| Regulatory Affairs Analyst San Jose, CA US GENERAL DESCRIPTION: Ensures regulatory compliance by completing the appropriate filings and documentation pertaining to incidents of injury, product approval and product registration and recall as required by the Food and Drug Administration. ESSENTIAL FUNCTIONS: Ensure that existing approvals and view job details | |||
| Senior Regulatory Affairs Specialist Allendale, NJ US Plan, organize and implement strategies and activities required to procure regulatory approval for new and revised product lines. Ensure compliance with all US, EU and SO international requirements and corporate policies and procedures regarding submissions for market approval of medical devices/com view job details | |||
| Clinical and Regulatory Affairs Specialist Scarborough, ME US Clinical Regulatory Affairs Specialist Date Posted 8/5/2011 Location Scarborough, ME Degree Required BA Min Salary $55,000.00 Max Salary $65,000.00 Job Type Full-Time Regular Min Experience 3 Years Position Id EB-8953044863 Job Description Job Function: The Clinical Regulatory Affairs Specialist is view job details | |||
| Regulatory Affairs Specialist Boston, MA US Regulatory Affairs Specialist in the Boston area. Requirements: Medical Device environment is highly preferred. **International experience is required** **Hands on experience putting regulatory submissions together ? Responsible for US and International product submission/registration activities, as view job details | |||
| Regulatory Affairs Specialist (Clinical Engineering) Indianapolis, IN US ABOUT US: TriMedx,a leading provider of comprehensive healthcare equipment services. TriMedx offers medical equipment management to improve healthcare delivery in healthcare systems throughout the U.S. And with the creation of the TriMedx Foundation, the company is able to support medical missions a view job details | |||
| Regulatory Affairs Director (Global Regulatory Leader) Thousand Oaks, CA US The Therapeutic Area team facilitates product development and global registration to achieve the desired regional labeling by developing and executing regulatory strategies and effective regulatory agency interactions. The Global Regulatory Leader (GRL) will lead one or more programs in the Therapeu view job details | |||
| Manager of Regulatory Affairs, Global Submissions Rockville, MD US For our rapidly growing facility in Rockville, Maryland, we are seeking a bright, professional, personable, and dependable addition to our team. Manager of Regulatory Affairs, Global Submissions Your major tasks will be: Working with global team members on Clinical Trial Applications, Investigationa view job details | |||
| Regulatory Affairs Mgr (Regional Representative) Thousand Oaks, CA US This role will support one or more programs in the therapeutic Area team within Amgen's regulatory Affairs department. The Therapeutic Area team facilitates product development and global registration to achieve the desired regional labeling by developing and executing regulatory strategies and effe view job details | |||
| Regulatory Affairs Sr Mgr (device) Thousand Oaks, CA US The RA CMC Group is responsible for generation of the global regulatory strategy and providing feedback to the team for plans and execution of the strategy. Facilitate product development and global registration by developing and executing regulatory strategies and effective regulatory agency intera view job details | |||
| Regulatory affairs & clinical trial management Auburn, WA US Job Title: Regulatory affairs & clinical trial management Profession: Biotechnology/Pharmaceuticals -> Clinical Development Professionals Regulatory affairs & clinical trial managementSyntrix Biosystems is currently seeking an entry level scientist to be part of a team that develops novel therapeuti view job details | |||
| Temp Regulatory Affairs Manager Branchburg, NJ US Title: Temp Regulatory Affairs Manager Location: NJ-Branchburg Other Locations: Position Summary: The Temp Regulatory Affairs Manager is responsible for: ? Approval of new products and new intended uses for existing products globally ? Supporting new product development teams by assessing regulatory view job details | |||
| Director, Regulatory Affairs Gaithersburg, MD US Title: Director, Regulatory Affairs Location: Gaithersburg, MD Req: 6163 Responsible for leading regulatory strategy, and coordinating regulatory projects, plans and schedules with PDT/GPT project team members and partners for submission of Investigational New Drug Applications and Biologic License view job details | |||
