Search Results: 642 vacancies
...years of demonstrated experience developing GUI and conducting user research, preferably in the medical arena.
• Experience in software architecting and software implementation.
• Experience with Balsamiq and Adobe XD.
• Experience working with FDA guidelines....
Suggested
2 days per week
3 days per week
...glove wear
PREFERRED QUALIFICATIONS:
Associates or Bachelor’s Degree
Experience working with SOPs, GDP, GMP, CLIA, and the FDA
Experience working in a highly regulated or high-volume retail environment
Excellent interpersonal, organizational, technical,...
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Minimum wage
Holiday work
Full time
Temporary work
Traineeship
Local area
Remote job
Relocation
Shift work
Afternoon shift
...to ensure compliance with all safety, company, and regulatory procedures. In addition, ensuring that the sanitation process meets all FDA and/or USDA and internal requirements.
The individual will ensure that the sanitation SOP is being followed and all activities are...
Suggested
Holiday work
Temporary work
Shift work
Night shift
Weekend work
...CPR) and AED certification
Fulfill state requirements (in state of licensure) for basic IV therapy
Satisfactorily complete the FDA approved training requirements for BioLife Medical Support Specialist
Two years in a clinical or hospital setting
What...
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Hourly pay
Minimum wage
Holiday work
Full time
Temporary work
Seasonal work
Local area
Remote job
...dispensing protocols, maintaining drug records and inventory control, formulating dosages, monitoring patients and ensuring compliance with FDA and DEA regulations.Prepares drug monographs and review of drugs requested for admission to formulary.Assists in reviewing the cost...
Suggested
Full time
Immediate start
Day shift
...dispensing protocols, maintaining drug records and inventory control, formulating dosages, monitoring patients and ensuring compliance with FDA and DEA regulations.Prepares drug monographs and review of drugs requested for admission to Hospital's Formulary.Assists in reviewing...
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Relocation package
Relocation bonus
...device manufacturing.
Five plus years in manufacturing / operations preferred.
Strong knowledge of medical device regulations (FDA, ISO 13485, etc.).
Demonstrated leadership and team management skills.
Excellent problem-solving and decision-making abilities....
Suggested
Temporary work
...out to prove that effective medicine for serious illnesses can also be fun and engaging.
Our flagship product, , is the first ever FDA-cleared prescription treatment delivered through a video game to treat children living with ADHD. This is only the beginning, as we...
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Contract work
For contractors
For subcontractor
...Minimum of 3 years of experience in pharmaceutical or medical device manufacturing or similar regulated industry with prior exposure to FDA 21 CFR 210/211, FDA 21 CFR 820, or ISO 13485 requirements
Preferred experience with bioresorbable polymers, device manufacturing,...
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....
Requirements:
Bachelor's degree in a scientific or related field.
5 years of QA experience in cGMP and FDA inspection.
Strong communication and organizational skills.
Proficiency in Microsoft Office.
bility to work independently...
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...antibodies (mAbs) to keep pace with evolving viral threats. In March 2024, Invivyd received emergency use authorization (EUA) from the U.S. FDA for its first mAb in a planned series of innovative antibody candidates.
THE HEART OF INVIVYD: OUR EMPLOYEES
Our team is...
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Local area
Remote job
...to track orders, manage inventory levels, and generate reports for analysis and decision-making
Understands various regulations (FDA, GFSI) and maintains compliance with purchasing of goods
Works with all production department to coordinate all purchasing within...
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...Job Description
Develops and manages the QA and QC system in a regulated radiopharmaceutical environment with regards to U.S. FDA cGMP and international regulations. Assists in all activities to verify that appropriate, current procedures are followed, and keeps the...
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For contractors
...novel therapeutics for non-alcoholic steatohepatitis (NASH), a liver disease with high unmet medical need.
The company has a recently FDA approved medicine, REZDIFFRA (resmetirom), a once daily, oral, thyroid hormone receptor (THR) ?-selective agonist, for the treatment...
Suggested
Holiday work
...QMS), Environmental Management Systems (EMS), and other regulatory requirements.
•Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive...
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For contractors
Shift work
...production department to troubleshoot and resolve technical problems.
Supports company policies and procedures, goals and objectives, FDA regulations, and good manufacturing practices.
Support Creation of PFMEA and assist with design reviews, and FMEA activities....
Holiday work
Local area
...Office applications which may include Outlook, Word, Excel, PowerPoint or Access.
**Preferred Qualifications:**
1. Basic knowledge of FDA, cooperative group, NCI and or OHRP regulatory guidelines
**Competencies:**
1. **Decision Making:** Ability to make decisions that...
Work experience placement
Immediate start
Shift work
...machinery and tools to complete assigned manufacturing activity including microscopes.
* Completion of documentation following cGMP and FDA guidelines.
* Follow clean room protocols for hygiene, gowning, & PPE.
* Adhere to and ensure compliance of Teleflex's Code of...
Worldwide
Shift work
...Develop and assist in the process and product monitoring, including the creation of a validation protocol (IQ, OQ, PQ) that comply with FDA regulations.
* Provide troubleshooting focus and direction for the team with details of root cause analysis.
* Utilizes Lean...
...and procedures when issues are identified.
Assist investigators and study teams in preparing and submitting IND applications to the FDA.
Preparation and submission of annual reports to the FDA; submission of regulatory documents to NIH/OBA, local bio safety...
Work experience placement
Local area
Immediate start
Remote job
Shift work
