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Red Lion Road-PA002SUMMARY:The main functions of a Validation Specialist are focused around the qualification of pharmaceutical packaging... ...determination of customer validation needs. The successful candidate will manage multiple projects under moderate supervision.This position...
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...the documentation to support Commissioning, Qualifications, and Validation. These people are responsible for protocol writing and... ...provide commissioning, qualification, validation, start-up, project management and consulting services related to operational readiness to FDA...
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...established gene and cell therapy, pharmaceutical, and biotechnology companies. We are an industry leader in providing project management, validation, engineering, quality/compliance, and consulting services to support our partners in finding ground-breaking treatments and...
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...Responsibilities:
Support all aspects of the Cleaning Validation Life Cycle for clients from development through qualification and monitoring .
Create/author/execute at a minimum , Validation Plans, V-cycle documents, Validation Summary Report, Qualification...
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...no one like you and that’s why there’s nowhere like RSM.
FDA Validation and IT Quality Director
The ERP and Automation Risk... ...GRC automation/implementation, security role design, security managed services, segregation of duties assessments, as well as ERP implementation...
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...Validation Supervisor Glaxo. Smith. Kline LLC - Details Responsible for the self-directed supervision of the day-to-day operations of Validation team members to support the value stream. Lead their team as a front-line leader (hands-on, on the floo Validation, Supervisor...
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...development, execution, review, and approval of equipment/software validations (including Computerized Laboratory Systems), System Life... ...for equipment/software related issues and consults with QA Management to resolve complex quality issues in a timely manner.
Responsibilities...
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...Job Description
Job Description Position: Validation Technician
Location: West Point, PA
Duration: 12 Months
Note: M-F/40hrs/week-100% onsite.
Job Description:
Candidate will work within the PCD metrology team that supports regulated equipment and...
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...largest and most mature advanced therapy manufacturing footprint in the world. We are an industry leader in providing project management, validation, engineering, quality/compliance, and consulting services to support our partners across the life science space in finding...
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...Must Have
Experience in cleaning validation in the biologics or vaccine industry to include the following:
Experience in authoring... ...clean hold times
EXCELLENT communication skills
Ability to manage, execute and troubleshoot on their own
Strong Microsoft...
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...largest and most mature advanced therapy manufacturing footprint in the world. We are an industry leader in providing project management, validation, engineering, quality/compliance, and consulting services to support our partners across the life science space in finding...
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Full time
...largest and most mature advanced therapy manufacturing footprint in the world. We are an industry leader in providing project management, validation, engineering, quality/compliance, and consulting services to support our partners across the life science space in finding...
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Full time
...with you.
Please find the urgent requirement I'm working on today and share the suitable resumes to call to
Role : Validation Lead
Location : KOP, PA Hybrid
Skills:
CSV, Computer System Validation, SAP Validation, Product Serialization, DSCSA...
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Immediate start
...continuous improvement through automation upgrades.
Develop validation documents per FDA cGMP and GAMP standards, functional specifications... ...IQ, OQ) for 21 CFR Part 11 compliance per FDA requirements
Manage, document, and implement these upgrades through changes control...
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...10 years Experience in Validating SAP systems in Manufacturing Experienced in CSV activities in Manufacturing related applications like... ...accuracy of the results and evidence and enables team on the defect management process Able to author Validation Plan and compile Validation...
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...Instrument Installation & operational qualification documentation, and calibration documentation.
Participate in computer system validation activities associated with new or upgraded equipment or software packages.
Support the purchase, installation, and equipment...
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...fill a position for a Laboratory-Based Cleaning Verification / Validation Analyst or Engineer working as a full-time employee of... ...and maintain supply inventory
~ Initiates and prepares change management documentation for deviations and document all Obvious Laboratory...
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Full time
...Immediate need for a talented Validation Engineer - I (Assistant) . This is a 06+ Months Contract opportunity with long-term potential and is located in West Point, PA(Onsite) . Please review the job description below and contact me ASAP if you are interested....
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...your future.
Your Role
This is an open application for Validation Engineers in the life science industry. We look forward to... ...advanced knowledge of risk-based validation approaches, quality management, and regulatory requirements and compliance.
Adaptability...
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...the documentation to support Commissioning, Qualifications, and Validation. These people are responsible for protocol writing and... ...provide commissioning, qualification, validation, start-up, project management and consulting services related to operational readiness to FDA...
Full time
Worldwide
Relocation
