Project Manager Biotech Manufacturing Jobs

641 jobs

Job Title : Advisor: Biotech (Manufacturing and Testing Manager) Requisition ID : 1400R52 Job Category : Sciences Job Type : Regular Primary Location : USA-MD: MARYLAND-FREDERICK Schedule : Full-time Remote Work Authorized: No Relocation Assistance: Not Available Travel : Yes, 20 % of the Time Clearance Level: None Employee Status : Regular Division: North American Public Sector...

. MAKE A POSITIVE IMPACT ON THE WORLD EVERY DAY Amaze yourself. Amaze the world. A job at EORM is unlike any other you’ve had. You’ll be challenged. You’ll be inspired. And you’ll be proud. Because whatever your job is here, you’ll be part of something big. This could be your ideal job if you are excited about biosafety and have several years experience in ergo and other general EH&S, and are i...

Our client, an exciting and rapidly growing Biotech firm, with manufacturing operations in the RTP, is actively recruiting for an Automation Engineer to manage all automation technology at two state-of-the-art lab facilities. This individual will be the subject matter expert for all automation activities including change control, validation, and documentation. This Automation Engineer will be res...

Senior Manager of Sales Analytics: My client, a specialty biotech company located in the SouthernCalifornia area, is committed to unlocking the potential biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. Their novel therapies have been used to treat more than 25 million patients. Their efforts are currentl...

External Manufacturing Ops Project Mgr-75015226-61058 Description Genzyme has pioneered the development and delivery of transformative therapies for patients affected by rare and debilitating diseases for over 30 years. We accomplish our goals through world-class research, collaboration with the global patient community, and with the compassion and commitment of our employees. With a focus on ra...

Contract Manufacturing Qlty Specialist- Day Shift-75012237-59879JC Description Genzyme has pioneered the development and delivery of transformative therapies for patients affected by rare and debilitating diseases for over 30 years. We accomplish our goals through world-class research, collaboration with the global patient community, and with the compassion and commitment of our employees. With ...

The Senior Manager, External Manufacturing is responsible for assigned manufacturing activities and projects at drug substance, drug product, and packaging CDMOs. He/she will also contribute to other Technical Operations activities in their area of expertise. Essential Functions: Coordinate production runs, including person-in-plant activities as necessary to support successful operations. Proj...

Manufacturing / Plant Engineer II - Utilities-00474085-50786JC Description Genzyme has pioneered the development and delivery of transformative therapies for patients affected by rare and debilitating diseases for over 30 years. We accomplish our goals through world-class research, collaboration with the global patient community, and with the compassion and commitment of our employees. With a fo...

Our client, a growing and dynamic pharmaceutical company, is currently hiring a Manager, Regulatory Affairs/CMC. Overall Purpose: The Manager of Regulatory Affairs is responsible for overseeing and managing the process of meeting requirements established by U.S. and international governmental agencies in introducing and maintaining new products in the marketplace. May also be responsible for su...

Job Title : Advisor: Biotech (Drug Product Sr. Manager) Requisition ID : 1400SBF Job Category : Sciences Job Type : Regular Primary Location : USA-MD: MARYLAND-FREDERICK Schedule : Full-time Remote Work Authorized: No Relocation Assistance: Not Available Travel : Yes, 20 % of the Time Clearance Level: None Employee Status : Regular Division: North American Public Sector Posting...

Our client, a growing and dynamic pharmaceutical company, is currently hiring a Manager, Regulatory Affairs/CMC. Overall Purpose: The Manager of Regulatory Affairs is responsible for overseeing and managing the process of meeting requirements established by U.S. and international governmental agencies in introducing and maintaining new products in the marketplace. May also be responsible for su...

Description CSC has an immediate position for a Sr. Process Validation Manufacturing Manager. This person will provide leadership and technical expertise to the Dynport Vaccine Company (DVC) product teams and DVC subcontractors with regard to development, design, optimization, qualification, validation and execution of manufacturing processes and analytical methods compliant with the current Food...

Description CSC has an immediate position for a Technical Development Manager. This position is located in Frederick, Maryland. Essential Job Functions The Technical Development Manager is responsible for overseeing and coordinating the technical development of DVC's recombinant vaccine against a bacteria, with the objective of achieving FDA licensure using the US FDA's "Animal Rule". The proje...

Contract Manufacturing Quality Spec- Evening Shift-75008663-58466 Description Genzyme has pioneered the development and delivery of transformative therapies for patients affected by rare and debilitating diseases for over 30 years. We accomplish our goals through world-class research, collaboration with the global patient community, and with the compassion and commitment of our employees. With a...

About The Opportunity: Our client is a clinical-stage biopharmaceutical company creating products to address a broad range of infectious diseases worldwide. Using innovative technologies, as well as new and efficient manufacturing approaches, the company produces potent candidates to combat diseases, with the goal of allowing countries to better prepare for and more effectively respond to rapidly...

Clinical Solutions Group/CSG is looking for CMC Regulatory Affairs personnel for a large pharmaceutical company in the Philadelphia area. The scope of work includes reviewing historical CMC registered files (BLAs/supplements/amendments) and authoring/compiling compliant CTD formatted documents within project timelines and with limited oversight. Requirements: • Minimum of a bachelors degree in a...

Provide supervision and implementation of all activities in the department, to ensure manufacturing goals are reached through maximum and efficient use of staff and materials. During the project phase: Drive all Operational Readiness activities for a Manufacturing building, ensuring consistency and comprehensiveness. Drive schedule definition for operational readiness activities Lead raw mater...

*Org Marketing Statement*All over the world, Pfizer colleagues are working together to positively impact health for everyone, everywhere. Each position at Pfizer touches and contributes to the success of our business and our world. That’s why, as one of the global leaders in the biopharmaceutical industry, Pfizer is committed to seeking out inspired new talent who share our core values and mission...

Org Marketing Statement All over the world, Pfizer colleagues are working together to positively impact health for everyone, everywhere. Each position at Pfizer touches and contributes to the success of our business and our world. That’s why, as one of the global leaders in the biopharmaceutical industry, Pfizer is committed to seeking out inspired new talent who share our core values and mission...

Job Title : Manager: Biotech (Senior Director: Regulatory Affairs) Requisition ID : 1400ORL Job Category : Sciences Job Type : Regular Primary Location : USA-MD: MARYLAND-FREDERICK Schedule : Full-time Remote Work Authorized: No Relocation Assistance: Not Available Travel : Yes, 10 % of the Time Clearance Level: None Employee Status : Regular Division: North American Public Sect...