| Sr. Regulatory Affairs Specialist Warwick, RI US Sr. Regulatory Affairs SpecialistDavol Inc.Warwick, RIThe position of Regulatory Affairs Specialist will provide technical and administrative regulatory support to ensure timely introduction of new products subject to medical products regulations. Provide regulatory support to marketed products. Pre view job details | |||
| Regulatory Affairs Specialist Rockville, MD US Regulatory Affairs Specialist Location Rockville, MD Job ID 2832 Employment Status Full-Time Regular Required Experience 2-5 years Required Education Bachelors Degree or Equivalent Required Travel No Relocation Available Yes Summary/Description Human Genome Sciences (HGS)is a biopharmaceutical compa view job details | |||
| Regulatory Affairs Project Manager Philadelphia, PA US Overview of Position/Company : Come work for a company that is experiencing significant growth and seeking to add a Regulatory Affairs Project Manager to the team! Job Description: The Project Managers primary responsibilities will include: Conduct regulatory reviews of technical summaries, clinical view job details | |||
| Manager, Regulatory Affairs (IND) Gaithersburg, MD US Responsibilities: At Kforce Clinical Research, we don't just offer jobs. We offer a rewarding career experience, complete with professional development opportunities and a great benefits package! We are intelligent business partners to some of the world's most valued pharmaceutical companies and hav view job details | |||
| Regulatory Affairs Mgr. / 9686 Somerville, NJ US Regulatory Affairs Mgr. / 9686 Company: ConsignMed Job#: 1115 Positions: 1 Job Type: Full Time - Contract Location: Somerville - NJ Department: Clinical Research Apply To This Job Email This Job Return To List Job Description Serve as the senior and principal regulatory affairs member of project dev view job details | |||
| Regulatory Affairs Specialist - RAS Pittsburgh, PA US Regulatory Affairs Specialist Overview of Position/Company: Up and coming cardiac company is seeking a Clinical Research Coordinator for a one month contract. Job Description: Our client is seeking a CRC for two high level, complex cardiology studies. Duties include, but are not limited to: Perform view job details | |||
| Associate Director, Regulatory Affairs Rockville, MD US Responsible for collection, preparation and assembly of documentation required for Investigational New Drug Applications (IND), Investigational Medicinal Product Dossiers (IMPD) and Clinical Trial Applications (CTA) for biologic oncology products. Responsible for supporting cross-functional activiti view job details | |||
| Regulatory Affairs Specialists Santa Rosa, CA US Provide worldwide premarket and postmarket regulatory affairs support; develop worldwide regulatory strategic level plans and complete premarket and postmarket regulatory deliverables for Class II and III medical devices, including project planning and coordination; assess device changes for worldwi view job details | |||
| Regulatory Affairs Specialist Warwick, RI US Regulatory Affairs Specialist Industry Title /Category: Medical Device/Regulatory/Clinical Affairs Job ID: 2011-5037 Career Level: experienced Location/Division: Warwick, RI/Davol Relocation: No Posted Date: 5/20/2011 Close Date: .. C. R. Bard, Inc. (NYSE: BCR)is a leading multinational developer, m view job details | |||
| Manager, Regulatory Affairs Silver Spring, MD US Manager, Regulatory AffairsJob Type:Full-Time PositionJob Category:RegulatoryLocation:Silver Spring, MDExperience Required:6-10 years direct regulatory experience in pharmaceutical/biotech industryEducation Level:Bachelor's DegreeRole Purpose/Position Overview Under the direction of the Director of view job details | |||
| Sr. Regulatory Affairs Specialist Minneapolis, MN US SR. Regulatory Affairs Specialist Ensure compliance to the FDA Quality System Regulations, European Requirements, and other regulatory requirements. Prepare required documentation (510(k)s, technical files, dossiers) for domestic and foreign submissions and registrations. Attend design review meetin view job details | |||
| Director of Regulatory Affairs Gaithersburg, MD US Responsibilities: At Kforce Clinical Research, we don't just offer jobs. We offer a rewarding career experience, complete with professional development opportunities and a great benefits package! We are intelligent business partners to some of the world's most valued pharmaceutical companies and hav view job details | |||
