Tuesday, August 21, 2012

Looking for SAP QM consultant with pharmaceutical industry exp....

Hello All,

Hope the day started on a good note to you. Please find below some of the requirements I am currently working on and let me know if you have any consultant who fits to the below requirement. If interested, please send me the below mentioned details, ASAP.

1.            Full Name:

2.            Contact number:

3.            Email Id:

4.            Current Location:

5.            Relocation:

6.            Visa Status (Citizen- GC-H1B)/ expiration date:

7.            Availability:

8.            Total Experience:

9.            Expertise:

10.          Rate (C-C, 1099, W2): $/hr

11.          Provide any 2 Client manager references of previous projects:

 

Title: SAP QM

Location: Vacaville, CA        

Duration: 3 months

Rate: $/hr maxx                 

Extensive knowledge and familiarity of SAP systems, including Quality Module (QM).

Extensive knowledge and ability to troubleshoot SAP issues.

Knowledge of analytical in-process, release, and stability testing.

Knowledge of general lab operations.

CSV validation experience/documentation experience.

Independently schedules and prioritizes workload to ensure the work is performed in a timely manner.

Lead assigned projects

Prepares new and revises existing standard operating procedures for systems to ensure compliance Have a basic understanding of the GMP system and environment Other duties as assigned

 

Skills

A minimum of 2-3 years lab experience in the pharmaceutical industry conducting QC testing and minimum of 2-5 years lab computer systems experience. Knowledge of FDAA/ICH guidelines, applicable State and Foreign regulations and standards routinely used in the industry (ANSI, ISO).

Strong computer skills (e.g.Excel) and communication skills.

Demonstrate competence to expeditiously perform root cause analysis and provide appropriate guidance Strong interpersonal skills, which include a professional demeanor when interaction with Novartis personnel. Sound and practical appropriate regulations with regards to Novartis. Diplomacy and persuasions used in obtaining cooperation for corrective action required for cGMP compliance. Ability to communicate clearly with a variety of individuals in various aspects of Novartis operations.

Strong written and verbal communication skills are essential May need to adapt to changing work shifts, both swing and/or graveyard on very short notice.

May use a computer for greater than 4 hours a day.

Deliver quality products and services on time to all customers, internal and external.

Monitor processes and products to identify opportunities for continuous improvement.

Contract position within BioPharma Operations reports to Head of QC   

Most of our qualified submissions lead to immediate client interview. Therefore, please do not submit Candidates who are close to confirmation / placement.

C H A N D U
chandu@paletteit.com
408-915-2629/757-271-6446

akkinenichandu@ymail.com

Fax: 866-564-4398

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