Senior Manufacturing Technician

Description

Qualifications

Education & Experience

Bachelors degree in Engineering, Industrial Technology, Pharmaceutical Sciences, Chemistry, Biology, Manufacturing Technology, or a related scientific or technical discipline.
Minimum of 5+ years of experience in a manufacturing environment.
Experience working in a cGMP pharmaceutical manufacturing environment preferred.
Respiratory, inhalation, aerosol, or Metered Dose Inhaler (MDI) manufacturing experience preferred.

Technical Skills

Hands-on experience operating, setting up, adjusting, and troubleshooting automated manufacturing equipment.
Ability to perform minor equipment repairs following approved procedures.
Experience with equipment changeovers, startups, line clearances, line setup, cleaning verification, and operational readiness activities.
Strong mechanical aptitude with knowledge of pneumatic, electromechanical, and automated production systems preferred.
Ability to identify equipment issues, troubleshoot problems, and support root cause investigations using established problem-solving methods.
Ability to read and interpret SOPs, equipment manuals, technical drawings, and manufacturing documentation.
Knowledge of manufacturing process controls and equipment performance monitoring.
Strong documentation skills with the ability to accurately complete production records and technical documentation.
Proficiency with manufacturing systems, electronic documentation systems, and Microsoft Office applications.
Ability to train and assist coworkers on established procedures and equipment operation.

Core Competencies

Strong analytical, mechanical, and problem-solving skills with excellent attention to detail.
Ability to prioritize assignments and work effectively in a fast-paced production environment.
Strong written and verbal communication skills.
Strong command of written and spoken English.
Physical & Work Environment Requirements
Ability to work safely in pharmaceutical manufacturing areas utilizing HFA propellants, compressed gases, APIs, excipients, cleaning agents, and other respiratory product components.
Ability to wear required PPE, including safety glasses, gloves, hearing protection, protective footwear, cleanroom gowning, and respiratory protection when required.
Must be medically qualified to wear respiratory protection, if applicable.
Ability to stand and walk for up to 12 hours per shift.
Ability to frequently bend, stoop, crouch, kneel, reach, and climb stairs.
Ability to safely use ladders and work platforms during equipment setup, inspection, cleaning, and changeovers.
Ability to lift, push, pull, and carry up to 50 pounds unassisted.
Ability to move pallets, drums, components, and equipment using pallet jacks, carts, drum-handling devices, and other approved equipment.
Ability to perform repetitive tasks requiring manual dexterity, including equipment assembly/disassembly, machine adjustments, component replacement, and documentation.
Ability to visually inspect equipment, components, materials, labels, and documentation for extended periods.
Ability to work in environments with varying temperature, noise, and humidity levels consistent with pharmaceutical manufacturing.
Must be able to safely work with pharmaceutical manufacturing materials while utilizing required engineering controls and PPE.

Skills

Gmp, Chemistry, Formulation, Laboratory, Batch record review, Cgmp

Top Skills Details

Gmp,Chemistry,Formulation,Laboratory,Batch record review,Cgmp

Additional Skills & Qualifications

As a Manufacturing Technical Associate, you will support the production and packaging of respiratory pharmaceutical products in a highly regulated manufacturing environment. This role is ideal for someone with strong hands-on technical skills who enjoys operating equipment, troubleshooting issues, and supporting manufacturing processes while maintaining high standards for quality and safety.

Key Responsibilities
Work in a pharmaceutical manufacturing environment, including classified and controlled areas supporting Respiratory Metered Dose Inhaler (MDI) manufacturing.
Perform manufacturing and packaging activities according to Batch Manufacturing Records (BMRs), Standard Operating Procedures (SOPs), cGMP requirements, safety procedures, and work instructions.
Operate, set up, adjust, monitor, and troubleshoot MDI manufacturing and packaging equipment.
Work with equipment used for:
Filling
Crimping
Propellant charging
Leak testing
Inspection
Packaging
Perform equipment setup, startup, changeovers, line clearances, disassembly, reassembly, and cleaning.
Meet established production, quality, and safety requirements.
Troubleshoot routine mechanical, pneumatic, equipment, and process-related issues.
Adjust machine settings to maintain established operating parameters.
Clear equipment jams, blockages, and material-flow interruptions.
Perform equipment resets and startup recovery following alarms or process interruptions.
Help minimize equipment downtime by identifying and resolving routine production issues.

Experience Level

Intermediate Level

Job Type & Location
This is a Permanent position based out of Fall River, MA.
Pay and Benefits
The pay range for this position is $52000.00 - $72800.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors. Weekly pay, benefits start day1, yearly bonuses, overtime potential, 401k savings plan and matching, health insurance medical/dental/vision, health savings account (HSA), flexible spending account (FSA), paid time off (PTO) vacation/sick/flex time, paid holidays, short-term disability (STD), long-term disability (LTD), parental leave, paid family leave, employee discounts, and other benefits.
Job Type & Location
This is a Permanent position based out of Fall River, MA.
Application Deadline
This position is anticipated to close on Nov 5, 2026.
Workplace Type
This is a fully onsite position in Fall River,MA. About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without
regard to race, sex, age, color, religion, national origin, veteran status, disability,
sexual orientation, gender identity, genetic information or any characteristic protected
by law.

If you would like to request a reasonable accommodation, such as the modification or
adjustment of the job application process or interviewing process due to a disability,
please email [email protected] for other accommodation options.

San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the
city and county of San Francisco, we will consider for employment qualified applicants
with arrest and conviction records.

Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who violates this law
shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI):
We may use Artificial Intelligence (AI) to support parts of our hiring process,
including sourcing, screening, and evaluating candidates. AI helps assess applications
and qualifications, but final decisions are made by our hiring team. By applying, you
acknowledge and agree that your application may be reviewed using AI tools.