Pharmaceutical Industry jobs in Remote

Indianapolis, Indiana

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Today

Minimum 1 week a month in Indiana during the basic/detailed design phase of the project. Full time on site during the Commissioning phase of the project Project based role, Duration 3 years The Automation Area Lead will be responsible the control system solution for an area within a project ensuring the solution is aligned with the overall program automation philosophy, standards and user requirements. The area lead will work in conjunction with the other members of the Project Team, including

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Third Party, Contract

Depends on Experience

Automation Area Lead DeltaV

Hybrid in Indianapolis, Indiana

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Today

Automation Area Lead DeltaV Indiana, IN (Hybrid) Minimum 1 week a month in Indiana during the basic/detailed design phase of the project. Full-time on-site during the Commissioning phase of the project Project-based role, Duration 3 years The Automation Area Lead will be responsible for the control system solution for an area within a project, ensuring the solution is aligned with the overall program automation philosophy, standards, and user requirements. The area lead will work in conjunction

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Contract, Third Party

Depends on Experience

Senior Developer - LabWare LIMS

Remote

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10d ago

Role Description: Seeking exceptional LabWare expertise that can configure complex code, provide in-depth application guidance and support L4 troubleshooting - Work closely with Product Owner, Quality Assurance and Business Process Owners to effectively and efficiently implement LIMS projects. - Assist with understanding the business requirements, analyze and suggest technical solution for LIMS projects - Create and review deliverables such as technical specification, design documents for LIMS

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Contract

$50 - $90

Senior Developer - LabWare LIMS 2

Remote

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10d ago

Title: Senior Developer - LabWare LIMS 2 Work Location: 100% Remote Position Type: Contract Duration: Long Term Job Description: Seeking exceptional LabWare expertise that can configure complex code, provide in-depth application guidance and support L4 troubleshootingWork closely with Product Owner, Quality Assurance and Business Process Owners to effectively and efficiently implement LIMS projects.Assist with understanding the business requirements, analyze and suggest technical solution for L

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Contract, Third Party

$100 - $110

Trade Business Analytics

Connecticut

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3d ago

Business Analytics role supports multiple customer groups and/or therapeutic areas & will be an expert in statistical methodologies for measuring marketing impact, will have a broad understanding of the pharmaceutical industry and a deep familiarity with industry data sources. The role requires using sophisticated analytics for projects including marketing mix modeling, ROI analyses on all relevant marketing programs/customer channels and promotional spends, customer profiling and segmentation,

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Contract

Dat Integrity CSV/CQV Lab Equipment Contractor | New York, New York | Onsite

Albany, New York

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Today

Title: CSV/CQV Lab Equipment Contractor Location: New York, New York | Onsite Duration: 12 months with 2 potential extensions ( 3 year long estimated project) Interview Process: One-step interview via Teams with hiring managers Responsibilities: Perform system administrative tasks, including commissioning and basic troubleshooting of equipment. This role will work with a variety of lab equipment, including SoloVPEs, Nova Flex2s, Kingfisher Apex, LabChips, Wave Rockers, and Sartochecks. Onboar

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Contract, Third Party

SAP SD Consultant

Hybrid in Pittsburgh, Pennsylvania

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9d ago

SAP SD Consultant Location: Pittsburgh, PA, USA (Hybrid) Experience: 89 Years Industry: Pharmaceutical Type: Contract (Rate: Please share your best competitive rates) Job Summary We are seeking an experienced SAP SD Consultant with strong pharmaceutical industry experience to support an ongoing customer project. The ideal candidate must be based in Pittsburgh, PA, and available to work in a hybrid onsite model. Key Responsibilities Work directly with business stakeholders to gather requiremen

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Contract

Depends on Experience

Quality Assurance(QA) Specialist

Morrisville, North Carolina

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13d ago

Description: Provide Quality and Compliance oversight for manufacturing of commercial and investigational products through Shop Floor presence.Responsible for performing inspection and disposition of raw materials and components by:Supporting incoming material release activities within the ERP system, ensuring compliance with applicable regulations and internal procedures.Obtaining Certificates of Analysis (CoA), Certificates of Compliance (CoC), and other required documentation from vendors in

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Contract

$35 - $38

SAP FICO Consultant

Hybrid in Pittsburgh, Pennsylvania

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9d ago

SAP FICO Consultant Location: Pittsburgh, PA, USA (Hybrid) Experience: 89 Years Industry: Pharmaceutical Rate: DOE Job Summary We are looking for a seasoned SAP FICO Consultant with strong functional knowledge and pharmaceutical industry experience. The consultant must be PA-based and available for a hybrid onsite schedule. Key Responsibilities Work with business teams to gather financial and controlling requirements. Configure and support SAP FI and CO modules (GL, AP, AR, Asset Accounting

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Contract

Depends on Experience

Excel Macro & Smartsheet Developer (Remote)

Remote

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21d ago

Excel Macro & Smartsheet Developer (Remote) We are looking to hire a candidate with the skills sets mentioned and experience for one of our clients within the pharmaceutical Industry. This is a REMOTE position. Job Summary: We are seeking a skilled Excel Macro and Smartsheet Developer to support automation, workflow optimization, and reporting needs. The ideal candidate must be proficient in both Excel Macros (VBA) and Smartsheet, with hands-on experience building automated solutions, dashboar

