Process Maintenance Technician at Project Farma

Indianapolis, Indiana, United States

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Not SpecifiedCompensation

Junior (1 to 2 years), Mid-level (3 to 4 years)Experience Level

Full TimeJob Type

UnknownVisa

Pharmaceutical, Life SciencesIndustries

Requirements

Minimum 3-5+ years of experience in mechanical maintenance within pharmaceutical, biotech, or regulated manufacturing environments
Strong mechanical aptitude with troubleshooting and critical thinking skills
Familiarity with demands of performing maintenance activities in a cGMP environment
Ability to interpret technical documentation and engineering drawings
Strong communication, organizational, and analytical skills
Comfortable working in confined spaces, heights, and around chemicals
Ability to use basic hand tools, power tools, and meters (DVM, Amp, and Ohm)
Willingness to work various shift patterns (8, 10, or 12 hours, days or nights, weekdays or weekends) and be 100% on-site

Responsibilities

Perform maintenance activities in compliance with cGMPs and SOPs
Assemble, disassemble, install, repair, and replace components for pharmaceutical-grade machinery and cleanroom equipment
Troubleshoot and resolve issues in mechanical, electrical, pneumatic, and PLC-controlled systems
Maintain accurate documentation including Maintenance and Calibration Records per cGMP standards
Inspect equipment for wear, irregularities, and potential failures
Collaborate with cross-functional teams (Quality, Engineering, Production) to ensure equipment reliability and compliance
Execute scheduled PMs and CMMS updates in a timely and accurate manner
Maintain tools and workspaces in accordance with cGMP housekeeping standards
Adhere to OSHA and site-specific safety protocols
Participate in continuous improvement initiatives and equipment reliability programs
Support audits and inspections by regulatory bodies and internal quality teams
Other duties as assigned

Skills

Key technologies and capabilities for this role

cGMPSOPsMechanical SystemsHydraulic SystemsPneumatic SystemsPLCTroubleshootingPMsCMMSCleanroom EquipmentCalibrationEquipment Maintenance

Questions & Answers

Common questions about this position

What experience is required for the Process Maintenance Technician role?

Minimum 3-5+ years of experience in mechanical maintenance within pharmaceutical, biotech, or regulated manufacturing environments is required, along with strong mechanical aptitude, troubleshooting, critical thinking skills, familiarity with cGMP environments, ability to interpret technical documentation and engineering drawings, and strong communication, organizational, and analytical skills.

Is this a remote position, or do I need to work on-site?

The role requires 100% on-site work at the client facility, with possible shift patterns including 8, 10, or 12 hours on days or nights, weekdays or weekends.

What is the salary or compensation for this position?

This information is not specified in the job description.

What is the company culture like at Project Farma?

Project Farma has a dynamic team of vibrant professionals passionate about delivering high-quality work, driven by innovation, thriving in a fast-paced environment, with opportunities for career acceleration and real impact.

What makes a strong candidate for this role?

A strong candidate has 3-5+ years in mechanical maintenance in pharma or regulated environments, strong troubleshooting and cGMP familiarity, and excels in cross-functional collaboration and compliance-focused maintenance.

Project Farma

Biomanufacturing services for cell and gene therapy

About Project Farma

Project Farma specializes in biomanufacturing, focusing on cell and gene therapy. The company develops and implements strategies for advanced therapy facilities, helping clients create treatments that modify genes to address diseases. Their services encompass the entire lifecycle of biomanufacturing projects, including facility construction, validation, quality assurance, regulatory compliance, and automation. Project Farma distinguishes itself by offering comprehensive, turnkey solutions that ensure facilities meet Good Manufacturing Practices (GMP), which is essential for producing safe therapies. Their goal is to enhance patient outcomes through effective project execution and they also emphasize philanthropy and professional development within their team.

Chicago, IllinoisHeadquarters

2016Year Founded

ACQUISITIONCompany Stage

Consulting, Biotechnology, HealthcareIndustries

51-200Employees

Benefits

Health Insurance

Dental Insurance

Vision Insurance

401(k) Company Match

Paid Vacation

Company Paid Maternity and Parental Leave

Continuing Education Assistance

Risks

Emerging biomanufacturing consulting firms increase market competition.

Rapid technological advancements may require significant investment to stay competitive.

Economic downturns could reduce demand from biotech startups.

Differentiation

Project Farma specializes in cell and gene therapy facility builds and compliance.

They offer turnkey solutions, managing projects from planning to execution.

Their focus on philanthropy and professional development sets them apart.

Upsides

Rising demand for cell and gene therapies boosts need for specialized facilities.

Advancements in automation enhance efficiency and cost-effectiveness of services.

Complex regulatory requirements increase demand for Project Farma's consulting expertise.

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