Biotech Validation Engineer - GMP & Aseptic
Legend Biotech US
Legend Biotech US is seeking a Validation Specialist to manage and execute site validation activities in compliance with regulatory requirements. The role involves controlling aseptic process validation, implementing changes, and working cross-functionally across technical teams. The ideal candidate has a Bachelor’s degree in engineering and at least 2 years of relevant experience in the pharmaceutical industry. Benefits include competitive pay, medical insurance, and retirement plans. #J-18808-Ljbffr Legend Biotech US
$120k
...Validation Specialist Legend Biotech is a global biotechnology company dedicated to treating, and one day... ...resulting from technical changes. Control Aseptic process validation and particle... ..., rationales, and approval for engineering and process changes to meet regulatory...SuggestedLocal areaWorldwide- ...Piper Companies is currently looking for an experienced ( CQV) Validation Engineer in Raritan, NJ to work for an innovative and growing... ...minimum of 30 days from the posting date. Keywords GMP, Pharmaceutical Manufacturing, Equipment Qualification, Equipment...Suggested
$87.1k - $94.6k
...Perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on... ...- Bachelor's degree (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience... ...industry - Essential experience in a GMP (Good Manufacturing Practice) environment...SuggestedFor contractorsWorldwide$72k - $116k
...and reports, ensuring qualification and validation activities meet internal and external compliance... ...in qualification/validation of typical GMP utilities, facilities, computer systems... ...facility. Bachelor’s degree in Engineering, Computer Science, Science, or related discipline...SuggestedTemporary workRelocation packageShift work$72.8k - $80.1k
...Direct small teams in document development and/or execution Qualifications and Experience - Bachelor's degree in a science or engineering field (or equivalent experience) - 2–4 years' experience in commissioning and qualification in a regulated industry -...SuggestedWorldwide$75k
...Facebook, Instagram ( , X ( and YouTube. ( Job Description An engineering professional that works with project engineers, stakeholders,... .... Responsibilities Develop, Execute and Implement Validation Documentation - Specification documents, SOPs, IQ/OQ/PQ...Temporary workLocal area- ...Job Title R3 Technology Inc. seeks Validation Engineer for its Hillsborough, NJ office. Responsibilities include gathering requirements to develop product-level requirements and assisting with the high-level systems view of product design. Conduct multi-disciplined...Work at officeRelocation
- ...Job Description We are seeking a Senior Validation Engineer with solid hands-on validation... ...validation summary reports as needed to support GMP manufacturing and laboratory systems... ...Partnering with Cellares enables academics, biotechs, and pharma companies to accelerate...Contract workFor contractorsFlexible hours
- Jacobs Management Group is seeking an experienced Electrical Engineer for their pharmaceutical manufacturing facility in Piscataway Township... ...experience. Proficiency in AutoCAD, regulatory inspections, and GMP compliance is essential. This hands-on position is critical for...
- ...motivated Senior Quality Validation Specialist, who will... ...process validation & engineering documents, test protocols... ...in support of GMP operations at the IDMO... ...lifecycle programs including aseptic process simulations,... ...Cellares enables academics, biotechs, and pharma companies...Flexible hours
$93.46k - $122.67k
Job Overview QA Validation Specialist III role at BioSpace, based in Raritan, NJ. Exempt level... ...therapy manufacturing plant in a sterile GMP environment. Key Responsibilities... ...recognition programs. EEO Statement Legend Biotech is a proud equal opportunity/affirmative...Work at officeFlexible hours- ...focused on Technology Quality Manufacturing and MES Services. This position requires a strong CSV and Quality expertise for leading validation activities across the SDLC in GxP systems with a desire for 7-10 years of relevant experience. Key responsibilities include...Remote work
- Creative Solutions Services, LLC is seeking a qualified candidate for a role focusing on validation in the pharmaceutical industry. Candidates should have over 3 years of experience in Computer System Validation and a strong background in FDA regulations. The position...
- Katalyst CRO is looking for a CSV Consultant in Raritan, NJ to support system validation activities in a regulated environment. The consultant will ensure compliance with FDA guidelines, contribute to validation documentation, and work within the System Development Lifecycle...