| REGULATORY AFFAIRS CMC NJ US Job ID: 331866 Job Title: REGULATORY AFFAIRS CMC Job Type: Contract Company: JUDGE GROUP Location: New Jersey Contact E-mail: cjm@judge.com Salary: Open Description: Responsible for: - compiling, preparing and reviewing submission documents for content with emphasis on CMC components of IND and IMPD view job details | |||
| Manager, Regulatory Affairs Novato, CA US As part of a Regulatory team, manage clinical and nonclinical aspects for the priority development project in the company, an enzyme replacement therapy for a lysosomal storage disorder. Create timelines and track deliverables to timelines to ensure that all submissions are submitted on-time. Develo view job details | |||
| Regulatory Affairs Senior Associate Boca Raton, FL US Regulatory Affairs Senior Associate Tracking Code 1369 Job Description This position assists in managing and participates in the planning, organizing and interpreting of regulatory documents for submission to governmental regulatory agencies. #160;Coordinate the compilation of documents needed to fi view job details | |||
| Senior Manager of Regulatory Affairs Washington, DC US Senior Manager of Regulatory Affairs Overview of Position/Company: Mid-sized Biopharmaceutical Company focused on the development of vaccines and therapeutics that assist the bodys immune system to prevent or treat disease is looking to add a qualified Senior Manager of Regulatory Affairs to their t view job details | |||
| Manager, Regulatory Affairs (CMC) Gaithersburg, MD US Responsibilities: At Kforce Clinical Research, we don't just offer jobs. We offer a rewarding career experience, complete with professional development opportunities and a great benefits package! We are intelligent business partners to some of the world's most valued pharmaceutical companies and hav view job details | |||
| REGULATORY AFFAIRS MANAGER Denver, CO US REGULATORY AFFAIRS MANAGER(Denver, CO) Apply Qualifications:Bachelor's and 5 years' experience OR Bachelor's and 7 years' experience Pay/Labor Grade:(not specified) Salary:(not specified) Paid Relocation Offered:N Function: Experienced Regulatory Affairs Professional Needed Description of Duties/Qua view job details | |||
| Sr Regulatory Affairs Spec Minneapolis, MN US The Senior Regulatory Affairs Specialist will represent regulatory affairs on new product and therapy development teams, product continuation teams, and other business initiatives. The Senior Regulatory Affairs Specialist will provide strategic guidance regarding global regulatory requirements and h view job details | |||
| Regulatory Affairs Associate Ann Arbor, MI US Job Title: Regulatory Affairs Associate Job Title Description: Regulatory Affairs Associate Location: Ann Arbor, MI Division: TCVS Ann Arbor, MI Job Type: Regular Description: Assist and make recommendations in preparing, organizing, and maintaining documentation sufficient to ensure regulatory comp view job details | |||
| Senior Regulatory Affairs Associate Somerset, NJ US Senior Regulatory Affairs Associate Job Overview: Our client is a leading medical device company looking to add a qualified Senior Regulatory Affairs Associate to their team in New Jersey! Job Description: The Senior Regulatory Affairs Associate serves as liaison between domestic/foreign governmenta view job details | |||
| ASSOCIATE DIRECTOR REGULATORY AFFAIRS NJ US Job ID: 330492 Job Title: ASSOCIATE DIRECTOR REGULATORY AFFAIRS Job Type: Contract Company: JUDGE GROUP Location: New Jersey Contact E-mail: cjm@judge.com Salary: Open Description: Associate Director/Director Regulatory Affairs Responsibilities: The Regulatory Affairs Associate Director/Director wil view job details | |||
| Regulatory Affairs Specialist Chelmsford, MA US Regulatory Affairs Specialist Department:Quality Assurance/Regulatory Affairs Office: ZOLL - Chelmsford, MA Location: Chelmsford, MA ZOLLMedical Corporation is committed to developing technologies that help advance the practice of resuscitation. With products for pacing, defibrillation, circulation, view job details | |||
| SR DIRECTOR Regulatory Affairs Fort Washington, PA US Title: SR DIRECTOR Regulatory Affairs Location: Pennsylvania-Fort Washington McNeil Consumer Healthcare Division of McNEIL-PPC, Inc is currently recruiting for a Senior Director, Regulatory Affairs for its location in Fort Washington, Pa. McNeil Consumer Healthcare Division of McNEIL-PPC, Inc market view job details | |||
| Sr Manager, Regulatory Affairs Cambridge, MA US JOB TITLE Sr Manager, Regulatory Affairs Requisition Number 6597BR Department Name Regulatory Therapeutics Location Cambridge, MA POSITION SUMMARY This Manager position serves as a liaison between the company and regulatory agencies for all assigned projects and is responsible for their day to day r view job details | |||
