Search Results: 301 vacancies
...Organize sample distribution/shipment
Coordinate testing at various sites for reagent qualification or requalification
Comply with FDA, EPA, DEP, DOT, OSHA, and client regulations and policies
Provide superlative service to clients by performing duties accurately...
Suggested
Holiday work
Full time
Monday to Friday
...pharmaceutical manufacturing, with at least 2 years in a supervisory or leadership role.
Thorough understanding of cGMP regulations, FDA guidelines, and other relevant regulatory requirements.
Strong leadership, communication, and interpersonal skills, with the...
Suggested
Permanent employment
Worldwide
...Product Introduction.
Experience in qualification, validation, and/or equipment lifecycle management.
Knowledge of cGMP regulations and FDA/EU guidance related to the manufacture of large molecule biotherapeutics.
Johnson & Johnson is an Affirmative Action and Equal...
Suggested
...Organize sample distribution/shipment
Coordinate testing at various sites for reagent qualification or requalification
Comply with FDA, EPA, DEP, DOT, OSHA, and client regulations and policies
Provide superlative service to clients by performing duties accurately...
Suggested
Permanent employment
...approval for departmental documents and coordinate document approvals against timelines.
Support internal and external audits, inspections, FDA pre-inspection readiness, certifications, tracking, and trending activities.
Support the maintenance program by reviewing, approving,...
Suggested
Work experience placement
Local area
...regulatory requirements.
Ensure that all documentation is compliant with internal requirements, regulatory requirements, including FDA, EMA, and ISO standards.
Attends the weekly management meeting to discuss timelines and weekly priorities.
Manage projects to...
Suggested
Local area
...and packaging of products.
Responsible for compliance with all clean room safety and production quality requirements.
Knowledge of FDA requirements Title 21 part 210 & 211 in Manufacturing, Processing, Packing, or Holding of Drugs and Finished Pharmaceuticals.
Will...
Suggested
Permanent employment
Work experience placement
Local area
Shift work
Weekend work
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...and quarterly safety meetings.
Perform and/or monitors MRI safety procedures on patients, employees, and visitors to comply with the FDA safety standards regarding ferrous objects, and implantable medical devices prior to those persons entering the MRI scan room....
Suggested
Permanent employment
Full time
Part time
Immediate start
Remote job
Saturday
...to assigned schedule.
Assist with development and implementation of owner change order requests.
Communicate with class, USCG, FDA and any other required regulatory agency to resolve any regulatory or inspection issues raised during construction of the vessel....
Suggested
Full time
Outdoor
Flexible hours
Monday to Friday
...improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.
**Equal Employment Opportunity**
Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants...
Suggested
Hourly pay
Contract work
Worldwide
Flexible hours
...Computer Science, or related field, MS in Statistics or Biostatistics is preferred.
Experience with producing outputs submitted to the FDA and other regulatory agencies.
Excellent organizational skill to prioritize multiple tasks and goals to ensure timely completion....
Suggested
Permanent employment
...Knowledge of OSHA requirements regarding safety, hazardous chemicals, etc.
•Working knowledge of GXP compliance as well as ICH and FDA guidelines.
Key Skills, Abilities, and Competencies
•Attention to detail, effectiveness and efficiency when performing work.
•...
Suggested
Contract work
Work experience placement
Flexible hours
...of 2-4 yrs. working experience in a cGMP Quality Control, analytical development, analytical transfer or validation department in an FDA-regulated industry.
Knowledge of principles, concepts, and practices in QC testing of protein biopharmaceuticals.
Hands-on...
Suggested
Contract work
Work experience placement
...Minimum of 2-4 yrs working experience in a cGMP Quality Control, analytical development, analytical transfer or validation department in a FDA-regulated industry.
•Knowledge of principles, concepts, and practices in QC testing of protein biopharmaceuticals.
•Hands-on...
Suggested
Work experience placement
...wait.
Position Summary :
The Assembly Technician is responsible for assembling medical devices in compliance with applicable FDA, state, OSHA, and ISO regulations and standards. The job requires the individual to be a team player with the ability to function...
Suggested
...Overview: Under the direct supervision of the Principal Investigator and/or other study team members, the individual will support an NIH/FDA-funded cigarillo smoking prevention messaging study for Black young adults and other health disparities-related research projects....
Hourly pay
Full time
...responsible for adherence to all policies and procedures surrounding research and maintaining up to date knowledge on the policies from IRB, FDA, ICH, GCP or other sources.
CONNECTING TO MISSION:
All individuals, within the scope of their position, are responsible for...
Full time
...alignment of QC priorities with the site priorities/strategy, also ensuring strategy deployment.
Leader in the Audit Room for ISO Audits, FDA Audits, Supplier Audits, and other applicable regulatory or non-regulatory body audits.
Inspect, test, or measure raw materials...
Local area
...and achieve company goals.
Establishes and ensures policy throughout the commercial manufacturing enterprise for the adherence to FDA, EMA, ANVISA and all other government agencies in which business is conducted.
Responsible for the product quality lifecycle of respective...
Contract work
...in consultation with study team; documents informational takeaways
* Evaluates materials to ensure alignment and consistency with GCP/FDA/NCI regulations
* Support departmental meetings, participate in conference calls, and assume responsibility for special projects as...
