| Location | Richardson, TX |
"Project Niche Skills"
"Visa Dependent Profiles Allowed"
POC: Sam Chavez
ATTENTION ALL SUPPLIERS!!!
READ BEFORE SUBMITTING:
UPDATED CONTACT NUMBER and EMAIL ID is a MANDATORY REQUEST from our client for all the submissions
We prioritize endorsing those with complete and accurate information
Avoid submitting duplicate profiles. We will Reject/Disqualify immediately.
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Please submit profiles within the max proposed rate.
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MANDATORY: Please include in the resume the candidate s complete & updated contact information (Phone number, Email address and Skype ID) as well as a set of 5 interview timeslots over a 72-hour period after submitting the profile when the hiring managers could potentially reach to them. PROFILES WITHOUT THE REQUIRED DETAILS and TIME SLOTS will be REJECTED.
Job Title: Consultant | Life Sciences | LIMS
Work Location & Reporting Address: Richardson, TX 75082 (Onsite. Open to candidates willing to relocate and work onsite from Day 1)
Contract duration: 12
MAX VENDOR RATE: #### per hour max
Target Start Date: 15 Nov 2026
Does this position require Visa independent candidates only? Yes
Must Have Skills:
Quality Manual and the relevant regulatory requirements
OT system
Quality management for IT and OT systems
Nice to Have Skills:
Detailed Job Description:
Primary focus is to ensure that the qualification of the OT system, quality management for IT and OT systems, ensuring that the required validation qualification deliverables are implemented according to the client s Quality Manual and the relevant regulatory requirements according to the client s procedures, author, review andor approve various validation qualification deliverables
Review approve validation qualification deliverables as provided by the supplier of the relevant systems, ensure that such deliverables are compliant to the client s requirements
Lead the project test resources in relation to the validation qualifications related activities of the project Act as the projects quality representative in relation to testing activities, engaging with local site QA andor QA eCPL
Report on the status of the various quality-related activities for key stakeholders
Engagement with the suppliers to advise the suppliers on the suitable completion of supplier provisioned validation qualification deliverables.
Minimum Years of Experience:
8 to 10+ years
Certifications Needed:
None
Top 3 responsibilities you would expect the Subcon to shoulder and execute:
Lead the project test resources in relation to the validation qualifications related activities of the project
Review approve validation qualification deliverables as provided by the supplier of the relevant systems, ensure that such deliverables are compliant to the Novartis requirements
Report on the status of the various quality-related activities for key stakeholders
Interview Process (Is face to face required?)
Virtual
Any additional information you would like to share about the project specs/nature of work:
Project Code: Novartis Pharma AG