QMS & SAP Validation Analyst (Contract)

Kashiv BioSciences LLC.
Piscataway, NJ, United States
2 months ago

Role details

Contract type
Temporary to permanent
Employment type
Full-time (> 32 hours)
Experience level
Starter
Experience required
1 year minimum
Compensation
$135,200.0 - $156,000.0
Working hours
Regular working hours
Job source

Tech stack

Data Integrity Laboratory Information Management Systems SAP (Applications) SAP Implementation Test Execution Engine Iq/oq/pq Test Scripts GXP

Job description

We are seeking a Validation Analyst to support validation of our Quality Management System (MasterControl) and SAP implementation (QM, Materials Management, Production modules). This role works under the direction of a senior validation lead and partners with Quality, IT, and business functions to deliver validation artifacts in compliance with 21 CFR Part 11, GxP, and EMA expectations., * Support validation of MasterControl QMS - authoring and executing IQ/OQ/PQ protocols, traceability matrices, and validation summary reports

  • Support SAP implementation and validation activities across QM, MM, and PP modules, including test script authoring and execution under senior oversight
  • Contribute to risk assessments, data integrity assessments, and change control documentation
  • Liaise with QA, IT, business process owners, and external SAP implementation partners
  • Support periodic review and maintenance of validated state for assigned systems
  • Assist in audit and inspection readiness for MasterControl and SAP

Requirements

Do you have experience in Test Execution (Quality assurance practices)?, Do you have a Master’s degree?, * Bachelor’s degree in Life Sciences, Engineering, IT, or a lab-based role in life sciences with 3+ years of relevant experience; OR Master’s degree with 1-2 years of relevant experience

  • Prior exposure to CSV activities in a GxP-regulated environment
  • Working understanding of 21 CFR Part 11, EU Annex 11, and EMA guidance
  • Experience authoring or executing validation protocols

Experience:

  • Exposure to MasterControl QMS (validation, administration, or end-user)
  • Exposure to SAP (any module, ideally QM, MM, or PP) in a GxP environment
  • Familiarity with GAMP 5 principles
  • Experience with ALCOA+ data integrity principles
  • Prior experience supporting enterprise system implementations in pharma, biotech, or medical device

Specialized Knowledge and Skills: ·

  • Familiarity with GAMP 5 principles and risk-based validation
  • Exposure to Caliber LIMS
  • Exposure to SAP (QM, MM, PP) in a GxP context
  • Prior experience and acting as a liaison across IT, Quality, Lab, and ERP (SAP Preferred) and related systems.

Work Environment & Physical Demands:·

  • This is an on-site position at our Piscataway, NJ location - OR - Chicago, IL location·
  • Must be able to work extended hours or weekend hours, as may be required.

Noise:·

  • No extraordinary noise levels.

Standing/Lifting:·

  • Very unlikely, but can be able to lift at least 20 lbs.

Benefits & conditions

2.42.4 out of 5 stars 20 New England Avenue, Piscataway, NJ 08854 $65 - $75 an hour - Contract

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