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554 jobs
Azurity Pharmaceuticals - US
4 days ago

Territory Manager - Queens, NY

RemoteNorth AmericaFull-time
United States

Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and…

analytics crm gdpr salesforce strategic-planning +1 skills
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Azurity Pharmaceuticals - US
4 days ago

Territory Sales Specialist - Des Moines, IA

RemoteNorth AmericaFull-time
United States

Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and…

crm gdpr veeva
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Azurity Pharmaceuticals - US
4 days ago

Territory Manager - GI - Kansas City

RemoteNorth AmericaFull-time
United States

Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and…

analytics crm gdpr salesforce strategic-planning +1 skills
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Azurity Pharmaceuticals - US
4 days ago

Territory Sales Specialist - Pittsburg, PA

RemoteNorth AmericaFull-time
United States

Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and…

crm gdpr veeva
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jobgether
4 days ago

Business Analyst, Veeva Migration / Business Analyst

RemoteNorth AmericaFull-time
United States

This Business Analyst role supports Veeva Vault eTMF migration initiatives within regulated life sciences environments. The position involves translating business requirements into migration specifications, managing data mapping and validation, and ensuring inspection readiness throughout the clinical document lifecycle.

ai data-quality gdpr jira servicenow +4 skills
69 300 – 104 439 $
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Simtra BioPharma Solutions
4 days ago

Quality Analyst I - Batch Review (weekend PM)

North AmericaContract
United States

Quality Analyst I responsible for compiling, reviewing, and releasing batch records for sterile injectable manufacturing on weekend PM shifts, primarily using Veeva and enterprise quality systems in an FDA-regulated cGMP environment.

veeva
Precision AQ
5 days ago

Senior Account Executive - Healthcare Marketing

Open 32d RemoteNorth AmericaSenior
United States

Precision AQ , the leading payer marketing agency, supports global pharmaceutical and life sciences clients in the achievement of commercial excellence. Are you looking for a rewarding career in a team-driven…

account-executive veeva
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Precision AQ
5 days ago

Senior Medical Editor - Healthcare Marketing

Open 20d RemoteNorth AmericaSenior
United States

Precision AQ is the top payer marketing agency in the country. We partner with global pharmaceutical and life sciences companies who are developing groundbreaking treatments to make medicines accessible and affordable.…

veeva
Precision Medicine Group
5 days ago

Senior Account Executive - Healthcare Marketing

Open 32d RemoteNorth AmericaSenior 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

Precision AQ , the leading payer marketing agency, supports global pharmaceutical and life sciences clients in the achievement of commercial excellence. Are you looking for a rewarding career in a team-driven…

account-executive veeva
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Precision Medicine Group
5 days ago

Senior Medical Editor - Healthcare Marketing

Open 20d RemoteNorth AmericaSenior 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

Precision AQ is the top payer marketing agency in the country. We partner with global pharmaceutical and life sciences companies who are developing groundbreaking treatments to make medicines accessible and affordable.…

veeva
Real Chemistry
5 days ago

Senior Account Manager, Med Affairs

Open 14d RemoteNorth AmericaSenior
United States

At Real Chemistry, making the world a healthier place isn’t just an aspiration—it’s our everyday reality. Our drive to transform healthcare is informed by our blend of deep scientific expertise, human-centred…

ai networking strategic-planning veeva
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Kyowa Kirin North America
5 days ago

CRM Manager, Omnichannel Customer Experience (OCX)

Open 76d RemoteNorth America
United States

Kyowa Kirin is a fast-growing global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines in four disease areas: bone and mineral; intractable…

cloud crm data-governance gdpr process-improvement +2 skills
125 000 – 166 700 $
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Simtra BioPharma Solutions
5 days ago

Specialist (m/w/d) QA CAPA Management

Europe
Germany

The Specialist (m/w/d) QA CAPA Management oversees customer-related deviation management and quality reporting within a pharmaceutical manufacturing environment. The role involves coordinating investigation strategies, approving CAPA measures, and representing quality processes during audits using GMP standards.

typescript veeva
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Simtra BioPharma Solutions
5 days ago

Specialist QA Supplier Quality Management (m/w/d)

Europe
Germany

The Specialist QA Supplier Quality Management oversees supplier qualification and monitoring within a GMP-regulated environment. The role involves managing the supplier quality system, handling deviations and CAPAs, and coordinating quality agreements and audits.

veeva
Simtra BioPharma Solutions
5 days ago

Specialist QA Document & Training (m/w/d)

Europe
Germany

The Specialist QA Document & Training manages GMP-compliant training and documentation systems, including LMS and eQMS, while supporting audits and process improvements. The role requires a background in natural sciences and experience in quality assurance within a pharmaceutical environment.

veeva
Simtra BioPharma Solutions
5 days ago

Specialist QA Change Control Management (m/w/d)

Europe
Germany

The Specialist QA Change Control Management oversees and improves the GMP-compliant change control processes at a biopharmaceutical manufacturing site. The role involves coordinating changes, moderating governance boards, ensuring data integrity, and supporting audits and international stakeholders.

veeva
Forge Biologics
5 days ago

Manager, Document Control (QA Operations)

Open 20d North AmericaFull-time 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

Manages a team overseeing compliant document control for a gene-therapy manufacturer, using an eQMS like Veeva Vault to maintain SOPs, batch records, and regulatory documentation.

accessibility smartsheet technical-writing vault veeva
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Forge Biologics
5 days ago

Specialist I, QA Operations

Open 17d North AmericaFull-time 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

Oversee quality assurance for AAV gene therapy manufacturing, reviewing batch records, ensuring cGMP compliance, and supporting cleanroom operations in a biotech facility.

process-improvement vault veeva
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Kymera Therapeutics
5 days ago

Senior Manager or Associate Director, Preclinical Safety Study Monitor

Open 34d North AmericaSenior 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

Who we are: Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically…

regulatory-compliance sharepoint veeva
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Kymera Therapeutics
5 days ago

Senior Specialist or Manager, Quality Systems

Open 67d North AmericaSenior 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

Who we are: Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically…

program-management vault veeva
85 000 – 200 000 $
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