IVD Assay Characterization & Validation Consultant
Consultant Specialists, Inc. (CSI)
Job Description
IVD Assay Characterization & Validation Consultant
\nHybrid – Indianapolis, IN (3 days onsite / 2 remote)
\nSeeking a hands‑on scientist to drive assay characterization, validation, and regulatory documentation for automated clinical chemistry assays. This role focuses on translating complex biochemical methods into scalable, manufacturable IVD products.
\n \nWhat You’ll Do
\n- \n
- Lead CLSI‑aligned assay characterization and validation protocol development \n
- Design studies for precision, linearity, interferents, stability, LoD/LoQ, and AMR \n
- Operate and troubleshoot automated chemistry analyzers (Cobas experience preferred) \n
- Execute multi‑day protocols (e.g., EP05), spike‑and‑recovery, and dilution workflows \n
- Conduct method comparison studies and resolve complex matrix behavior issues \n
- Analyze datasets using validation software; build statistical models and bias metrics \n
- Author MVRs, DHF documentation, and FDA Q‑Sub technical packages \n
- Support regulatory strategy and frame technical questions for FDA interactions \n
- Mentor lab staff on SOPs, protocols, and analytical best practices \n
What You Bring
\n- \n
- BS/MS/PhD in Clinical Chemistry, Biochemistry, Biomedical Engineering, or related field \n
- 2+ years in IVD assay development/validation in FDA/ISO‑regulated environments \n
- Strong CLSI fluency and hands‑on experience with automated analyzers \n
- Familiarity with FDA 510(k) matrix expansion and Q‑Sub processes \n
- Exceptional experimental rigor, analytical problem‑solving, and data integrity \n
- Ability to communicate complex findings across scientific, engineering, and regulatory teams \n
- Self‑directed, detail‑driven, and comfortable in fast‑paced development settings \n
About the Organization
\nFocused on advancing near‑patient diagnostic solutions that support diabetes management and continuous monitoring. The Indianapolis site manufactures high‑volume blood glucose monitoring products and is expanding into sensor manufacturing for next‑generation continuous glucose monitoring systems.
- ...IVD Assay Characterization & Validation Consultant Hybrid – Indianapolis, IN (3 days onsite / 2 remote) Seeking a hands‑on scientist to drive assay characterization, validation, and regulatory documentation for automated clinical chemistry assays. This role focuses...SuggestedRemote work
- ...Job Description IVD Assay Scientist \n Location: Indianapolis, IN (Hybrid... ...to support our client's development, characterization, and validation of automated clinical chemistry assays... ...-owned company providing top-tier consulting and staffing solutions across industries...SuggestedFull timeContract workRemote work
- ...Pharma GroupContact: ApplicationsEmail: ****@*****.*** Overview: We are seeking an IVD Assay Characterization & Validation Consultant to drive the technical characterization, execution, analytical verification, and regulatory documentation for...SuggestedHourly payContract workFlexible hoursNight shift
$48 - $53 per hour
...Job Description Job Description Pay Range: $48.00hr - $53.00hr Job Overview: We are seeking an IVD Assay Characterization & Validation Consultant to drive the technical characterization, execution, analytical verification, and regulatory documentation for automated...SuggestedHourly payContract workTemporary workLocal areaFlexible hoursNight shift- ...we’re improving health and improving lives.Labcorp is seeking a Validation Specialist, Immunoassay to join ourteam in Indianapolis, IN!... ...Monday-Friday 8am-5pmJob Responsibilities:Performs procedures for assay performance verification, clinical testing as required in all...SuggestedTemporary workCasual workInternshipMonday to FridayFlexible hours
- ...Engineering Services Pharmaceutical Manufacturing Client Contract Consulting Opportunity Position Overview Brooksource Engineering... ..., equipment, and systems are designed, qualified, and validated to meet quality and regulatory requirements. The consultant...Contract work
- ***THIS IS A 6-MONTH CO-OP STARTING JANUARY 4, 2027 THROUGH JUNE 25TH, 2027. TO QUALIFY, THE CANDIDATE HAS TO BE ACTIVELY ENROLLED IN AN ACADEMIC PROGRAM- NO RELOCATION STIPEND PROVIDED*** MilliporeSigma is a global leader in life science research and biopharmaceutical...Full timeTemporary workWork at officeRelocation
- ...architecture, engineering, construction, system integration, and consulting firm committed to helping our clients realize their most... ...the power of business to build a better world.Job Description:Validation Engineer III Who You’ll Work With You will join one of our 45...Full timeWork at officeFlexible hours
$84.9k - $157.7k
...improve how our equipment performs. You'll also design and execute validation activities to keep our processes aligned with Roche's... ...and time scopes for each project.Ensures process changes are characterized and implemented following validation policies and procedures....Full timeLocal areaRelocation packageNight shiftRotating shiftWeekend work- ...documentation for reagent manufacturing cell and equipment, including validations, assembly drawings, work instructions, BOMs, and routings.... ...and design control processes, including feasibility, characterization, verification, validation, design transfer.Technical...Full timePart time
$72.8k - $80.1k
Are You Ready? CAI is a professional services company established in 1996 that has grown to nearly 800 people worldwide. For mission-critical and regulated industries needing to deliver essential solutions in high-stakes environments, we provide accelerated operational...Worldwide- ...Validation Engineering Roles Join one of our 45 offices in the US as part of a committed team of over 1500 professionals, working directly with clients on projects that shape the world around us. As a contract professional with BW Design Group, you'll be welcomed into...Contract workWork at officeImmediate start
