Biotech Start Up Jobs

343 jobs

Senior Project Manager – Life Science & Biotech Industries Job Qualifications: Bachelor of Science, Engineering discipline 10+ years PM experience PE registration preferred PMP Certification preferred LEED Accreditation preferred FDA regulated manufacturing experience required cGMP compliance/verification Job Description: Qualified candidates will offer 7+ years of project management exp...

Our client, a prestigious research institute that develops innovative engineering solutions for healthcare, is seeking a motivated and skilled Research Project Coordinator to start ASAP! This temporary role is an excellent way to gain experience in a research capacity among some of the brightest minds in the field. In the role, you would manage the administrative components of the laboratory's res...

Thriving biotechnology company is currently looking to hire a polished and professional Executive Assistant to provide comprehensive support to a growing team. In this role, you will be responsible for managing a wide range of support functions including, but not limited to, preparing correspondence and memoranda; managing complex calendars including scheduling meetings, appointments and video con...

Senior Process Engineer – Biotech - Downstream Overall Description The Colonial Group specializes in the placement of outstanding talent in Manufacturing for the Biotech, Chemical, General Manufacturing, Food, and CPG industries. Our clients understand our decades of industry experience give us unique insights and access to top talent at all levels. We are a nationally recognized, award-winning ...

Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron markets medicines for eye diseases, colorectal cancer, and a rare inflammatory condition and has product candidates in development in other areas o...

Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron markets medicines for eye diseases, colorectal cancer, and a rare inflammatory condition and has product candidates in development in other areas o...

Serves as primary contact point between the sponsor and the investigational site. A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilities include sit...

Serves as primary contact point between the sponsor and the investigational site. A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilities include sit...

Serves as primary contact point between the sponsor and the investigational site. A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilities include sit...

Serves as primary contact point between the sponsor and the investigational site. A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilities include sit...

Serves as primary contact point between the sponsor and the investigational site. A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilities include sit...

Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron markets medicines for eye diseases, colorectal cancer, and a rare inflammatory condition and has product candidates in development in other areas o...

Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron markets medicines for eye diseases, colorectal cancer, and a rare inflammatory condition and has product candidates in development in other areas o...

Our client, an exciting and growing medical device/diagnostics sponsor company located in the Southern CA area is looking for a Director of their Medical Affairs division. The Director of Medical Affairs will lead the post-market scientific and technical activities for the company's biomarker tests, starting with the FDA-cleared tests already on the market. Key areas of focus include medical educ...

MANUFACTURING TECHNICIAN Pleasanton, CA - not Bart accessible Contract Length: 1 year Anticipated Start Date: May 4th 2015 Full time 40 hours a week– shifts vary Pay rate: $17-18.70/ depending on shift Duties: · Work in a team based environment to manufacture high quality custom oligonucleotides in a high throughput, fast paced setting. Essential Functions include but are not limited to the...

Responsibilities will include, but are not limited to: Oversight of CRO who will develop, program, test and maintain clinical trial databases and data entry screens using Rave in accordance with company standards. Review computer validation/edit checks for in-house and outsourced studies. Develop, program, test and maintain computer validation/edit checks in SAS. Develop, program, test and mainta...

Performs the role of Clinical Trial Assistant (CTA) supporting the Local Trial Manager and Site Manager to ensure optimal management of all documents with logistical and administrative tasks related to trial start-up, execution and closing of clinical trials. Performs regulatory document review and approval, including site specific Informed Consents. Ensures trial related activities are in complia...

The Clinical Research Associate monitors activities at clinical study sites to assure adherence to Good Clinical Practices (GCPs), SOPs and study protocols. Reviews regulatory documents as required and prepares site visit reports. Responsible for multiple projects and must work both independently and in a team environment. May participate in the study development, start-up and close-out process in...

EN ES ZN FR RU BookmarksPost a Job Home Vacancies Post a Job Contact us Now Hiring Aunite Annes and Fresh City $10per hour to Start Home Massachusetts Worcester / central MA General labor Now Hiring Aunite Annes and Fresh City $10per hour to Start Job Details ID #15540614 State Massachusetts City Worcester / central MA Date 2015-04-26 Deadline 2015-07-25 Category General labo...

4 Weeks Annual Vacation Fantastic Benefits Package Skokie, Greater Chicago LanzaTech’s award winning technology is revolutionizing the way the world thinks about waste carbon by treating it as an opportunity instead of a liability. LanzaTech’s unique process provides a sustainable pathway to produce platform chemicals that serve as building blocks to products that have become indispensable in our ...