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Fulltime Msat Process Engineer Jobs in Indiana (NOW HIRING)

Ambu

Engineer, Process

Noblesville, IN · On-site

Production, NV - IE Employment Type: Full-time Req ID: 10361 Objective: Responsible for engineering related support of manufacturing equipment and processes including continuous improvement, scrap ...

Eli Lilly and Company

Process Safety Lead

Indianapolis, IN · On-site

$98K - $128K/yr

The Engineering Technology Center (ETC) is a group of skilled engineering practitioners who possess ... Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly ...

Eli Lilly and Company

Process Safety Lead

Indianapolis, IN · On-site

$98K - $128K/yr

The Engineering Technology Center (ETC) is a group of skilled engineering practitioners who possess ... Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly ...

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Fulltime Msat Process Engineer information

What engineers make $200,000 a year?

Fulltime MSAT Process Engineers typically do not earn $200,000 annually; such high salaries are more common in senior or specialized engineering roles like software engineers, petroleum engineers, or aerospace engineers with extensive experience, advanced skills, and often in leadership positions. Compensation varies based on industry, location, and level of expertise, with some senior engineers in high-demand fields reaching or exceeding this salary level.

What engineers make $300,000 a year?

Senior engineers in specialized fields such as software engineering, petroleum engineering, and certain aerospace engineering roles can earn $300,000 or more annually, especially with extensive experience, advanced skills, and leadership responsibilities. High compensation often involves working in high-demand industries, holding managerial or executive positions, or possessing rare expertise and certifications.

What does an MSAT engineer do?

An MSAT (Manufacturing Science and Technology) engineer is responsible for supporting the manufacturing process of biopharmaceutical products, ensuring process consistency, troubleshooting issues, and optimizing production methods. They often work with process development, validation, and equipment calibration, using tools like chromatography and bioreactors. The role requires strong technical skills, knowledge of GMP regulations, and collaboration with cross-functional teams.

What engineer makes $500,000 a year?

Fulltime MSAT Process Engineers typically do not earn $500,000 annually; such high salaries are more common in executive or specialized roles within the tech industry. Engineers in high-level management, senior technical leadership, or with extensive experience and unique skills may reach this level, often supplemented by bonuses or stock options.
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Fulltime Msat Process Engineer jobs near you
Principal MSAT Engineer (AVI & Device)

Principal MSAT Engineer (AVI & Device)

INCOG BioPharma Services

Fishers, IN • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

The Principal MSAT Engineer for Automated Vision Inspection & Device is an exciting role in a fast-growing team with lot of growth opportunities. This role is responsible for overseeing and enhancing the visual inspection program to ensure the highest quality standards for Biopharmaceuticals products. This role involves providing expert guidance on inspection methodologies, leading training programs, optimizing systems, and ensuring compliance with regulatory requirements. The person in this role will also leverage in-depth technical knowledge and strong analytical skills to drive product quality and patient safety.

Essential Job Functions:

• Lead the design, development, and implementation of risk-based strategies for visual inspection of different products (e.g., syringes, cartridges, vials)

• Serve as go-to expert on visual inspection processes, equipment and quality standards.

• Conduct root cause analysis and implement corrective and preventive actions (CAPA) for quality-related events.

• collaborate with cross-functional teams involving process engineering, operations, quality assurance to identify and implement process improvements.

• Ensure compliance with FDA and global regulatory bodies by keeping inspection processes and documentation up to date.

• Act as a subject matter expert for the development and maintenance of internal strategy documents and execution documents to support visual inspection programs.

• Participate in internal and external audits, providing expert insights and support.

• Explore and evaluate new technologies and methodologies in visual inspection.

Special Job Requirements:

• Bachelor’s degree in Chemistry, Engineering, or a related field; Advanced degree preferred.

• 10+ years of experience working in a GMP-regulated environment

• 5+ years of experience in visual inspection for biopharmaceutical products

• In-depth knowledge of visual inspection standards, practices, and equipment

• Familiarity with regulatory guidance (FDA, EMA) and experience in regulatory inspections.

Additional Preferences:

• Proven record of developing training programs and mentoring inspection team

• Experience with automated visual inspection systems


Additional info about INCOG BioPharma Services:

At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business.

If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus.

INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics.

By submitting your resume and details, you are declaring that the information is correct and accurate.

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