Science Regulatory Jobs

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65 Science Regulatory jobs found on Monster.

Jobs 1 to 20 of 65
JURISolutions Richmond, VA
Job Description JURISolutions is partnering with a corporate client on a search for an attorney with pharmaceutical industry experience, who has also sat on medical review committees as well as promotional review committees in a legal/regulatory capacity. Experience with the regulations and compliance issues pertaining to these committees is required. Other in-house responsibilities will be expec...
The Human Service Counselor provides ongoing individual and group treatment for residents in accordance with accepted clinical standards and practice in the field of licensure. Provide training/modeling to paraprofessional staff regarding positive patient interactions with the overall goal of increasing treatment effectiveness. Serve as a member of the treatment team and as the treatment team faci...
Immediate needs INDUSTRIAL HYGIENE MANAGER SUMMARY The Industrial Hygiene Manager will have responsibility for developing, communicating, implementing, and monitoring Potent Chemical Control and Industrial Hygiene Programs for the company. To ensure compliance with applicable regulatory requirements, act as a resource and subject matter expert for internal and external customers in the matters ...
Job Description : The Product Manager guides the development of products and processes designed for the Life Sciences regulatory operations and regulatory affairs market. This candidate will work in the Product Management group to lead the identification of requirements for future software products and releases by working with internal subject matter experts, customers and experts in the industry...
Danaher Corporation Miami, FL
Senior Staff Regulatory Affairs Specialist-DIA002235Danaher Company Description (1000 character limit)Beckman Coulter develops, manufactures and markets products that simplify, automate and innovate complex biomedical testing. Our diagnostic systems are found in hospitals and other critical care settings around the world and produce information used by physicians to diagnose disease, make treatmen...
The Audit Associate Director will be responsible for independently leading the planning, conduct and reporting of routine and non-routine R&D audits of activities, data, facilities and processes to assure adherence to corporate and R&D policies, Biogen Idec internal standards, and compliance with regulatory requirements and guidelines. The Audit Associate Director will manage Audit Manager(s) and ...
The GCP Quality & Compliance Director will provide global strategic leadership for GCP quality and oversight for Biogen Idec R&D. This role will provide expertise and guidance related to relevant and current GCP regulations, guidelines, and will partner with Quality and Compliance groups within Dev Sci. functions to enable transparency & escalation of R&D quality and compliance issues. As an exper...
The Associate Director, Quality Analytics will provide global leadership for R&D Quality Analytics (QA). The incumbent will develop builds & manage the system for aggregation of R&D quality metrics from multiple systems and functions that contribute to the R&D Quality Management System (QMS). The Associate Director will provide analytical and statistical expertise for the setting of “tolerance” le...
The Product Manager guides the development of products and processes designed for the Life Sciences regulatory operations and regulatory affairs market. This candidate will work in the Product Management group to lead the identification of requirements for future software products and releases by working with internal subject matter experts, customers and experts in the industry. Product Manager ...
University of Kansas Medical Center Kansas City, KS, 66101
The Silver City Health Center LMSW is a member of the interdisciplinary Care Team. The LMSW will have primary responsibility for coordinating all psychosocial community services under the general direction of the SCHC Director of Clinical Services. The LMSW must comply with regulations of the Kansas Behavioral Sciences Regulatory Board. The LMSW is responsible for assessing problems and determinin...
The Sr. Staff Regulatory Specialist develops, designs, manages and integrates Beckman Coulter’s regulatory strategies and programs. As a regulatory process expert to development center teams, the incumbent creates and integrates advanced regulatory strategies for global registrations and compliance activities; provides regulatory leadership in promotional material review, experimental designs, dat...
KVC Health Systems Topeka, KS, 66604
KVC is looking for dedicated professionals with a Bachelor's or Master's degree in a field that is able to be licensed by the State of Kansas Behavioral Science Regulatory Board (BSRB), from an accredited college or university. KVC Behavioral HealthCare, Inc. Job Description/Performance Expectations Department: Permanency Position Title: Therapeutic Case Manager Reports to: Permanency Supervisor S...
KVC Health Systems Independence, KS, 67301
Preference will be given to applicants who have current or recent experience with current contractors in the Kansas child welfare system. KVC Behavioral HealthCare, Inc. Job Description/Performance Expectations Department: Permanency Position Title: Therapeutic Case Manager Reports to: Permanency Supervisor Supervises: N/A FLSA Status: Exempt I. Minimum Requirements: Education: Bachelors or Master...
KVC Health Systems Pittsburg, KS, 66762
KVC is looking for dedicated professionals with a Bachelor's or Master's degree in a field that is able to be licensed by the State of Kansas Behavioral Science Regulatory Board (BSRB), from an accredited college or university. KVC Behavioral HealthCare, Inc. Job Description/Performance Expectations Department: Permanency Position Title: Therapeutic Case Manager Reports to: Permanency Supervisor S...
Senior Editor - Business Management amp; Communications (Non-clinical Editing) Requisition ID -00434641 The Position Description: Works with a high level of independence across the gRED and Roche organizations to ensure a consistently high editorial quality of regulatory documents and meet aggressive deadlines, and other duties, as assigned. Responsibilities: As lead editor, substantively e...
Senior Editor - Business Management & Communications (Non-clinical Editing) Requisition ID-00434641 Description Description: Works with a high level of independence across the gRED and Roche organizations to ensure a consistently high editorial quality of regulatory documents and meet aggressive deadlines, and other duties, as assigned. Responsibilities: As lead editor, substantively edits, ...
MONSANTO COMPANY USA, Missouri
Description The Regulatory function is seeking a US Biotechnology Regulatory Affairs Oilseeds Team Lead who will lead the development and submission of regulatory submissions in order to obtain and maintain approvals for Monsanto's biotechnology derived soybean and canola products in the United States and support approval efforts globally. The successful candidate will lead a team of regulatory ...
*Org Marketing Statement*Global Marketing and Commercial Development (GMCD) is a newly created group that uniquely combines early commercial development and in-line marketing tasks within the Global Innovative Pharma (GIP) business of Pfizer. While the group sits in the center of assessing and developing early assets, it also supports the life-cycle of strategic in-line GIP portfolio through its r...
Topeka Public Schools Topeka, KS, 66604
Reports To: Coordinator of Social Work Services Position Purpose: Children are affected by many social forces that impact their role as students. Families can be in a state of change, or be experiencing economic and employment pressures; personal safety may be at risk due to drug/alcohol abuse, violence, or poor nutrition and health. Unmet physical and emotional needs of children affect their ab...
Sonya M Recruiting LLC Mobile, AL
The Senior Consultant applies expertise and in-depth knowledge of science, regulatory affairs, and product development to coordinate and execute strategies for clearance and approval of in vitro diagnostic (IVD) products and new medical devices. The Senior Consultant is responsible for the implementation of high quality programs that adhere to all regulatory specifications and meet customer expect...

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Science Career Tools

Science Regulatory/Quality Assurance, Other

Salaries

$24,960.00 - $79,040.00
Typical Salary for Science Regulatory/Quality Assurance, Other
(51 Respondents)
Source: Monster.com Careerbenchmarking Tool

Education / Training

Bachelor's
51.1%
Master's
22.2%
Associates
15.6%
Doctorate
6.7%
Some College Coursework Completed
4.4%
(45 Respondents)
Source: Monster.com Careerbenchmarking Tool

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