| Sr Mgr Regulatory Affairs Newark, DE US Sr Mgr Regulatory Affairs Company Siemens Healthcare Diagnostics Inc. Division SMSD - Diagnostics Functional Area QA - Quality Assurance/Regulatory Affairs/Regulatory Compliance Location DE - Newark Req ID 93797 Job Type Regular Job Time Full-Time Experience Level Senior Level Required Education Bac view job details | |||
| Associate Director, Regulatory Affairs Cambridge, MA US JOB TITLE Associate Director, Regulatory Affairs Requisition Number 6267BR Department Name Regulatory Therapeutics Location Cambridge, MA POSITION SUMMARY This Associate Director position is established to play a key role in the planning and management of regulatory submissions to global health auth view job details | |||
| Regulatory Affairs Manager Short Hills, NJ US Our client in Central New Jersey is seeking a Regulatory Generalist to perform the following functions for 2-4 months. Can work remotely 2 days per week. General Regulatory tactical work IRB Renewals Country documentation Maintain current knowledge of relevant regulations, including proposed and fin view job details | |||
| Director, Regulatory Affairs Bridgewater, NJ US Director, Regulatory Affairs Job ID: 1996 Location: US-NJ-Bridgewater Category: R&D - Regulatory Affairs Pos. Type: Full Time More information about this job: Overview: Provide Regulatory Oversight to Project teams Review and assess Core Safety Information for labeling impact Review and Assess Adver view job details | |||
| Regulatory Affairs Specialist Liberty, MO US Kelly Scientific Resources is seeking candidates for Regulatory Affairs Specialist positions in the Kansas City metro area. Positions vary from short-term temporary to long-term temporary as well as temp-to-hire. Job Description: Provides support on regulatory projects for clients and guidance on re view job details | |||
| Sr. Regulatory Affairs Specialist Osseo, MN US Sr. Regulatory Affairs Specialist Job Purpose:Responsible for Regulatory Affairs support of the product development process, submissions and regulatory compliance. Key Responsibilities: Begins to act as a company representative, developing and maintaining positive relationships with device reviewers view job details | |||
| Manager, Regulatory Affairs West Chester, PA US Manage Regulatory activities for the division. Represent global regulatory affairs position and implications of regulatory science on product development teams. Develop global, regional and multi-country regulatory strategy for individual new or modified products and update strategy based upon regul view job details | |||
| Executive Director, Regulatory Affairs NE Jersey, NJ US Job Descriptions: Duties and Responsibilities Within therapeutic areas of responsibility: #xbf;Coordinates interaction of his/her direct reports with regulatory agencies. Provides support to staff in communications with agencies. Has established relationships with agencies. Maintains corporate credi view job details | |||
| Director of Regulatory Affairs Baltimore, MD US Director Regulatory Affairs, Commercial Products Location: Ellicott City, MD Position will report to the Vice President, Regulatory Affairs Position Description: This position will be primarily responsible for managing regulatory activities involving assigned marketed products including (1) review o view job details | |||
| Sr. Regulatory Affairs Specialist Minneapolis, MN US The Regulatory Affairs Specialist or Senior Regulatory Affairs Specialist originates appropriate documents to obtain and maintain clinical and/or marketing privileges consistent with applicable government requirements where AMS conducts business. All positions are responsible for following applicabl view job details | |||
| Regulatory Affairs Manager San Jose, CA US Regulatory Affairs Manager Location: US-CA-San Jose Category: QA Quality Control Position Type: Full Time Experience (Years): .. Posted Date: 10/11/2011 Company Name: Olympus America Inc. Company URL: Olympus America Inc Information URL: About Olympus Corp of the Americas More information about this view job details | |||
| Manager, Regulatory Affairs Warren, NJ US Manager, Regulatory Affairs Job ID: 12004 Location: Warren, NJ - 33 Offsite Territory: Full/Part Time: Full-Time Regular/Temporary: Regular Category: Executive Department: Executive - 4101 Return to Previous Page About Celgene Celgene Corporation is committed to delivering innovative therapies desig view job details | |||
