Manufacturing Technical Associate

Nesco Resource; Fall River (MA); On-site; USD 40,000 - 57,000; Full time

Benefits offered by this job

Benefits starting day 1

Onsite role

12-hour shifts

Job summary

Nesco Resource, a well-regarded pharmaceutical company in Fall River, MA, seeks a Manufacturing Technical Associate for a full-time, permanent role with benefits starting on day 1. The on-site position features 12-hour shifts (7:00–19:00 or 19:00–07:00) on a rotating 3-4-4-3 schedule and starting pay up to $35/hour plus shift differential.

You will support the production of respiratory pharmaceutical products, operate and troubleshoot automated manufacturing equipment, ensure cGMP compliance,

Qualifications

• Bachelor's degree in Engineering, Industrial Technology, Pharmaceutical Sciences, Chemistry, Biology, Manufacturing Technology, or a related field.

Responsibilities

• Operate, setup, adjust, monitor, and troubleshoot Respiratory MDI manufacturing and packaging equipment.
• Execute manufacturing and packaging processes per BMRs, SOPs, and cGMP requirements.
• Perform startup, changeovers, line clearances, cleaning, and routine adjustments to maintain production readiness.
• Document production and equipment activities accurately per cGMP.

Skills

Manufacturing equipment operation

Troubleshooting

Changeovers

Production documentation

Reading SOPs

Education

Bachelor's degree in Engineering or related technical field

Job description

Work for a well-regarded pharmaceutical company in Fall River, MA as Manufacturing Technical Associate. This is a full time, permanent position with benefits starting on day 1!

What you need to know:

• Starting Pay: up $35/hour plus shift differential
• 100% Onsite role
• 12-hour shifts, either 7:00 AM-7:00 PM or 7:00 PM-7:00 AM, following a rotating 3-4-4-3 schedule (3 days on, 4 days off, followed by 4 days on, 3 days off)

The Manufacturing Technical Associate supports the production of respiratory pharmaceutical products in a highly regulated manufacturing environment. This role requires hands‑on experience operating, setting up, adjusting, and troubleshooting automated manufacturing equipment while maintaining compliance with cGMP, quality, safety, and production requirements.

Key Responsibilities

• 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 Respiratory Metered Dose Inhaler (MDI) manufacturing and packaging equipment, including filling, crimping, propellant charging, leak testing, inspection, and packaging systems.
• Perform equipment startup, changeovers, line clearances, disassembly, reassembly, cleaning, and routine adjustments to maintain production readiness.
• Troubleshoot mechanical, pneumatic, electromechanical, equipment, and process-related issues, including jams, blockages, alarms, and material flow interruptions, using approved procedures and equipment manuals.
• Perform minor equipment repairs within established procedures and operating parameters; investigate recurring issues and elevate complex electrical, automation, engineering, validation, or maintenance concerns.
• Prepare manufacturing rooms and equipment by verifying calibration status, pressure differentials, environmental conditions, and equipment readiness.
• 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.
• Monitor equipment performance, support root cause investigations, corrective actions, and continuous improvement initiatives, and communicate opportunities for operational improvements.

Qualifications and Experience

• Bachelor's degree in Engineering, Industrial Technology, Pharmaceutical Sciences, Chemistry, Biology, Manufacturing Technology, or a related scientific or technical discipline.
• Minimum of five years of manufacturing experience .
• Demonstrated experience operating, setting up, adjusting, troubleshooting, and performing minor repairs on automated manufacturing equipment.
• Experience with equipment changeovers, startup activities, line clearances, cleaning verification, and production documentation in a cGMP environment.
• Respiratory, inhalation, aerosol, or Metered Dose Inhaler (MDI) manufacturing experience preferred.
• Advanced knowledge of pharmaceutical manufacturing operations and cGMP requirements preferred.
• Strong mechanical aptitude and working knowledge of pneumatic, electromechanical, and automated production systems preferred.
• Ability to identify equipment issues and support root cause investigations using established problem-solving methods.
• Ability to read and interpret SOPs, equipment manuals, technical drawings, manufacturing records, and process control documentation.

Physical and Environmental Requirements

• Ability to work in classified and controlled pharmaceutical manufacturing environments, including areas using hydrofluoroalkane (HFA) propellants, compressed gases, active pharmaceutical ingredients (APIs), excipients, cleaning agents, and other respiratory product components, while following established safety procedures and training requirements.
• Ability to wear required PPE, including safety glasses, gloves, hearing protection, protective footwear, cleanroom gowning, and respirators when required, for extended periods.
• Must be medically qualified to wear respiratory protection when applicable and able to work safely with manufacturing materials using required engineering controls and PPE.
• Ability to stand and walk continuously for up to 12 hours per shift.
• Ability to frequently bend, stoop, crouch, kneel, reach, climb stairs, and work around manufacturing equipment.
• Ability to operate equipment controls, perform machine adjustments, assemble and disassemble equipment components, install change parts, and complete routine maintenance and documentation tasks.
• Ability to lift, push, pull, and carry up to 50 pounds unassisted and handle heavier loads using approved material‑handling equipment.
• Ability to move pallets, drums, components, and equipment using pallet jacks, drum‑handling devices, carts, and other approved equipment.
• Ability to safely ascend and descend ladders and work platforms during equipment setup, inspections, cleaning, and changeovers.
• Ability to perform repetitive tasks requiring manual dexterity and work in varying temperatures, noise levels, and humidity conditions consistent with pharmaceutical manufacturing operations.

Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.