Veeva Vault GxP Analyst

Business Analyst for Veeva Vault GxPLaiba Technologies LLC is seeking a skilled Business Analyst to join our team in Jersey City, NJ. As a Business Analyst for Veeva Vault GxP, you will be responsible for coordinating with various stakeholders to ensure efficient project delivery.Key Responsibilities:Develop and execute system test scripts for Veeva Vault...

Must Have's: Exposure to Technologies 1. Veeva Vault Administration 2. Veeva QualitDocs 3. Veeva QMS Domain/Process 1. Quality 2. Medical Devices, Customer & service excellence 3. Knowledge in Life science domain and GxP principles. Responsibilities: Perform onsite QMS lead role and work with business team and program team in managing the deliverables as per...

Job Title: QMS Lead RoleAbout the Role:We are seeking a highly skilled QMS Lead to join our team at Omni Inclusive. As a QMS Lead, you will be responsible for managing the delivery of quality management systems and ensuring compliance with GxP principles.Key Responsibilities:Develop functional requirements, design, testing, training, and implementation of...

GxP Business AnalystLocation: Foster City, CADuration: 12 Months+Requirements:This is a client-facing role so it requires communication to be 10/10Looking for candidates having around 8 years of experienceGxP Documentation is a mustMust have a Bachelor's degree from the USResponsibilities:Apply client change processes and tools to create a strategy to...

Job Title: Quality Management Systems LeadWe are seeking a highly skilled Quality Management Systems Lead to join our team at Omni Inclusive. As a key member of our organization, you will be responsible for managing the implementation and maintenance of our quality management systems, ensuring compliance with regulatory requirements and industry...

Job Title: Senior Manager, R&D Information SystemsAt Gilead Sciences, we're committed to creating a healthier world for all people. As a Senior Manager, R&D Information Systems, you'll play a critical role in driving the success of our Quality Information Systems team.Job Summary:We're seeking an experienced professional to lead the development and...

GxP Business AnalystLocation: Foster City, CA ( 3 days onsite)Duration: 12 Months+ Requirements:This is a client-facing role so it requires communication to be 10/10Looking for candidates having around 8 years of experienceGxP Documentation is a mustMust have a Bachelor's degree from the USResponsibilities:Apply client change processes and tools to create a...

Job DescriptionAt Gilead Sciences, we're committed to creating a healthier world for all people. As a Senior Manager, R&D Information Systems, you'll play a critical role in driving our mission forward.OverviewThe Quality Information Systems team within PDM Quality is responsible for Business Systems Ownership and Business Administration support of all of...

Job DescriptionOmni Inclusive is seeking a highly skilled QMS Lead Role to join our team. As a QMS Lead, you will be responsible for managing the deliverables as per Gilead Releases and working closely with the business team and program team.Key Responsibilities:Develop functional requirements, design, testing, training, and implementation of Veeva Vault...

Cash Vault Services Analyst Job DescriptionGardaWorld is a leading provider of cash management solutions, and we are seeking a highly skilled Cash Vault Services Analyst to join our team. As a Cash Vault Services Analyst, you will play a critical role in ensuring the accuracy and integrity of our cash management operations.Key Responsibilities:Balance and...

Job Title: CMC Regulatory Affairs Data Entry SpecialistFladger Associates is seeking a highly skilled Regulatory Affairs Data Entry Specialist to join our team in Foster City, CA. As a key member of our Regulatory Affairs team, you will be responsible for performing data entry using our Company RIM System to support key CMC RA stakeholders.Key...

Job DescriptionJob DescriptionWe are seeking a Regulatory Affairs Assistant - II for a very important client. Specific Job Responsibilities• Perform data entry using Gilead RIM System to enter relevant information to support key CMC RA stakeholders.• Work collaboratively to support the team by executing routine data entry, such as the input of...

We are seeking a Regulatory Affairs Assistant - II for a very important client.Specific Job Responsibilities• Perform data entry using Gilead RIM System to enter relevant information to support key CMC RA stakeholders.• Work collaboratively to support the team by executing routine data entry, such as the input of submission related dates, regulatory...

Description: Job Title: CMC Regulatory Affairs, Data Entry Contractor PositionContract Duration: 6 months (we would like to start with 6 months, with the potential to extend if the person is highly competent and a good resource for our team)Location: Remote- If the candidate is in the Foster City, CA area, we would prefer that they are onsite 2-3 days if...

Specific Job Responsibilities• Perform data entry using Gilead RIM System to enter relevant information to support key CMC RA stakeholders.• Work collaboratively to support the team by executing routine data entry, such as the input of submission related dates, regulatory assessment comments.• Ensure completeness, correctness and consistency of...

Location: Foster City, CA (Hybrid)Contract: 6-months initial contractPay range: $50.00 - $63.00 per hourSpecific Responsibilities: Perform data entry using the RIM system to input relevant information that supports key CMC Regulatory Affairs stakeholders.Collaborate with the team to execute routine data entry tasks, such as entering submission-related dates...

Job SummaryWe are seeking a highly organized and detail-oriented CMC Regulatory Affairs professional to join our team at Unicon Pharma Inc.The successful candidate will be responsible for performing data entry using Gilead RIM System, collaborating with the team to support key CMC RA stakeholders, and ensuring the completeness, correctness, and consistency...

Job Title: CMC Regulatory Affairs Assistant II - Data EntryWe are seeking a highly skilled and detail-oriented individual to join our team as a CMC Regulatory Affairs Assistant II - Data Entry. This is a remote opportunity with the possibility of working on-site in Foster City, CA.Key Responsibilities:Perform data entry using RIM System to enter relevant...

Job DescriptionInnova Solutions is seeking a highly skilled Regulatory Affairs Assistant - II to join our team. As a key member of our Regulatory Affairs team, you will be responsible for performing data entry using our Client RIM System to support key CMC RA stakeholders.Key Responsibilities:Perform data entry using Client RIM System to enter relevant...

Regulatory Affairs Assistant - IIWe are seeking a highly skilled Regulatory Affairs Assistant - II to join our team at ATR International. This role is a great opportunity for someone who is passionate about advancing therapeutics against life-threatening diseases, while working with a collaborative team in Regulatory Affairs.Key Responsibilities:Perform data...