Validation Specialist
TechDigital Group
The Validation Specialist, Computerized Systems, is responsible for performing initial and routine validation activities for GxP computerized systems. Primary responsibilities include: qualification of laboratory instruments, setup of computers and instruments, troubleshooting of system related issues, and technical writing and execution. Executes validation projects, system qualification, and implements industry best practices for the design and delivery of GxP computerized systems. 1. Required Competencies: Knowledge, Skills, and Abilities: Working understanding of validation concepts and requirements. Intermediate written and verbal communication skills. Knowledge of cGMP. Critical reasoning and decision making skills. Knowledge of validation industry and regulatory requirements. Ability to work independently and participate in a team. Work and time management skills. Working proficiency in Microsoft Word, Outlook, Excel, PowerPoint, and Project. 2. Duties and Responsibilities: Performs validation document generation, program management, and protocol execution activities. Interface with Engineering, and end user groups to support development of life cycle documents and system requirements. Design the validation approach with technical oversight, provide the scientific rationale and acceptance criteria, and generate validation protocols. Execute validation studies, perform data analysis, and write protocol summaries, reports, and technical reports. Protocol execution and project activities. Execute qualification activities with oversight. Participate in department and site project teams. Perform qualification activities according to site objectives and timelines. Edit department SOPs and generate basic revisions as required. Execute CAPA plans, risk assessments, investigations, and root cause analysis. Working understanding of site quality GxP systems supporting document management, change controls, deviations, CAPAs. Defend validation protocols in internal and external audits as a subject matter expert with limited supervision. Interact and collaborate with departments (on and offsite) as well as vendors, consultants and other external service providers. Perform general administrative and organizational activities. Management of time and work deliverables, regular interface and reporting to management. Complete regulatory, site, and department training requirements on a timely basis. Perform other tasks as assigned. 3. Education and Experience: Bachelor's degree preferred, preferably in Science or Engineering. 8 years relevant work experience required. An equivalent combination of education, experience and training may substitute. 4. Working Conditions The incumbent may be required to gown and operate in classified manufacturing environments. This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job. #J-18808-Ljbffr TechDigital Group
- Senior Validation Specialist Warren, NJ--Onsite Work Schedule: Mon - Fri, Business Hours The Senior Validation Specialist, Computerized Systems, is responsible for performing initial and routine validation activities for GxP computerized systems. Primary responsibilities...SuggestedWork experience placement
- 1. PURPOSE AND SCOPE OF POSITION: The Validation Engineer supports the successful implementation of laboratory equipment and systems at multi-use sites through interaction with internal customers and external service providers. The incumbent in this role contributes to...SuggestedFor contractorsWork at officeImmediate start
$80k - $100k
Support validation activities for manufacturing equipment, facilities, utilities, processes, and computerized systems in accordance with... ...to support compliant and reliable operations. The Validation Specialist will work cross-functionally with Quality, Operations, Engineering...SuggestedContract workWork at officeWork from home- An established industry player is seeking a Validation Specialist for Computerized Systems to ensure compliance with GxP standards. In this pivotal role, you will be responsible for performing initial and routine validation activities, including qualification of laboratory...Suggested
- An established industry player is seeking a Validation Qualification Specialist to ensure compliance in laboratory equipment and systems. This role involves developing qualification protocols, managing projects, and providing exceptional customer service within a dynamic...Suggested
$60 - $65 per hour
...message the job poster from Talent Groups We are looking for a Validation Associate with 7+ years of experience in Computer System... ...new job is posted. Sign in to set job alerts for “Validation Specialist” roles. Massachusetts, United States $60.00-$65.00 16 hours ago...16 hoursFull timeContract work- ...Qualification activities within pharmaceutical manufacturing. The role requires over 5 years of experience in Equipment and Computer System Validation, strong knowledge of cGMP, and bilingual capabilities in English and Spanish. Responsibilities include developing documentation,...
- ...developing documentation, and ensuring compliance with cGMP. Ideal candidates will have over 5 years of experience in equipment validation and be fluent in English and Spanish. This position offers an opportunity to contribute to safety and efficacy standards in life...
- Experic, LLC is seeking a Validation Specialist for their Cranbury, NJ office. This role involves supporting validation activities for manufacturing and computerized systems in line with cGMP guidelines. Key responsibilities include preparing and reviewing validation documentation...Work at office
- An established industry player is seeking a Senior Validation Specialist to oversee validation activities for GxP computerized systems. This role involves qualifying laboratory instruments, troubleshooting system issues, and ensuring compliance with industry standards....
