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Manufacturing Technical Associate - 2nd Shift

Aequor Technologies LLC
  • Fall River, MA
  • $30–$40 Per Hour
  • Instant Apply
9 days ago

Job Description

Manufacturing Technical Associate - 2nd Shift
Onsite in Fall River, MA
Full-Time
2nd shift 3:00pm - 11:30pm
Rotating shifts - 4 on 3 off - 3 on - 4 off

Responsibilities/ Accountabilities
  • Must be willing to work in a pharmaceutical manufacturing setting, including classified and controlled environments supporting Respiratory Metered Dose Inhaler (MDI) manufacturing.
  • Execute manufacturing and packaging processes in accordance with Batch Manufacturing Records (BMRs), Standard Operating Procedures (SOPs), cGMP regulations, safety requirements, and established work instructions.
  • Operate, set up, adjust, monitor and troubleshoot MDI manufacturing and packaging equipment, including filling, crimping, propellant charging, leak testing, inspection, and packaging systems.
  • Perform routine manufacturing activities while achieving established production, quality, and safety requirements.
  • Perform equipment setup, startup, changeovers, line clearances, disassembly, reassembly, and cleaning activities in accordance with approved procedures.
  • Troubleshoot routine mechanical, pneumatic, equipment, and process-related issues using established procedures, operating parameters, equipment manuals, and approved work instructions to minimize equipment downtime. (Including but not limited to: adjusting machine settings to maintain established operating parameters; clearing equipment jams, blockages, and material flow interruptions; performing equipment resets and startup recovery following alarms or process interruptions; troubleshooting filling, crimping, leak-testing, inspection, and packaging equipment performance issues.)
  • Assisting with the investigation of recurring equipment issues and escalating complex electrical, automation, engineering, validation, or maintenance concerns to appropriate personnel.
  • Monitor equipment performance and communication opportunities for operational improvements to management.
  • Prepare rooms and equipment for manufacturing operations, including verification of calibration status, pressure differentials, environmental conditions, and equipment readiness.
  • Ensure line clearance requirements are completed and documented before initiating manufacturing activities.
  • Receive, transfer, verify, and reconcile manufacturing materials according to approved procedures and batch documentation.
  • Complete production and equipment documentation accurately, legibly, and contemporaneously in compliance with cGMP requirements.
  • Participate in troubleshooting activities, investigations, corrective action implementation, and continuous improvement initiatives as assigned.
  • Assist with equipment qualification, validation, and commissioning activities as directed by management, Engineering, Validation, or Quality personnel.
  • Assist with training and onboarding of manufacturing personnel on established equipment operation, setup procedures, and departmental practices.
  • Ensure adherence to quality standards throughout all stages of manufacturing and packaging operations.
  • Wear appropriate personal protective equipment (PPE) and follow respiratory manufacturing containment and safety requirements.
  • Perform duties through the safe use of equipment according to Health & Safety procedures and equipment manuals.
  • Flexible to work extended hours to meet manufacturing schedules when required.
  • Maintain discipline and comply with company policies and procedures.
  • Participate in safety-related programs, committees, and initiatives.
  • Enforce and follow safety regulations and ensure work areas remain clean and inspection ready.
  • Adhere to companies Safety, Health, and Environmental policies.
  • Work under general supervision while performing assigned responsibilities independently within established procedures and approved operating parameters.
  • Other duties as assigned by Manufacturing Management.
Education Qualifications
  • Bachelor's degree in engineering, Industrial Technology, Pharmaceutical Sciences, Chemistry, Biology, Manufacturing Technology, or a related scientific or technical discipline.
Experience
  • Minimum seven (7+) years of experience in pharmaceutical manufacturing, respiratory manufacturing, medical device manufacturing, or other regulated manufacturing environments.
  • Demonstrated experience operating, setting up, troubleshooting, adjusting, and performing minor repairs on automated manufacturing equipment.
  • Experience performing equipment changeovers, startup activities, line clearances, and production documentation in a cGMP environment.
  • Respiratory, inhalation, aerosol, or Metered Dose Inhaler (MDI) manufacturing experience preferred.
Skills/ Competencies
  • Advanced knowledge of pharmaceutical manufacturing operations and cGMP requirements.
  • Demonstrated ability to independently operate, set up, troubleshoot, adjust, and perform minor repairs on manufacturing equipment following approved procedures.
  • Strong mechanical aptitude with working knowledge of pneumatic, electromechanical, and automated production systems.
  • Ability to identify equipment issues, perform troubleshooting activities, and support root cause investigations using established problem-solving methods.
  • Experience performing equipment changeovers, line setup, cleaning verification, and operational readiness activities.
  • Ability to read and interpret SOPs, batch records, equipment manuals, technical drawings, and manufacturing documentation.
  • Working knowledge of manufacturing process controls and equipment performance monitoring.
  • Strong documentation skills with the ability to accurately complete production records and technical documentation.
#INDQU
 

Numbers & Facts

LocationFall River, MA
IndustryStaffing/Employment Agencies
Salary$30–$40 Per Hour
Company Size100 to 499 employees

Skills

  • Aerosolsunmatched
  • Automationunmatched
  • Biologyunmatched
  • Biotech and Pharmaceuticalunmatched
  • Calibrationunmatched
  • Chemistryunmatched
  • Commissioningunmatched
  • Continuous Improvementunmatched
  • Corrective Actionunmatched
  • Current Good Manufacturing Practice (cGMP)unmatched
  • Disassemblersunmatched
  • Documentationunmatched
  • Drug Manufacturingunmatched
  • Electricityunmatched
  • Electromechanicsunmatched
  • Equipment Maintenance/Repairunmatched
  • Equipment Validationunmatched
  • Housekeeping/Cleaningunmatched
  • Identify Issuesunmatched
  • Industrial Engineeringunmatched
  • Maintain Complianceunmatched
  • Manufacturingunmatched
  • Manufacturing Equipment Maintenanceunmatched
  • Manufacturing Managementunmatched
  • Manufacturing Operationsunmatched
  • Manufacturing Technologyunmatched
  • Manufacturing/Industrial Processesunmatched
  • Medical Equipmentunmatched
  • Metered Dose Inhalersunmatched
  • Onboardingunmatched
  • Operational Communicationsunmatched
  • Operational Improvementunmatched
  • Operations Managementunmatched
  • Operations Processesunmatched
  • Performance Analysisunmatched
  • Problem Solving Skillsunmatched
  • Procedure Developmentunmatched
  • Process Control Engineeringunmatched
  • Production Scheduleunmatched
  • Production Systemsunmatched
  • Quality Metricsunmatched
  • Record Keepingunmatched
  • Regulationsunmatched
  • Regulatory Complianceunmatched
  • Root Cause Analysisunmatched
  • Safety Processunmatched
  • Safety Trainingunmatched
  • Safety/Work Safetyunmatched
  • Standard Operating Procedures (SOP)unmatched
  • System Start-Upunmatched
  • Technical Drawingunmatched
  • Technical Writingunmatched
  • Testingunmatched
  • Time Managementunmatched

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