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Sterile Processing Consultant Jobs in Indiana (NOW HIRING)

Red Star

Sterile Packaging Manager

IN · On-site

Partner with Operations to optimize sterile packaging equipment, manufacturing processes, and production readiness while providing technical consultation to contract manufacturing partners and ...

Red Star

Sterile Packaging Manager

Larwill, IN · On-site

Partner with Operations to optimize sterile packaging equipment, manufacturing processes, and production readiness while providing technical consultation to contract manufacturing partners and ...

Red Star

Senior Sterile Packaging Engineer

Larwill, IN · On-site

Partner with Operations to optimize sterile packaging equipment, manufacturing processes, and production readiness while providing technical consultation to customers and contract manufacturing ...

Red Star

Senior Sterile Packaging Engineer

IN · On-site

Partner with Operations to optimize sterile packaging equipment, manufacturing processes, and production readiness while providing technical consultation to customers and contract manufacturing ...

Red Star

Senior Sterile Packaging Engineer

Larwill, IN · On-site

$85 - $110/hr

Partner with Operations to optimize sterile packaging equipment, manufacturing processes, and production readiness while providing technical consultation to customers and contract manufacturing ...

Johnson & Johnson

Sr. Sterilization Scientist

Warsaw, IN · On-site

$88K - $120K/yr

... consultation processes. DePuy Synthes, is recruiting for a Senior Sterilization Scientist , to be ... located in West Chester, PA; Warsaw, IN; Raynham, MA or Palm Beach Gardens, FL . About MedTech ...

Jj

Sr. Sterilization Scientist

Warsaw, IN

$88K - $120K/yr

... consultation processes. DePuy Synthes, is recruiting for a Senior Sterilization Scientist , to be ... located in West Chester, PA; Warsaw, IN; Raynham, MA or Palm Beach Gardens, FL . About MedTech ...

Eliquent Life Sciences, Inc

CQV Engineer

Indianapolis, IN · On-site

$80K - $95K/yr

... sterilization, shipping, and processes validation and facilities, utilities, systems, equipment ... consultants. QUALIFICATIONS AND REQUIREMENTS: * Bachelors Degree in engineering, science, or ...

CYNET SYSTEMS

Fermentation Technician

Indianapolis, IN · On-site

$23/hr

Apply advanced sterile techniques for inoculating and sampling shake flasks. * Conduct fermenter ... Proactively suggest process or experimental design enhancements, and participate in continuous ...

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Sterile Processing Consultant information

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How much do sterile processing consultant jobs pay per hour?

As of Aug 25, 2026, the average hourly pay for sterile processing consultant in Indiana is $26.16, according to ZipRecruiter salary data. Most workers in this role earn between $18.99 and $31.59 per hour, depending on experience, location, and employer.

What is a sterile processing consultant?

A Sterile Processing Consultant is a healthcare professional who advises medical facilities on best practices for sterilization, decontamination, and infection control. They assess sterilization processes, ensure compliance with industry regulations, provide staff training, and recommend improvements to enhance patient safety. Their expertise helps hospitals, surgical centers, and other healthcare facilities maintain high standards in instrument reprocessing and regulatory compliance.

What are some typical challenges a sterile processing consultant faces in healthcare environments?

Sterile Processing Consultants often encounter challenges such as addressing outdated or inconsistent sterilization procedures, training staff on best practices, and ensuring regulatory compliance across various departments. They may also navigate resistance to change when introducing new technologies or process improvements. The role frequently involves cross-functional collaboration with surgical, nursing, and administrative teams to optimize workflow and maintain patient safety standards. These challenges make the role both dynamic and essential for upholding healthcare quality.

What are the key skills and qualifications needed to thrive as a sterile processing consultant?

Success as a Sterile Processing Consultant requires deep knowledge of sterilization protocols, instrument decontamination, and healthcare compliance standards, often backed by experience in sterile processing and a related certification such as CRCST or CBSPD. Familiarity with tracking systems, autoclaves, and documentation software is commonly necessary. Outstanding analytical skills, attention to detail, and the ability to communicate effectively with clinical and support staff differentiate top performers. These abilities help ensure healthcare facilities meet strict safety standards, prevent infections, and implement improvements efficiently.

What are the most commonly searched types of Sterile Processing Consultant jobs in Indiana?

The most popular types of Sterile Processing Consultant jobs in Indiana are:

What are popular job titles related to Sterile Processing Consultant jobs in Indiana?

For Sterile Processing Consultant jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Sterile Processing Consultant jobs in Indiana look for?

The top searched job categories for Sterile Processing Consultant jobs in Indiana are:

Sterile Processing Consultant jobs near you
Infographic showing various Sterile Processing Consultant job openings in Indiana as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 90% Physical, 4% Hybrid, and 6% Remote job distribution, with an average salary of $54,416 per year, or $26.2 per hour.

