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Eu Jobs in Indiana (NOW HIRING)

BSI Prof Serv EHS West

Familiarity with the Medical Devices Regulation (EU)2017/745 and/ or Medical Devices Directive 96/42/EEC is an advantage. * At minimum, an awareness of the requirements of IEC 60601 family of ...

BSI Group

Familiarity with the Medical Devices Regulation (EU)2017/745 and/ or Medical Devices Directive 96/42/EEC is an advantage. * At minimum, an awareness of the requirements of IEC 60601 family of ...

IntelliPro Group Inc.

IT Engineer

Whitestown, IN · On-site

We continue leading global talent solutions with a dynamic presence in over 160 countries, including the USA, China, Canada, Singapore, Japan, Philippines, UK, India, Netherlands, and the EU.

IntelliPro Group Inc.

IT Engineer

Whitestown, IN · On-site

$25 - $30/hr

We continue leading global talent solutions with a dynamic presence in over 160 countries, including the USA, China, Canada, Singapore, Japan, Philippines, UK, India, Netherlands, and the EU.

Codis

Quality Associate

Seymour, IN · On-site

The Quality Associate performs all activities in accordance with Codis' Standard Operating Procedures (SOPs) and applicable regulations (FDA, EU, USP/NF, etc.). Primary Responsibilities * Perform and ...

Codis

Quality Associate

Seymour, IN · On-site

The Quality Associate performs all activities in accordance with Codis' Standard Operating Procedures (SOPs) and applicable regulations (FDA, EU, USP/NF, etc.). Primary Responsibilities * Perform and ...

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Eu information

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$38.5K

$90.8K

$131.8K

How much do eu jobs pay per year?

As of Aug 20, 2026, the average yearly pay for eu in Indiana is $90,790.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,900.00 and $106,600.00 per year, depending on experience, location, and employer.

What are EU jobs?

EU jobs refer to employment opportunities within the institutions, agencies, and bodies of the European Union. These jobs can range from policy development and administration to translation, law, finance, and technical roles. EU jobs are typically based in major cities such as Brussels, Luxembourg, and Strasbourg, but can also be found across member states. Positions are open to citizens of EU member countries and often require multilingual skills, relevant qualifications, and sometimes passing a competitive selection process. Working for the EU offers attractive benefits, job security, and the chance to contribute to European policymaking and integration.

What are some common challenges faced by EU policy analysts when working on cross-border legislative projects?

EU Policy Analysts often encounter challenges such as navigating complex regulatory frameworks that differ across member states, coordinating with diverse stakeholders, and ensuring compliance with both national and EU-level policies. Effective communication and adaptability are crucial, as analysts frequently work in multicultural teams and must balance varying interests and priorities. Staying updated on legislative developments and building strong networks within EU institutions can help address these challenges and contribute to successful policy outcomes.

What are the key skills and qualifications needed to thrive as an EU policy analyst, and why are they important?

To thrive as an EU Policy Analyst, you need a strong background in political science, European law, or international relations, often supported by a relevant degree and fluency in multiple European languages. Familiarity with EU institutions, legislative processes, and research tools such as Eur-Lex and Eurostat is essential. Excellent analytical thinking, cross-cultural communication, and adaptability are soft skills that set candidates apart in this role. These skills ensure effective policy analysis, stakeholder engagement, and informed decision-making in the complex EU regulatory environment.

What is the difference between Eu vs Data Analyst?

AspectEuData Analyst
Required CredentialsBachelor's degree, relevant certificationsBachelor's degree, data analysis certifications
Work EnvironmentFinancial institutions, consulting firmsCorporate, tech, healthcare sectors
Industry UsageEuropean Union projects, compliance rolesData interpretation, reporting, insights

Eu professionals typically focus on European Union regulations and compliance, often requiring similar credentials as Data Analysts. While Data Analysts interpret data across various industries, Eu roles are more specialized in EU-related policies and standards. Both roles involve analytical skills, but their application contexts differ significantly.

What are the most commonly searched types of Eu jobs in Indiana?

The most popular types of Eu jobs in Indiana are:

What are popular job titles related to Eu jobs in Indiana?

For Eu jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Eu jobs in Indiana look for?

The top searched job categories for Eu jobs in Indiana are:

Eu jobs near you
Infographic showing various Eu job openings in Indiana as of August 2026, with employment types broken down into 78% Full Time, 18% Part Time, 1% Temporary, and 3% Contract. Highlights an 81% Physical, 7% Hybrid, and 12% Remote job distribution, with an average salary of $90,790 per year, or $43.6 per hour.

