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📑 Refer a friend: Career Developers Inc, a well-established staffing agency/consulting firm, is celebrating 30 years in business. Previously in Ramsey, NJ for 25 years and now headquartered in sunny West Palm Beach, FL, we offer comprehensive commercial and government staffing services nationwide (GSA Contract holder). With a port ...

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📑 Job Description: The incumbent supports activities for Veeva electronic Document Management System (EDMS) based on Veeva Vault - QualitDocs. In the role, the incumbent is primarily responsible for supporting the Veeva Vault - Quality Suite platform which may include supporting platform enhancements updates, and/or end- ...

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📑 Position Details: Our client, a world-leading Pharmaceutical Company in Jacksonville, FL is currently looking for a Veeva Vault Administrator to join their expanding team.Job Title: Veeva Vault Administrator / REMOTE WORK Duration: 9 months contract, extendable up to 24 mont ...

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📑 Title: Technical Project Coordinator Duration : 6+ Months.Location: Parsippany, NJ.Rate: OpenRequirementsJob Description :Strong Master Data and Customer Relationship Data Management Solution Architect to collaborate with both Veeva and the Analyti ...

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📑 Role: Veeva Solutions Architect Location: Palo Alto, CA - Onsite Required Duration: Long-Term Rolling Contract ROLE AND RESPONSIBILITIES: Manage & Maintain Veeva Vault Clinical operations (CTMS, eTMF) & Vault RIM Analyze, develop, and implement R ...

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📑 Job Details: 2-4 years experience with Veeva Vault Platform and Clinical Vault applications Good Understanding of clinical studies and operational datasets Working experience of Data and Content Migration<br / ...

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📑 Job Description: Veeva QualityDocs and GxP Training System AdministratorJob Title: Veeva Veeva QualityDocs and GxP Training System Administrator AdministratorThe Veeva QualityDocs and GxP Training System Administrator is responsible for the management of Veeva QualityDocs and GxP Training.</ ...

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📑 Global system experience working with Regulatory Affairs Strategy, Intelligence, Regulatory Information Mgt & Operations, and/or Submission Publishing domains in support of market authorization. Experience working with Clinical Operations team in the Quality space to manage Audits, Inspections, Vendor Oversight, and ...

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📑 Job SummaryWe are looking for a Veeva CRM Subject Matter Consultant for our Life Sciences client. This role is key in implementing and optimizing Veeva CRM solutions within the organization's Sales Force Operations. It requires a deep understanding of the Veeva CRM platform, its capabilities, and how it can be leveraged to meet ...

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📑 Position: Content Central Librarian 58123-1Location: Lawrence Township NJ 08648Duration: 12 months (possibility of extension for the right candidate depending on performance)Pay rate: $47.96/ hour on W2 Top 3-5 skills:< ...

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📑 Job Details:Job Title: Interactive Visual Aid (IVA) SpecialistLocation: Mettawa, IL (Hybrid, Onsite 3 days/week) or RemoteDuration: 12 Months (With Possible Extension)Position Type: Full-Time, ContractPosition Overview:The Digital ...

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📑 CONTENT MANAGEMENT-CONTENT CENTRAL LIBRARIANPrinceton Pike, NJPay Rate is $46.95 per hour. Top 3-5 skills:1. Scientific background, familiarity with different medical reference types, and medical terminology. Experience managing reference/core ...

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📑 IMMEDIATE CONTRACT NEED! (16 MONTH CONTRACT). OPEN TO REMOTE IN U.S. (EST HIGHLY PREFERRED).Looking for someone with hands on experience supporting and implementing Veeva Vault RIM Registrations platform is required. Veeva certification desiredIn this role, you will partner with Regulatory Affairs business a ...

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📑 Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countrie ...

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📑 Immediate need for a talented Manufacturing Systems Validation Specialist . This is a 06+ Months Contract opportunity with long-term potential and is located in Summit, NJ (Onsite). Please review the job description below and contact me ASAP if you are interested.Job ID:(phone number removed)Pay Range: $47 - ...

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📑 Immediate need for a talented Manufacturing Systems Validation Specialist . This is a 06+ Months Contract opportunity with long-term potential and is located in Summit, NJ (Onsite). Please review the job description below and contact me ASAP if you are interested.Job ID ...

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📑 Director, IT GxP Systems The Director, IT GxP Systems will work to maintain a stable GxP systems environment to enhance performance, uptime, and compliance. This person will implement IT GxP policies, procedures, and best practices and serve as the organization’s Director, IT GxP Systems.This is ...

