Search Results: 914 vacancies
...Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following... ...position:
~ Senior Automation Specialist for Medical Devices
Qualifications:... ...Bradley, Software Validation and Design Review.
Must be fully bilingual (English / Spanish...
Suggested
Holiday work
Weekend work
...Requirements:
Bachelor's degree in Medical Technologist
Minimum one year of experience as a Medical Technologist or Similar position.
Valid Medical Technologist license.
Must have a valid driver's license and passport.
Bilingual communication skills (English...
Suggested
Holiday work
Weekend work
...and five years of experience in Validation Life Cycle within the Medical Device Industry.
Bilingual (English and Spanish)... ...analysis related to equipment performance.
Support the periodic review of equipment/system qualifications studies.
Generate & execute...
Suggested
Flexible hours
...processes at the center level
Job Description
1 Perform final QA review and release for all shipment and associated documents, to... ...for health care benefits, including choices of plans for medical and prescription drug, dental, and vision coverage; Company-provided...
Suggested
Holiday work
Full time
Temporary work
Local area
Immediate start
Shift work
...Assess process performance by observation of floor operations and review of performance data.
Evaluate, plan, and implement solutions... ...our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch...
Suggested
Flexible hours
Shift work
...opportunity. Join the Kelly® team as a Regulatory Compliance Review Analyst to work at a leading Puerto Rican company in the distribution... ...offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident...
Suggested
Holiday work
Permanent employment
Temporary work
Local area
Flexible hours
...procedures reflect current operations. Serve as a document owner.
2. Assess process performance by observation of floor operations and review of performance data. Evaluate, plan, and implement solutions for process improvement opportunities.
3. Provide troubleshooting...
Suggested
...ensure information is provided in a timely, accurate, and complete manner.
Support the facilitation of daily huddles and weekly review boards to drive the performance of investigations as required.
Pull deviation investigation metrics and associated CAPA and EC metrics...
Suggested
Shift work
Rotating shift
QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented,... ...process performance by observation of floor operations and review of performance data. Evaluate, plan, and implement solutions for...
Suggested
Shift work
...experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas,... ...and configuration assurance processes for the control of review, revision, distribution, production, retrieval of records...
Suggested
...AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job)
Review and approve product MPs.
Approve process validation protocols... ...our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality...
Suggested
Flexible hours
Shift work
...engineering and technical solutions, MTG has the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, PR, Boston, MA & San Francisco, CA and we serve life sciences...
Suggested
...experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas,... ...life cycle.
Hands-on experience in the development and/or review of decommissioning life cycle documentation and reports....
Suggested
Work experience placement
...Bachelor's Degree in Life Sciences or Engineering and previous exposure in Investigation activities within the Pharmaceutical or Medical Devices industry.
Excellent reading, writing, and speaking skills in Spanish and English.
Shift: Administrative and according...
Suggested
Flexible hours
Shift work
...procedures reflect current operations. Serve as a document owner. Assess process performance by observation of floor operations and review of performance data. Evaluate, plan, and implement solutions for process improvement opportunities. Provide troubleshooting support...
Suggested
...Quality Agreements and support audits.
A Day in the Life:
Documentation / Client Focus (80%)
Develop/Preparation/approval and review Material Specifications, Requirements and Methods.
Review and approve protocols and reports.
Manage Change controls, CAPAs,...
Shift work
...respect, teamwork, creative talent, enthusiasm, and diligence.
Preferred Experience
Experience in change control, nonconformance review, preventive maintenance review, minor deviations, work orders, and job plans.
FUNCTIONS
- Approve process validation protocols...
Full time
Contract work
Local area
...MAKES YOU A FIT:
The Technical Part:
Bachelor's Degree in Engineering and two (2) years of exposure within the Pharmaceutical & Medical Devices Industry.
Bilingual: Spanish and English
Soft Skills: Communication skills
Shift: 1st Shift.
Experience in:...
Flexible hours
Shift work
...Equipment safety assessment.
Environmental assessment.
Reviews and approves all subcontractor's safety plans.
Verifies that... ...our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality...
For subcontractor
Flexible hours
Shift work
Description:
The primary responsibility of this role is to generate detailed reports based on environmental assessments conducted on various properties.
Responsibilities:
Conduct environmental assessments on designated properties.
Collect...
Full time
Contract work
Remote job
