Top 40 Quality assurance associate ii Jobs in Indianapolis, In

Associate Director-Quality Assurance-Site Data Integrity
Eli Lilly —Indianapolis, IN
- $115,500 - $169,400 a year
- Full-time
- Management
- 5 years
- System design
- Health insurance
- Dental insurance
8d
Associate Director, Quality Assurance (Clinical Research Preferred)
IQVIA —Indianapolis, IN
- $88,600 - $246,600 a year
- Full-time
- Remote
- Nursing
- Bachelor's degree
- Mentoring
- Work from home
Quality Assurance Analyst II
Katalyst Healthcares & Life Sciences —Indianapolis, IN
- Contract
- Mid-level
- Continuous improvement
- Communication skills
Quick Apply
QA Engineer II
Vignesh Technological Solutions —Indianapolis, IN
- Computer Science
- Mid-level
- Under 1 year
Associate Director-Quality Assurance-Site Data Integrity
Information Technology Senior Management Forum —Indianapolis, IN
- $115,500 - $169,400 a year
- Full-time
- 5 years
- System design
- English
- Health insurance
- Dental insurance
7d
Sr. Associate, QA Analytical (R2 – R3)
Eli Lilly —Indianapolis, IN
- $155,126.00 - $178,394.90 a year
- Full-time
- Mid-level
- Travel
- 1 year
- Health insurance
- Dental insurance
QA Analyst II
Vignesh Technological Solutions —Indianapolis, IN
- Computer science
- Oracle
- Computer Science
Sr. Principal Associate, Flow Mentor, Manufacturing Quality Assurance - Lilly Medicine Foundry
Eli Lilly —Indianapolis, IN
- $65,250 - $169,400 a year
- Weekends as needed
- 5 years
- Bachelor of Science
- Engineering
- Health insurance
- Dental insurance
Sr. Principal Associate - GQA Advisor
Eli Lilly —Indianapolis, IN
- $65,250 - $169,400 a year
- Full-time
- Bachelor of Science
- Office
- Bachelor's degree
- Paid holidays
- Disability insurance
Site QC Head (Associate Director)
Novartis —Indianapolis, IN
- $138,600 - $257,400 a year
- Full-time
- 5 years
- Organizational skills
- Experience equivalent to degree accepted
- Health insurance
- 401(k) matching
Quality Assurance Associate - 1st Shift
Hyster-Yale Group —Avon, IN
- Full-time
- Forklift
- High school diploma or GED
- Ability to lift 50 pounds
- Profit sharing
- Health insurance
Quality Assurance Associate - 1st Shift
Hyster-Yale Materials Handling —Avon, IN
- Full-time
- Background check
- 5 years
- Forklift
- Health insurance
- Dental insurance
Quick Apply
2d
Associate, MFG Quality
Adidas —Indianapolis, IN
- $19.15 an hour
- Overtime
- Computer literacy
- Basic math
- English
- Paid parental leave
- Health savings account
QUALITY SUPERVISOR II
Pilkington North America Inc. —Shelbyville, IN
- Monday to Friday
- Computer literacy
- Mid-level
- 3 years
Quick Apply
Associate Quality
FedEx Supply Chain, Inc —Indianapolis, IN
- Ability to walk for extended periods
- 5 years
- Engineering
- Paid jury duty
- Paid parental leave
2d
Senior Specialist, Quality Control Chemist II (2nd Shift)
Cardinal Health —Indianapolis, IN
- $68,500 - $88,020 a year
- Monday to Friday
- Microsoft Word
- Ability to walk for extended periods
- Mid-level
- Paid parental leave
- Health savings account
QC Inspector II
Abbott Laboratories —Westfield, IN
- $14.55 - $29.15 an hour
- Full-time
- Mid-level
- High school diploma or GED
- Warehouse
- Health insurance
- Tuition reimbursement
2d
QA Associate, 3rd Shift
INCOG BioPharma Services —Fishers, IN
- Full-time
- Mid-level
- Office
- Bachelor's degree
Quality Assurance Associate_Shift_1
Neovia —Greenwood, IN
- $18.45 an hour
- Basic math
- High school diploma or GED
- Bachelor's degree
Quick Apply
Quality Control Specialist II
AeroSafe Global —Indianapolis, IN
- $22 - $28 an hour
- Full-time
- Bachelor of Science
- Mid-level
- Bachelor's degree
- Health savings account
- AD&D insurance
Quick Apply

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Associate Director-Quality Assurance-Site Data Integrity

Eli Lilly -
Indianapolis, IN

Apply Now

Job Details

Full-time
$115,500 - $169,400 a year
8 days ago

Benefits

Health insurance
Dental insurance
401(k)
Flexible spending account
Employee assistance program
Vision insurance
Life insurance

Qualifications

Data integrity assurance
Content creation for technical audiences
Management
Technical documentation
Pharmaceutical regulatory compliance
English
GMP
Project management experience in manufacturing
Inclusive leadership practices
Data quality management
Manufacturing facility experience
Data integrity and documentation
Pharmaceutical company experience
Project management experience in healthcare
Quality standards in production
Collaboration with manufacturing teams
Manufacturing
Technical writing experience within technology
Legal compliance
Cross-functional communication
Pharmaceutical manufacturing facility experience

Full 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.