$80k - $95k
Amneal Pharmaceuticals in Piscataway Township is seeking a Maintenance Engineer to take ownership of all maintenance, troubleshooting, and continuous improvement of manufacturing equipment. The role plays a vital part in ensuring smooth production of oral solid dosage...$40 - $50 per hour
...Job Description Job Description GMP Production Support Engineer Full Time, Direct Hire Monday-Friday 7am-4:30pm OR 6pm-6am (5 days on/5... ...candidate has GMP manufacturing, process support, MSAT, biotech/pharma production, or equipment support experience, plus...Full timeMonday to Friday$80k - $90k
Amneal Pharmaceuticals is seeking a Process Engineer in Piscataway Township. The role involves planning and executing Process and Cleaning Validation assignments while collaborating with cross-functional teams. A Bachelor's Degree in Pharmaceutical/Biomedical Engineering...- ...Overview Validation Manager role at WhiteCrow Research. Our client is a global injectables... ..., systems, and process changes with Engineering, Manufacturing, and Quality. Manage validation... ...with sterile injectable manufacturing, aseptic processes, utilities, and equipment...Full time
$90k - $110k
Amneal Pharmaceuticals is seeking a Project Engineer to support engineering projects in sterile/aseptic manufacturing. This role encompasses project management from... ...Engineering and have 3+ years of experience in a GMP environment. A competitive salary ranging from $90,...$91.7k - $135k
...Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description Job Description The Engineer III, Manufacturing Engineering, at Thermo Fisher Scientific will play a crucial role in enhancing production processes and systems...Temporary workWork at office- Katalyst CRO in Raritan, NJ, is seeking an experienced CSV validation professional to lead end-to-end CSV activities in adherence to regulatory... ...risk-based validation strategies. Experience in Pharma or biotech, strong leadership skills, and a comprehensive understanding...
- Experienced Validation lead to support end to end validation ownership of a Unified Regulatory Platform (URP) built on Veeva and AWS based cloud stack 8+ years' experience in Computer System Validation or Quality management or Business Analysis in GxP application area...
- ...capabilities with marketing objectives. Apply your expertise in engineering principles and financial acumen to enhance diagnostic... ...installation, scale-up, optimization, automation, trouble shooting and validation of manufacturing processes or equipment. Aids in the...Work at office
- ...Manufacturing Engineer • Floor Oriented • 5-7 years of manufacturing / process engineering experience • bility to read prints • Proven record of continuous improvement • Fiberglass experience is a plus • utomotive / Agricultural experience is preferred...
$76k - $96.5k
...Job Title: Manufacturing Engineer Job Description This Manufacturing Engineer role focuses on sustaining engineering and supporting the production of complex, high-value semiconductor capital equipment in a low-volume, high-complexity, engineer-to-order environment...Permanent employmentRelocationShift work- ...Process Engineer The Process Engineer position is responsible for the design, operation, installation, and maintenance in all areas of... ...publications. Ensure that manufacturing conforms to all ISO and GMP procedures. Participate in all training required and assigned...Flexible hours
$90k - $210k
...Senior Process Engineer We are seeking an innovative and highly... ...from Process Development into GMP manufacturing facilities, as... ...from customers Lead Master Validation Plan creation in order to support... ...of experience within the biotech/biopharma industry in cGMP Operations...Flexible hours- A leading technology consulting firm is looking for an Experienced Validation Lead to support the end-to-end validation of a Unified Regulatory Platform built on Veeva and AWS cloud technology. The ideal candidate will have over 8 years of experience in Computer System...
- EY is seeking an Identity Verification Engineer to design and implement identity proofing workflows and passwordless authentication using 1Kosmos or Microsoft Verified ID. You will configure biometric verification, liveness detection, and identity assurance controls while...Remote job
- ...have managed teams of at least 6-8 engineers and consultants on defined... ...utilities, upstream and downstream biotech equipment, single use disposable, or aseptic fill finish manufacturing, we’d... ...provide commissioning, qualification, validation, start-up, project management...Full timeWorldwide
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