Resultados de la búsqueda: 34 vacantes
...For process onwer services in the Manufacturing area.
WHAT MAKES YOU A FIT:
The Technical Part:
Bachelor's Degree with five (5) years of Manufacturing Operations experience within the pharmaceutical or regulated industry.
Bilingual (English & Spanish)....
...infrastructures and business processes, as well as the involved project management.
Job Description
~ Initiate, revise, and approve manufacturing procedures. Ensure all procedures reflect current operations. Serve as a document owner.
~Assess process performance by...
...SUMMARY
With minimal supervision, support the execution of manufacturing/quality systems such as non-conformances, process validation, procedures, training, and new product introductions. Apply process, operational, scientific expertise, basic compliance knowledge, and...
...Assessment
Requirements
Shift, Education & years of experience needed;
Doctorate degree OR Master's degree and 3 years of Manufacturing Operations experience
OR Bachelor's degree and 5 years of Manufacturing Operations experience
OR Associate’s degree and 10...
...QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world...
...QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world...
QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world...
...YOU WILL: (The day-to-day on the job)
Review and approve product MPs.
Approve process validation protocols and reports for manufacturing processes.
Request Quality on incident triage team.
Approve Environmental Characterization reports.
Release of sanitary...
...In support of Quality Assurance program acts as the technical specialist.
Review and approve product MP’s.
Approve process... ...being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality talent. We're FITS!...
Inteldot has over 14 years in the life science industry with allocations a cross Puerto Rico, United Sates, Europe and Japan. This is a great opportunity for one of our leading clients in Puerto Rico .
Description:
Perform one or more of the following duties...
...CSV Specialist for laboratory equipment.
Skills:
Laboratory instruments qualification
Validation Cycle
Requirements
Bachelor Degree in Science
At least 5 years of experience in related area
Biligual (Spanish/English)
Technical Writing...
...EXPERIENCE REQUIRED
:
• You will perform review, approval and tracking of cGMP processes, procedures, testing (methods) in manufacturing, documents and records, batch record review, MES, EBR, SAP, Trackwise; including but not limited to Deviation’s, CAPAs, and validations...
...travel/lodging/transportation expenses (employees only)
General Description:
With minimal supervision, support the execution of manufacturing/quality systems such as non-conformances, process validation, procedures, training, and new product introductions. Apply process...
...Investigations Specialist with experience in regulated industries. Strong knowledge... ...investigation process as it applies to manufacturing issues and complaints.
Understanding... ...processes and systems involved in the manufacture of bio pharmaceutical.
Strong knowledge...
Candidates qualifications / expertise;
• Perform Trackwise system queries, deviations
• Participate in triage process
• Perform oversight of the process and procedures/GMP tasks
• Manage Change Controls and deviations for review and approval as QA contact...
...product MPs. Approve process validation protocols and reports for manufacturing processes. Request Quality on incident triage team. Approve... ...that operations for licensed pharmaceutical products are manufactured, tested, and stored, according to current Good Manufacturing...
...practices.
~ Keep abreast of any safety and environmental law or regulation changes that impact the client.
~ Participate in manufacturing meetings to discuss workplace safety and regulatory concerns and opportunities.
~ Actively role model all company and assigned...
...under the highest ethics standards for the following position:
Specialist QA
Shift: Mon/Tue then Fri/Sat/Sun on alternate weeks from 5... ...MPs.
~Approve process validation protocols and reports for manufacturing processes.
~Request Quality on incident triage team.
~...
Expertise required:
Aseptic Techniques, Change Control and New Product Introduction.
Requirements
Education and years of experience requirements;
Doctorate degree or Master's degree and 3 years of directly related experience
or Bachelor's degree and ...
...(and in the US as well!). Our company is flexible, family-oriented and focused on our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality talent. We're FITS!
Are you the Next Piece?...