| Director, Regulatory Affairs Cambridge, MA US Requisition Number- 16933BR Job Title- Director, Regulatory Affairs Location- US-MA-Cambridge Job Category- Regulatory Job Description- I. Position Summary: This position is responsible for leading a Regulatory CMC biologics team. Responsibilities include directing innovative CMC regulatory strategi view job details | |||
| Regulatory Affairs Manager I Maple Grove, MN US Regulatory Affairs Manager I Requisition ID 36262 Full/Part Time Full Time Location Maple Grove MN Description Regulatory Manager I (IC Stent Franchise ndash; Drug Eluting Stents) PURPOSE STATEMENT Provides direction and leadership to employees who are responsible for planning, developing, and coord view job details | |||
| Regulatory Affairs Manager Harrisburg, PA US GENERAL PURPOSE OF JOB (Overall Summary): The Regulatory Affairs Manager will work with the Director of Corporate Compliance and Regulatory Affairs to implement the regulatory strategy to move products to clearance/approval as quickly as possible while remaining in compliance with applicable regulat view job details | |||
| Associate Director, Regulatory Affairs Fort Washington, PA US Associate Director, Regulatory Affairs Fort Washington, PA DESCRIPTION: Intuitive Technology Solutions is searching for an Associate Director of Regulatory Affairs to join the team of a Global Pharmaceutical Company located in the Greater Philadelphia Area. The ideal candidate will be responsible fo view job details | |||
| Associate Director of Regulatory Affairs Santa Clara, CA US At Abbott, every day is filled with new discoveries and leading-edge innovation. Our professionals are passionate about life, health care and their contributions. With more than $35 billion in sales in more than 130 countries, we're not just poised to enhance the health of the world we're positioned view job details | |||
| Manager, Global Regulatory Affairs Morristown, NJ US Summary: The Global Regulatory Affairs Manager manages all regulatory aspects for the Rxbranded products. Participates on the product development teams and managesmarketed product maintenance by providing global regulatory guidance andstrategy as well as US executional components. Interacts with FDA view job details | |||
| CMC Director of Regulatory Affairs Cambridge, MA US Job Title: CMC Director, Regulatory Affairs Job Code: GRDRA Position Description:Reporting to the Senior Director, Regulatory Affairs, the Director of CMC Regulatory Affairs will be responsible for developing and implementing CMC regulatory strategies as well as coordinating all aspects of CMC regul view job details | |||
| Regulatory Affairs Associate Los Angeles, CA US Company Description: Full service nationwide Staffing Firm for Permanent and Contract staffing in the Executive, Information Technology, Manufacturing, Engineering, Financial, Banking, Oil & Gas, Biotechnology, Sales & Distribution industries. Job Description: REGULATORY AFFAIRS ASSOCIATE Client is view job details | |||
| Regulatory Affairs Associate Ann Arbor, MI US Job Title: Regulatory Affairs Associate Job Title Description: Regulatory Affairs Associate Location: Ann Arbor, MI Division: TCVS Ann Arbor, MI Job Type: Regular Description: Assist and make recommendations in preparing, organizing, and maintaining documentation sufficient to ensure regulatory comp view job details | |||
| Associate II, Regulatory Affairs Broomfield, CO US Job Title: Associate II, Regulatory Affairs Profession: Biotechnology/Pharmaceuticals -> Clinical Development Professionals Job ID 91950BRPosting Title Associate II, Regulatory AffairsDivision SandozBusiness Unit Sandoz - United StatesCountry USAWork Location Broomfield, COCompany/Legal Entity USA S view job details | |||
| Principal Regulatory Affairs Specialist Marlborough, MA US Job Title: Principal Regulatory Affairs Specialist Profession: Biotechnology/Pharmaceuticals -> Clinical Development Professionals Job: IRC27912Add To Basket Refer Apply NowJavaScript enabled browser required.DescriptionJob Title Principal Regulatory Affairs Specialist Location Marlborough, MA, US D view job details | |||
| Regulatory Affairs Associate II Gaithersburg, MD US Job Title: Regulatory Affairs Associate II Profession: Biotechnology/Pharmaceuticals -> Clinical Development Professionals Regulatory Affairs Associate II Location MD, GaithersburgJob Description This Regulatory CMC position will be responsible for collection, preparation and assembly of CMC documen view job details | |||
