(Sr.) Engineer Technician

AFE; New Jersey; Hybrid; USD 85,000 - 105,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401(k) retirement plan

Parental leave

Paid time off

Flexible spending account

Health savings account

Life and AD&D insurance

Disability coverage

Commuter benefits

Job summary

GenScript USA Inc/ProBio Inc. in New Jersey seeks an Engineering Technician to manage manufacturing and laboratory equipment, supporting GMP maintenance programs and vendor activities.

The role ensures proper documentation and cross-functional collaboration across maintenance teams. The position requires a High School Diploma with 5 years in pharma/biotech facilities, strong CMMS, GMP knowledge, and excellent communication.

Qualifications

• High School Diploma with 5 years of facilities maintenance/operations experience in pharma/biotech or related environment.
• Knowledge of cGMP, GXP, GAMP, SDLC regulations.
• Proficiency with CMMS.
• Proficiency with Microsoft Office.
• Excellent verbal and written communication skills.
• Ability to lift up to 50 lbs and work in confined spaces, heights, and varying conditions.

Responsibilities

• Maintains and performs corrective and preventative maintenance and calibrations on GMP and non-GMP equipment.
• Supports troubleshooting, testing, repair and optimization of instruments, equipment and control systems.
• Participates in continuous improvement of the site Maintenance Program.
• Maintains calibration standards and vendor documentation.
• Assists in start-up, commissioning, and turnover of new systems.
• Performs preventative and predictive maintenance on related clean utilities and systems that support Process Manufacturing.
• Maintains water rooms and related equipment including pumps, motors, DI water system, WFI stills, clean steam generators and piping.
• Maintains all site refrigerators and freezers.
• Troubleshoots and repairs clean utility equipment and Water for Injection point-of-use flushing.
• Maintains documents and records on all validated equipment and systems.
• Interfaces with departments, contractors on scheduling repairs and maintenance of clean utility systems.
• Maintains up-to-date training records.
• Communicates with management regarding change documentation.
• Follows cGMPs and coordinates with Facilities Management for planned/unplanned work.
• Performs additional duties as required.

Skills

CMMS

Microsoft Office

Verbal & written communication

GMP/GXP knowledge

Troubleshooting

Maintenance planning

Education

High School Diploma or GED

Tools

CMMS Software

Microsoft Office Suite

Job description

About GenScript

Founded in 2002 in New Jersey, GenScript Biotech Corporation accelerates innovation in biotech and healthcare by providing researchers and companies with the building blocks needed to develop groundbreaking treatments and products. Guided by its mission to Make People and Nature Healthier Through Biotechnology, and its role as a well-recognized biotechnology company, GenScript has a team of approximately 6,165 employees and has served more than 200,000 customers across over 100 countries and regions.

About ProBio

ProBio, a subsidiary of GenScript, is a global CDMO offering end-to-end services from discovery to GMP for plasmids, antibodies, and cell & gene therapies. We bring together multidisciplinary expertise to accelerate development and manufacturing through customized, and comprehensive services. ProBio has established companies in the United States, the Netherlands, South Korea, and China (Hong Kong, Shanghai, and Nanjing) and other regions to serve global customers, and has helped customers in the United States, Europe, Asia Pacific and other regions obtain more than 150 IND approvals since October 2017

Position Overview

The Engineering Technician is responsible for the manufacturing and laboratory equipment at the site. This includes performing activities and overseeing outside vendor activities required to support the Preventative Maintenance and Corrective Maintenance program in accordance with Good Manufacturing Procedures (GMP) regulations and company Standard Operating Procedures (SOPs). This includes ensuring that these activities are properly documented. Instrument services may be performed in but not limited to GMP, Good Lab Practices (GLP), Non-GMP process and laboratory areas. The incumbent works cross-functionally with internal departments and external resources as appropriate on maintenance and repair-related issues.

Responsibilities

• Maintains and performs corrective and preventative maintenance and calibrations on GMP and non-GMP equipment.
• Supports other departments to troubleshoot, test, repair and optimize instruments, equipment and control systems.
• Participates in the continuous improvement efforts within the site Maintenance Program.
• Assists in the maintenance and review of calibration standards and vendor calibration documentation.
• Provides support for start-up, commissioning, and turnover of new systems.
• Perform preventative and predictive maintenance on related clean utilities and systems that support Process Manufacturing.
• Maintains water rooms and related equipment. This includes, but may not be limited to, pumps, motors, Deionized Water System, WFI stills, Clean Steam Generators and related piping.
• Maintains all site refrigerators and freezers.
• Troubleshoots and repairs all related clean utility equipment and systems and Water for Injection (WFI) point of use flushing.
• Maintains documents and records on all validated equipment and systems.
• Interfaces with other departments, contractors and disciplines on scheduling repairs and maintenance of clean utility systems.
• Maintains up to date training records.
• Communicates with management regarding change documentation, as necessary.
• Follows current Good Manufacturing Practices (cGMPs).
• Communicates and coordinates with each department and within Facilities Management when planned and unplanned work events occur.
• Perform additional job duties as required.

Qualifications

• High School Diploma (or GED) with a minimum 5 years of facilities maintenance/operations experience in a pharmaceutical, biotechnology or related environment OR the equivalent combination of education and experience. Advanced knowledge of Preventive Maintenance and calibration disciplines within a cGMP Biotechnology, Pharmaceutical or related manufacturing environment.
• Knowledge of cGMP, GXP, Good Automated Manufacturing Practice (GAMP), Software Development Life
• Cycle (SDLC) regulations, knowledge of pharmaceutical, manufacturing and laboratory systems and equipment.
• Proficiency with Computerized Maintenance Management Systems (CMMS).
• Proficiency with Microsoft Office.
• Excellent verbal and written communication and skills.
• Ability to lift up to 50 lbs. and work in confined spaces, heights, and varying environmental conditions.
• Must be able to stand, walk, bend, and climb ladders for extended periods.
• Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals.
• Ability to write routine reports and correspondence.
• Ability to work holidays and varying shift times/hours if required.
• Must be able to respond to site emergencies .
• Ability to work independently and collaboratively, as required, in a fast‑paced, matrixed, team environment consisting of internal and external team members.
• Analytical thinker with excellent problem‑solving skills and the ability to adapt to changing priorities and deadlines.
• Excellent planning, organization and time management skills including the ability to support and prioritize multiple projects.
• Refrigeration Technician background a plus but not required.

Pay range is estimated between $85k - $105k based on skill set and experience.

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Benefits

Benefits include medical, dental, and vision insurance as well as a 401(k) retirement plan with a company match that vests fully on day one. We offer paid parental leave after just three (3) months of employment, and a paid time off policy that includes vacation time, personal time, sick time, floating holidays, and company holidays. Additional benefits include flexible spending and health savings accounts, life and AD&D insurance, short- and long-term disability coverage, legal assistance, and supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance. We also provide commuter benefits, well‑being initiatives, and peer‑to‑peer recognition programs; demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work.

GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.

GenScript USA Inc./ProBio Inc. maintains a drug‑free workplace.

Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.