Hi, Good Morning.
I hope you are doing great!! We are seeking for Sr.Validation Engineers for Duluth, GA. It is a 6+ months contract assignment and it is through one of my preferred vendor. Could you please go through the below job description and please send me your consultants updated resumes ASAP!! Writing, Review, Approval and remediation of validation protocols. •Training of validation SOP’s and Global Policies. •Review, and Approval of validation SOP’s and Global Policies. •Prepare final reports for IQ/OQ, and PQ. Participate in CRB approvals. •Support validation activities for large capital procurement projects (i.e. New manufacturing sites.) *Skills:* *Skills Type and Proficiency: * Minimum Required: Knowledgeable of cGMP and FDA regulations with regards all area of validation. Good technical writing and communication skills. Good PC skills. Preferred Level: Expert knowledge of cGMP, and FDA regulations with regards to all areas of validation. Excellent technical writing skills. Excellent communication and project management skills. Good documentation management skills. Excellent PC skills. Education: Education/Degrees/Certificates: Minimum Required: BS Degree Preferred Level: BS Engineering / Biology / Chemistry Experience Yrs and Type of Experience: Minimum Required: 5+ years experience in writing and execution of validation protocols. Experience in cGMP and FDA regulations. Knowledgeable of cGMP and FDA regulations with regards validation. Good technical writing and communication skills. Good PC skills. -- *Thanks&Regards,* * Kiran Kumar,* * 847-307-5966.* -- You received this message because you are subscribed to the Google Groups "Hot List" group. To unsubscribe from this group and stop receiving emails from it, send an email to [email protected]. To post to this group, send email to [email protected]. Visit this group at http://groups.google.com/group/directclienteq. For more options, visit https://groups.google.com/d/optout.
