02/05/20 1:54 PM
Greetings,
Title- Validation Analyst
Location: Peapack, NJ
Duration: 1+ Year
Description-
• Ability to identify perform validation of pharma applications in a manufacturing industry
• Ability to author SOP’s and manuals
• Ability to follow the SLDC with focus on Agile development projects
• Experience in ALM and Trackwise for Quality Management and Test management
• Ability to work without any supervision
• Good business analytical skills
• Have knowledge of IIOT framework and applications supporting it
• Excellent knowledge of 21CFRPart11, GMP, Compliance FDA regulations etc.
• Skills and experience working in diverse, multi-disciplined work groups, able to prioritize and allocate their time to meet the business day-to-day demands in a fast paced environment.
• Engaged hands-on individuals that have the abilty to self-direct and take initiative when an opportunity arises that requires attention and support.
1. A successful candidate will possess a minimum of 5 years of experience within a GxP environment at a pharmaceutical industry.
2. Experience and knowledge of GAMP process, GMP, 21CFR Part 11, excellent written and verbal communication skills, and strong adherence to Good Documentation Practices.
3. Additional skills of experience with HPALM, Trackwise.
Regards,
Naman Shukla
Next Level Business Services, Inc.
Consulting| Analytics| Staff Augmentation
US: +1 (904)-406-8313: Cell : +1 (314) 548-9670 |Fax: +1 (608) 646-8326
11340 Lakefield Drive, Suite #200, Johns Creek, GA 30097
E-mail: naman.shukla@nlbservices.com| Web: www.nlbservices.com
Hangout : naman.shukla@nlbservices.com
linkedin.com/in/naman-shukla-a5124228
An ISO 27001 and 20000-1 Certified & Minority Business Enterprise (CMBE)
If you would prefer to no longer receive any emails from this Company, you may opt out at anytime by clicking here.Greetings,
Title- Validation Analyst
Location: Peapack, NJ
Duration: 1+ Year
Description-
• Ability to identify perform validation of pharma applications in a manufacturing industry
• Ability to author SOP’s and manuals
• Ability to follow the SLDC with focus on Agile development projects
• Experience in ALM and Trackwise for Quality Management and Test management
• Ability to work without any supervision
• Good business analytical skills
• Have knowledge of IIOT framework and applications supporting it
• Excellent knowledge of 21CFRPart11, GMP, Compliance FDA regulations etc.
• Skills and experience working in diverse, multi-disciplined work groups, able to prioritize and allocate their time to meet the business day-to-day demands in a fast paced environment.
• Engaged hands-on individuals that have the abilty to self-direct and take initiative when an opportunity arises that requires attention and support.
1. A successful candidate will possess a minimum of 5 years of experience within a GxP environment at a pharmaceutical industry.
2. Experience and knowledge of GAMP process, GMP, 21CFR Part 11, excellent written and verbal communication skills, and strong adherence to Good Documentation Practices.
3. Additional skills of experience with HPALM, Trackwise.
Regards,
Naman Shukla
Next Level Business Services, Inc.
Consulting| Analytics| Staff Augmentation
US: +1 (904)-406-8313: Cell : +1 (314) 548-9670 |Fax: +1 (608) 646-8326
11340 Lakefield Drive, Suite #200, Johns Creek, GA 30097
E-mail: naman.shukla@nlbservices.com| Web: www.nlbservices.com
Hangout : naman.shukla@nlbservices.com
linkedin.com/in/naman-shukla-a5124228
An ISO 27001 and 20000-1 Certified & Minority Business Enterprise (CMBE)
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