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Veeva Vault Platform- San Francisco, CA Onsite at San Francisco, California, USA

Email: [email protected]

Hi Professional,

I hope you are doing good.

Please find below requirement and let me know your interest

Veeva Vault Platform

Location: San Francisco, CA Onsite

Duration: Long term

Role name:

Lead

Role Description:

Provide consulting,
author proposals, design, build, Configure and support Veeva QMS, Veeva
Vault based applications to meet business process and application
requirements2. Provide training and support to employees on Veeva QMS,
as well as on QMS procedures and best practices, in general.3. Knowledge
on handling events QARs, CAPAs,Change controls, qualification document
review and compliance4. Stay updated on industry trends and regulatory
changes to ensure continuous compliance.5. Lead the development and
execution of QMS processes, including document control, change
management, and CAPA (Corrective and Preventive Actions).6. Collaborate
with cross-functional teams to assess and enhance quality processes
throughout the product lifecycle.7. Drive continuous improvement
initiatives to optimize QMS efficiency and effectiveness.8. Prepare and
present reports on quality metrics and compliance status to
management.9. Support the on-going regulatory compliance of the IT
components for defined servicesto ensure the proper integration and
functionality of the Veeva QMS system.10. Strong project management
skills with a focus on delivering results within deadlines.11. Review
and approve regulatory system changes and documentation12. Solves a
range of straightforward problems through knowledge and technical
experience in own discipline with a moderate level of guidance13.
Support periodic reviews of the entire system and compile related
reports during operation phase14. Understands how the team integrates
with other teams to achieve overall objectives of the area and builds
knowledge of the organization, processes, customers, and key business
drivers.

Competencies:

Veeva Vault Platform

Experience (Years):

10 & Above

Essential Skills:

IT Manufacturing
Domain (Qualification implementation and
Advisory in

Veeva

QMS
) Minimum

6 years
of

IT
experience in

pharma
domain for implementing and managing

Veeva

QMS
. Minimum of

Bachelors Degree
or applicable experience within

information/Computer systems
with focus on Qualification of Mfg.
applications Must have experience on implementation, consulting for

Veeva

QMS
in Life Sciences. Deep knowledge of

Veeva

QMS
,

Veeva
Vault configuration, developing them in live projects
based on client requirement. Previous experience in the

biotechnology
/

Pharmaceutical
/

Life Science
or related industry implementing and validating
computer systems that manage regulated information Working knowledge of

IT infrastructure
qualification processes and

IT
operating procedures Thoroughly familiar with
Quality GxP

IT compliance
requirements. Strong planning and

analytical skills
combined with ability to work with
geographically distributed teams in a rapid development model. Awareness of

ITIL
and Support Project Methodology. Ability to
familiarize himself / herself independently with entirely new subjects and
thus provide comprehensive and innovative solutions Excellent written and
verbal communications skills Solid grasp of

Information security
and standard methodologies Working
knowledge of Document and Object record

migration
from

legacy application
to

Veeva
Vault. Good technical knowledge in core technologies
and platforms such as

Java
, .Net,

XML
,

HTML
,

PL/SQL API.
In-depth knowledge of

quality management principles
and industry regulations (e.g.,

FDA
,

ISO
). Qualified on Global Quality tracking systems for
initiation handling and

closure
of

investigation

Desirable Skills:

Good communication skills Manufacturing domain
experience/ ISA 95 Certifications in relevant quality management systems and
regulatory affairs are a plus. Any certfication related on Veeva vault QMS

Best Regards,

Vinod
| Sr. IT Recruiter|
Email:
[email protected]

--

Keywords: information technology procedural language California
Veeva Vault Platform- San Francisco, CA Onsite
[email protected]

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Tue May 21 01:22:00 UTC 2024

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shareyourresume001@gmail.com wrote:
Hi Professional,

I hope you are doing good.

Please find below requirement and let me know your interest

Veeva Vault Platform

Location: San Francisco, CA          Onsite

Duration: Long term

Role name:

Lead

Role Description:

Provide consulting,
       author proposals, design, build, Configure and support Veeva QMS, Veeva
       Vault based applications to meet business process and application
       requirements2. Provide training and support to employees on Veeva QMS,
       as well as on QMS procedures and best practices, in general.3. Knowledge
       on handling events QARs, CAPAs,Change controls, qualification document
       review and compliance4. Stay updated on industry trends and regulatory
       changes to ensure continuous compliance.5. Lead the development and
       execution of QMS processes, including document control, change
       management, and CAPA (Corrective and Preventive Actions).6. Collaborate
       with cross-functional teams to assess and enhance quality processes
       throughout the product lifecycle.7. Drive continuous improvement
       initiatives to optimize QMS efficiency and effectiveness.8. Prepare and
       present reports on quality metrics and compliance status to
       management.9. Support the on-going regulatory compliance of the IT
       components for defined servicesto ensure the proper integration and
       functionality of the Veeva QMS system.10. Strong project management
       skills with a focus on delivering results within deadlines.11. Review
       and approve regulatory system changes and documentation12. Solves a
       range of straightforward problems through knowledge and technical
       experience in own discipline with a moderate level of guidance13.
       Support periodic reviews of the entire system and compile related
       reports during operation phase14. Understands how the team integrates
       with other teams to achieve overall objectives of the area and builds
       knowledge of the organization, processes, customers, and key business
       drivers.

Competencies:

Veeva Vault Platform

Experience (Years):

10 & Above

Essential Skills:

IT Manufacturing
 Domain (Qualification implementation and
  Advisory in

Veeva

QMS
) Minimum

6 years
 of

IT
 experience in

pharma
 domain for implementing and managing

Veeva

QMS
. Minimum of

Bachelors Degree
 or applicable experience within

information/Computer systems
 with focus on Qualification of Mfg.
  applications Must have experience on implementation, consulting for

Veeva

QMS
 in Life Sciences. Deep knowledge of

Veeva

QMS
,

Veeva
 Vault configuration, developing them in live projects
  based on client requirement. Previous experience in the

biotechnology
 /

Pharmaceutical
 /

Life Science
 or related industry implementing and validating
  computer systems that manage regulated information Working knowledge of

IT infrastructure
 qualification processes and

IT
 operating procedures Thoroughly familiar with
  Quality GxP

IT compliance
 requirements. Strong planning and

analytical skills
 combined with ability to work with
  geographically distributed teams in a rapid development model. Awareness of

ITIL
 and Support Project Methodology. Ability to
  familiarize himself / herself independently with entirely new subjects and
  thus provide comprehensive and innovative solutions Excellent written and
  verbal communications skills Solid grasp of

Information security
 and standard methodologies Working
  knowledge of Document and Object record

migration
 from

legacy application
 to

Veeva
 Vault. Good technical knowledge in core technologies
  and platforms such as

Java
, .Net,

XML
,

HTML
,

PL/SQL API.
 In-depth knowledge of

quality management principles
 and industry regulations (e.g.,

FDA
,

ISO
). Qualified on Global Quality tracking systems for
  initiation handling and

closure
 of

investigation

Desirable Skills:

Good communication skills Manufacturing domain
  experience/ ISA 95 Certifications in relevant quality management systems and
  regulatory affairs are a plus. Any certfication related on Veeva vault QMS

Best Regards,

Vinod
| Sr. IT Recruiter|
Email: 
vinod.t@siriinfo.com

Keywords: information technology procedural language California 
Veeva Vault Platform- San Francisco, CA Onsite
shareyourresume001@gmail.com

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Location: San Francisco, California