- ## Validation EngineerApply: Indianapolis, IN: Columbus, OH: Full time: Posted 2 Days Ago: R021372**About Us:**BW Design Group is a fully... ..., engineering, construction, system integration, and consulting firm committed to helping our clients realize their most critical...Full timeFor contractorsWork at office
- ...Validation / CQV Engineer (Commissioning, Qualification & Validation) Indianapolis, IN | Up to 40% Travel Help Bring Critical Manufacturing Systems Online We are looking for a Validation / CQV Engineer to join our Indianapolis, IN team to support commissioning...Full timeH1bImmediate start
$111.2k - $166.8k
...the US. Your RoleValidation is the backbone of pharmaceutical manufacturing quality — and in this role, you will own it. As a Sr. Validation Engineer, you will lead and execute validation activities across a complex aseptic manufacturing site, with a primary focus on...Shift workWeekend work- DescriptionINCOG BioPharma is seeking a highly motivated Senior Validation Engineer with validation expertise to join our team. The Senior Validation Engineer is a key individual contributor role within the INCOG BioPharma Validation Department. The Senior Validation Engineer...Full timeH1bVisa sponsorshipWork visa
- ...Services \n Pharmaceutical Manufacturing Client \n Contract Consulting Opportunity \n \n Position Overview \n Brooksource... ...processes, equipment, and systems are designed, qualified, and validated to meet quality and regulatory requirements. The consultant...Contract work
- DescriptionTSMS - Senior Process Validation EngineerThe Senior Process Validation Engineer - Technical Services and Manufacturing Sciences (TSMS) will be responsible for leading all facets of Process Validation, GMP Floor Support, and Continued Process Verification in...Full timeH1bWork at officeVisa sponsorshipWork visa
- ...Engineers by filling resource gaps, ensuring projects remain on track during critical milestones. Document and support Computer Systems Validation (CSV) tasks as needed to meet regulatory requirements. Requirements: Bachelor's degree in Engineering, Science, or related field....
- DescriptionThe Senior Manager of Validation Engineering is responsible for understanding and implementing validation requirements for a sterile injectables manufacturing and packaging facility. The ideal candidate has practical experience in qualification and validation...Full timeH1bVisa sponsorshipWork visa
$104.8k - $192.2k
...answers for the most pressing issues of today and tomorrow. EY teams work across a full spectrum of services in assurance, consulting, tax, strategy and transactions. Fueled by sector insights, a globally connected, multi-disciplinary network and diverse ecosystem...For contractorsSummer holidayFlexible hours- ...Job Description Job Description Validation Consultant – Analytical Development Equipment Location: Indianapolis, IN Engagement: Contract Industry: Pharmaceutical / Radiopharmaceutical Manufacturing Genovice is seeking an experienced Validation...Contract work
- ...Job Description Job Description E2i is a small systems integrator that has specialized in automation, validation, informatics, control panel design, and fabrication for the last 36 years. Our mantra is Quality People. Quality Results. At E2i, self-growth is at the...
- Job-ID32302816Reference26-00646 Job Summary:We are seeking a Sr. Validation & Compliance Engineer to support commissioning, qualification, and validation (CQV) activities for equipment, utilities, and facilities within a regulated pharmaceutical/biotech manufacturing environment...
- ...Process Validation Engineer We are seeking a Process Validation Engineer to support validation and qualification activities in a GMP-regulated manufacturing environment. The ideal candidate will have experience with process validation, equipment qualification, CSV,...
- ...-enabled, great place to work in the world. Through our Reinvention Services we bring together our capabilities across strategy, consulting, technology, operations, Song and Industry X with our deep industry expertise to create and deliver solutions and services for our...Full timeWork experience placementLive inWork at officeLocal area
- ...are robust, reproducible, and compliant? INCOG BioPharma's Quality Assurance team is expanding, and we're looking for a process validation professional with hands-on experience and a strong command of the three-stage process validation life cycle.The Senior QA Process...Full timeH1bVisa sponsorshipWork visa
- ...Senior Validation Engineer supporting radiopharmaceutical GMP operations at RayzeBio (Bristol Myers Squibb subsidiary) in Indianapolis. Responsible for developing and maintaining commissioning, qualification, and validation documentation for facility systems, utilities...Work experience placement
$107.9k - $130.75k
...importantly, on patients. Learn more about RayzeBio: The Senior Validation Engineer, CQV Sterility Assurance supports the... ...partners with Quality, Manufacturing, Engineering, QC, Operations, consultants, contractors, and project teams to ensure systems, equipment,...Hourly payFull timeFor contractorsWork experience placementSummer workLive inWork at officeLocal areaImmediate startFlexible hours- ...: Monday-Friday, First Shift; Onsite Full-Time Position. Position Summary: The primary purpose of this job is to provide Validation/Quality Engineering support for operations to ensure Quality System and Medical Device Regulatory requirements are adhered to. This...Full timeLocal areaWorldwideMonday to FridayShift workDay shift
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to IVD Assay Characterization & Validation Consultant. Be the first to apply!
- validation consultant Indianapolis, IN
- senior design verification engineer Indianapolis, IN
- verification engineer Indianapolis, IN
- computer system validation engineer Indianapolis, IN
- verification & validation engineer Indianapolis, IN
- validation engineer Indianapolis, IN
- validation specialist Indianapolis, IN
- validation officer
- software verification engineer
- physical verification engineer





