| Open Roles - 2/5/2024 at Remote, Remote, USA |
| Email: [email protected] |
| These are hot roles!! 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 analyzing business requirements, designing solutions, and implementing changes to streamline our Veeva RIM Registration process and SAP integrations Responsibilities: Analyze 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 Change/Remove SubscriptionPowered by Zoniac Siliconstar Tech, 320 Decker Drive, Suite 100, Irving, Texas 75062 Phone: 972 256 8154 Keywords: quality analyst business analyst sfour information technology wtwo California |
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| Mon Feb 05 19:10:00 UTC 2024 |