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Open Roles - 2/7/2024 at Remote, Remote, USA
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Role: Veeva RIM Validation Engineer

Client: Pharma

REMOTE

Pay Rate: $65hr W2 / 72hr c2c max 

12 plus months

Pharma/ Biotech/ Life Sciences/ Medical Device/ Healthcare or Manufacturing experience is a must

Looking for Business Analyst with Registration experience and someone who can write test scripts.

8-10 year of overall experience

Looking for candidates local from Cali or nearby States, not accepting far off east coast based candidates

Job Description

Person should understand how data is set up in registration module and how it will interact with SAP systems.

BA Registration

Our company is seeking an experienced Business Analyst with expertise in Veeva RIM Registrations and Integrations with SAP to join our team

The successful candidate will be responsible for analysing business requirements, designing solutions, and implementing changes to streamline our Veeva RIM Registration process and SAP integrations

Responsibilities:

Analyse business requirements related to Veeva RIM ( Validation ) Registrations and SAP integrations, and identify gaps in existing processes

Design solutions and provide recommendations for process improvements related to Veeva RIM ( Validation ) Registrations and SAP integrations

Implement changes to streamline the Veeva RIM Registration process and SAP integrations

Collaborate with cross-functional teams to develop and implement Veeva RIM Registration and SAP integration projects

Provide support and guidance to end-users in the Veeva RIM ( Validation ) Registration process and SAP integrations

Identify and mitigate risks related to Veeva RIM ( Validation ) Registration and SAP integration projects

Document business processes, requirements, and system configurations related to Veeva RIM Registrations and SAP integrations

Requirements:

Bachelor's degree in Business Administration, Information Technology, or related field

3+ years of experience as a Business Analyst, with a focus on Veeva RIM ( Validation ) Registrations and Integrations with SAP

Strong understanding of the Veeva RIM Registration process and experience working with Veeva Vault RIM

Role: QA SOP Analyst (Documentation Specialist)

Rate:                   $60hr c2c Okay with H1s

Duration:             12 Months

Location:              Remote

Candidate should be from California to Mid-West Not accepting far off East candidates

 MOSTLY REMOTE BUT NEED TO ATTEND SOME ONSITE METTINGS. (Foster City, CA)

Not looking for more than 10 years

Pharma, Medical, Life science or Biotech industry background is required

Primary responsibilities for role:

Develop SOP's for over 20 different laboratory systems/equipment and a new digital platform. Client is going from a Paper-Based system to a digital platform system.

Interface with SME's that are implementing the new digital platform and the Laboratory Technicians.

Attend required onsite/remote meetings.

Update client and PTS Advance management on progress and any areas that have become a bottleneck which is causing delays.

Requirements:

Education and Experience by level:

Minimum Education: Bachelor's Degree

At least 4+ years of technical documentation experience within the Life Science industry including gathering required information and developing documentation to include SOPs, implementation plans, admin guides

3+ years of experience managing technical documentation including version control and developing processes to make document creation and maintenance more efficient

2+ years of experience reviewing technical documentation to identify areas of improvement and quality

Demonstrates strong technical documentation skills and ability to adapt to changing circumstances.

Displays flexibility with assignment.

Completes SOP's in a timely manner and can identify and present to management areas that are causing project delays.

Communicates effectively and promptly at all levels of the organization, supporting department objectives and management decisions.

Able to promote team approach.

Application Question(s):

What level of experience do you have with developing SOP's within a Laboratory Environment

Have you developed SOP's for a Pharmaceutical, Biotech and/or Medical Device company

Have you ever developed SOPs for any lab equipment

Any experience with QMS, Trackwise or similar system

Have you ever worked in a supervisory role

Position: Sr. Supply Chain Business Analyst

Duration:

 12+ months

Location: Hybrid at Foster City, CA ( Not looking for far off east coast based candidates, looking from Cali or nearby States

Client: Pharma

$75/hr c2c or $70hr W2

Okay with H1s

PHARMA IS A MUST OR HEALTHCARE OR PHARMA MANUFACTURING OR ANY MEDICAL DEVICE INDUSTRY EXP..

Not looking for profiles beyond 17 years pf experience

           SAP familiarity

           Pharma background

           Analytical skills

Must-Have skills:

At least 8 years of experience with SAP Supply Planning & Manufacturing

Experience in Pharma industry and specifically for Clinical Supplies

Experience in Chemicals & Biologics

Experience designing end-to-end processes for supply planning of clinical supplies  using internal and CMO supplies

Experience with S4/HANA Supply Chain Systems

Experience leading design workshops & testing sessions

Experience creating process flow diagrams and presenting solutions to senior management

Experience writing test scripts and doing extensive testing of integrations

Experience with any testing management system

Supply Chain Management

Delivery Manager

Pharma Experience

Client Expectation Management

Stakeholder presentations

Resource Management.

Experience in Pharma industry preferred

SAP familiarity

Pharma background

Analytical skills 

Duties:

Provide focused delivery of all aspects of project management, project scope definition, risk management, adaptable project scheduling, resource hiring and management

Change management and consistent project documentation and reporting.

Guide and direct implementation of infrastructure, systems, applications and technical  

Integration 

activities.

Must be results-oriented and ensure successful completion of the projects on time, on budget and within 

the defined scope while leading through influence and with solid soft skills and tact.

Bachelors degree in computer science or equivalent. 

Thanks,

Ashley

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Siliconstar Tech, 320 Decker Drive, Suite 100, Irving, Texas 75062 Phone: 972 256 8154

Keywords: quality analyst business analyst access management sfour information technology wtwo California
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Wed Feb 07 22:09:00 UTC 2024

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