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- ...The Computer Systems Validation (CSV) Specialist, Level 3 Location : Portsmouth, NH. Relocation assistance is available for eligible... ...managing CAPAs and deviations. ~ Background in biotech, pharma, or medical device industry. ~ Strong attention to detail and...SuggestedRelocation package
$100k - $110k
...A prominent pharmaceutical company seeks a Senior Validation Specialist in Bristol, TN. The role focuses on validating processes, equipment, and systems while ensuring compliance with regulatory standards. Ideal candidates possess strong technical writing and analytical...SuggestedFull time- ...Skye Blue Consulting has been engaged to find a Validation Manager for one of our top clients in Western North Carolina. The client is a small (but growing!) pharma firm with competitive salaries, great benefits and is located in the beautiful foothills area. Job Description...Suggested
- ...A leading engineering firm in North Carolina is seeking a Lead Validation Engineer to oversee commissioning and qualification activities for automation and process systems. This role will ensure validation strategies align with regulatory expectations while mentoring...Suggested
- ...A leading pharmaceutical company is seeking an Associate Director of Validation to oversee the validation function for manufacturing operations. The role requires developing validation strategies, coordinating multidisciplinary teams, and ensuring compliance with regulatory...Suggested
- ...A leading clinical research organization in North Carolina seeks a Lead Validation Engineer to oversee commissioning and qualification activities for automation and process systems. This senior-level position involves coordinating with various stakeholders while ensuring...SuggestedContract work
$83 - $101 per hour
...A recruitment firm is seeking a Computerized System Validation SME in Gaithersburg, MD. This role will oversee validation of GxP-impacting computerized systems, ensuring compliance and quality throughout the lifecycle. The ideal candidate will have over 8 years of experience...SuggestedContract work- ...A leading IT staffing company is seeking a validation specialist to manage commissioning and validation activities within the pharmaceutical sector. You will be responsible for ensuring compliance with regulatory standards and driving the validation life cycle. The ideal...Suggested
- ...A global pharmaceutical company is seeking a Director for Commercial Manufacturing Validation in Boston. The candidate will ensure compliance in validation programs for development and commercial products. Key responsibilities include leading validation strategies, maintaining...SuggestedFull time
- ...include the development of processes and equipment characterization, establishing testing strategies, and ensuring compliance with validation protocols. A Bachelor's degree in a relevant field along with 5 years of experience in the pharmaceutical or medical device...Suggested
$173.2k - $216.5k
...A leading global pharmaceutical company is seeking a Director of Commercial Manufacturing Validation. This role ensures compliance across development and commercial portfolios while leading cross-functional technical teams. The ideal candidate has extensive experience...SuggestedFull timeFlexible hours$90k - $100k
...manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and... ...Overview: This role serves as the site SME for all cleaning validation and verification activities related to intermediate and API manufacturing...SuggestedLocal area- ...Job Description Job Description Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance,...Suggested
$130k - $160k
...Affiliate Overview Eidos Therapeutics, an affiliate within BridgeBio Pharma, is a commercial?stage biopharmaceutical company focused on... ...(ATTR?CM). What Youll Do The Manager, Computer System Validation (CSV), QA will report to the Associate Director, Quality Assurance...SuggestedWork at officeRemote work$173.2k - $216.5k
...Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc... ...for the position of Director, Commercial Manufacturing Validation . This role functions within SMPA's Global Technology and Quality...SuggestedFull timeFlexible hours$103.1k - $185.6k
...Job Summary: The Director of Validation will lead all validation activities across pharmaceutical and medical device manufacturing operations with a strong focus on sterile/aseptic manufacturing environments. The scope of responsibility encompasses all planning and implementation...Contract workTemporary workPart timeLocal areaRemote work- ...Job Description Job Description Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance,...For contractorsWeekend work
$75.79k - $113.68k
SUMMARY This position is responsible for establishing and maintaining the validated state for software-based computerized systems in use at Bora Pharmaceuticals Inc. according to the Validation Policy for Computerized Systems and in compliance with FDA and other regulatory...Work at officeLocal area- ...Pharmaceutical testing and manufacturing laboratory in Wilmington, is seeking a qualified candidate for the position of Computer System Validation Specialist. Responsibilities: Performs and leads computer system validation projects related to authoring and executing...
- ...Company Overview: Quality Agents, LLC provides expert validation and quality assurance services to the pharmaceutical and biotechnology industries. Our team ensures that equipment, systems, and processes used in the development and production of drug products meet...Full timePart timeInternship
- ...manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning and Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure that our clients can keep on providing the world with...
- ...organizations across the globe, and the development of our staff continues to grow PharmEng Technology. We are seeking an experienced Validation Engineer in Dorado, Puerto Rico. Objectives of this Role: Write and execute, Installation Qualification (IQ), and...Weekend work
- ...leading Pharmaceutical testing and manufacturing laboratory in Wilmington, is seeking a qualified candidate for the position of Validation Engineer. This position, in the Manufacturing and Formulations Services department, requires a Bachelors degree or higher in a scientific...Full time
- ...We are seeking to identify a skilled QA Validation Specialist (Contract) to join a leading pharmaceutical team supporting critical cGMP qualification and validation activities. This 6-month contract offers $38–40/hr. and hands-on ownership of equipment, facility...Contract work
- ...Job Description Job Description Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance,...Weekend work
- ...Job Description Job Description Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance,...
- ...Job Description Job Description Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance,...Weekend work
- ...inspections (FDA, OH Board of Pharmacy) and internal audits. Manage validation activities, including site Validation Master Plan, and approve... ...accurate documentation. Bonus Points: ~10+ years in pharma/biotech/medical device industry or similar ~7+ years in...Work at officeMonday to FridayFlexible hours
- ...Medical Safety Expert. This role is central to developing and validating an AI-powered adverse event (AE) detection engine that can accurately... ...of experience in pharmacovigilance or drug safety within a pharma, biotech, or CRO environment. ~ At least 2 years of...Hourly payContract workFor contractorsFlexible hours
$155k - $410k
...Software; Semiconductor; or, Telecommunications; - Life Sciences: Pharma, Bio Pharma, & Specialty Pharma;ÊMedical Device, Medical... ...operations. Key experience: (e.g., process engineering, process validation) and strong management consulting intrinsics such as...Full timeTemporary workH1b





