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Remote G Code Programmer Jobs in Monroe, MI (NOW HIRING)

THOMSON REUTERS

Lead Research Engineer

Ann Arbor, MI · On-site +1

$100K - $132K/yr

... remote teams. * Be an Agile Person:With a strong sense of urgency and a desire to work in a fast ... Take pride in writing clean, reusable, maintainable and well-tested code * Experience in ...

micro1 AI

Director of Biostatistics

Toledo, OH · Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Experience preparing submission-ready deliverables for regulatory agencies (e.g., FDA, EMA) is a ...

micro1 AI

Director of Biostatistics

Ann Arbor, MI · Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Experience preparing submission-ready deliverables for regulatory agencies (e.g., FDA, EMA) is a ...

TALENT Software Services

Be Seen First

Senior Electrical Designer

Ann Arbor, MI · Remote

$80K - $160K/yr

Utilizes digital tools and design software (e.g., CAD, BIM, 3D modeling) to create, modify, and ... codes and standards suitable for the project. * May apply basic engineering principles and ...

Leidos

Senior Transmission Line Engineer

Ann Arbor, MI · On-site +1

$73K - $132K/yr

This position is 100% REMOTE but candidate must reside in Michigan to be considered. You should ... Knowledge of NESC, ACI, AISC, and ASCE code requirements; construction specifications; material ...

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All JobsG Code Programmer JobsRemote G Code Programmer JobsRemote G Code Programmer Jobs in Monroe, MI

Remote G Code Programmer information

See Monroe, MI salary details

$11

$36

$63

How much do remote g code programmer jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for remote g code programmer in Monroe, MI is $36.60, according to ZipRecruiter salary data. Most workers in this role earn between $23.80 and $47.64 per hour, depending on experience, location, and employer.

What is the difference between Remote G Code Programmer vs CNC Machinist?

AspectRemote G Code ProgrammerCNC Machinist
CredentialsKnowledge of G-code, CAD/CAM software, sometimes certifications in CNC programmingTechnical training, certifications in machining or manufacturing
Work EnvironmentPrimarily remote, computer-based tasksOn-site manufacturing or machine shop
Industry UsageDesigning and programming CNC machines remotelyOperating CNC machines directly in production
Search & Comparison IntentUnderstanding programming roles, remote work optionsHands-on machining skills, on-site work

The main difference is that Remote G Code Programmers focus on writing and optimizing G-code instructions remotely, often using CAD/CAM software, while CNC Machinists operate and set up CNC machines directly in manufacturing environments. Both roles require knowledge of G-code, but their work settings and responsibilities differ significantly.

What are popular job titles related to Remote G Code Programmer jobs in Monroe, MI?

For Remote G Code Programmer jobs in Monroe, MI, the most frequently searched job titles are:

What cities near Monroe, MI are hiring for Remote G Code Programmer jobs?

Cities near Monroe, MI with the most Remote G Code Programmer job openings:

Remote G Code Programmer jobs near you
Infographic showing various Remote G Code Programmer job openings in Monroe, MI as of August 2026, with employment types broken down into 100% Contract. Highlights an 100% Remote job distribution, with an average salary of $76,125 per year, or $36.6 per hour.

Mgr, Drug Product Development & Manufacturing

ESPERION THERAPEUTICS INC

Ann Arbor, MI • Remote

$138K - $176K/yr

Full-time

Medical, Retirement, PTO

Posted 15 days ago

Job description

Company Overview


Our Mission: At Esperion, we are working tirelessly to deliver innovative medicines that help patients reach their goals today, tomorrow, and into the future.


Esperion is a fully remote based company with a corporate headquarters located in Ann Arbor, MI. The Company offers a competitive salary including a performance-based bonus program and a comprehensive benefits package including a 401(k) matching plan and health insurance, and paid time off and holidays.


Position Title: Manager, Drug Product Development and Manufacturing

The Manager, Drug Product Development and Manufacturing is a technical role that supports the development, technology transfer and manufacturing of device combination drug products at contract manufacturing organizations (CMOs). A key component of this technical role is supporting the manufacturing of commercial combination products as well as providing technical expertise for additional development and supply-chain expansion efforts. This is a remote, work from home position with approximately 25% travel.


Preferred Location: Remote – US


Essential Duties and Responsibilities*

  • Support activities for commercial manufacturing of device combination drug products at CMOs, including technical review of drug product batch records, on-site “person-in-plant” technical oversight, and support of other manufacturing activities at CMOs as required.
  • Collaborate within Tech Ops and internal project teams including Supply Chain, Quality Control, Quality Management, Regulatory Affairs, as required, for timely execution of combination product manufacturing activities.
  • Provide engineering and technical knowledge to support injection moulding, valve actuator assemblies, metering mechanisms, dimensional tolerances and functional performance, spray pattern and aerodynamic particle size distribution (APSD).
  • Maintain technical documentation of device history (DHF), process validation and commercial manufacturing, and support combination device regulatory filings.
  • Collect, analyze, and summarize data for continuous process verification (CPV) and provide input into remediation plans for identified gaps.
  • Support combination product / device-related technical activities, including coordination with device suppliers/partners on components, specifications, and technical issue resolution.
  • Partner with Quality and Regulatory to help ensure device/combination-product documentation expectations are met (e.g., device master record/device history record inputs where applicable) and support inspection readiness.
  • Ensure manufacturing changes and investigations consider combination-product requirements, including interface with design controls and risk management activities as applicable.
  • Create and review technical documents, reports, updates and presentations for cross-functional teams and management.

*additional duties and responsibilities as assigned


Qualifications (Education & Experience)

  • Bachelor’s degree in Pharmaceutical Sciences, Engineering, Chemistry or closely related field from an accredited college or university, with minimum 4 years of experience with development and commercialization of device combination drug products.
  • Drug device combination product experience required, including familiarity with applicable device quality system requirements (e.g., 21 CFR Part 820/4 and ISO 13485) and risk management principles (e.g., ISO 14971) as applicable.
  • Experience in a GMP device manufacturing in pharmaceutical industry either in a research and development, process development, manufacturing, or contract manufacturing role;
  • Experience with human factor and user error engineering, dose accuracy and delivery performance, container closure systems, and extractables/leachables.
  • Solid background in device combination development, technology transfer of manufacturing processes, troubleshooting and process improvements, including experience supporting combination products and device-component interfaces
  • Experience working with contract manufacturers
  • Hands on experience with quality systems in a regulated environment, including change control, risk management, CAPA and deviations. Working knowledge and experience with SOPs and ICH guidelines.
  • Experience working in a multi-cultural, multi-lingual environment is necessary with a demonstrated ability to contribute successfully to a multi-disciplinary team environment.
  • Ability to work in a dynamic group that takes a multi-disciplined team approach to executing and achieving departmental and corporate goals.
  • Experience in statistical analysis, interpretation, and summary (control charts) of trending data preferred.
  • Self-motivated, organized, and be reliable and responsive as needed to perform responsibilities.
  • Demonstrated alignment with Esperion’s Vision, Mission, Values and Culture.
  • Proficient with office and applicable business systems including: Trackwise, Veeva, etc.
  • Excellent written and verbal English communication skills.
  • Domestic and international travel required (up to 25 %).