Senior Principal QA - Supplier & Material Management, Gene Therapies

Eli Lilly and Company

Lebanon, IN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 17 days ago

Eli Lilly and Company rating

8.8

Company rating: 8.8 out of 10

Based on 63 frontline employees who took The Breakroom Quiz

11th of 86 rated pharmaceutical

Job description

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work-but it's work worth doing. If you're driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.
Position Overview:
The Sr. Principal - Materials and Supplier Management QA provides technical and administrative leadership for materials and supplier quality systems across Lilly's Advanced Therapies pharmaceutical manufacturing site. This role leads the start-up and routine operation of QA functions overseeing Materials Management and Logistics operations, including supplier governance, warehouse quality support, and regulatory compliance. The role partners cross-functionally with supply chain, procurement, customer service, and warehouse operations to ensure materials and suppliers meet Lilly Quality Standards.
Key Responsibilities:
Leadership & Quality Culture
  • Work with the Associate Director of Quality Assurance to support the development of the vision, strategy, and quality culture for the overall site QA organization, with focus on materials management, supplier and service provider governance, and logistics activities.
  • Foster a strong quality culture including maintaining open communications and promoting teamwork and employee participation in the work group.
  • Support a safe work environment, including supporting and leading safety efforts for your team and adhering to HSE corporate and site goals.

Materials & Supplier Management
  • Establish and maintain the site material supplier program, partnering with other Lilly manufacturing sites and global materials management teams.
  • Develop and maintain the approved supplier list, Quality Agreements, material and supplier risk assessments, and periodic reviews of supplier performance.
  • Coordinate and write Supplier, Service Provider, and Affiliate Quality Agreements, ensuring compliance with associated requirements.
  • Provide input, guidance, and recommendations for supplier/service provider approval and certification activities.
  • Responsible for materials and supplier complaint handling; maintain complaint database and track supplier responses.
  • Provide quality assurance support to the warehouse and logistics for all operational needs, including incoming material receipt, sampling, testing, and material approvals.
  • Network with cross-functional resources to ensure establishment of the materials management quality system and facilitate facility (e.g., warehouse) qualification.
  • Serve as technical resource to review and approve materials management documents (e.g., qualification documents, change controls, procedures, quality agreements).
  • Review and approve GMP documentation including procedures, deviations, technical reports, specifications, and change controls.
  • Provide input and guidance for site activities (e.g., new product/process development, tech transfer, change controls) as materials/vendor management quality SME.
  • Perform materials SAP data steward functions.
  • Support regulatory inspection activities by providing documentation, subject matter expertise, and inspection readiness support.
  • Demonstrate knowledge and application of US, EU, Japanese, and other applicable regulations in pharmaceutical manufacturing and material/supplier management.
  • Support development of the overall site operational readiness plan, including development of quality processes and approval of operational procedures and controls.
  • Provide subject matter expertise for material/vendor management quality during new product/process development and technology transfers.

Basic Requirements:
  • Bachelor's degree in a science, engineering, or pharmaceutical-related field of study, or equivalent industry experience.
  • Must have prior experience in Gene and Cell Therapies.
  • 9+ years in pharmaceutical Quality Assurance, including specific Materials QA experience.
  • 3+ years of experience working with and managing suppliers and materials in a regulated environment.
  • 1+ years of experience with SAP or other inventory/material management systems
  • Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.

Additional Skills / Preferences:
  • Demonstrated knowledge of US, EU, Japanese, and other applicable regulations in pharmaceutical manufacturing and material/supplier management.
  • Excellent interpersonal, written, and oral communication skills.
  • Strong technical aptitude and ability to train and mentor others.
  • Demonstrated problem-solving and decision-making skills.
  • Strong knowledge of Quality Management Systems and applicable regulatory requirements.
  • Previous experience with material management computer systems, including SAP, Veeva QDocs, TrackWise, or similar systems.
  • Demonstrated technical writing skills.
  • Previous facility or area start-up experience.
  • Previous regulatory inspection readiness and inspection execution experience.
  • Previous experience with deviation and change management systems.

Additional Information:
  • Position Location: US: Lebanon IN LP2
  • Travel Percentage (%): Position may require travel (10-25%) or potentially a short duration assignment at another Lilly site to establish material management system knowledge
  • Shift Information: Ability to work 8-12 hour days - Monday through Friday at the Lebanon, Indiana gene therapy site

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women's Initiative for Leading at Lilly (WILL).
Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is
$65,250 - $169,400
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
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About Eli Lilly

Sourced by ZipRecruiter

Eli Lilly, based in Indianapolis, IN, US, is one of the pioneers in the pharmaceutical industry with a rich history dating back to 1876. This global pharmaceutical company focuses on discovering, developing, manufacturing and selling pharmaceutical products in approximately 120 countries. The company's product categories include endocrinology, oncology, cardiovascular, neuroscience, and immunology. Having invested over $9 billion in research and development in the past decade, Eli Lilly is also committed to creating high-quality medicines that meet real needs. As a recipient of several awards and recognitions, Eli Lilly is known for its focus on life-saving research and drug development. Their mission is to make medicines that help people live longer, healthier, and more active lives.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Indianapolis, IN, US

Year founded

1876

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