...Responsibilities
Set-up, maintain, operate, test and inspect product, and perform repairs on associated departmental equipment in conformance to FDA, GMP’s, ISO 13485 standards and finished product specifications.
Minimize scrap generation from processes and promote workplace...
Suggested
Hourly pay
Temporary work
Local area
Flexible hours
Shift work
Afternoon shift
...is to set-up, maintain, operate, test and inspect product, and perform repairs on associated departmental equipment in conformance to FDA, GMP’s, ISO 13485 standards and finished product specifications. Minimize scrap generation from processes and promote workplace...
Suggested
Temporary work
Local area
Flexible hours
Shift work
Day shift
...being evaluated to participate in a research study for various health conditions, in compliance with study protocol, SOPs, GCP, ICH, and FDA Regulations.
Key Responsibilities
Essential Job Duties: Responsibilities may include but are not limited to:
Reviewing the...
Suggested
Full time
Temporary work
Flexible hours
...operate, supply, sample and record movement of materials associated with production machinery and ancillary equipment in conformance to FDA, GMP’s, ISO13485 standards, and finished product specifications; sample and inspect production, stage material accordingly and report...
Suggested
Hourly pay
Temporary work
Local area
Flexible hours
Shift work
Afternoon shift
Monday to Friday
...us as we continue to grow.
The Principal Investigator conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes. Working with a local and central team drives clinical...
Suggested
Full time
Temporary work
Local area
...and also assist/advise with all maintenance technicians, and perform repairs on associated departmental equipment in conformance to FDA, GMP’s, ISO 13485 standards and finished product specifications. Minimize scrap generation from processes and promote workplace safety...
Suggested
Hourly pay
Full time
Temporary work
Flexible hours
Shift work
Day shift
...required, utilizing problem-solving tools as needed.
Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, GLP, QSR, and cGMP regulations.
Support execution of validations for lab equipment, lab methods, or facility projects.
Perform...
Suggested
Hourly pay
Full time
Temporary work
Local area
Flexible hours
Shift work
Day shift
...engineering preferred or other related scientific field, or related sterilization experience
~4-8 years professional experience within an FDA regulated industry, preferably medical devices
~4-8 years working experience in a quality or regulatory role preferred
~4-8 years...
Suggested
Full time
Contract work
Temporary work
Work experience placement
Local area
Flexible hours
3 days per week
