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Director Statistical Programming Jobs in Indiana

Linamar

CMM Programmer

Albion, IN

... providing statistical reports reflecting process control, process capability and gauge ... Ability to work independently (self-directed) and in a team-oriented environment. What Linamar Has ...

Avalign Technologies

Sr. Quality Engineer

Greenwood, IN

$80.80K - $109.50K/yr

... statistical process controls to achieve required reliability and consistency. Conduct or direct ... Partner with operations and engineering to ensure strict adherence to the MRB process. Submit ...

Linamar

CMM Programmer

Albion, IN · On-site

... providing statistical reports reflecting process control, process capability and gauge ... Ability to work independently (self-directed) and in a team-oriented environment. What Linamar Has ...

Pwc

Data Strategy & Governance -Director

Indianapolis, IN · On-site

$155K - $410K/yr

You will leverage skills in data manipulation, visualisation, and statistical modelling to support ... Data Engineer / Azure Solutions Architect - Google Professional Data Engineer - DAMA CDMP ...

Culver Tool and Engineering LLC

Quality Engineer

Plymouth, IN · On-site

$65.40K - $84.50K/yr

Oversight of CMM programming schedule as directed * Participate in project management as needed ... Strong Understanding of statistical analysis * Problem-Solving prowess * Must be respectful and ...

Ametek

Senior Manufacturing Engineer

Pierceton, IN · On-site

$84.20K - $115.20K/yr

Will also direct personnel to work with operations and regulatory teams to ensure processes are ... process control methods, statistical analysis, DOE, ISO standards and FDA quality system ...

Ametek

Senior Manufacturing Engineer

Pierceton, IN

Will also direct personnel to work with operations and regulatory teams to ensure processes are ... process control methods, statistical analysis, DOE, ISO standards and FDA quality system ...

WEG Electric Corp

Mechanical Engineer

Bluffton, IN

Specify system components or direct modification of products to ensure conformance with engineering ... Statistical analysis for component tolerance stack-up requirements. * Provide feedback to sales and ...

WEG Electric Corp

Mechanical Engineer

Bluffton, IN · On-site

Specify system components or direct modification of products to ensure conformance with engineering ... Statistical analysis for component tolerance stack-up requirements. * Provide feedback to sales and ...

WEG Electric Corp

Mechanical Engineer

Bluffton, IN · On-site

Specify system components or direct modification of products to ensure conformance with engineering ... Statistical analysis for component tolerance stack-up requirements. * Provide feedback to sales and ...

Venteon

Supplier Quality Engineer

Bluffton, IN · On-site

$75K/yr

This is a Full Time, Permanent, Direct Hire Position offering Competitive Compensation, Bonus ... Proficient in Microsoft Office; experience with ERP/QMS systems and statistical software preferred.

Pwc

Payer Platform Delivery Lead, Director

Indianapolis, IN · On-site

$155K - $410K/yr

... and engineering teams - Actively engaging in business development and client collaboration ... At PwC, we recognize that conviction records may have a direct, adverse, and negative relationship ...

Placon Corporation

Quality Manager

Elkhart, IN · On-site

... statistical analysis. * Knowledge of Microsoft Office Suite. * Must be able to plan and direct one ... Supervision Engineering calculations and the ability to manage multiple priorities and complex ...

Placon Corporation

Quality Manager

Elkhart, IN · On-site

... statistical analysis. * Knowledge of Microsoft Office Suite. * Must be able to plan and direct one ... Supervision Engineering calculations and the ability to manage multiple priorities and complex ...

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Director Statistical Programming information

See Indiana salary details

$146.1K

$266.6K

$327.3K

How much do director statistical programming jobs pay per year?

As of May 30, 2026, the average yearly pay for director statistical programming in Indiana is $266,578.00, according to ZipRecruiter salary data. Most workers in this role earn between $247,900.00 and $306,900.00 per year, depending on experience, location, and employer.

What Is the Job of a Director Statistical Programming?

The job of a director of statistical programming oversees the development and implementation of SAS programs to produce statistical analysis datasets. In this career, your responsibilities include managing the team that generates tables and graphs using the SAS programs for applications such as clinical studies. Other duties include participating in the planning and review of statistical analysis and studying reports, abstracts, and manuscripts as required. You collaborate with project leads to contribute to department operations and standards, such as CDISC for clinical research.