| Manager, Regulatory Affairs Cambridge, MA US Job Code: CPSLMRAFunctional area: Regulatory Affairs To apply, send email with a subject of Job Code CPSLMRA Please include a CV and cover letter with your email message. Position description: The Manager of Regulatory Affairs participates in the development and implementation of regulatory strategy view job details | |||
| Technical Writer Regulatory Affairs Orangeburg, NY US Job Title: Technical Writer Regulatory Affairs Profession: Computer Engineering and Information Technology -> Technical Writing/Documentation -- Job Title: Technical Writer Regulatory Affairs State/ Province: New York City: Orangeburg Description: Essential Function: -- The Technical Writer is respo view job details | |||
| Regulatory Affairs and Safety PM Thousand Oaks, CA US Our major biotech client is looking for a Regulatory Affairs and Safety PM for 1 YEAR positions in Thousand Oaks, CA. *Client is looking for candidates with traditional project management experience in the pharmaceutical industry. Ideally candidates that have managed project deliverables with cross view job details | |||
| Director, Regulatory Affairs Minneapolis, MN US UnitedHealth Group is an innovative leader in the health and well-being industry, serving more than 55 million Americans. Through our family of companies, we contribute outstanding clinical insight with consumer-friendly services and advanced technology to help people achieve optimal health.What mak view job details | |||
| Sr. Regulatory Affairs Associate Pleasanton, CA US Job Title: Sr. Regulatory Affairs Associate Profession: Biotechnology/Pharmaceuticals -> Clinical Development Professionals Company Overview Seeing things in a different light is just the beginning at CooperVision. Our visionaries put ideas into action, raise the bar on product excellence and create view job details | |||
| Manager, Regulatory Affairs Los Angeles, CA US Job Title: Manager, Regulatory Affairs UCLA Title: Manager Job No.: H60306 Work Hours: M-F hours: TBA Work Location: A7-248 CHS Job Type: Career Duration: Indefinite Minimum Salary: $36.30 / $6317 Maximum Salary: $68.20 / $11867 Layoff Referral Deadline: 01/11/2012 Bargaining Unit: 99 Job Duties: Th view job details | |||
| Consultant, Regulatory Affairs US Consultant, Regulatory Affairs Department: Consulting and Reimbursement Services Location: India - Haryana - Gurgaon Employment Type: Full Time Job Type: Regular Company Profile: PAREXEL International is a growing, fast-paced, global Clinical Research Organization (CRO) that has helped bring to mark view job details | |||
| Regulatory Affairs Coordinator Leawood, KS US Our client is looking to hire an individual who will be responsible for regulatory activities to support research studies. Duties: Maintain the Trial Master File and/or Regulatory Binder Assure timeliness in aspects of study start up Work with IRB submissions Ensure study budgets are in place and ad view job details | |||
| Senior Regulatory Affairs Head Mexico City, MX value= Apply to job id=button1 name=button1 onClick= javascript:ApplyNow(); > Job ID 90108BR Position Title Senior Regulatory Affairs Head Division Pharma Business Unit General Medicines - Latin America Country Mexico Work Location Mexico City Company/Legal Entity Mexico Novartis Farmac?utica, S.A. view job details | |||
| Regulatory Affairs Associate DE Regulatory Affairs Associate Regulatory Affairs Associate to work in our office in Cambridge, MA. Regulatory Affairs represents the interface between the Company and the Regulatory Authorities. The group supports our customers by being responsible for the clinical development and approval of regulat view job details | |||
| Director, Global Regulatory Affairs South San Francisco, CA US Title: Director, Global Regulatory Affairs Location: California-South San Francisco Janssen Alzheimer Immunotherapy Research Development, LLC (JAI), a member of the Johnson Johnson Family of Companies, is recruiting for a Director, Global Regulatory Affairs, to be based in South San Francisco, CA. J view job details | |||
| Regulatory Affairs Specialist CMC South San Francisco, CA US Regulatory Affairs Specialist We are actively seeking an experienced Regulatory Affairs Specialist to join a fast growing biopharmaceutical company in the bay area. Key Responsibilities: - In charge of US regulatory activities for marketed products including clinical, safety, and preclinical issues. view job details | |||
| Manager, Regulatory Affairs US Requisition #: 4241 Posting Job Title: Manager, Regulatory Affairs Department: Regulatory & Clinical Affairs Dept Group: Quality & Regulatory Location: HQ Country: United States State: California City: San Diego Job Summary: Job Responsibilities . Participate on product development core teams as reg view job details | |||