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📑 The Fountain Group are a national staffing firm and are currently seeking a Regulatory Affairs Lead for a prominent Pharmaceutical client of ours. This position is in Bridgewater, NJ (Hybrid Role). Details for the position are as follows: Job Description: Pay: (phone number removed)/hr on ...

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📑 Job Title- PRC Coordinator Duration- 08/30/2024 3 months-up-to 6 months.Cambridge ,MAJob Summary:This role is a contract role (Short-term assignment)---the assignment could be as short as 3 months-up-to 6 months.Job Summary: The US Commerc ...

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📑 Agile Methodology Good to have -Clinical domain, Oracle Apex knowledge, DevOps, New Billing/ Strategic/ Non- Exclusive 2024 - PDC Release 4.2.1 & 4.3 (Veeva)Senior PM, Good to have -Clinical domain, Oracle Apex knowledge, DevOps, Additional requirement : New Billing/ ...

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📑 This role is a contract role (Short-term assignment)---the assignment could be as short as 3 months-up-to 6 months.Job Summary: The US Commercial Regulatory Affairs Promotional Review Committee (PRC) Coordinator is responsible for facilitating the promotional review committee process of assigned products for ...

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📑 Title: Vendor Quality SpecialistLocation: Fully RemoteContract: 6 months with possibility of conversion Support the GLP/GMP vendor management program, including maintaining the Approved Supplier List, performing vendor risk assessments, audit planning, scheduling, pre-audit meeting schedul ...

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📑 This is an exciting opportunity to lead GxP Quality Systems within a promising Cell & Gene Therapy company revolutionizing cancer immunotherapies! You'll be responsible for providing Quality Systems oversight and support for the development and operations of a commercial scale state-of-the-art cGMP cell therapy manufacturing and laboratory facil ...

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📑 Title: Validation - Specialist, MSEO Manufacturing Systems ValidationLocation: Summit NJ 07901Duration: 6 months (Possibility of extension for the right candidateComments:Minimum 50% onsite required every week (Candidate is supposed to align the onsite days with the man ...

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📑 Responsibilities: Sound understanding of Electronic Batch Records (EBR) and Review by Exception (RBE) and Recipe Authoring/Validation. Ability to work extended hours or a modified work schedule to assist manufacturing operations support model, including 12x7 on-call support rotation <b ...

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📑 Job Description:Minimum 50% onsite required every week (Candidate is supposed to align the onsite days with manager and be available onsite when manager requests)REQUIRED COMPETENCIES: Knowledge, Skills, and Abilities:* Sound understanding of Electronic Batch Records (EBR) and Review by Exception (RBE) and Recipe Authoring/V ...

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📑 VALIDATION SPECIALIST SUMMIT NJ Hybrid Role!The pay ranges between $55.00 - $57.60 an hour!Required Skills: Bachelor's degree in a life sciences, engineering or technology discipline required . Minimum of 2+ ...

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📑 Job Title: Validation - Specialist, MSEO Manufacturing Systems ValidationJob ID: (phone number removed)Location: Summit, NJ, 07901Duration: 06 Months contract on W2 Job Description: Minimu ...

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📑 Immediate opportunity for an Environmental Health & Safety Specialist II to work with multi-national pharmaceutical company dedicated to pharmaceutical research and vaccine development. The HSE Associate Level Service Provider serves an important and highly visible role helping to ensure that site HSE Management System (HSE-MS) requirements are ...

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📑 Role: Validation Engineer, RIMLocation: Remote A High School Diploma with 6+ years of relative experience OR an Associates Degree with 5+ years of relative experience OR A Bachelor's Degree with 4+ years of relevant experience or a Master's Degree (M.S./MBA)with 2+ years of relevant exp ...

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📑 Terumo Medical Corporation (TMC) develops, manufactures, and markets a complete, solutions-based portfolio of high-quality medical devices used in a broad range of applications for numerous areas of the healthcare industry. TMC places a premium on providing customers with world-class products, training and education programs that drive clear eco ...

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📑 Hybrid 50%The U.S. Omnichannel Strategy team leads omnichannel planning, execution, and measurement in close partnership with Brand, Agency, Business Insights and Production teams. In this role, you will be responsible for the management and execution of omnichannel engagement plans to support a Client brand. You will serve as a dedicated p ...

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📑 Job Description: Provide Data and Business analysis support to the Enterprise Master Data Management organization focusing on Customer Master.Data Analysis Support for Ex-US Next Gen Customer Master: Works independently on large volume data sets, data analysis and comparison be ...

