Validation specialist h1.location_city
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Validation specialist • usa
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We are seeking an experienced Validation Specialist to support validation activities for Syringe Assembly Machines (SAM) in a GMP-compliant pharmaceutical environment.The ideal candidate will posse...[show_more][last_updated.last_updated_30]
Coordinate with department supervisors to ensure assigned tasks are completed according to established timelines.Develop, update, and maintain procedures and forms within the electronic document ma...[show_more][last_updated.last_updated_variable_days]
Validation Engineer / Specialist.Are you hungry to learn, grow, and own your career inpharmaceutical validation? We're looking for a.Validation Engineer /Specialist.Support IQ, OQ, PQ protocols for...[show_more][last_updated.last_updated_variable_days] They are interested in temperature mapping experience, specifically CTUs, stability chambers, or similar environments.Strong lab instrument experience.Experience with risk assessments, URS, IQ/OQ/P...[show_more][last_updated.last_updated_30] 
Stantec’s Buildings team is on a mission to become the world’s leading integrated design practice.Our architects, engineers, interior designers, consultants, sustainability specialists, and technol...[show_more][last_updated.last_updated_variable_days]
You will assure that merchandise meets established quality standards and will implement activities within the product specification validation and item approval process.West Chester, PA headquarter...[show_more][last_updated.last_updated_variable_hours] As Qualification Specialist in the Equipment Integration team, you are responsible for caring about the GMP requirements.The team is responsible for transferring existing Lab Equipment from Spark N...[show_more][last_updated.last_updated_30] 
Job Title: Validation Specialist IV.Contract (Possible extension based on work performance).Equipment Validation Specialist exists to ensure all critical GMP equipment and systems are validated and...[show_more][last_updated.last_updated_30] As Qualification Specialist in the Equipment Integration team, you are responsible for caring about the GMP requirements.The team is responsible for transferring existing Lab Equipment from Spark N...[show_more][last_updated.last_updated_30] 
As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers.Our global presence provides opportuni...[show_more][last_updated.last_updated_variable_days]
Position SummaryThe QA Systems & Validation Specialist is responsible for ensuring that all GMP-related changes, systems, and validation activities comply with regulatory requirements and site Qual...[show_more][last_updated.last_updated_30]
This role is essential in maintaining the accuracy of validation processes, identifying root causes of failures, and implementing corrective actions to enhance efficiency and quality.Responsibiliti...[show_more][last_updated.last_updated_30] Algorithm Validation specialist for CSV validation of ML algorithms for various imaging systems built by data scientists.Strong understanding of clinical imaging workflows and machine learning (ML)...[show_more][last_updated.last_updated_30] 
Kelly Science is seeking a Validation Engineer for a growing company located in Marlborough, MA.Employment Type: Full Time; 3 month contract with possible extension.Work Schedule: Monday-Friday 8am...[show_more][last_updated.last_updated_variable_days]
The core responsibilities of the Validation Specialist III include but are not limited to performing Outbound Calls to Insurance Agents/Regional offices or utilizing various electronic means such a...[show_more][last_updated.last_updated_30]
The VP, Fraud/GEN AI Validation COE is responsible for performing model validation for all the fraud models, and ensure they are meeting the related MRM policies, standards, procedures as well as r...[show_more][last_updated.last_updated_variable_days]
Validation Specialist, Computerized Systems.The Validation Specialist, Computerized Systems, is responsible for performing initial and routine validation activities for GxP computerized systems.Pri...[show_more][last_updated.last_updated_1_day]
We are seeking a knowledgeable and detail-driven.DRG) assignment and inpatient medical record coding.This role plays a key part in supporting revenue integrity, reducing audit risk, and ensuring ac...[show_more][last_updated.last_updated_30]
Company Overview TestPros is a successful and growing business, established in 1988 to provide Information Technology (IT) technical support services to a wide range of Commercial and U.Federal, St...[show_more][last_updated.last_updated_30]
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Katalyst HealthCares & Life SciencesAlbany, NY[job_card.30_days_ago]
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Job Description:
Job Description:
- We are seeking an experienced Validation Specialist to support validation activities for Syringe Assembly Machines (SAM) in a GMP-compliant pharmaceutical environment. The ideal candidate will possess a strong understanding of the validation lifecycle and documentation required to ensure compliance with industry standards and regulations.
- Perform validation activities for Syringe Assembly Machines, including installation, operational, and performance qualification (IQ, OQ, PQ).
- Develop, review, and execute validation protocols and reports in compliance with GMP standards.
- Troubleshoot and resolve equipment-related issues during validation activities.
- Collaborate with cross-functional teams, including Engineering, Quality Assurance, and Manufacturing, to ensure successful validation.
- Maintain detailed and accurate documentation in accordance with regulatory requirements.
- Support continuous improvement initiatives to optimize equipment performance and compliance.
- Minimum of years' experience in the validation of Syringe Assembly Machines or equivalent equipment in a GMP pharmaceutical environment.
- Solid understanding of Validation Life Cycle documentation, including risk assessments, protocols, and reports.
- Familiarity with regulatory standards such as FDA, EU GMP, and ISO guidelines.
- Strong analytical, problem-solving, and communication skills.
- Ability to work independently and as part of a team to meet project deadlines.
- Bachelor's degree in Engineering, Life Sciences, or a related field.
- Experience with automated manufacturing equipment in sterile environments.
- Compensation: Competitive hourly rate based on experience.