Search Results: 96 vacancies
...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,...
Suggested
Minimum wage
Holiday work
Full time
Temporary work
Traineeship
Local area
Remote job
Relocation
Shift work
Afternoon shift
...operations, food safety and quality goals.
Food Safety Requirements/Responsibilities:
Comply with all Plant, State and Federal, FDA, HACCP, and SQF regulations.
Conduct verification of monitoring activities to assure finished product comply with food safety and...
Suggested
Holiday work
Relocation
...Promote environmental responsibility and support the company's ESG goals.
Accountable for the EHS Management System.
Quality/FDA
Produce first-quality products for commercial sales. Expand process control, quality, and process improvement.
Manage the customer...
Suggested
Local area
...Qualifications
ARRT registration.
Current Rad Tech license in the state of practice.
Must meet and maintain mammography specific ACR & FDA/MQSA requirements.
Must meet and maintain the ARRT Advanced Mammography Certification.
Current Basic Life Support (BLS) for...
Suggested
Hourly pay
Full time
Night shift
Weekend work
...in core scientific discipline
* Familiarity with large molecule drug substance manufacturing
* Knowledge of current USP/Ph. Eur./FDA/ISO/GMP standards and guidance
* Ability to work with independently with guidance or in team environments under deadlines
* Well...
Suggested
Local area
...role develops and implements company policies and ensures compliance with local, state, and federal regulations and other agencies i.e. FDA, OSHA, ISO 13485.
RESPONSIBILITIES
* Responsible for ensuring the safety of everyone on site. Ensures environmental, health, and...
Suggested
Temporary work
Local area
...knowledge.
Education and Experience
•High school diploma or GED required
•Minimum of 3 years in a quality control environment or FDA regulated manufacturing environment or ASQ/CQI Certification
•Minimum of 1 year developing measurement routines in vision systems...
Suggested
Shift work
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...~ Bachelor's Degree from accredited university
~3+ years of technical writing in a relevant field
~ Experience working within FDA design control guidelines
~ Experience writing technical development reports for both internal and external customers
~ Ability to...
Suggested
Holiday work
Temporary work
For contractors
Flexible hours
...discipline
~7+ years experience in Quality Engineering
~ At least 2 years of medical device QE experience
~ Strong knowledge of FDA QSR and ISO 13485
~ Ability to independently solve problems, lead projects, and influence teams
Preferred Qualifications:...
Suggested
Flexible hours
...quality experience, include 3 years of medical device experience and at least 3 years of team leadership experience.
Significant FDA and Notified Body inspections and audits experience.
Deep understanding and clear ability to interpret and apply medical device standards...
Suggested
Flexible hours
...allowing for college students
Job Description:
Degree required: High School, Associate Degree or above
Knowledge of cGMP/FDA regulated industry
Basic mathematical skills
Strong technical and compliance writing capability
Proficient in MS...
Suggested
...develop and coach production leads and employees
Ensure quality, safety and good manufacturing processes (GMPs) are followedComply with FDA, USDA and HACCP standards
Identify and resolve employee, customer, and/or supplier concerns
Reasonable accommodations may be...
Suggested
Holiday work
Temporary work
Immediate start
Shift work
Weekend work
Saturday
Afternoon shift
3 days per week
...compliance with company policy and within the guidelines of BioFire Diagnostics Quality System. Adheres to Regulatory requirements, including FDA, ISO, Legal, Ethical and BioFire specific procedures.
+ Source a variety of raw materials, equipment, chemicals, injected molded...
Suggested
Contract work
...activities/procedures (during screening and clinical procedures) are completed on schedule and in accordance with the protocol, the FDA and the IRB requirements.
+ Performs non-medical activities such as distribution of scrubs, locks, DVDs, movies, games, front desk...
Suggested
Work experience placement
Relief
...experience will be strongly preferred. Materials handling experience within the medical device industry, including working with the FDA regarding control of materials for instruments and chemistry, preferred. Valid driver's license and clean driving record.
Skills:...
Suggested
Relocation bonus
Shift work
Sunday
Day shift
...tickets in asset management system.
Complies with regulatory agencies requirements. This includes but is not limited to DEA, SBOP, FDA, OSHA, etc.
Maintains inventory of controlled substances including checking into management system, daily audits, and final...
Temporary work
Local area
...negotiating, and finalizing partnerships with bio-pharmaceutical companies is essential.
* Experience negotiating product approvals with the FDA, EMA, PMDA and other global regulatory authorities is essential.
* Network of contacts and colleagues in the pharmaceutical...
...degree in chemistry or related field.
Preferred Requirements:
Pharmaceutical industry experience and an understanding of cGMP, FDA, EMA, USP, NRC, and ICH guidelines.
Experience with radioanalytical instruments and techniques (such as alpha and gamma...
Holiday work
Temporary work
Flexible hours
...experience will be strongly preferred. Materials handling experience within the medical device industry, including working with the FDA regarding control of materials for instruments and chemistry, preferred. Valid drivers license and clean driving record.
**Skills:*...
Relocation bonus
Night shift
...technical training while qualifying and ensuring that all staff adhere to measurement protocols and cGMP requirements to comply with FDA standards.
•Prepares system documentation, including user requirement documents, specification documents, test plans and user manuals...
Temporary work
