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BioPharma Consulting JAD Group
1 views 3 days ago

QA Validation Specialist - Cell and Gene Therapy

NewBe an early applicant North AmericaContract
United States

QA Validation Specialist providing quality oversight of commissioning, qualification and validation at a cGMP cell and gene therapy manufacturing facility and QC labs in Boston. Day to day involves reviewing/approving IQ/OQ/PQ, CSV, process and cleaning validation documents, CMMS records, and SOPs in Veeva, plus supporting change controls, deviations and audits on a 6-12 month contract.

CMMS Risk Assessment Veeva
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jobs.servier.com
3 days ago

【契約社員】Marketing Assistant

NewBe an early applicant Contract

. MAIN FOCUS AND MISSION: The Marketing Assistant provides accurate and timely administrative and operational support to the Marketing Head and Marketing team. The role coordinates meetings, schedules, expenses,…

Veeva
jobs.servier.com
3 days ago

Senior Manager, Scientific Communications and Publication, Neurology

Open 1d Senior

About Servier Servier Pharmaceuticals is an independent, commercial-stage biopharmaceutical company built to think differently about what long-term impact can look like in healthcare. Launched in 2018 and backed by the…

Veeva
jobs.servier.com
3 days ago

Sr. Manager, IT Application Management, Digital

Open 1d Senior

Sr. Manager, IT Application Management, Digital About Servier Servier Pharmaceuticals is an independent, commercial-stage biopharmaceutical company built to think differently about what long-term impact can look like…

Analytics Automation CRM CSS HTML +6 skills
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jobs.servier.com
3 days ago

Associate Director, IT Application Management (Market Access & Patient Services)

Open 1d Hybrid

Associate Director, IT Application Management ( Market Access & Patient Services) About Servier Servier Pharmaceuticals is an independent, commercial-stage biopharmaceutical company built to think differently about…

Agile AI Analytics API Automation +13 skills
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careers.molnlycke.com
3 days ago

Field Sales Tianjin, North Region

NewBe an early applicant

Sales Representive Tianjin Make your next step a big one If you're ready to have an impact in a career that makes a difference, Mölnlycke could be your next step. You’ll be helping to equip medical professionals around…

CRM Veeva
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careers.molnlycke.com
3 days ago

Field Sales Wuhan, Central Region

NewBe an early applicant

Sales Representive Wuhan Make your next step a big one If you're ready to have an impact in a career that makes a difference, Mölnlycke could be your next step. You’ll be helping to equip medical professionals around…

CRM Veeva
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careers.molnlycke.com
3 days ago

Field Sales Xi'an, West Region

NewBe an early applicant

Sales Representive Xi'An Make your next step a big one If you're ready to have an impact in a career that makes a difference, Mölnlycke could be your next step. You’ll be helping to equip medical professionals around…

CRM Veeva
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Deloitte
3 days ago

Manager Regulatory Affairs Advisory / Life Sciences (m/w/d)

NewBe an early applicant Hybrid

Du willst im Bereich Strategy, Risk & Transactions – Advisory – Regulatory & Compliance innovative Lösungen entwickeln? Dann gestalte die Zukunft der Regulierung mit uns! Unser Team entwickelt mit Kunden aller Branchen…

Veeva
LEO Pharma
3 days ago

Maintenance Support Professional

NewBe an early applicant Contract

Application deadline: November 15th, 2026 Location: Ballerup 2750, Denmark, Denmark Contract type: Permanent Job ID: 4919 Help secure reliable operations today — and support the transition into LEO Pharma’s future…

CMMS Corrective Action Root Cause Analysis Veeva
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careers.reckitt.com
3 days ago

Sales Commercial Excellence Manager - Trade

NewBe an early applicant

We are Reckitt Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world.…

AI Automation CRM Performance Management Power BI +1 skills
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Kyverna
3 days ago

Associate Director, Regulatory Affairs, Advertising, Promotion & Labeling

NewBe an early applicant RemoteNorth America
United States

The Associate Director, Advertising, Promotion and Labeling will execute regulatory oversight for advertising, promotion, medical communications, and product labeling from pre-launch planning through lifecycle…

Veeva
Revolution Medicines
2 views 3 days ago

Senior QA Manager, GMP GxP Auditing & Vendor Management

NewBe an early applicant North AmericaFull-timeSenior
United States

Senior QA manager at an oncology biotech who leads GMP/GxP internal and external audits, runs the supplier/vendor quality program, drafts quality and technical agreements, maintains audit schedules and KPIs (using tools like Veeva), and prepares teams for regulatory inspections. Requires 8+ years pharma/biotech and 5+ years as a GMP lead auditor, with up to 25% travel.

Ccpa Cmos Corrective Action Program Management Risk Assessment +2 skills
164K – 205K $
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Vera Therapeutics, Inc.
3 views 3 days ago

Manager, Regulatory Operations

NewBe an early applicant RemoteContract

Vera Therapeutics is a commercial-stage biotechnology company focused on the pursuit of truth in science to transform medicine in autoimmune disease, starting with the kidney. Vera Therapeutics’ flagship commercial…

SharePoint Vault Veeva
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Eikon Therapeutics
1 views 3 days ago

Associate Director, Clinical Data Management

Open 25d North America H-1B sponsor history — This employer has had H-1B petitions approved by USCIS in the last five fiscal years, per the USCIS H-1B Employer Data Hub. The approval belongs to the employer and is not a commitment to sponsor this role.
United States

Eikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biology to discover novel treatments for life-threatening…

Data Quality Veeva
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ORIC Pharmaceuticals
2 views 3 days ago

Senior Regulatory Affairs Manager

NewBe an early applicant HybridNorth AmericaSenior
United States

We are seeking an experienced Regulatory Affairs professional to join our team and help advance the clinical development of oncology products at ORIC. In this role, you will collaborate closely with colleagues across…

Assembly Regulatory Compliance Strategic Planning Veeva
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Miltenyi Biotec
1 views 3 days ago

Supervisor, Warehouse *PC 1277

NewBe an early applicant North AmericaFull-time
United States

Your Role: Responsible for daily supervision of eight to ten assigned team of hourly MM Associates within a GMP warehouse and manufacturing environment. The team’s duties include but, are not limited to receiving,…

Corrective Action ERP GCP SAP SAP MM +1 skills
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Intuitive Surgical
4 views 3 days ago

Clinical Marketing Manager, Ion

NewBe an early applicant RemoteNorth America
United States

Primary Function of Position Joining the Ion Clinical Marketing team is an opportunity to develop and execute national and regional strategic marketing initiatives that help hospitals turn their investment in Ion into…

Accessibility Cloud Veeva
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OnHires
1 views 3 days ago

Senior Business Systems Analyst, Content Supply Chain & AI (Pharma Commercial)

NewBe an early applicant HybridNorth AmericaContractSenior
United States

Contract role bridging a global pharma company's commercial teams, system integrators, and AI/ML developers. The analyst owns functional requirements for content supply chain workflows, supports Adobe content platforms (Workfront, Experience Manager, Express, Firefly) and Veeva Vault, and documents AI-assisted content production with API-based integrations.

Agentic AI AI API Assembly Cloud +6 skills
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Orion Innovation
6 views 4 days ago

Computer Systems Validation Engineer

Open 45d North AmericaContract
United States

Orion Innovation is a premier, award-winning, global business and technology services firm. Orion delivers game-changing business transformation and product development rooted in digital strategy, experience design,…

Automation E-commerce ERP Oracle SAP +3 skills
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