Show me jobs with…
Near this location
For International Job Search Please   Click Here
Regulatory Affairs
Most Pharmaceutical, Biotechnology, Medical Device and Life Science companies are hiring for Regulatory Affairs professionals. Our clients are no different and on this page you will find their open regulatory career opportunities.
Search Jobs by Category

Posted By

Name... @ Company

   


Image not available



Category Country State

Manager, Maintenance (Millsboro, DE)

Merck & Co. - Millsboro, DE

Education: Associate’s degree in Engineering or other Scientific/Technical Area OR Master’s License in Trade (Electrical, HVAC, HVAC/R, Plumbing, etc.) Required: • A minimum of 8 years’ industry experience as an engineer, supervisor, or technical lead in a maintenance department that supports a manufacturing setting. • 3 year’s management and or lead role experience (people/budget/or...more

From Merck & Co. - 2/16/2018 5:49:54 AM

Global Program Regulatory Manager

Novartis Pharmaceuticals - East Hanover, NJ

Minimum requirements Science based BS or MS with requisite experience and demonstrated capability. Advanced degree (MD, Ph D, PharmD) preferred. English Experience with regulatory submission and approval processes in 1 or more major regions. • Experience in a global/matrix environment or cross-functional teams in the pharmaceutical industry. • Experience in HA negotiations. • 2-4 years involvement...more

From Novartis Pharmaceuticals - 2/16/2018 5:49:38 AM

Team Lead - Medical Safety Review

Merck & Co. - Rahway, NJ

Education: • M.D. or D.O. and equivalent Required: • Minimum of 3 years clinical practice experience, following training or prior industry experience in safety, clinical development and/or medical affairs • Relevant Safety Systems Experience (i.e. Argus, ARIS-G, etc). • Minimum 3 years People Management Experience • Minimum of 8 years of professional experience and/or pharmaceutical in...more

From Merck & Co. - 2/15/2018 5:46:44 AM

Regulatory Information Manager

AstraZeneca Pharmaceuticals - Gaithersburg, MD

Essential Requirements •Minimum 1 year hands-on experience with tracking of regulatory information. •University degree or equivalent experience in life sciences or technical field. •Ability to provide global expertise on requirements for tracking of regulatory submissions and approvals. •Ability to assess data, documentation and processes for regulatory impact/compliance with relevant regulat...more

From AstraZeneca Pharmaceuticals - 2/15/2018 5:46:03 AM

Medical Information Specialist

CSL Behring - King of Prussia, PA

Main Responsibilities and Accountabilities: 1. Leads efforts in researching, writing, and reviewing database of accurate, evidence-based, balanced medical information SRLs and FAQs for US and Global Medical Affairs that results in effective communication with our internal and external stakeholders. Establishes and conducts periodic review of current literature for evaluation and inclusion in resp...more

From CSL Behring - 2/14/2018 5:44:13 AM

Director, Vaccines Policy

Merck & Co. - Upper Gwynedd, PA

Education: • Bachelor's degree required. Skills and qualifications: • At least 5 years of demonstrated success working in the public policy arena and/or government • At least 1 year working internationally or in a global context • Knowledge of health and immunization systems • Demonstrated leadership ability to identify strategic priorities, bring together different ...more

From Merck & Co. - 2/14/2018 5:41:54 AM

Biobank Program Manager (NCI)

Leidos Biomedical Research, Inc. - ROCKVILLE, MD

PREFERRED QUALIFICATIONS Candidates with these desired skills will be given preferential consideration: - Experience managing a large network of specimen collection activities - Experience in the ethical, legal, and regulatory aspects of biobanking and human subjects research - Knowledge of best practices in biobanking operations and biobanking data standards - Experience in bios...more

From Leidos Biomedical Research, Inc. - 2/13/2018 5:47:42 AM

Senior Specialist, Regional Dossier Publisher

Merck & Co. - Carolina, PR

Requirements: • Bachelor's Degree or higher degree in Life Sciences or IT. • Minimum three (3) years of pharmaceutical industry experience. • Knowledge of Liquent Insight Publisher and other publishing tools will be considered as a plus. • Strong documentation management skills. • Strong analytical and customer service skills with the ability to work with varying g...more

From Merck & Co. - 2/13/2018 5:47:18 AM

Sr. Specialist, Regulatory Affairs, CMC - Post Approval

Merck & Co. - Rahway, NJ

Education Requirement: •B.S. in a science, engineering, or a related field (advanced degree preferred). Fields of study include Pharmacy, Chemical Engineering, Biology, Microbiology, Virology, Molecular Biology, or Biochemistry. Required Experience and Skills: •At least two (2) years of relevant experience, including biological/pharmaceutical research; manufacturing, testing or a related fie...more

From Merck & Co. - 2/13/2018 5:47:18 AM

Associate Director, Regional BPIM

Merck & Co. - Carolina, 

Requirements: •Bachelor's Degree in a Science or Information Technology discipline required. Advanced degree preferred (engineering or scientific discipline, MBA). •Five (5) years or more of experience in Pharmaceutical Industry. •Regulatory Affairs and/or Regulatory Operations will be considered as a plus. •Three (3) or more years of experience in implementing and/or supporting information...more

