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Program Control Manager Jobs in Indiana (NOW HIRING)

Implements shipping program, coordinates physical distribution, order fulfillment, inventory management and control, and contract management activities. * Performs a combination of manual and ...

Oversee welder, fitting, rubber lining, and painting training programs. * Witness and document ... Collaborate closely with production and management teams to drive quality and safety improvements.

Inventory Control Lead

Mooresville, IN · On-site

$24.13 - $27.16/hr

... Inventory Control program. Develop and maintain productive, effective, and professional ... Support the Inventory Control Supervisor and Manager, ensuring the processes and procedure of the ...

Inventory Control Lead

Mooresville, IN · On-site

$24.13 - $27.16/hr

... Inventory Control program. Develop and maintain productive, effective, and professional ... Support the Inventory Control Supervisor and Manager, ensuring the processes and procedure of the ...

Showing results 41-60

Program Control Manager information

See Indiana salary details

$33.7K

$101.7K

$160.1K

How much do program control manager jobs pay per year?

As of Sep 13, 2026, the average yearly pay for program control manager in Indiana is $101,669.00, according to ZipRecruiter salary data. Most workers in this role earn between $67,300.00 and $130,800.00 per year, depending on experience, location, and employer.

How does a program control manager collaborate with project managers and finance teams to ensure successful program delivery?

Program Control Managers work closely with project managers to track project progress, monitor budgets, and manage schedules. They regularly coordinate with finance teams to ensure accurate forecasting, cost reporting, and compliance with financial policies. This collaborative approach helps identify potential risks or issues early, allowing for proactive solutions that keep programs on track. Open communication and cross-functional teamwork are essential for aligning program objectives with organizational goals and ensuring successful outcomes.

What are the key skills and qualifications needed to thrive as a program control manager, and why are they important?

To thrive as a Program Control Manager, you need strong analytical abilities, expertise in project management, and a background in finance or business administration, often supported by a relevant degree. Familiarity with project management software (such as Microsoft Project or Primavera), Earned Value Management Systems (EVMS), and certifications like PMP or PMI-SP is typically expected. Excellent communication, attention to detail, and problem-solving skills enable effective collaboration and proactive risk management. These skills ensure accurate project tracking, budget adherence, and successful delivery of program objectives.

What is the difference between Program Control Manager vs Project Scheduler?

AspectProgram Control ManagerProject Scheduler
Primary FocusOverseeing program budgets, schedules, and performance metricsDeveloping and maintaining project timelines and schedules
Required CredentialsTypically requires project management certifications (PMP), experience in program oversightOften requires scheduling software proficiency, certifications like PMI-SP
Work EnvironmentStrategic, cross-project coordination, often in corporate or government sectorsDetailed schedule planning, often within project teams
Industry UsageCommon in large-scale programs, defense, aerospace, constructionUsed across various industries for individual projects

The Program Control Manager and Project Scheduler roles are related but distinct. The Program Control Manager oversees multiple projects, focusing on overall program performance, budgets, and schedules, often requiring broader management skills and certifications. The Project Scheduler concentrates on creating and maintaining detailed project timelines. Both roles are essential for successful project delivery but serve different levels of project management within organizations.

What does a program control manager do?

A program control manager oversees the planning, monitoring, and controlling of large projects or programs to ensure they meet scope, schedule, and budget goals. They develop schedules, track progress, analyze variances, and implement corrective actions, often using tools like earned value management systems. Strong organizational, analytical, and communication skills are essential for success in this role.

What cities in Indiana are hiring for Program Control Manager jobs?

Cities in Indiana with the most Program Control Manager job openings:

Infographic showing various Program Control Manager job openings in Indiana as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 18% Part Time, and 4% Contract. Highlights an 96% Physical, 2% Hybrid, and 2% Remote job distribution, with an average salary of $101,669 per year, or $48.9 per hour.

Sr. Manager/Associate Director, Analytical Development & Quality Control

Indianapolis, IN • Hybrid

Genezen
Biotechnology Research and Development • 51 - 200 employees

Full-time

Posted 25 days ago


Job description

JOB SUMMARY

The Senior Manager/Associate Direct, Analytical Development & Quality Control provides scientific, and operational leadership for analytical development and QC functions supporting viral vector programs (AAV, LVV, RVV). This role is accountable for integrating Analytical Development and Quality Control into a unified, phase-appropriate analytical lifecycle that supports both scientific innovation and GMP execution. This role is responsible for coordinating phase-appropriate analytical lifecycle activities that support method development, GMP execution, regulatory readiness, and data integrity.

This role partners across Analytical Development, Quality Control, Quality Assurance, Regulatory Affairs, Manufacturing, and Process Development to ensure analytical activities are aligned with program needs, GMP expectations, and inspection readiness requirements

ESSENTIAL JOB FUNCTIONS

Analytical Development & Lifecycle Management

  • Manage and support analytical method development, qualification, validation, transfer, and lifecycle activities in alignment with ICH Q2/Q10/Q14 principles and program requirements.
  • Implement and maintain method transfer processes, including acceptance criteria, readiness assessments, documentation, and ongoing performance monitoring.
  • Contribute to the development and optimization of analytical platforms and reference standards supporting viral vector characterization.
  • Support development and execution of sampling strategies to ensure representative, compliant testing and clear alignment with program and quality requirements.

