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Stationary Engineer Grade 3

Pharmaceutics InternationalHunt Valley, Maryland, United StatesOnsite
This job is no longer open

Basic Function:


The Stationary Engineer reports to the Director of Facilities and provides mechanical services to all GMP manufacturing (aseptic and oral solid dose), product development, packaging, and office areas.      Primary responsibility is for all Steam systems with secondary responsibility for other mechanical systems as needed.  Requirements of the position include both mechanical and electrical understandings.

Responsibilities:


  • Completes all PM’s and safety task on all on site boilers and steam systems

  • Ensure the 450k square feet of facility at Pii meets the appropriate cGMP standard, assist in monitoring the environmental conditions of the cGMP areas and ensure all parameters meet the cGMP requirements

  • Uses independent judgment and critical thought processes to analyze, troubleshoot and repair a variety of operating and complex building and manufacturing equipment.

  • Works independently with minimal supervision.  

  • Reads and interprets blueprints, electrical schematics, technical manuals, pneumatic schematics, and equipment specifications.  

  • Interacts constructively as a team member in a team environment, supporting team goals and objectives.

  • Performs preventive maintenance on all base building and critical system equipment.

  • Troubleshoots equipment breakdowns and performs mechanical, pneumatic, and electrical maintenance

  • Provide guidance to less experienced maintenance technicians

  • Will recommend parts/supply purchases for equipment that supports manufacturing/lab areas including spare parts inventory

  • Completes GM training meeting deadlines and schedules

  • Escalates issues to Engineering management when required (i.e., safety, complexity, need for contractors)

  • Works in a safe and compliant manner using PPE and observing safety precautions

  • Performs other duties as assigned.

Education & Experience: 


  • High School Diploma or GED  
  • 3 years of experience with facilities maintenance, preferably in a pharmaceutical environment
  • Basic math and computer skills (WORD, EXCEL) 
  • Minimum Grade 3 Stationary License in the state of MD.

Physical Requirements:

  • Hear and speak to employees and business associates on the phone, Teams and in person in English
  • Exposure to manufacturing/laboratory environment such as noise, dust, odors, and fumes 
  • Occasionally required to lift up to 50 lbs. 
  • Regularly required to sit, stand, bend, kneel, reach and move about the facility including climbing stairs, climbing ladders, gowning for clean areas.
  • Regularly required to document work in handwriting or in a computer system
  • Ability to hear and discern mechanical sounds for troubleshooting.
  • Ability to hold and manipulate hand tools.
  • Ability to see and read and understand measurement tools in English and Metric units
  • Ability to write on paperwork orders and in logbooks.  
  • Ability to use a computer monitor, keyboard, and pertinent software.
  • Ability to use PPE (respirators, gloves, safety shoes, goggles, etc.)
  • Ability to receive training and take tests to demonstrate knowledge acquisition. 32 To 40 (USD) Hourly

This job is no longer open

Life at Pharmaceutics International

Pii (Pharmaceutics International, Inc) is a multinational contract formulation and pharmaceutical development, Clinical Trial Materials (CTM), and commercial manufacturing company with corporate headquarters in Hunt Valley, Maryland, USA. Founded in 1994, Pii manufactures a wide range of dosage forms covering solid, semi-solid and aseptic filling. This service is complemented by full analytical and regulatory support.
Thrive Here & What We Value- Collaborative work environment that fosters sharing of ideas- Diverse customer and employee base (internally and externally)- Emphasis on quality standards and compliance with regulatory requirements- Adheres to Pii policies and procedures in carrying out maintenance assignments achieving excellence in timeliness, quality of work, documentation, inspection, and communicating skills.- Responsible for following all relevant regulations (e.g., FDA, OSHA, EPA, etc.)- Demonstrates ability to comprehend and follow all applicable SOPs- Results-oriented and efficient- Creative and open-minded who fosters an environment in which sharing of ideas is encouraged- Demonstrate the ability to work closely with a diverse customer and employee base (internally and externally)- Ability to work well in a cross-functional team environment- Energetic, execution-focused, self-motivated, and organized individual who is accustomed to working in a deadline-focused, high-pressure entrepreneurial environment- Demonstrates excellent personal organizational skills.- Selfmotivated and team-oriented with the ability to work with minimal supervision and limited direction.- Can accommodate nonroutine work schedules, and be able to respond to call-ins.- Good understanding of cGMPs, industry, and regulatory standards and guidelines.</s>
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