USA-Process & Master Data Governance Manager I

Job Description

Immediate need for a talented USA-Process & Master Data Governance Manager I. This is a 03+months contract opportunity with long-term potential and is located in Swiftwater, PA (Onsite). Please review the job description below and contact me ASAP if you are interested.

Job ID: 26-26461

Pay Range: $50/hr - $68/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location).

Key Responsibilities:

• Ensure site on-time implementation of data remediation activities through support of master data configuration and data migration and SOP revisions
• Responsible for the master data management process, including the updating of specifications, analysis, and supporting the approval and verification process
• Ensure that the LIMS complies with all relevant regulatory standards
• Support the business in the creation and updating of training materials as changes to the system occur

Key Requirements and Technology Experience:

• Key skills; LabWare LIMS
• System validation and master data management
• Sample plans / Sampling plans
• Item codes and Product specifications
• 21 CFR Part 11 data integrity
• Manager Notes:
• Approximately 1–3 years of hands-on LabWare LIMS experience.
• Candidate should have direct experience working with:
• Product specifications
• Sample plans / Sampling plans
• Item codes,
• LIMS master data
• Candidate should be comfortable working within LabWare LIMS and performing routine master data activities.
• Strong practical experience with the specific master data components above is more important than having extensive overall LIMS experience.
• Working knowledge of aseptic processes, biology, chemistry, life sciences with strong supervisory skills
• Knowledge of cGMPs and regulatory requirements with Strong analytical & balanced decision-making skills
• 1-3 years of experience in use and administration of a LabWare LIMS, including LIMS Basic
• Strong working knowledge of laboratory processes including cGMP’s in a pharmaceutical environment
• Experience in system validation and master data management
• Familiar with 21 CFR Part 11 data integrity best practices in a pharmaceutical environment
• Excellent written and verbal communication skills and the ability to lead and participate in teams
• Experience or familiarity with the Laboratory Environment
• Experience with SQL and database structures

Our client is a leading Healthcare Industry, and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration.

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