Search Results: 180,427 vacancies
...Job Description
Job Description The FDA Center for Tobacco Products requires the assistance of minors (Youth Participant) to attempt the purchase of tobacco products from local tobacco retailers. The Chaperone will accompany the FDA Commissioned Inspector and Youth...
Suggested
Contract work
Part time
Local area
Flexible hours
Weekend work
Overview:
POSITION SUMMARY: Responsible for assisting with overall management of glasswares operation to include oversight of staff as appropriate, glass sterilization, glasswares receiving and distribution process and ensuring contract requirements are met in a professional...
Suggested
Contract work
...of audit results into each client's supplier risk management framework.
What you'll need:
You will need to have expertise in US FDA Pharmacovigilance regulations. You will need experience managing PV agreements with multiple parties and assertiveness dealing with...
Suggested
Local area
...Job Description
FDA Plant Manufacturing Process Engineer
\n\n\n\n \n
A four year engineering degree; three or more years of process engineering experience on an FDA compliant manufacturing line; and three or more years of manufacturing plant project management...
Suggested
Permanent employment
Full time
Remote job
...all assigned medical centers. Specifically, responsible for study start-up activities and regulatory management of industry sponsored, FDA regulated clinical trials. This position will be in support of the Research Management Office (RMO), located at the Home Office in...
Suggested
For contractors
Home office
**Job Description**
Protective Security Officer (PSO), DHS/FPS -FDA (Operations) Beltsville, MD, United States of America AddThis Sharing Buttons **Overview**
BTI Security is committed to hiring high caliber security professionals. Our industry-low turnover rate shows...
Suggested
Hourly pay
Permanent employment
Full time
Contract work
Part time
Local area
Are you ready to join a thriving team where exceptional care is our priority? Fox Dental Associates in Asheville, NC is seeking a talented Dental Assistant to become an integral part of our established practice. We prioritize a team-centered approach, reflecting our commitment...
Suggested
Full time
...Medical officers at FDA perform duties that:
ensuring all human drugs manufactured for interstate sale are safe and effective with truthful and informative product labeling
ensuring the safety, potency, purity and effectiveness of vaccines, blood products, certain...
Suggested
Permanent employment
...The Clinical Trial Reviewer is a full-time physician position with the FDA. It is a hybrid role where candidates must live within commutable distance of the FDA Headquarters in Silver Spring, MD, and willing to report to the office at least one day per week. The team follows...
Suggested
Permanent employment
Full time
Weekend work
1 day per week
...Meaningful & Mission-Driven
Physicians generally contribute to the overall health and wellbeing of their communities in very meaningful... ...respected but working with the Food and Drug Administration (FDA) offers physicians a way to contribute to the overall public good...
Suggested
Permanent employment
...The Clinical Trial Reviewer is a full-time physician position with the FDA. It is a hybrid role where candidates must live within commutable distance of the FDA Headquarters in Silver Spring, MD and willing to report to the office at least one day per week. The team follows...
Suggested
Permanent employment
Full time
Weekend work
1 day per week
...The Clinical Trial Reviewer is a full-time physician position with the FDA. It is a hybrid role where candidates must live within commutable distance of the FDA Headquarters in Silver Spring, MD and willing to report to the office at least one day per week. The team follows...
Suggested
Permanent employment
Full time
Weekend work
1 day per week
...primarily on medical device postmarket compliance and enforcement matters; work on pre-market matters is also likely.Prefer experience with FDA device enforcement matters, postmarket compliance issues, quality systems requirements, recalls, adverse event reporting,...
Suggested
Work experience placement
$20 per hour
Join Our Front Desk Team at Fox Dental Associates in Asheville, NC!
Position: Front Desk Coordinator
Are you driven by dedication, possess exceptional organizational skills, and have a true passion for dentistry and patient care? Fox Dental Associates in Asheville...
Suggested
Full time
Private practice
Monday to Friday
...experience required, including working knowledge of 21 CFR 820 and ISO 13485 requirements
~ Familiarity with international standards and FDA guidance documents for medical electrical equipment
~ Knowledge of applicable regulations, standards, and laws including: CPSIA,...
Suggested
Flexible hours
...Description
*Applications will be reviewed on a rolling-basis.
FDA Office and Location: A research opportunity is available immediately in the Division of Cell Therapy (DCT2), within the Office of Cellular Therapy and Human Tissue (OCTHT) at the Center for Biologics...
Permanent employment
Full time
Contract work
Immediate start
Flexible hours
...thoroughly familiar with GMP regulations for the life sciences industry. We are currently looking for someone who used to work for the FDA and/or has extensive experience with mock FDA Audits.
As an SQA Quality Auditor, you will have at least four years’ experience and...
Local area
...research opportunities are currently available at the Center for Drug Evaluation and Research (CDER), Food and Drug Administration (FDA) in Silver Spring, Maryland.
The Division of Quantitative Methods and Modeling (DQMM) in the Office of Research and Standards (ORS...
Full time
Contract work
...Description
*Applications will be reviewed on a rolling-basis.
FDA Office and Location: A research opportunity is available in the Office of Quality Surveillance (OQS), Office of Pharmaceutical Quality (OPQ), Food and Drug Administration (FDA) located in Silver...
Permanent employment
Full time
Contract work
Part time
Remote job
Notes: Firm is seeking an associate with 4-6 years of experience in drug and medical device regulatory compliance issues, specifically current good manufacturing practice (CGMP) matters. Prior industry experience in pharmaceutical manufacturing or a scientific background...