- Validation Qualification Specialist This role is 100% Onsite Work Schedule: Mon - Fri, Business Hours 1. PURPOSE AND SCOPE OF POSITION: The Validation Engineer supports the successful implementation of laboratory equipment and systems at multi-use sites through interaction...For contractorsWork at officeImmediate start
$30 - $35 per hour
A pharmaceutical and biotechnology company is seeking a QC Specialist/Scientist for a contract position in Kentucky. The role involves performing method validation primarily for HPLCs, as well as GCs and FTIRs. Candidates should have experience with basic analytical techniques...Hourly payFull timeContract work- A leading technology services provider is seeking a Computer Validation Specialist in New Jersey to ensure compliance with regulatory requirements and contribute to validation deliverables for computer systems. You will prepare and approve validation documents, conduct...
$102.1k - $153.2k
..., engineers, interior designers, consultants, sustainability specialists, and technologists are passionate about the power of design.... ...that support and enhance our communities. The Commissioning and Validation role provides crucial services to confirm equipment and...Full timeTemporary workPart timeWork experience placementCasual workWork at officeLocal areaImmediate startFlexible hours- Current job opportunities are posted here as they become available. MV04-020526 Validation Specialist - Utilities & Facilities (Electrical) Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology...
- A leading financial services firm is looking for a Business Validation Associate to support the Open Banking team. This role involves validating operations and ensuring compliance with regulations. You will collaborate with cross-functional teams, handle customer disclosures...Full timeWork at office
$55 per hour
...based AI opportunity provider seeks mathematicians for evaluating and improving AI systems. Contributors will design math problems, validate simulations using Python, and enhance AI logic. A relevant degree and 3+ years of experience are required. The role is part-time...Contract workPart timeFlexible hours- ...leading consulting firm is looking for a Credit Risk Modeler for remote, project-based opportunities. The role involves performing validations of credit decisioning models and demands a solid understanding of predictive accuracy. Candidates should have at least 5 years of...Remote workFlexible hours
- A leading solutions provider in biotech is seeking a Validation Specialist focused on Utilities and Facilities. The ideal candidate will have over five years of experience and a strong background in electrical systems within GMP environments. Responsibilities include supporting...
- A leading services supplier in biotechnology is seeking a Validation Specialist with over 5 years of experience in Utilities and Facilities C&Q for a biotech facility. The ideal candidate will have a Bachelor’s degree in Engineering and expertise in electrical systems within...
$110k - $150k
New York Life seeks a Research Senior Associate in New York, NY, to support product innovation through analysis and validation of new concepts. The ideal candidate will have strong analytical and problem-solving skills and experience managing complex projects. This hybrid...- A leading services supplier seeks a Validation Specialist with over 5 years of experience to support utilities and facilities commissioning and qualification activities for a biotech facility. The ideal candidate will have a strong knowledge of electrical systems in GMP...
- A leading service supplier in engineering and validation is looking for a Validation Specialist in Kentucky. The ideal candidate will have over 5 years of experience in Utilities and Facilities C&Q within biotech environments, focusing on electrical systems. You'll support...
- ...services company is seeking a detail-oriented Scheduler Application Specialist to ensure that job scheduling workflows function correctly... ...in a remote setting. This contract position is essential for validating and improving scheduling reliability. #J-18808-Ljbffr...Contract workRemote work
- A leading insurance firm is looking for a Model Validation Specialist to oversee the validation of AI and ML models. This role involves close collaboration with technical and business teams to ensure compliance and quality. Candidates should have an advanced degree in a...Work at officeRemote work
$70k - $90k
...Full-time $70000.00-$90000.00/year Are you hungry to learn, grow, and own your career inpharmaceutical validation? We’re looking for a Validation Engineer /Specialist who wants hands‑on experience and a clear pathto leadership. What You’ll Do SupportIQ, OQ, PQ...Full time$70k - $100k
Validation Engineer / Validation Specialist (CQV, GMP, Life Sciences) Location: New York City Salary: $70-100K + Bonus + Benefits Are you looking to build a career in validation, commissioning, and qualification (CQV) within the pharmaceutical / life sciences industry...$60 per hour
A leading AI systems firm is seeking experienced quantitative professionals. In this fully remote role, you will evaluate AI-generated quantitative analysis and help shape the future of AI models. With a flexible schedule and competitive pay of up to $60 USD/hour, this ...Remote workFlexible hours$80k - $100k
...individual and team success. Located in Monmouth Junction, New Jersey, Tris Pharma has an immediate opening for a Method Validation Documentation Specialist. Position Summary The Method Validation (MV) Documentation Specialist supports the MV department by creating,...Full timeContract workWork experience placementWork at officeLocal areaImmediate start- ...job opportunities are posted here as they become available. Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading... ...the highest ethics standards for the following position: CQV specialist Position Summary The CQV Specialist will support commissioning...Weekend work
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