Job Description :
Hi ,
Hope you are doing well.
We are hiring a Validation Analyst at Peapack, NJ – Contract with one of our Clients.
Below is the Job Description. If you''re interested please give me a call back at or you can E-Mail me at
Please attach your updated Resume
Position: Validation Analyst
Location: Peapack, NJ
Duration: 12 Months
Role Description
Relevant Experience
5 years of experience within a GxP environment at a pharmaceutical industry.
Technical/Functional Skills:
Excellent experience with CSV, 21CFR Part 11, Manufacturing systems, IIOT exposure is a advantage, FDA regulations, Inspections, Business Analyst, HP ALM, Trackwise.
Experience Required
A successful candidate will possess a minimum of 5 years of experience within a GxP environment at a pharmaceutical industry.
Experience and knowledge of GAMP process, GMP, 21CFR Part 11, excellent written and verbal communication skills, and strong adherence to Good Documentation Practices.
Additional skills of experience with HPALM, Trackwise.
Roles & Responsibilities:
Successful candidate will possess:
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