Job Description

The Site Data Leader will have primary responsibility for data management activities within the site. This includes data integrity. He/she will be an advocate for data management across the manufacturing site and will chair the site data lead team.

The Site Data Leader will ensure that a robust Data Integrity Program exists within the site providing strong project management leadership to advance the site’s agenda. This requires interface with the Manufacturing & Quality (M&Q) Data Management organization, serving as a global data management subject matter expert to facilitate and drive improvements in M&Q data-related corporate quality standards, business processes, organizational design, and governance necessary for ongoing data integrity effectiveness.

This role will partner with functional area data experts to anticipate and resolve key data management and integrity issues while driving solutions that impact the site and align with corporate objectives. This role will leverage a deep understanding of GMP data flows (electronic and paper), the application of data management and integrity principles in operational processes, and Computer System Validation methodologies to ensure regulatory compliance, consistency, and sustainment.

This role will be responsible for ensuring the site’s data integrity training program facilitates the sustainment of its data integrity continuous improvement journey. The Site Data Leader will also be responsible for advancing data management standards to ensure consistency and consumability of data to drive process improvements.

Job Requirements

Experience in leading inspection readiness with effective results obtained through interaction/discussion with regulatory officials related to data integrity expertise in areas as necessary.
Demonstrated proficiency in planning and the ability to carry out tasks with a high degree of independence as well as being able to work in a team environment.
Strong project management and organizational skills are a must.
Demonstrated ability to interpret and apply standards to different situations by understanding site needs and applying good problem-solving skills.
Demonstrated ability to write technical documents, develop business presentations and effectively communicate concepts to a wide range of personnel including senior leadership.
Ability to influence and contribute to strategy and agenda in the area of data integrity.
Strong knowledge and technical expertise in areas of cGMPs, production practices, and quality systems.
Recognized understanding of regulations governing data integrity.
Ability to build relationships across dimensions of difference, ask questions & invite others to contribute.
Demonstrated business acumen.
Speak up with ideas as well as concerns and ensure the psychological safety of others.
Demonstrated learning agility and ability to think creatively; try new ideas and apply learnings.
Highly motivated, enthusiastic to learn and share ideas and solutions effectively with management and colleagues.
Strong collaboration with colleagues at all levels.
Demonstrated courage & integrity.
Demonstrated success in influencing without authority.
Ability to take initiative, to be assertive, to lead by example and to build high-quality relationships.
Highly flexible, adapting to changes in priorities, requirements and processes is required.

Basic Qualifications

Bachelor’s degree or higher in the sciences, engineering, or related field.
Fluency in English (Read / Write) is required.
Minimum of 5 years of experience in pharmaceutical manufacturing
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 Preferences

Understanding and working knowledge of domestic and international data integrity regulations and other policies/regulations as applicable.
Understanding of IT system design, controls, and usage.
Ability to communicate effectively with all levels and functions in the organization.
Ability to work on multiple concurrent project initiative.

Other Requirements

Available to travel (domestic and international) on an average of

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
$115,500 - $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.

#WeAreLilly

Apply Now

Refine Your Search

quality assurance associate ii jobs in indianapolis, in

Associate Director-Quality Assurance-Site Data Integrity

Associate Director, Quality Assurance (Clinical Research Preferred)

Quality Assurance Analyst II

QA Engineer II

Associate Director-Quality Assurance-Site Data Integrity

Sr. Associate, QA Analytical (R2 – R3)

QA Analyst II

Sr. Principal Associate, Flow Mentor, Manufacturing Quality Assurance - Lilly Medicine Foundry

Sr. Principal Associate - GQA Advisor

Site QC Head (Associate Director)

Quality Assurance Associate - 1st Shift

Quality Assurance Associate - 1st Shift

Associate, MFG Quality

QUALITY SUPERVISOR II

Associate Quality

Senior Specialist, Quality Control Chemist II (2nd Shift)

QC Inspector II

QA Associate, 3rd Shift

Quality Assurance Associate_Shift_1

Quality Control Specialist II

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