Search Results: 97 vacancies
...Description
*Applications will be reviewed on a rolling-basis.
FDA Office and Location: A research opportunity is available within the Food and Drug Administration (FDA) in The Center for Drug Evaluation and Research (CDER), located at St. Louis, Missouri.
The...
Suggested
Permanent employment
Full time
Contract work
...Description
*Applications will be reviewed on a rolling-basis.
FDA Office and Location: A research opportunity is available in the Division of Pharmaceutical Quality Research II (DPQR II), Office of Pharmaceutical Quality Research (OPQR), Office of Pharmaceutical...
Suggested
Permanent employment
Full time
Contract work
...following 5S principles.
Work with the department Associate Team Leaders and Team Leaders to ensure compliance with all cGMP, ISO and FDA guidelines for warehouse activities.
May need to drive a truck for material transport of product from one location to another....
Suggested
Holiday work
Relocation bonus
Day shift
...of Cisco networking
~ Experience working with integrators / outside contractors is preferred
~ Knowledge of cGMP, validation and FDA industry experience preferred
Education:
Associate's Degree or additional education a plus
Note: Any pay ranges displayed...
Suggested
Contract work
For contractors
Remote job
...Functions
Ensure a safe and quality working environment through training, awareness, and compliance to safety guidelines, SOP's and FDA regulations.
Participate and perform effectively in a team environment and interact with multiple departments to ensure the...
Suggested
Holiday work
Work experience placement
Outdoor
Flexible hours
Shift work
Rotating shift
...is responsible for assisting in administration of the quality functions at a site to assure adherence to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable regulatory standards. The Quality Technician supports manufacturing and servicing operations...
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For contractors
Local area
...Department, and adherence to this policy is a condition of employment. Full vaccination means having received a Food and Drug Administration (FDA) Emergency Use Authorization (EUA) approved vaccine or vaccine series, consisting of two doses of either of the two-dose vaccines or...
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Hourly pay
Holiday work
Full time
Temporary work
Part time
Relief
Currently hiring
Shift work
Weekend work
Afternoon shift
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...myIRB
Add people to DOA log & send for PI signature via DocuSign
Add people to OnCore (investigators only)
Create FDF and update FDA 1572 (investigators only) & send to sub-I/PI via DocuSign
Misc. Startup Tasks
Add or update study team in myIRB
Add sub-Is...
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...Department, and adherence to this policy is a condition of employment. Full vaccination means having received a Food and Drug Administration (FDA) Emergency Use Authorization (EUA) approved vaccine or vaccine series, consisting of two doses of either of the two-dose vaccines or...
Suggested
Hourly pay
Holiday work
Full time
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...manner under the close supervision of a senior staff member. Perform research activities according to Food and Drug Administration (FDA) regulations, ICH Guidelines, Good Clinical Practices (GCP) and standard operating procedures.
Essential Duties and Responsibilities...
Suggested
Holiday work
Full time
Monday to Friday
...Quality Assurance analyses/functions in the processing of raw materials to finished goods and ensure compliance to company, customer, FDA, DOC, USDA and GMP specifications and regulations.
Perform the Quality Assurance functions of production lines and/or the Quality...
Suggested
Holiday work
Worldwide
Shift work
...following 5S principles.Work with the department Associate Team Leaders and Team Leaders to ensure compliance with all cGMP, ISO and FDA guidelines for warehouse activities.Provides training to others within the department.Identifies areas that need improvement within the...
Suggested
Shift work
...Technician, you'll be responsible for filling and packaging finished products, making sure they meet our quality standards and comply with FDA regulations. You'll also handle staging and loading items onto trucks, following our standard procedures to keep things running...
Suggested
Holiday work
Temporary work
...clinical research data;
Attend all relevant study meetings;
Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research;
Recruit and screen patients for clinical trials and...
Suggested
Full time
Part time
Work experience placement
...departmental leadership.
Must maintain operational compliance with US and international regulatory agencies and guidelines (i.e. FDA, EU, HC, TGA, PIC/S, ISO, USP, NRC, cGMP, etc.).
Requirements
High school diploma or GED equivalent is required....
Suggested
Holiday work
Work experience placement
Immediate start
Outdoor
Shift work
Monday to Friday
...compliance, with particular focus on In Vitro Diagnostic Regulation (EU) 2017/746 (IVDR; maintaining compliance with requirements of FDA 21 CFR 820, CMDR SOR 98-292, ISO 13485:2016, and other applicable International Medical Device Regulations.
Qualifications:...
Temporary work
Shift work
Day shift
2 days per week
3 days per week
Monday to Friday
...environment.
+ Enjoy working in areas outside of usual comfort zone and love to learn new technologies.
+ Ability to perform in an ISO/ FDA regulated environment.
+ Familiarity with or interest in biology, microbiology and biochemistry.
Knowledge and Skills Required...
Work experience placement
...high speed manufacturing
equipment.
Knowledge of planning and scheduling principles.
Knowledge of quality systems and FDA controls.
Computer program functional knowledge including Word, Excel, and PowerPoint.
Additional Information:
Extensive...
Relocation
Afternoon shift
...improvement of warehousing, distribution and maintenance aspects of the packaging facility to meet production goals while ensuring GFSI, FDA and OSHA compliance. This position is expected to supervise the warehousing and maintenance staffs. In addition, they will be...
Full time
Temporary work
Immediate start
Relocation
Shift work
All shifts
...While working in a cGMP environment, he/she must maintain operational compliance with U.S. and international regulatory agencies (i.e. FDA, NRC, Health Canada, OSHA, etc.)
Author Change Controls, Protocols, Corrective and Preventive Action items and Periodic Reviews....
For contractors
