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Document Control
Document Control Regulatory Affairs is an exciting career that requires a dynamic individual capable of handling a multitude of job tasks. Finding a position in Document Control is easy at HireLifeScience.com. We offer excellent job opportunities across the United States and have simplified the hiring process. By clicking on the job title that matches your qualifications you can apply directly to the hiring company. Whether you are embarking on a new career or looking for an advanced position HireLifeScience.com has the right Document Control career for you!
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QA Document Coordinator (NCI)

Leidos Biomedical Research, Inc. - FREDERICK, MD

KEY ROLES/RESPONSIBILITIES Reporting to the QA Document Control Supervisor, the QA Document Coordinator will: - Receive, scan, sort and file documentation according to the organizational filing system (electronic and paper-based) - Develop and maintain electronic and paper file structures - Use and understand the electronic document management system (eDMS) to file/retrieve electronic ...more

From Leidos Biomedical Research, Inc. - 8/6/2018 6:40:10 AM

QA Document Coordinator (NCI)

Leidos Biomedical Research, Inc. - FREDERICK, MD

KEY ROLES/RESPONSIBILITIES Reporting to the QA Document Control Supervisor, the QA Document Coordinator will: - Receive, scan, sort and file documentation according to the organizational filing system (electronic and paper-based) - Develop and maintain electronic and paper file structures - Use and understand the electronic document management system (eDMS) to file/retrieve electronic ...more

From Leidos Biomedical Research, Inc. - 8/6/2018 6:40:10 AM

The HireLifeScience.com Career Fair 2018 - Edison, NJ

HireLifeScience.com - Edison, NJ

Required qualifications to attend: Attendance is free. Candidates must possess a 4 year life science related degree and 2 years professional experience working for a Life Science related company. An invitation to attend will be sent if the minimum qualifications are met. A general overview of job categories companies will be hiring for: -Research & Development -Clinical Research -Laboratory...more

From HireLifeScience.com - 7/30/2018 7:52:49 AM

Regulatory Submissions Manager

Amicus Therapeutics - Cranbury, NJ

QUALIFICATIONS AND BACKGROUND REQUIREMENTS - BS or MS in scientific discipline or equivalent required. Project Management certification (i.e. PMP) and/or RAC certification preferred. - 3-8 years of regulatory affairs experience with drugs and/or biologics; at least 2 years' experience in regulatory submissions management; at least 1-2 years' experience in global markets. - Experience...more

From Amicus Therapeutics - 7/16/2018 6:32:08 AM

BioAnalytical Document Coordinator

Covance, Inc. a division of LabCorp® - Salt Lake City, UT

Education/Qualifications - Bachelor of Science (BS) degree in science or related field is highly preferred - Strong ability in utilizing Microsoft Word and Excel including the use of Word Templates Experience - Minimum of 2 years of related experience - Excellent communication, presentation, and interpersonal skills - Proven detail orientation skills with the ability to pri...more

From Covance, Inc. a division of LabCorp® - 6/29/2018 6:36:40 AM

Principal Medical Communications Scientist

AstraZeneca Pharmaceuticals - Gaithersburg, MD

Main Duties and Responsibilities As a Principal MCS, you will •provide expert communications leadership to late-stage drug projects (Phase 3 onwards) in a world-leading biopharmaceutical company •lead a strategy-driven approach to authoring clinical documents for submissions.  You will liaise with senior project staff, prospectively develop a storyboard for the submission, and plan docume...more

From AstraZeneca Pharmaceuticals - 4/17/2018 5:43:58 AM
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