Quality Control Operations & Stability

  • Lead QC laboratory operations supporting in-process, release, and stability testing.
  • Provide technical decision authority for analytical readiness, method suitability, and QC support of batch disposition.
  • Oversee stability strategies, including protocol design, trending, and shelf-life justification.
  • Direct investigations (OOS, OOT, deviations) and ensure effective CAPA implementation.
  • Ensure QC operations maintain appropriate independence and objectivity in support of quality decisions.

Laboratory & Shared Infrastructure Governance

  • Own governance of shared laboratory infrastructure, including equipment lifecycle management, scheduling prioritization, and resource allocation.
  • Ensure appropriate segregation and controls for GMP and non-GMP activities within shared laboratory spaces. 

Microbiology, EM & Contamination Control

  • Serve as SME for aseptic processing, contamination control, and microbiological monitoring.
  • Oversee environmental monitoring programs, trending, and control strategies.
  • Ensure microbiological controls support product quality and regulatory compliance.

Regulatory Compliance & Inspection Readiness

  • Ensure compliance with cGMP, GLP, FDA, EMA, and applicable regulatory requirements.
  • Serve as primary SME during regulatory inspections and client audits for analytical and QC functions.
  • Support regulatory filings, responses, and analytical justification strategies.
  • Maintain continuous inspection readiness across laboratory operations.

Data Integrity, Systems & Continuous Improvement

  • Oversee LIMS, analytical systems, and data integrity (ALCOA+, Part 11) across all laboratory functions.
  • Implement digital solutions, automation, and process improvements to enhance efficiency and compliance.
  • Establish and monitor performance metrics (e.g., turnaround time, right-first-time, deviation trends).

Client & Cross-Functional Leadership

  • Act as executive scientific partner for clients and internal stakeholders.
  • Drive alignment across Process Development, Manufacturing, QA, and RA on analytical strategy and readiness.
  • Support proposals, scope definition, and client program execution.
  • Lead analytical aspects of technology transfer and commercialization.

Organizational Leadership

  • Lead a hybrid organization with direct oversight of QC and indirect leadership of AD via scientific leads.
  • Build and develop high-performing teams through coaching, performance management, and succession planning.
  • Establish a culture of scientific excellence, accountability, and continuous improvement.

 KNOWLEDGE, SKILLS, AND EXPERIENCE

EDUCATION / CERTIFICATIONS / LICENSES

Essential/Desired

BS in Molecular Biology, Biochemistry, Chemistry or related field

Essential

MS in Molecular Biology, Biochemistry, Chemistry or related field

Desired

ON-THE-JOB EXPERIENCE

 

Minimum 4 years in a leadership role

Essential

Minimum 8 - 10 years progressive experience in analytical development, quality control, or related discipline within biopharma or CDMO environments

Essential

Extensive experience supporting viral vector products across clinical development phases and regulatory submissions

Essential

Demonstrated success leading analytical development, method validation, and QC Operations in a cGMP environment

Essential

SKILLS / ABILITIES

 

Strong understanding of analytical methods used for viral vector characterization including:

  • qPCR and ddPCR
  • ELISA
  • Flow cytometry
  • Cell-based potency assays
  • Genome integrity assays
  • Empty/full capsid analysis

Essential

Extensive knowledge of cGMP, GLP, FDA, EMA, and ICH requirements.

Essential

Excellent communication skills and ability to thrive in fast paced, dynamic environment

Essential

Experience with environmental monitoring programs, contamination control, and aseptic manufacturing support.

Essential

Familiarity with laboratory systems, LIMS, data integrity principles, and automation technologies.

Essential

Proven leadership experience, with a track record of building and managing high-performing teams

Essential

PHYSICAL DEMANDS

While performing the duties of this job, the employee is required to meet the following physical demands:

Work Environment

  • Frequently required to work in a BSL 2 environment with personal protective equipment/aseptic gowning
  • Regularly required to work around large machinery and typical utilities seen in pharmaceutical facilities
  • Occasionally exposed to moving mechanical parts; high, precarious places; toxic or caustic chemicals; hazardous waste; and risk of electrical shock
  • Occasionally exposed to extremely loud noise levels
  • Spending time on the floor during activity execution (maintenance, construction, commissioning and qualification) is required

Movement

  •  Frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and arms
  • Occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl

Lifting

  • Frequently lift and/or move up to 10 pounds
  • Occasionally lift and/or move up to 25 pounds

Vision

  • Frequently utilize close vision and the ability to adjust focus

Communication

  • Frequently required to communicate by talking, hearing, using telephone and e-mail