| High Priority Position: QA Specialist with cGMP manufacturing environment, FDA & Biotech/Pharmaceutical industry Exp. at NC || Day One Onsite || Kindly dont share Fake/Mismatched/Junk Profiles || || W2 or 1099 (No C2C) at Industry, Texas, USA |
| Email: [email protected] |
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http://bit.ly/4ey8w48 https://jobs.nvoids.com/job_details.jsp?id=2310879&uid= Dear Professional, Hope you are doing great today... This is BABU, BDM FROM PANTAR SOLUTIONS INC, we are an Information Technology and Business Consulting firm specializing in Project-based Solutions and Professional Staffing Services. Please have a look at below position which is with our Client and let me know your interest ASAP. I would really appreciate if you could send me your MOST RECENT UPDATED RESUME: QA Specialist with cGMP manufacturing environment, FDA & Biotech/Pharmaceutical industry Exp. Morrisville, NC || Day One Onsite || || W2 or 1099 (No C2C) Long Term Note: This role is not remote. The role will require presence onsite at the Morrisville location and on 2-2-3 shift to support GMP operations. This is an alternating shift that includes weekends on a rotating basis, as the manufacturing process is a 7-day a week process. Kindly dont share Fake/Mismatched/Junk Profiles Need strong QA Specialist with cGMP manufacturing environment, manufacturing, KNEAT, SlingShot, Blue Mountain RAM, VEEVA, batch record review, analytical analyses, FDA requirements and guidance documents, Biotech/Pharmaceutical industry Exp. Consultant LinkedIn profile must have been created before 2018/2019 Need 8 - 10+yrs of IT Exp. Profiles || Need Passport number, I94, Travel History documents during submission for H4EAD/E3/TN1/H1/GC EAD/GC Provide Quality and Compliance oversight for manufacturing of commercial and investigational products through Shop Floor presence. Responsible for performing inspection and disposition of raw materials and components by: Working within our ERP system (Slingshot) to ensure compliant material release. Acquiring Certificates from Vendors to support Release per Master Specification. Reviewing the required documentation (CoA, CoC, CoS, etc.) to ensure that the material meets testing specification. Ensure rejected and or released materials are transferred to the appropriate areas by collaborating with appropriate stakeholders. Upon release, archiving the completed Mater Specification within document control room. Proactively assess and identify risk for mitigation and communication to stakeholders. Responsible for completing assigned training and other tasks in a timely manner and representing Quality in meetings and providing meeting feedback to the team as required. As required, advise and provide quality oversight and compliance guidance based on the company procedures and standards for the SMPA Quality Management System. Responsible for completing the logbook and Work Order reviews for Manufacturing, Engineering, Quality, and Warehouse to ensure that the entries are complete and adhere to company policies and procedures. This role will be on site and on 2-2-3 shift to support GMP operations alternating shifts that include weekends on a rotating basis, as the manufacturing process is a 7-day a week process. Responsible for providing QA review/approval of the completed Manufacturing batch records in a timely manner and ensuring that the entries adhere to the company policies and procedures. Skills Experience in a cGMP manufacturing environment, with strong working knowledge of FDA requirements and guidance documents. Relevant experience and knowledge of manufacturing, batch record review, and/or analytical analyses for the biotech/pharmaceutical industry. Integrity, entrepreneurial spirit, ownership mentality, and a commitment to excellence. Be flexible and contribute positively to the team's success, take on additional tasks as required and adjust to changing business needs. Strong organizational skills and ability to work on multiple projects with tight timelines and minimal oversight. Working experience in KNEAT, SlingShot, Blue Mountain RAM and VEEVA is preferred. Education B.S. in chemistry, biological or pharmaceutical sciences, or related discipline At least 3 years of experience in the biotech/pharmaceutical industry within research and development or commercial organizations. PLEASE NOTE: If for any reason this does not interest you or you felt uncomfortable by any part of this email, I sincerely apologize. Please consider this E-mail as a request for referrals and feel free in forward this email to anyone whom you might find a fit. Thanks & Regards, Babu Pantar Solutions Inc 1908 Cox Rd, Weddington, NC 28104 Email: babu (dot) s (at) pantarsolutions (dot) com Keywords: quality analyst information technology green card wtwo North Carolina High Priority Position: QA Specialist with cGMP manufacturing environment, FDA & Biotech/Pharmaceutical industry Exp. at NC || Day One Onsite || Kindly dont share Fake/Mismatched/Junk Profiles || || W2 or 1099 (No C2C) [email protected] http://bit.ly/4ey8w48 https://jobs.nvoids.com/job_details.jsp?id=2310879&uid= |
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| 03:28 AM 03-Apr-25 |