Discussion:
Need:-Maximo Validation Lead
saurabh sharma
2015-07-06 17:11:22 UTC
Permalink
Hi,





Role:- Maximo Validation Lead

Location:-Foster City CA

Duration:-12 Months



*Job Title*

Maximo Validation Lead

*Relevant Experience*

*(in Yrs)*

5 +

*Technical/Functional Skills*

Computer System validation

GMP practices

GaMP approach

Good Communication

Excellent document skills

21-CFR PART 11 assessment, Annex 11 assessment

GMP assessment

CAPA procedures in Pharmaceutical industry



*Experience Required*

Knowledge of Computer System Validation

Understanding of software implementations in pharmaceutical industry

Knowledge of GMP, GaMP practices

Good documentation skills

Understanding of IQ, OQ and PQ procedures

Experience on CAPA/deviation procedures in pharmaceutical industry



Nice to have :

Maximo functionality awareness

*Roles & Responsibilities*

Lead the validation activity for Maximo implementation program

Coordinate with business groups and technical team for successful
validation of Maximo

Understands the business needs and application constraints to come up with
a strong validation strategy

Work cohesively with the validation engineers during IQ, OQ, PQ activities

Ensure the implemented system in 21-CFR PART 11 / Annex 11 compliant

Perform reviews and assessment of the documents produced during the
implementation

*Generic Managerial Skills*

Lead the validation team for Maximo implementation program

Estimate time, schedule and cost for validation activities for Maximo
implementation

Communicate and coordinate with the business and technical teams

Ensure validation activities are happening in according to the client’s
computer system validation plan





*Saurabh Sharma*

*Sr. Recruiter – IT Services*



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*SAP AND IT CONSULTING SERVICES *

9622 Blackberry Terrace Dr, Spring, TX 77379

T: 281 954 5503 | 281 954 5922

Email: ***@e-infionics.com <***@e-infionics.com> |
***@gmail.com

Web: www.e-infionics.com



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