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📑 On-Board Services is hiring a Validation Specialist in Summit, NJ!For immediate consideration please send your resume to Subject Line: Position Title and State you are Located.About Us:On-Board Services, Incorporated is an on-site contract service provider for a local m ...

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📑 Job Description: Minimum 50% onsite required every week (Candidate is supposed to align the onsite days with manager and be available onsite when manager requests) REQUIRED COMPETENCIES: Knowledge, Skills, and Abilities: Sound understanding of Ele ...

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📑 Specialist, MSEO Manufacturing Systems ValidationJob Number: (phone number removed)Be part of a company that delivers life-changing healthcare solutions. Eclaro is looking for a Specialist, MSEO Manufacturing Systems Validation for our client in Summit, NJ.Eclaro’s client is a leader in th ...

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📑 Job Overview: We are seeking a highly motivated and experienced Manager/Senior Manager to join our CMC Quality Control department. This role will oversee our external stability programs, supporting both commercial and clinical programs across all modalities and molecules. The successful candidate will work closely with internal QC repres ...

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📑 *This position is onsite in Ridgefield, CT & remote*Currently seeking a Global Case Management Associate (GCM) to join our Patient Safety & Pharmacovigilance (PSPV) team located at our Ridgefield, CT facility. The GCM will provide case processing and auditing support.Duties & Responsibilities:< ...

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📑 NEED 3 Total CWs* Job Title: Technical Writer Location: Bothell, WA TOP SKILLS: - Minimum of 5-8 years' experience in a GMP laboratory environment. At least 5 years' experience in writing and reviewing standard operating procedures. - Experienc ...

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📑 Hybrid 50% The U.S. Omnichannel Strategy team leads omnichannel planning, execution, and measurement in close partnership with Brand, Agency, Business Insights and Production teams. In this role, you will be responsible for the management and execution of omnichannel engagement plans to support a Client brand. You ...

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📑 Hybrid - 3 days onsite, 2 remote Managing the preparation of regulatory submissions for IND, ANDA, NDA, 510K, AdProm, and other electronic submission types o Creating timelines for regulatory filings o Providing and maintain templates for authoring. o Overseeing authoring and reviewing of regulat ...

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📑 Data Entry SpecialistKelly Services is seeking a diligent and detail-oriented individual to join our team as an SFE & Trade Contractor as a Data Entry Specialist. In this role, you will collaborate directly with the Sales Forces Effectiveness (SFE) Team and the Ax Trade Team, focusing on operational support for our Ax ...

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📑 Responsibilities: Business Analyst with IT GxP process and Business Process implementation experience. This person will need to be able to work in a very fast-paced and dynamic environment. Experience working in the Biotech/Pharma Industry. Develop and optimize test scripts usi ...

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📑 Responsibilities: Supports delivery of projects involving implementation and/or management of Regulatory InformationSupports Data & Content Migration into Regulatory Information Management System, involves.Source to target data model mapping.Data quality assessment<b ...

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📑 Main Responsibilities include:• Supports delivery of projects involving implementation and/or management of Regulatory Information• Supports Data & Content Migration into Regulatory Information Management System, involves:o Source to target data model mapping< ...

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📑 Medical Affairs Content DeveloperGlobal & US Medical CommunicationsThis position will be hybrid, so the candidate will be expected to work from the Nutley, NJ office 2 or 3 times a week.Description:This role is responsible for the creation and development of scientific and medical cont ...

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📑 About Accord BiopharmaAt Accord Biopharma we go beyond the biology of medicine to see diseases from a patient’s perspective. Our focus is innovating high quality therapies that enhance the overall treatment experience. Accord Biopharma is the US biopharmaceutical division of Intas Pharmaceuticals Ltd. Intas is a verticall ...

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📑 Job description : We are looking for Senior Manager with experience in Digital analytics in pharma / life science, which includes the oversight of promotional activities, measure and optimize various marketing measures, HCP eligibility, targeting measurement and impact analysis of digital and MCM campaigns. </p ...

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📑 Title: USA - Regulatory Affairs Ops Specialist I Location: Round Lake IL Hybrid - 3 days onsite, 2 remote Duration: 12 Months Pay Rate:$ 28.00/hr on W2 to $ 32.00/hr on W2 Managing the preparation of regulatory submissions for IND, ANDA, NDA, 510K, Clientrom, and other ...

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📑 Kelly Science & Clinical is seeking a Regulatory Affairs Ops Specialist near Round Lake, IL.Long term contract = ~1 year contract Shift: Monday - Friday 1stHybrid - 3 days onsite, 2 remoteCompensation: based on experience ...

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