| Manager, Regulatory Affairs (IND) Gaithersburg, MD US At Kforce Clinical Research, we don't just offer jobs. We offer a rewarding career experience, complete with professional development opportunities and a great benefits package! We are intelligent business partners to some of the world's most valued pharmaceutical companies and have evolved to creat view job details | |||
| Sr. Regulatory Affairs Specialist Warwick, RI US Sr. Regulatory Affairs Specialist Industry Title /Category: Medical Device/Regulatory Affairs Job ID: 2012-5391 Career Level: experienced Location/Division: Warwick, RI/Davol Relocation: No Posted Date: 1/6/2012 Close Date: .. C. R. Bard, Inc. (NYSE: BCR)is a leading multinational developer, manufac view job details | |||
| Head of Medical of Regulatory Affairs Mongkok, CN Title: Head of Medical of Regulatory Affairs Location: China-Mongkok Johnson Johnsonis the world s most comprehensive and broadly based healthcare Company, touching the lives of nearly a billion people every day. Our Family of Companies throughout the world compete in consumer, pharmaceutical and me view job details | |||
| Associate Director, Regulatory Affairs North Billerica, MA US Job Ref LMI 9511 Job Title Associate Director, Regulatory Affairs Job Type Full-time Location North Billerica Description Lantheus Medical Imaging, Inc., a worldwide leader in diagnostic medicine for more than 50 years, is dedicated to creating and providing pioneering medical imaging solutions to i view job details | |||
| Manager, Regulatory Affairs Silver Spring, MD US Manager, Regulatory AffairsJob Type:Full-Time PositionJob Category:RegulatoryLocation:Silver Spring, MDExperience Required:6-10 years direct regulatory experience in pharmaceutical/biotech industryEducation Level:Bachelor's DegreeRole Purpose/Position Overview Under the direction of the Director of view job details | |||
| Principal Regulatory Affairs Specialist Indianola, PA US Job Title: Principal Regulatory Affairs Specialist Interest Category: Clinical & Regulatory Affairs Job Type: Full Time City: Indianola Description: The Principal Regulatory Affairs Specialist at MEDRAD will provide World-wide Regulatory leadership to the MEDRAD Interventional Pittsburgh (MIP) organ view job details | |||
| Director, Quality and Regulatory Affairs ON CA Title: Director, Quality and Regulatory Affairs Location: North America-Canada-ON-Concord Other Locations: Scope of Role: The Director, Quality Regulatory Affairs provides strategy and direction to ensure all Quality and Regulatory Affairs systems are established, implemented and maintained in accor view job details | |||
| Regulatory Affairs Senior Associate Boca Raton, FL US Regulatory Affairs Senior Associate Tracking Code 1369 Job Description This position assists in managing and participates in the planning, organizing and interpreting of regulatory documents for submission to governmental regulatory agencies. Coordinate the compilation of documents needed to file a view job details | |||
| Manager, Global Regulatory Affairs Elverson, PA US Our client in the Elverson, PA area is currently hiring a Global Regulatory Affairs Manager for a permanent opportunity. This position will be responsible for leading the activities of Regulatory Affairs with an emphasis on global regulatory strategies, regulatory submissions, and interaction with g view job details | |||
| Regulatory Affairs Director Saint Louis, MO US Our client, a leader in the pharmaceutical industry, is currently seeking qualified candidates for their Regulatory Affairs Sr. Manager/Director opening. This is a direct placement opportunity. Job Duties and Responsibilities: *Leads and directs regulatory programs in order to meet established corpo view job details | |||
| Regulatory Affairs Specialist Saint Louis, MO US Regulatory Affairs Associate needed for local CRO. REQUIREMENTS: BA Degree Minimum of 1 year of Regulatory experience MAJOR DUTIES AND RESPONSIBILITIES:- Reviews and manages incoming registration requests from affiliates and distributors. Prepares simple dossier and other documents required for subm view job details | |||
| Principal Regulatory Affairs Specialist Marlborough, MA US Key Responsibilities: Prepares submissions to obtain and maintain global regulatory approvals for clinical research and commercial distribution of Endoscopy products. Provides technical guidance and regulatory training/mentoring to other Regulatory Affairs employees and cross-functional teams. Acts view job details | |||