From Merck & Co. - 2/13/2018 5:47:17 AM

Executive Director, Regulatory Affairs CMC PCV Franchise

Merck & Co. - West Point, PA

Skills: • Develop and maintain expert knowledge of current global regulatory CMC requirements for investigational submissions, original registrations and post-approval changes. This includes knowledge of the regulatory guidance for bacterial polysaccharide conjugate vaccines. • Identify and resolve technical and operational problems associated with regulatory strategy and submissions using ...more

From Merck & Co. - 2/12/2018 5:44:25 AM

Associate II, Regulatory Affairs

Novartis Pharmaceuticals - Wilson, NC

Minimum requirements Bachelor's in a scientific related field required At least three years of pharmaceutical experience required, and at least one year of regulatory experience preferred. Computer knowledge, problem solving skills, strong working knowledge of regulatory and drug development processes, strong technical knowledge, innovative and creative, possesses good judgment and leadership ab...more

From Novartis Pharmaceuticals - 2/12/2018 5:43:52 AM

Director Regulatory Affairs - OTC

Novartis Pharmaceuticals - Fort Worth, TX

Minimum requirements •Bachelors degree in relevant discipline. •English •10 years directly related experience

From Novartis Pharmaceuticals - 2/12/2018 5:43:52 AM

Associate Scientist I

AstraZeneca Pharmaceuticals - Gaithersburg, MD

Position Requirements: Requires an in depth understanding and experience of the principles and concepts within the area of device development in the pharmaceutical industry. Expected to demonstrate up to date technical knowledge.  Requires some knowledge of the drug development process and the importance of the application of device development capability to this process.  Requires a basic knowl...more

From AstraZeneca Pharmaceuticals - 2/12/2018 5:43:17 AM

Senior Data Reviewer/Data Reviewer, Office of Data Reliability

Sun Pharma - New Brunswick, NJ

Minimum Bachelor of Science (B.S.) in Chemistry, Pharmacy, Biochemistry or related field; Master's Degree in Organic Chemistry is desirable. Experience: Minimum 5+ years of experience in a pharmaceutical company in quality assurance/quality control, analytical development and batch record review. Competencies: Technical: Knowledge of strict compliance of approved QC Laboratory testing p...more

From Sun Pharma - 2/9/2018 5:53:41 AM

Documentation Specialist/QC Support (NCI)

Leidos Biomedical Research, Inc. - FREDERICK, MD

PREFERRED QUALIFICATIONS Candidates with these desired skills will be given preferential consideration: - College entry level math skills - Strong oral and written communication skills - Experience in quality assurance or control for technical documents, or similar - Knowledge of File Maker Pro, Study Log, Freezerworks, or similar Expected Competencies: - Strong multitaski...more

From Leidos Biomedical Research, Inc. - 2/9/2018 5:53:23 AM

Investigator, PK Sciences

Novartis Pharmaceuticals - East Hanover, NJ

Minimum requirements Ph.D. in a relevant discipline, Pharm D. with appropriate post-doctoral training, or equivalent. Excellent oral and written communication skills as well as organizational and project management skills will be required. Coaching, mentoring, and people management skills will also essential Investigator: 3+ years of relevant post-doctoral, industry or government experience. Know...more

From Novartis Pharmaceuticals - 2/9/2018 5:52:50 AM

Assoc. Director Global Regulatory Affairs CMC - Change Control Team Lead

Merck & Co. - Rahway, NJ

Education: • Bachelor's degree or higher in a scientific discipline. • A minimum of six (6) years in the pharmaceutical and/or medical device industry with a minimum of three (3) years in CMC Regulatory Affairs Required: • Strong experience in manufacturing change control, global regulatory CMC strategy development, planning and execution of submissions • Strong aptitude for understandin...more

From Merck & Co. - 2/9/2018 5:52:37 AM

Director, Global Regulatory Affairs Lead - Oncology

Merck & Co. - Upper Gwynedd, PA

Education: •B.S. Degree in biological science, chemistry or related discipline, with minimum of 10 years drug development or clinical •experience or regulatory affairs •M.S. with minimum of 10 years drug development or clinical experience or regulatory affairs •M.D. with minimum of 5 years regulatory experience •PhD with minimum of 7 years relevant regulatory experience Required: •A...more

From Merck & Co. - 2/9/2018 5:52:37 AM

Director, Global Regulatory Affairs Lead - Oncology

Merck & Co. - Upper Gwynedd, PA

Education: • B.S. Degree in biological science, chemistry or related discipline, with minimum of 10 years drug development experience in regulatory affairs • M.S. with minimum of 10 years drug development experience in regulatory affairs • M.D. with minimum of 5 years regulatory experience • PhD with minimum of 7 years relevant regulatory experience Required: • Ability to achie...more

From Merck & Co. - 2/9/2018 5:52:37 AM
Page 1 of 5 1 2 3 4 5 >
 Go To 
 
Page Size   Total Records: 93