| CSV Computer System Validation Specialist - Contract Role -Raritan, NJ (Onsite from Day-1) at Raritan, New Jersey, USA |
| Email: [email protected] |
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http://bit.ly/4ey8w48 https://jobs.nvoids.com/job_details.jsp?id=544330&uid= From: Jitendra Kashyap, IDC Technologies Inc [email protected] Reply to: [email protected] Hi Hope you are doing well! We have urgent openings for one of our Client. If you are interested and available in the job market please respond to my mail with your updated resume along with expected hourly rate. Role: CSV/ Computer System Validation Specialist Location: Raritan, NJ (Onsite from Day-1) Contract Role Mandatory Skills CSV, 21 CFR part 11, Data integrity, Archiving Detailed JD: Provide compliance leadership, direction and oversight to project teams in the area of Computer System Validation Responsible for the quality oversight of GxP regulated computerized systems (e.g. manufacturing plant systems, laboratory systems and enterprise applications). Manage the release of regulated systems for GxP production use Participate in the review and approval of technical changes, Quality Incidents, CAPAs and procedures Contribute to establishing and deploying processes, compliance-driven standards, and procedures (as required), determining boundaries for harmonization and alignment versus differentiation, and ensuring they remain current with FDA and global regulatory requirements for GxP computerized systems Participate in evaluating the current Crucell quality systems for GxP computerized systems, and implement improvements to comply with the current FDA/EU standards Provide quality guidance on GxP regulatory requirements (including but not limited to 21 CFR Parts 210, 211, 58, 820, 11 and EU Annex 11 EU) In addition, this individual will lead and participate in project teams and may participate in regulatory inspections and client audits Minimum Qualifications: Bachelors or Masters degree in science, computer science, or relevant area English, fluently spoken and written Thorough knowledge of cGMP, in manufacturing and R&D within GxP regulated industries A minimum of 7 years relevant working experience in a pharmaceutical or biotechnology company of which preferably 3 years in validation or QC, and in QA/CSV In-depth knowledge of computerized quality systems Experience with GMP inspections Competences: Communicative skills Negotiation skills Convincing Team player Accuracy Problem solver Please reply with your updated resume and required details: Full Name (as per legal docs): Contact Number: Current Location: Expected Rate/Salary: Work authorization/Visa Status: Best time to take call: Availability to start: Waiting for your earliest response Regards, Jitendra Kashyap IDC Technologies Inc Email: [email protected] ____________________________________ Empowering Technologies Services Remote Services | IT Services | BPO | IT Consulting | Staffing Solutions | ________________________________ Keywords: quality analyst rlang information technology New Jersey http://bit.ly/4ey8w48 https://jobs.nvoids.com/job_details.jsp?id=544330&uid= |
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| 08:01 PM 18-Aug-23 |