| Senior Regulatory Affairs Specialist Marlborough, MA US Key Responsibilities: Prepares submissions to obtain and maintain global regulatory approvals for clinical research and commercial distribution of products. Provides technical guidance and regulatory training/mentoring to other Regulatory Affairs employees and cross-functional teams. Acts as company view job details | |||
| Regulatory Affairs Project Manager Pleasanton/East Bay, CA US Regulatory Affairs Project Manager Location: CA-Pleasanton/East Bay Job Code: 1761 # of Vacancies: 1 Description Seeing things in a different light is just the beginning at CooperVision. Our visionaries put ideas into action, raise the bar on product excellence and create the next generation of cont view job details | |||
| Director Regulatory Affairs - Devices US Director Regulatory Affairs - Devices Job Title: Director Regulatory Affairs - Devices Job Type: Full-Time Location: Glory Park, Wooburn, United Kingdom Job Description: GENERAL SUMMARY Responsible for leadership and development of regulatory services for designated geographic areas or globally. Thi view job details | |||
| Regulatory Affairs Specialists Job Santa Rosa, CA US Regulatory Affairs Specialists Requisition80746 CategoryRegulatory Affairs and QA BusinessCardioVascular DivisionEndoTher Regulatory - US LocationUSA-CA-Santa Rosa RelocationRelocation eligibility to be determined Job TypeFull Time - Regular Exempt/Non-ExemptExempt ShiftFirst Travel Percentageless t view job details | |||
| Manager, Regulatory Affairs US Manager, Regulatory Affairs Job ID: 6634 # Positions: 1 Location: US-PA-West Chester Experience (Years): 7 Posted Date: 1/17/2012 Category: Regulatory/Clinical Affairs - General More information about this job: Overall Responsibilities: Manage Regulatory activities for the division.Represent global view job details | |||
| Director, Global Regulatory Affairs Woodcliff Lake, NJ US Director, Global Regulatory Affairs Department Name Clinical Development/Research Location/Territory Name Woodcliff Lake, NJ Job Description Provide global regulatory strategic support for multiple pipeline projects with in vitro companion diagnostic device development components. Lead program effor view job details | |||
| Director of Regulatory Affairs Baltimore, MD US Director Regulatory Affairs, Commercial Products Location: Ellicott City, MD Position will report to the Vice President, Regulatory Affairs Position Description: This position will be primarily responsible for managing regulatory activities involving assigned marketed products including (1) review o view job details | |||
| Regulatory Affairs Associate Ann Arbor, MI US Job Title: Regulatory Affairs Associate Job Title Description: Regulatory Affairs Associate Location: Ann Arbor, MI Division: TCVS Ann Arbor, MI Job Type: Regular Description: Assist and make recommendations in preparing, organizing, and maintaining documentation sufficient to ensure regulatory comp view job details | |||
| Director of Regulatory Affairs Philadelphia, PA US Director of Regulatory Affairs Department: Performance Improvement (905) Schedule: Regular Full time Shift: Day Hours: 7:00AM-3:30PM FTE: 1.00 Job Details: - Bachelors Degree within Related Field - 3 - 5 Years in Hospital Setting - 3 - 6 Years Related Experience The Director of Regulatory Affairs is view job details | |||
| Director of Regulatory Affairs Gaithersburg, MD US At Kforce Clinical Research, we don't just offer jobs. We offer a rewarding career experience, complete with professional development opportunities and a great benefits package! We are intelligent business partners to some of the world's most valued pharmaceutical companies and have evolved to creat view job details | |||
| Regulatory Affairs Project Manager Allegan, MI US Regulatory Affairs Project ManagerTracking Code2009721Job Description Perrigo seeksRegulatory Affairs Project Manager: Allegan, MI. Assemble and review data and information required for ANDA and NDA submissions and amendments for new drug products. Work closely with all relevant departments to ensur view job details | |||
| Principal Regulatory Affairs Specialist Plymouth, MN US Principal Regulatory Affairs Specialist Job Requisition #: 11284 Date Posted: 06/27/2011 Category: Regulatory Affairs Location: Plymouth - MN - USA About Us St. Jude Medical develops medical technology and services that focus on putting more control into the hands of those who treat cardiac, neurolo view job details | |||
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