Process Maintenance Technician at Precision for Medicine

Indianapolis, Indiana, United States -

Full Time

Start Date

Immediate

Expiry Date

21 Jan, 26

Salary

240000.0

Posted On

23 Oct, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Mechanical Maintenance, Troubleshooting, Critical Thinking, cGMP Compliance, Technical Documentation, Communication, Organizational Skills, Analytical Skills, Hand Tools, Power Tools, PLC Troubleshooting, HVAC Systems, Utility Maintenance, Aseptic Processing, ISO Standards, FDA Audit Processes

Industry

Pharmaceutical Manufacturing

Description

Welcome to the forefront of innovation in cutting edge patient centered treatments! We are seeking the best and the brightest to join our high performing organization as a Project Engineer. As a leader within the life science industry, we are constantly pushing the boundaries of what is possible and redefining the standards of excellence. Our dynamic team is composed of vibrant professionals who are passionate about delivering high quality work for our partners and changing the lives of patients across the globe. If you are looking for a career accelerator, are driven by innovation, thrive in a fast-paced environment, love to travel, and are ready to make a real impact, then Project Farma wants you to join our team. The Process Maintenance Technician plays a critical role in ensuring the reliability and performance of production and support equipment in a regulated pharmaceutical manufacturing environment. This role involves executing reactive, preventive, and predictive maintenance, troubleshooting mechanical, hydraulic, pneumatic, and control systems, and supporting GMP-compliant operations. The technician may work one of various shift patterns, including 8, 10, or 12 hours, occurring on days or nights, weekdays or weekends, and be 100% on-site at the client facility. Key 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. Metrics for Success PM completion rate and CMMS accuracy Equipment uptime and reliability Compliance with GMP documentation standards Audit readiness and deviation reduction Responsiveness to unplanned maintenance events Experience Required 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). Other Preferred Certification in First Aid or CPR Familiarity with ISO standards and FDA audit processes. Experience supporting equipment qualification (IQ/OQ/PQ). Experience with aseptic processing, HVAC systems, and utility maintenance is a plus. Technical diploma or degree in Mechanical Engineering or equivalent. Proficiency in troubleshooting PLCs, HMIs, and automated systems. Skilled in using lathes, mills, grinders, and precision instruments. Examples of our core services within the life science space, include: Capital Project Management (including Project Controls and Scheduling); Facility Management & Builds; Tech Transfers; Validation Life Cycle (including Commissioning and Qualification, Process Validation, Computer System Validation, etc.); GxP Automated Systems; Due Diligence & Business Strategy; Quality, Regulatory, & Compliance. In return for your skills, knowledge, and passion, we offer a wide range of benefits including: Competitive salary based on experience Annual bonus (discretionary) Medical, Dental, and Vision insurance effective your first day of employment 401k Plan with company match Paid Time Off and Company Paid Holidays Company Paid Maternity and Parental Leave Continuing Education Assistance Who are we? As a Patient Focused, People First delivery team, we are committed to advancing manufacturing to achieve operational excellence and accelerate speed to market for next-generation medicines. Our manufacturing playbook has led to the creation of the largest and most mature advanced therapy manufacturing footprint in the world. We are an industry leader in providing project management, validation, engineering, quality/compliance, and consulting services to support our partners across the life science space in finding ground-breaking treatments and solutions. We believe that our culture of philanthropy, teamwork, training and development and commitment to the patient is the foundation to our teams’ and partners’ long-term success. Project Farma is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability status, age, or veteran status or any other characteristics protected by applicable law. PerkinElmer is committed to a culturally diverse workforce. Applicants must be authorized to work in the United States on a full-time basis. We will not sponsor applicants for current or future work visas for this position. This position may require significant travel to support project and business needs. We cannot employ anyone with an invalid driver's license. Precision is required by law in some states or cities to include a reasonable estimate of the compensation range for this role. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Precision, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. This role is also eligible for a discretionary annual bonus, health insurance, retirement savings benefits, life insurance and disability benefits, parental leave, and paid time off for sick leave and vacation, among other benefits. Reasonable estimate of the current range $50,000—$240,000 USD Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice. Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com. It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.

Responsibilities

The Process Maintenance Technician ensures the reliability and performance of production and support equipment in a regulated pharmaceutical manufacturing environment. This includes executing maintenance activities, troubleshooting systems, and maintaining compliance with GMP standards.