Rate $6065/hr on C2C Job Type: Contract Client TekWissen / Cognizant Job Description: This is an onsite role to help with commissioning efforts of a DeltaV system and mentor other Junior and Intermediate Engineers. The client and t More...

Location: Raritan NJ Hybrid Type: 12 months contract Job Details: 10 years experience in Computer System Validation or Quality management or Business Analysis in GxP application area Has working experience in any one or two of the following domains Clinical Development an More...