oq Jobs in indiana

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HVAC SME

Zachary Piper Solutions, LLC

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Bloomington, Indiana, USA

Full-time

Piper Companies is seeking a BioPharma HVAC Subject Matter Expert (SME) to join an expansion project team of a new facility build for a CDMO out in Bloomington, IN. The role has an onsite expectation and slated through 2026 and potentially beyond. The SME will lead the implementation, and qualification of complex HVAC systems for the new GMP manufacturing facility. This role requires deep technical knowledge and hands-on experience with HVAC systems designed for cleanrooms, controlled environmen
Posted 8 days ago | Updated 5 hours ago

Manufacturing Engineer I

Freudenberg Group

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Jeffersonville, Indiana, USA

Full-time

Working at Freudenberg: We will wow your world! Responsibilities: Lead the identification, development, and qualification of manufacturing processes improvements. Deploy GROWTTH tools to create simple, robust, and innovative manufacturing processes for new and sustaining products Create and maintain quality system documentation such as process failure mode effects analysis, process flow charts, process validation plans, validation protocols, manufacturing procedures, etc. Supports the developm
Posted 13 days ago | Updated 13 hours ago

Equipment Validation Engineer

Apex Systems

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Indianapolis, Indiana, USA

Full-time

Job#: 2073087 Job Description: Role: Equipment Validation Engineer Location: Indianapolis, IN (On-Site) Type: Long Term Contract Apex Systems, a global leader in Technology Services, is searching for an Equipment Validation Engineer in Indianapolis, IN for a large Life Sciences client. This is a long term contract with an immediate start date. This role requires on site support 5 days a week due to the nature of the role. See below for more details! Duties and Responsibilities: Supports the
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Posted 5 days ago | Updated 8 hours ago

Validation (CQV) Engineer

Tech Rakers

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Indianapolis, Indiana, USA

Contract

Title: Validation (CQV) Engineer Qualifications and Requirements Bachelor's degree in Engineering, Pharmaceutical Science, or related technical field4-8 years of experience in a CQV role within pharmaceutical, biotech, or medical device industriesWorking knowledge of GMP regulations, Computerised System Validation and GAMP5Hands-on experience with qualification protocols for pharmaceutical manufacturing equipment and utilitiesFamiliarity with automation systems used in pharmaceutical manufacturi
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Posted 16 days ago

Trackwise Digital Architect

VeridianTech

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Texas, USA

Full-time

Trackwise Digital Architect Remote Requirement Experience with designing and implementing IT systems. Experience with understanding specifications, evaluate current application, gather requirements, and work closely with stakeholders to deliver the right solution Experience working and implementing systems using TrackWise Digital platform. Hands on experience in TrackWise Digital Application setup: Permission Sets, Configuring Platform Custom Settings, Configuring Remote Site Settings, E-s
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Posted 60+ days ago | Updated moments ago

Computer System Validation Specialist

SGS Consulting

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Remote

Contract

Job Title: Computer System Validation (CSV) Specialist Duration: 08 Months + (Possible Extension) Location: Wilmington, DE 19803 (Remote) Schedule: M-F: 08 AM 05 PM Kindly Do not apply if you are not or Permanent Resident of USA. Qualifications: The official position title is Computer System Validation (CSV) specialist to support the Newark manufacturing facility with validation of new and existing computerized systems.This role will primarily support the Newark manufacturing facility but may r
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Posted 14 days ago

Sr. R&D Engineer

Medtronic

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Remote or Irvine, California, USA

Full-time

We anticipate the application window for this opening will close on - 24 Jun 2025 Position Description: Sr. R&D Engineer for Covidien, LP (a Medtronic company) located in Irvine, CA. Multiple positions available. Responsible for providing R&D and quality engineering support to ensure the successful development of Medtronic Neurovascular devices, design transfers, scale-up and ongoing operational support; work with Design and Quality control of Class II and Class medical devices (bare-metal or
Posted 13 days ago | Updated 7 hours ago

Senior Principal Process Engineer (AME) - Neurovascular - Irvine, CA (Onsite)

Medtronic

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Remote or Irvine, California, USA

Full-time

We anticipate the application window for this opening will close on - 23 May 2025 At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life For over a decade, Medtronic has been at the forefront of transforming stroke care, leading the fight against both acute ischemic stroke (AIS) and hemorrh
Posted 3 days ago | Updated 7 hours ago