What are the key skills and qualifications needed to thrive as a Director of Statistical Programming, and why are they important?

To thrive as a Director of Statistical Programming, you need advanced expertise in statistical analysis, programming languages such as SAS or R, and a strong background in clinical trial data, typically supported by a degree in statistics, mathematics, or a related field. Familiarity with regulatory submission processes, CDISC standards, and project management tools is essential, as are relevant certifications like SAS Certified Professional. Leadership, effective communication, and strategic thinking are key soft skills for managing teams and collaborating across departments. These skills ensure high-quality data outputs, regulatory compliance, and successful execution of complex clinical development projects.

How does a Director of Statistical Programming typically collaborate with cross-functional teams in a pharmaceutical or biotech company?

A Director of Statistical Programming regularly works with biostatistics, clinical data management, regulatory affairs, and medical writing teams to ensure that statistical deliverables meet project timelines and regulatory requirements. They coordinate programming efforts across multiple studies, provide leadership and mentorship to programming staff, and help resolve technical or resource-related challenges. Effective collaboration is essential to streamline workflows, maintain data integrity, and ensure clear communication of statistical results within the organization.

What does a Director of Statistical Programming do?

A Director of Statistical Programming oversees teams responsible for the programming and analysis of clinical trial data, ensuring the accuracy and integrity of statistical outputs. They set departmental strategies, manage resources, and ensure compliance with regulatory requirements and industry standards. This role also involves collaborating with other departments, such as biostatistics and clinical operations, to support the successful delivery of statistical analyses for drug development and regulatory submissions. They play a key leadership role in mentoring staff and advancing programming processes and technologies.
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Director Statistical Programming jobs near you
Infographic showing various Director Statistical Programming job openings in Indiana as of May 2026, with employment types broken down into 9% As Needed, 78% Full Time, 9% Part Time, 3% Contract, and 1% Summer. Highlights an 74% Physical, 8% Hybrid, and 18% Remote job distribution, with an average salary of $266,578 per year, or $128.2 per hour.
Senior/Principal Process Engineer - API External Manufacturing Peptides

Senior/Principal Process Engineer - API External Manufacturing Peptides

Eli Lilly and Company

Indianapolis, IN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 days ago

Eli Lilly and Company rating

8.8

Company rating: 8.8 out of 10

Based on 62 frontline employees who took The Breakroom Quiz

11th of 70 rated pharmaceutical

Job description

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.
Position Brand Description:
The position of API EM Engineer [Synthetic Peptide Synthesis and Purification] reports to the API EM Engineering Associate Director and provides technical leadership and expertise in conjunction with API EM contract manufacturer personnel in the reliable supply and commercialization of medicines with safety first and quality always by:
  • Developing and sustaining process knowledge in order to ensure the execution of the appropriate product, process, and operational control strategy at a number of Contract Manufacturers (CMs)
  • Direct and Indirect interaction with CM personnel to ensure reliable supply via the CM execution of the operational control strategy
  • FUME assessment to ensure an understanding of risk presented to the operational control strategy
  • Participation with internal or CM resources in the equipment specification, procurement, and IQ/OQ/PQ
  • Participation with internal and CM resources to assess the HSE and PSM elements of the CM that impact Lilly products
  • Engaged with internal and external resources in developing capabilities with new or evolving technologies that may impact delivery of internal or external portfolio assets.
  • Adherence to the expectations of the Lilly Red Book when carrying out interactions with API EM's CMs.

Key Objectives/Deliverables:
Coach and Mentor Process Team Members
  • Utilize past experiences with unit operation control to provide insight and feedback to members of the CM Joint Process Team (JPT).
  • Champion the application of statistical thinking and use of data to monitor process performance and make engineering decisions with CM members of the JPT.
  • Support and peer review root cause analysis around FUME and operational incidents.
  • Peer review documentation of learning points, technical studies, and incident investigations.

Scale-Up & Tech Transfer
  • Lead/support tech transfers and scale-up from development through PV and commercial supply.
  • Translate process intent into operating strategies, equipment fit/gap, batch documentation, and PV readiness at CMs.
  • Support engineering runs and PV readiness through parameter optimization and performance trending.