Sterile Packaging Manager

IN • On-site

Red Star
Restaurants • 51 - 200 employees
Learn more about Red Starexternal

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 7 days ago

Job description

ABOUT US: Red Star is a vertically integrated U.S.-based contract manufacturer specializing in injection molding, precision machining, cleanroom assembly, and sterile packaging for the medical device industry. From concept through high-volume production, our teams work together to solve complex manufacturing challenges and help bring innovative medical devices to market.
SUMMARY: The Sterile Packaging Manager leads and oversees sterile packaging activities. This role partners cross-functionally with Regulatory, Product Development, Operations, Supply Chain, and Quality to develop and execute sterile packaging strategies from concept through commercialization and post-market support. Serving as an organizational subject matter expert, this position ensures sterile packaged products meet requirements for sterility assurance, packaging integrity, shelf life, transportation, distribution, and regulatory compliance.
The Sterile Packaging Manager provides leadership for packaging design and development, validation strategy, process controls, and technical documentation, including Design History File (DHF) requirements. The role establishes procedures and standards related to sterile packaging while leading continuous improvement initiatives and developing team members and cross-functional project teams.
ESSENTIAL DUTIES AND RESPONSIBILITIES: (includes the following but other duties may be assigned)
  • Lead the strategy, development, implementation, and lifecycle management of sterile packaging designs across product lines in partnership with product development teams to ensure packaging, labeling, and sterilization requirements are achieved.
  • Lead sterile packaging activities and provide coordination for sterilization requirements for new product introductions, design changes, and sustaining engineering initiatives.
  • Oversee the design, evaluation, and approval of packaging components and sterile packaging systems for medical device products.
  • Review, approve, and maintain packaging, labeling, and related technical documentation to ensure compliance with applicable requirements.
  • Lead risk assessment activities related to product, packaging, sterilization, and process changes to maintain sterility assurance and package integrity across all applicable entities.
  • Establish validation strategies and oversee execution of sterile packaging-related validation and verification activities, including sealing validations, OQ/PQ studies, design of experiments, transit testing, aging studies, and ongoing process monitoring.
  • Ensure effective monitoring, control, and continuous improvement of sterile packaging processes across internal and external manufacturing locations.
  • Develop and maintain procedures, business processes, work instructions, and training programs related to sterile packaging and sterilization activities.
  • Provide leadership and technical oversight for creation and approval of protocols, reports, technical justifications, and validation documentation.
  • Ensure packaging validation programs remain current, effective, and compliant at all applicable facilities.
  • Lead design transfer activities and ensure critical process parameters are defined, documented, transferred, and controlled based on process capability and risk.
  • Partner with Operations to optimize sterile packaging equipment, manufacturing processes, and production readiness while providing technical consultation to contract manufacturing partners and customers as needed.
  • Manage sterile packaging project timelines, priorities, and resource allocation to support business objectives and product launch commitments.
  • Lead investigations and corrective actions associated with post-market surveillance signals, nonconformances, and quality events related to sterile packaging.
  • Represent sterile packaging functions during customer, internal, regulatory, and certification audits.
  • Supervise, coach, and develop assigned team members and provide leadership to cross-functional project teams.

QUALIFICATION REQUIREMENTS:
  • Bachelor's degree in Packaging Engineering, Packaging Science, Engineering, or related technical discipline.
  • Minimum 5-7 years of progressive experience in sterile packaging within medical device, pharmaceutical, or related regulated industry; medical device experience strongly preferred.
  • Previous experience leading projects, initiatives, teams, or direct reports preferred.

OTHER SKILLS and ABILITIES:
  • Strong leadership, project management, and cross-functional collaboration skills.
  • Knowledge of applicable standards including ISO 11607, ISO 11137, relevant ASTM standards, and quality system requirements.
  • Experience with manufacturing processes, process validation, statistical analysis, and risk management methodologies.
  • Ability to influence decision-making and drive execution across multiple stakeholders and facilities.

BENEFITS:
  • Health, dental, and vision insurance
  • Paid time off and paid holidays
  • 401(k) with company match
  • Bonus opportunities

PHYSICAL DEMANDS AND WORK ENVIRONMENT:
While performing the duties of this job, the employee is regularly required to sit, talk, and hear. The employee is frequently required to stand, walk, and use hands to handle or feel objects, tools, or controls. The employee may occasionally be required to reach with hands and arms and lift and/or move up to 20 pounds.
The employee will typically work in a manufacturing environment and may be exposed to high noise levels from machinery, moving machine parts, and other physical hazards. The physical demands and work environment characteristics described here are representative of those an employee may encounter while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

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