Reliability Engineer II

Medtronic

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Warsaw, Indiana, USA

Full-time

We anticipate the application window for this opening will close on - 5 May 2025 At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life Act boldly. Compete to win. Move with speed and decisiveness. Foster belonging. Deliver resultsthe right way. That's the Medtronic Mindset - our cultural n
Posted 30 days ago | Updated 7 hours ago

Engineer, Inspection/Packaging

Novo Nordisk Inc

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Bloomington, Indiana, USA

Full-time

About the Department At Novo Nordisk, we want to make a difference. For more than 100 years, we have led the way in diabetes care. Being part of Novo Nordisk allows our employees to embark on life-changing careers, and the opportunity to help improve the quality of life for millions of people around the world. Our Bloomington, Indiana site is a state-of-the-art facility where we have an integrated model from process and formulation to clinical and commercial biomanufacturing and drug product f
Posted 20 hours ago | Updated 7 hours ago

Validation Engineers II

Merck KgaA

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Indianapolis, Indiana, USA

Full-time

Work Location: Indianapolis, Indiana Shift: No Department: LS-SC-POEME Indianapolis Validation Engineering (1204795) Recruiter: Ashley Hennessy This information is for internals only. Please do not share outside of the organization. NOTICE OF FILING This notice is posted as the result of the filing of an Application for Alien Labor Certification with the Department of Labor for the job opportunity listed below. Any person may provide documentary evidence bearing on this Labor Certification Ap
Posted 31 days ago | Updated 7 hours ago

Sr. Electrical Engineer - Neuro

Medtronic

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Remote or Minneapolis, Minnesota, USA

Full-time

We anticipate the application window for this opening will close on - 16 May 2025 At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life The Electrical Engineer for Medtronic NEUROMODULATION/PELVIC HEALTH RPE will be responsible for device electrical hardware design for market released impla
Posted 6 days ago | Updated 7 hours ago

Process Engineer

Novartis

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Indianapolis, Indiana, USA

Full-time

Job Description Summary The Process Engineer will execute engineering activities (design, implementation, maintenance, etc.) within technical area of expertise by using reliable and cost-effective technical solutions, ensuring technical quality to enable the overall site / project objectives. Responsible for execution of maintenance and calibration activities and commissioning activities for projects at site level. Supervise plant engineering team providing technical assistance to the function a
Posted 47 days ago | Updated 7 hours ago

Computer Systems Validation Engineer

Corporate Solutions General, Inc.

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Remote or San Francisco, California, USA

Full-time, Part-time, Contract, Third Party

Computer System Validation Engineer (CSV) SFO, CA Onsite Contract Client : Cellares Minimum 10+ Years experience required .5 year in Pharma domain Job Roles and Responsibilities: * Develop, execute, and document test protocols for system qualification, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ). * Ensure that software is properly validated and compliant with internal and external standards, such as FDA 21 CFR Part 11, GxP, an
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Posted 20 hours ago

MES Consultant

BOTG LLC

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Remote

Full-time

Location: Remote Job Type: Full-Time / Contract Industry: Life Sciences / Pharmaceuticals / Manufacturing About the Role: We are seeking experienced MES (Manufacturing Execution System) Consultants with strong backgrounds in Electronic Batch Records (EBR) and Master Batch Record (MBR) design, along with hands-on recipe authoring experience. This is a remote position, ideal for professionals with a solid understanding of GMP-regulated environments, especially in pharmaceutical or biotech manufact
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Posted 2 days ago

LIMS and QC Applications Consultant

Expedite Technology Solutions

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Remote or Bridgewater, New Jersey, USA

Full-time, Contract

Solution Architecture and Design: Lead the design and development of LabVantage LIMS solutions tailored to business and laboratory needs. Develop system workflows, configurations, and integrations with other enterprise systems (e.g., S4 Hana ERP, MES, ELN, SDMS). Define data models, interface designs, and system configurations. Implementation and Deployment: Oversee installation, configuration, and validation of LabVantage LIMS applications. Develop and execute project plans, ensuring timely an
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Posted 28 days ago | Updated moments ago

Serialization Execution System

KK Associates

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Indianapolis, Indiana, USA

Full-time, Third Party, Contract

Position:- :- Serialization Execution System (Validation) Location: - Indianapolis, IN JD:- SCADA, PLC, Systech, Serialization, Automation, Packaging line and vision systems Provide tier2 support to the Serialization Execution System. Assist existing teams in software qualification and validation activities and further assist the Serialization support team in managing serialized lines. Develop a global, repeatable, and logical process to effectively resolve any issues arising from the instal