Resultados de la búsqueda: 145 vacantes
The Document Control performs a wide range of duties including the following:
Copy, scan and store documents
Check for accuracy and edit files, like contracts
Review and update technical documents (e.g. manuals and workflows)
Distribute project-related copies...
...For Documentation Support services in the Utilities area.
WHAT MAKES YOU A FIT:
The Technical Part:
Bachelor’s Degree and three to five (3-5) years of exposure in document control within the Pharmaceutical or Medical Device industry.
Bilingual, Spanish and...
...preferably experience with Minitab
Ability to speak, write and understand English to comply with written procedures, instructions, SOPs and other documents
Works with minimum supervision.
**Weil Group is proud to be an Equal Employment Opportunity Employer**...
...framework for measuring and improving our performance. Compliance Specialist 2018 2 Job Description GIDEP).
Act as a point of contact... ....
Generate product certificate of compliance or test documents for required customer orders.
Work with all necessary internal...
...Review and approval of Electronic Batch Records and related documentation to support Drug Substance Disposition Process. • Performs SAP... ...deviations from established procedures are investigated and documented per procedures • Collaborates cross functionally as needed to...
...Expertise
1. Initiate, revise, and approve manufacturing procedures. Ensure all 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...
...Possess excellent writing skills that include closing the gap between a highly technical investigation into a simple and concise document that can be understood by non-technical reviewers.
Communication and escalation of complaints, site representation on the product...
...The Validation Specialist I should have experience in validation life cycle and will also c ontribute intermediate to advanced level... ...technical support such as manufacturing support, regulatory documentation and continued process verification.
Responsible for providing...
...on the job)
Initiate, revise, and approve manufacturing procedures. Ensure all 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...
...Procurement Specialist
JOB SUMMARY : This position is responsible for research and procure all materials required... ...related duties as assigned.
Evaluate bid and construction documents (drawing, specifications and understand)
REQUIREMENTS:
Bachelor...
...fields.
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Job Description
Specialist QA with experience in:
Aseptic Technics
Change Control
New Product Introduction
Qualifications
Doctorate degree...
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...
...Employees
• Respect for Diversity
• Nimble
• Fight for What’s Right
STILL INTERESTED? Please continue !
A Patient Care Specialist 2 (PCS2) contributes to AHF by embodying
our commitment to excellence in patient care and operational
efficiency. Through...
...cGMP processes, procedures, testing (methods) in manufacturing, documents and records, batch record review, MES, EBR, SAP, Trackwise;... ...that deviations from established procedures are investigated and documented per procedures
• Ensures that production records and testing...
...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...
$30 - $37 por hora
...is a contract role for one year
As a Junior Validation Specialist at our pharmaceutical facility, you will be integral in ensuring... ...focus on generating System Development Life Cycle (SDLC) documentation, performing validations, and qualifying systems crucial for pharmaceutical...
...America.
Responsibilities:
Participates and support all activities related with documentation store, supply, etc.
Administers the electronic documentation system (check in, document/CRs release, and controlled documents issuance).
Qualifications Requirements/...
mirus Consulting Group is a local company based in Humacao, Puerto Rico that provides computer system validation and information technology consulting services to pharmaceutical companies and other organizations across the Island and parts of the United States. Its services...
...incidents, near misses and property damage incidents.
~ Ensure follow-up is done to minimize future exposure and proper records/documents are maintained.
~ Conduct, coordinate and track various training to support company programs.
~ Perform safety audits and inspections...
...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...
