Hi Friends,

*Need MES software consultant*

*Please respond to [email protected]*

Peapack, NJ

2 years

*F2F interview *

* *

They are using a product called Rockwell Automation's PMX software. This is
a software specifically to life sciences. It communicates between LIMS,
ERPs, DMS's etc and the plant floors. MES is manufacturing enterprise
systems.

* *

*Overview:*

The candidate has an opportunity to work closely with manufacturing and
technical IT resources to develop business requirements for the Core MES
application. Responsibilities include the creation of requirement documents,
assisting in application design, testing and debugging new development in
accordance with the SDLC. The role also performs supportive application
related activities as well as communicates within the PGM IT center team and
with end-user teams.  Another key responsibility is the design, development,
and support of interfaces to other core solutions. Candidate must possess a
good understanding of Pfizer's business functions, its applications, and be
able to document the business's needs for use in technical designs.
Additional responsibilities:
- Ensures technical development is aligned with business requirements.
- Coordinates the creation and maintenance of testing plans.
- Coordination and execution of functional testing.
- Responsible for overseeing the completion of system configuration.
- Act as the point person for the Help Desk activities for the MES
application issues
- Travel to customer sites to provide support as a subject matter expert for
the Pfizer core MES solution.
- Be required to work in both independent and team environments
- Ensure that the system design is in accordance per specifications
- Develop, configure, and/or unit test applications per requirements and
design specifications
- Perform system integration testing activities
- Provide applications support during and post-production implementation

*Qualifications:*

·        Experience working with MES software solutions (preferable RA PMX)
- MUST

·        Experience with all responsibilities necessary for development role
of a project and can work well and deliver in both team and independent
environments – MUST

·        Knowledge of full lifecycle software development and systems
integration processes, including the creation of associated documentation
(e.g., design and functional specifications) and testing protocols (e.g.,
pharmaceutical system validation processes such as the IQ/OQ/PQ protocols)
– MUST

·        Excellent Written and Verbal communication Skills with the ability
to interact with business and IT resources at various levels (e.g., users,
project  management, sponsors, stakeholders) – MUST

·        Strong knowledge of relational databases, specifically Oracle –
MUST

·        Strong proficiency in a number of programming languages or
constructs (i.e. Python, Microsoft .NET, SQL, and Java) – MUST

·        Proficiency with Windows 2000/03 Server, and VMWare Environments,
including operating system-specific administration and scripting languages –
PREFERRED

·        Experience providing support and enhancements for applications,
including having the ability to manage multiple, high-priortity tasks  –
PREFERRED

·        Strong knowledge of web application servers like BEAWeblogic,
Tomcat, Apache, and WebSphere – PREFERRED

·        Bachelors Degree, with a preference in Computer Science –
PREFERRED

 Knowledge or Familiarity  working within the Pharmaceutical industry –
PREFERRED


-- 
James
Astoline Inc
Phone : 732-889-1407
E-mail : [email protected]
www.astoline.com

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