Develop and Sustain Process Knowledge
  • Identify process knowledge gaps that impact equipment and process capability.
  • Develop or support the capture of key process knowledge (examples include material and energy balances, kinetics, chemistry, process modeling, and equipment design basis).
  • Enable the development and maintenance of process knowledge. infrastructure such as key models, report history, lab models, and literature.
  • Utilize optimization resources and tools for process analysis and process improvement studies.
  • Review and track key process engineering metrics.

Provide Process & Equipment Support
  • Identify systemic issues affecting production and reliable supply from CMs
  • Lead or participate in root cause analysis and countermeasure development and implementation for major safety, quality, or throughput incident investigations. Perform reviews of incident documentation for technical accuracy.
  • Review and approve documentation and engineering decisions.

Process Optimization & Continuous Improvement
  • Support development and technical analysis for on-going continuous improvement activities.
  • Review and identify cost reduction opportunities, as well as process capacities and bottlenecks. Assist in prioritization of opportunities with respect to overall business objectives.
  • Work with the CMs to ensure the application of statistical thinking and methods to understand process variability and capability.
  • Perform and promote optimization of unit operation cycle time, loading, and yield performance.
  • Engage with late phase development and Engineering Technical Center resources to ensure staying contemporary with key engineering disciplines and developing portfolio platforms (e.g. continuous manufacturing operations).

Equipment Capability and Asset Management
  • Create an appropriate methodology to ensure visibility of the ongoing state of qualification of key FUME systems at the CMs.
  • Review equipment and process system user requirements and qualification plans to ensure that the equipment and systems are appropriate for the intended purpose.
  • Act as customer representative for review of Contact Manufacturer (CM) requests for capital projects targeted at both short and long term needs.

Oversight of HSE and PSM
  • Serve as the liaison for API EM and Global HSE on health, safety, and environmental (HSE) and process safety management (PSM) oversight at the relevant contract manufacturing sites.
  • Leverage internal Lilly experts in HSE and PSM to ensure appropriate risk reduction at CMs.
  • Participate in Lilly HSE and PSM audits of contract manufacturing sites as applicable.
  • Maintain key HSE and PSM metrics for review within API EM.

Adherence to Business, Quality, and Financial Systems
  • Understand and follow all applicable Lilly policies and procedures with respect to interactions and oversight of API contract manufacturing sites. These include but are not limited to: Financial Responsibility and Reporting (FRAP); Lilly Red Book; Lilly contract manufacturing standards; Lilly engineering standards, and Lilly Quality policies and best practices.

Basic Requirements:
  • Bachelor of Science degree in Chemical Engineering, or another engineering discipline with 5 years chemical manufacturing experience.
  • 3+ years of work experience in a manufacturing/process engineering related to peptides or small molecules
  • Demonstrated experience in scale-up and/or technology transfer (internal plant or external CMO).
  • 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:
  • Experience with SM and/or peptide unit operations and purification/isolation steps relevant to drug substance manufacturing.
  • Experience in typical unit operations for API Manufacturing manufacturing.
  • Deep technical knowledge of API / Drug Substance manufacturing equipment and unit operations.
  • Demonstrated ability to apply fundamental chemical engineering principles to process understanding, problem solving, and process improvement.
  • Demonstrated ability to function in a team environment as a technical leader and as a member of teams.
  • Demonstrated ability to manage and prioritize competing priorities and to appropriately communicate verbally and in writing to various audiences.
  • Develop and implement innovative approaches to problems
  • Process Hazard Analysis experience
  • Successful application of root cause analysis and systematic problem solving
  • Strong Computer skills in a variety of software packages ( e.g Batch Plus, JMP, Visio, Aspen, Dynochem, OSI PI, MS Office Suite).
  • Visualize an operation/process and reflect it in a model.

Other Information:
  • The normal schedule for this position is Monday-Friday, 8 hours/day. However, teleconferences may routinely occur outside of these hours due to the time zones of contract manufacturers. OUS travel may routinely be required to support process start-ups, troubleshooting, and commercial manufacturing. This travel is typically in the range of 15% to 25% annually, depending on the needs of the process(s).
  • Must complete assigned training curriculum.
  • No certifications required.
  • Tasks require entering manufacturing and laboratory areas and will require wearing appropriate PPE.

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 Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.
Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is
$66,000 - $171,600
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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