Resultados de la búsqueda: 79 vacantes
...you are curious, anxious to explore all possibilities without anyone telling you to (while also following instructions, of course). It means you’re creative, with such an eye for detail that nothing gets past you. If this sounds like you, and if you have a commitment...
...the root of the problem and satisfying your client’s need to fix it. Sprinkle on a love of the scientific method, teamwork and,... ...occasion, depending on the nature and complexity of the complaint, the specialist may be responsible of conducting and documenting the...
...Lead the review and administration of customer contract reviews as it pertains to quality and compliance requirements.
Complete... ...framework for measuring and improving our performance. Compliance Specialist 2018 2 Job Description GIDEP).
Act as a point of contact for...
...technology consulting services to pharmaceutical companies and other organizations across the Island and parts of the United States. Its services include the assessment and validation of automation equipment, network infrastructures and business processes, as well as the...
...and, above all else, being ethical and you just might have what it takes to take on this new challenge. Bring it on!
AS A PIECE... ...In support of Quality Assurance program acts as the technical specialist.
Review and approve product MP’s.
Approve process validation...
Minimum Requirements
Mid-level individual contributor on a project or work team, 3-5 years of experience required.
Bachelor Degree in Engineering
Experience within Medical Devices and/or Pharmaceutical industries.
Experience in equipment IQ, OQ and PQ, Validation...
...The Validation Specialist I should have experience in validation life cycle and will also c ontribute intermediate to advanced level of pharmaceutical support skills under scientific and administrative direction.
Apply sound scientific methods and analysis while...
...in the company’s controlled document processes to ensure correct handling of documents from the ground up
Oversee document through its entire lifecycle (inception to archival)
Check and edit incoming documents and prepare for distribution
Create document filing...
...fields.
Log on now to our website qrcgroup.com / to learn more about our services and solutions!
Job Description
Specialist QA with experience in regulated industries to:
Perform Trackwise system queries, deviations
Participate in triage process...
...fields.
Log on now to our website qrcgroup.com / to learn more about our services and solutions!
Job Description
CSV Specialist for validation of laboratory instruments with LIMS connection (HPLC, Gas Chromatographer, Instron pull testers)...
...Validation Specialist with experience in regulated industry, validating/qualifying laboratory equipment, manufacturing equipment, processes, utilities and facilities.
Tasks:
Execute complete validation cycle
Change Control
Equipment qualification (manufacturing...
...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...
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 ...
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...
Our Client is looking for a highly motivated, organized and energetic Recruiter to join our team in our Puerto Rico office. The Recruiter will research, develop and implement effective recruiting and staffing strategies to attract a diverse pool of qualified talent for...
For Engineering support services in the Engineer area.
WHAT MAKES YOU A FIT:
The Technical Part:
Bachelor’s Degree in Engineering and one (1) year of exposure within the Pharmaceutical & Medical Devices Industry.
Bilingual: Spanish and English
Soft Skills...
...collection and reporting including but not limited to air, storm water and surface water discharge.
~ Ensure the company meets all its legislative compliance obligations with OSHA, CAL/OSHA, EPA, AQMD, ADA, and fire codes.
~ Serve as primary contact for all regulatory...
Description:
Perform one or more of the following duties and responsibilities in support of site Quality Assurance program under minimal supervision. Review and approve product MPs. Approve process validation protocols and reports for manufacturing processes. Request...
JOIN OUR TEAM!
PharmaLex is a highly successful and growing consulting company for the Healthcare industry around the world. PharmaLex offers professional development, plus a stimulating and collaborative work environment. We are committed to providing exciting career...
...are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:
~Specialist QA
Description:
Perform one or more of the following duties and responsibilities in support of the Quality Assurance program...