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Contract

$50

SAP FICO Solution Consultant

Remote

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6d ago

Job Title: SAP FICO Solution Consultant Location: Remote Job Description: We are seeking an experienced SAP Finance Solution consultant to lead the design, development, and implementation of SAP Finance (FICO) solutions across enterprise environments. Apart FICO with GXP, Deep exposure to Gross-to-Net and Rebate processes used in Life Sciences/Pharma will be key on this role Experience of GxP in the pharmaceutical industry for regulations and quality guidelines. Key Responsibilities Lead the a

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Third Party, Contract

Depends on Experience

Databricks/Unity Catalog Data Governance Lead - Remote

Remote

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7d ago

Databricks/Unity Catalog Data Governance Lead - Remote We are looking to hire a candidate with the skills sets mentioned and experience for one of our clients within the pharmaceutical Industry. Role Overview The Data Governance Lead is responsible for establishing and operationalizing governance standards across the PSG data ecosystem, with a strong emphasis on Databricks and Unity Catalog as foundational components of the platform. This role focuses on unifying fragmented data sources into a

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Contract

Scrum Master / PM Data Platform & Databricks - Remote

Remote

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6d ago

Scrum Master / PM Data Platform & Databricks - Remote We are looking to hire a candidate with the skills sets mentioned and experience for one of our clients within the pharmaceutical Industry. This is a REMOTE position. Job Summary: We are looking for a highly skilled Scrum Master/Project Manager with strong experience in the data domain to lead Agile delivery and project oversight across data engineering and cloud-based initiatives. This role requires hands-on familiarity with DataBricks, AW

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Contract

CSV Engineer

Indianapolis, Indiana

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Today

Responsibilities: Interface with client Subject Matter Experts, Site and Area Management, Quality Assurance, and other stakeholders for validation planning. Guide the creation and updates of project validation planning deliverables such as Validation, Security, and Test Plans. Support execution of validation activities in alignment with the approved Validation Plan and CSV documentation standards. ssist Project CSV Leads in generating/editing CSV documents and electronic testing templates. Recom

Full-time

Clinical SAS Programmer

Raleigh, North Carolina

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Today

Responsibilities: Review protocols for CDISC conformance. Review Case Report Forms and eCRFs with CDISC CDASH and SDTM conformant elements. Write and manage SAS code for mapping clinical data to SDTM data structures in conformance with Emmes' SDTM Implementation Guide, project standards, and the study protocol. Create DEFINE specifications for mapping of SDTM and ADaM compliant datasets. Review and QC submission ready SDTM datasets, define.xml, and supporting documentation, as appropriate. Provi

Full-time

Quality Assurance Engineer - Process and Validation (930)

Petersburg, Virginia

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Today

About Civica Civica is a 501(c)(4) social welfare organization established in 2018 by health systems and philanthropies to reduce chronic generic drug shortages and related high prices in the United States. Civica is led by an experienced team of healthcare and pharmaceutical industry leaders. Today, more than 55 health systems have joined Civica. They represent over 1,500 hospitals and one-third of all U.S. hospital beds. Civica has also begun to supply the U.S. Department of Veteran's Affairs

Full-time

Associate Microbiologist (356)

Colonial Heights, Virginia

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Today

About Civica: Critical shortages of essential generic injectable drugs are an ongoing crisis in U.S. healthcare and have reached an all-time high. Over 300 essential medications are currently reported to be in shortage, according to industry and FDA reports. Shortages put patients at risk and waste hospital resources. Civica is a market-based nonprofit solution created in 2018 by health systems and philanthropies for the express purpose of preventing and mitigating drug shortages. Today, near

Full-time

AI GenAI Data Science Internship

Indianapolis, Indiana

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Today

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined

Full-time

USD 65.00 per hour

Sr Manager, RWE Analytics

Plainsboro Township, New Jersey

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Today

Job Title: Sr Manager, RWE Analytics Location: Plainsboro, NJ Hybrid - 3 days onsite, 2 days work from home Work Schedule: Mon-Fri, 8:30 AM-5:30 PM (45 hours/week) Minimum Requirements: 3+ years of experience working in the pharmaceutical industry analyzing RWE studies Must have experience analyzing claims, EHR, registry and linked data sources PhD or Master's in Epidemiology, Biostatistics, Public Health, or related field is required Job Summary The Senior Scientist, Health Economic Resources

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Contract

Validation Engineer

Austin, Texas

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Today

Summary: We are seeking a talented Validation Engineer to join our team. As a Validation Engineer, you will play a crucial role in ensuring the quality and compliance of our manufacturing processes and systems. You will be responsible for designing, implementing, and executing validation protocols to ensure that equipment, facilities, and processes meet regulatory requirements and industry standards. Roles & Responsibilities: Design and develop validation protocols for SCADA technology used in t

Full-time

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Pharmaceutical Industry jobs in Remote