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Senior Project / Program Manager - Pharma
SOUTH SAN FRANCISCO, CA, UNITED STATES
Zifo is looking for a Senior Project/Program Manager with experience in running the project portfolio. The Project Manager will be responsible for the delivery of various technical solutions for large biopharma customers.RequirementsHigh level PM Job Description: Lead and manage new...
Senior Manager, Clinical Trial Supplies, Oncology - JOB ID: 1344CA
PALO ALTO, CA, UNITED STATES
...skills. The Senior Manager, Clinical Trial Supplies (CTS), Oncology will work as an integral member of the Ascendis Global CTS Oncology team, managing all aspects of Investigational Medicinal Products (IMP), Clinical Trial Supplies, Comparators and ancillary products used in Ascendis Oncology...
Senior Manager, Clinical Trial Supplies, Oncology - JOB ID: 1344CA
PALO ALTO, CALIFORNIA, US
...skills. The Senior Manager, Clinical Trial Supplies (CTS), Oncology will work as an integral member of the Ascendis Global CTS Oncology team, managing all aspects of Investigational Medicinal Products (IMP), Clinical Trial Supplies, Comparators and ancillary products used in Ascendis Oncology...
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Associate Director, IT Product Ownership - Job ID: 1407
PALO ALTO, CA, UNITED STATES
Ascendis Pharma is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe, and the United States. Today, we're advancing programs in Endocrinology Rare Disease and Oncology.Here at Ascendis, we pride ourselves on exceptional science, visionary leadership, and...
Associate Director, IT Product Ownership - Job ID: 1407
PALO ALTO, CALIFORNIA, US
Ascendis Pharma is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe, and the United States. Today, we're advancing programs in Endocrinology Rare Disease and Oncology. Scroll down for a complete overview of what this job will require Are you the right...
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US_Process Engineer III
SOUTH SAN FRANCISCO, CA, UNITED STATES
...devices for parenteral pharmaceutical therapeutics at .The candidate has in depth experience in high volume manufacturing processes and methodologies and process development to support clinical and commercial production activities within s device development programs. This includes engaging...
Process Engineer III
SOUTH SAN FRANCISCO, CA, UNITED STATES
...devices for parenteral pharmaceutical therapeutics at .The candidate has in depth experience in high volume manufacturing processes and methodologies and process development to support clinical and commercial production activities within 's device development programs. This includes engaging...
QA Specialist
FOSTER CITY, CA, UNITED STATES
Responsibilities: Performs a wide variety of activities to ensure compliance with applicable quality objectives and regulatory requirements. Serves as Analytical Operation Lead for clinical and commercial projects. Leads quality investigations/deviations/quality event escalation...
Associate Director Global PV Operations, Oncology - Job ID: 1405
PALO ALTO, CA, UNITED STATES
...etc.) Provides pharmacovigilance expertise to Ascendis or CRO/Vendor staff when needed Pharmacovigilance related responsibilities over GVP, Patient Support Programs (PSPs) and other Service Providers (SPs) vendors. These activities include, but is not limited to: Ensuring SP/vendor...
Associate Director Global PV Operations, Oncology - Job ID: 1405
PALO ALTO, CALIFORNIA, US
...Report, etc.) Provides pharmacovigilance expertise to Ascendis or CRO/Vendor staff when needed Pharmacovigilance related responsibilities over GVP, Patient Support Programs (PSPs) and other Service Providers (SPs) vendors. These activities include, but is not limited to: Ensuring SP/vendor...
Engineer Senior
THOUSAND OAKS, CA, UNITED STATES
Fully OnsiteStandard business hours Notes from hiring manager:Looking for hands on STRONG engineer experience with proper training/ background in technical side/ mathematics. NOT LOOKING for quality lab/ bench top/ science work. The job seeker needs to be practical with troubleshooting...
Engineer Senior
THOUSAND OAKS, CA, UNITED STATES
FULLY ONSITE AT USTO Standard business hours Copy of AMAGJP(phone number removed) 2 resumes attached of a ideal candidate for this role NOTES FROM HIRING MANAGER: Looking for hands on STRONG engineer experience with proper training/ background in technical side/ mathematics. NOT...
GxP Validation Lead
ALAMEDA, CA, UNITED STATES
...applications) for GxP compliance Assist building a standardized method of enabling / implementing the SOPs for the GxP applications and getting the teams to adopt the standard approach Manage and execute validation plans and validation documents for new systems in scopeAnalyze and propose...
Validation Lead
OAKLAND, CA, UNITED STATES
Responsibilities : Act as a Validation Lead for multiple products (applications) for GxP compliance Assist building a standardized method of enabling / implementing the SOPs for the GxP applications and getting the teams to adopt the standard approach Manage and execute validation...
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Clinical Research Coordinator II Registered Nurse
WINSTON-SALEM, NORTH CAROLINA, UNITED STATES
...safety, quality, compliance and stewardship. At Novant Health, one of our core values is diversity and inclusion. By engaging the strengths and talents of each team member, we ensure a strong organization capable of providing remarkable healthcare to our patients, families and communities...
Quality Assurance Manager
GROTON, CT, UNITED STATES
Position Details: Our client, a world-leading Pharmaceutical Company in Groton, CT is currently looking for a Manufacturing Quality Manager to join their expanding team.Job Title: Manufacturing Quality Manager / Pharma Industry / Hybrid Work Duration: 20 months contract, extendable up to 36...
Clinical / Scientific - Quality Assurance Manager
CHESTERFIELD, MO, UNITED STATES
Position Details: Our client, a world-leading Pharmaceutical Company in Groton, CT is currently looking for a Manufacturing Quality Manager to join their expanding team.Job Title: Manufacturing Quality Manager / Pharma Industry / Hybrid Work Duration: 19 months contract, extendable up to 36...
Quality Assurance Manager
GROTON, CT, UNITED STATES
Position Details: Our client, a world-leading Pharmaceutical Company in Groton, CT is currently looking for a Manufacturing Quality Manager to join their expanding team.Job Title: Manufacturing Quality Manager / Pharma Industry / Hybrid Work Duration: 20 months contract, extendable up to 36...
Manager 2 - Process Excellence
TITUSVILLE, NJ, UNITED STATES
Position Details: Our client, a world-leading Pharmaceutical Company in Titusville, NJ or Horsham, PA is currently looking for a Project Manager to join their expanding team.Job Title: Project Manager / Pharma Patient Assistance programs / Hybrid Work Duration: 9 months contract...
Project Manager Ad Agency
METTAWA, IL, UNITED STATES
...be nice to have1. pharma experience2. client facing3. Advanced level experience on PM software & Smart Sheets.PRIMARY FUNCTION / PRIMARY GOALS / OBJECTIVESThe Sr. Project Manager works closely with their assigned account manager to help coordinate daily activities and the ongoing...
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