Compounding Technician III (Mon-Fri 5:30a-2:00p)

Fagron Tech; Canton (MA); On-site; USD 75,000 - 110,000; Full time

Benefits offered by this job

401(k) with company match

Medical, vision, and dental

Health Savings Account (HSA)

Job summary

Fagron US is seeking a Sterile Compounding Technician III to perform advanced sterile compounding and pharmaceutical manufacturing in accordance with MBRs, SOPs, cGMP. This role requires expert aseptic technique, cleanroom operation, and precise batch documentation.

You will mentor Technicians I and II, assist with training and qualifications, and collaborate with Quality teams to address manufacturing and compliance concerns while supporting production readiness and continuous improvement.

Qualifications

• High school diploma or equivalent.
• Substantial experience in sterile compounding, aseptic processing, or pharmaceutical manufacturing.
• Advanced knowledge of aseptic techniques, cleanroom practices, and contamination prevention.
• Strong understanding of cGMP requirements, batch records, and GDP (Good Documentation Practices).
• Demonstrated ability to independently perform complex manufacturing activities and troubleshoot production issues.
• Strong attention to detail, problem-solving, communication, and organizational skills.
• Ability to mentor and provide technical guidance to other technicians.

Responsibilities

• Independently perform advanced sterile compounding and manufacturing activities in accordance with approved MBRs, SOPs, and cGMP requirements.
• Demonstrate advanced proficiency in aseptic techniques, material handling, mixing, filtration, filling, and equipment operation.
• Support production setup, line clearance, material reconciliation, and manufacturing readiness.
• Complete and review assigned batch production records, equipment logs, and manufacturing documentation in accordance with GDP.
• Identify and troubleshoot production issues, equipment malfunctions, documentation discrepancies, and potential contamination risks.
• Serve as a technical resource and provide guidance to Compounding Technicians I and II and newly hired personnel.
• Assist with hand-on training, aseptic technique demonstrations, and employee qualification activities when authorized.
• Support equipment setup, cleaning, operational checks, and coordination of maintenance activities.
• Collaborate with production leadership and Quality teams to address manufacturing and compliance concerns.
• Assist with daily production coordination, workflow efficiency, and manufacturing schedules.
• Support investigations, inspections, corrective actions, and continuous improvement initiatives.
• Maintain required aseptic qualifications and promote compliance with safety, quality, and contamination prevention standards.

Skills

Aseptic processing

Cleanroom operations

Batch documentation

cGMP knowledge

Troubleshooting

Mentoring others

Communication

Education

High school diploma or equivalent

Job description

About The Job

The Sterile Compounding Technician III is responsible for performing advanced sterile compounding and pharmaceutical manufacturing activities in accordance with approved Master Batch Records (MBRs), Standard Operating Procedures (SOPs), current Good Manufacturing Practices (cGMP), and applicable regulatory requirements.

This position requires advanced proficiency in aseptic processing, cleanroom operations, batch documentation, and equipment handling. The Technician III independently performs complex manufacturing activities, supports troubleshooting and process improvements, and serves as a technical resource for other technicians.

Key Responsibilities

• Independently perform advanced sterile compounding and manufacturing activities in accordance with approved MBRs, SOPs, and cGMP requirements.
• Demonstrate advanced proficiency in aseptic techniques, material handling, mixing, filtration, filling, and equipment operation.
• Support production setup, line clearance, material reconciliation, and manufacturing readiness.
• Complete and review assigned batch production records, equipment logs, and manufacturing documentation in accordance with Good Documentation Practices (GDP).
• Identify and troubleshoot production issues, equipment malfunctions, documentation discrepancies, and potential contamination risks.
• Serve as a technical resource and provide guidance to Compounding Technicians I and II and newly hired personnel.
• Assist with hand-on training, aseptic technique demonstrations, and employee qualification activities when authorized.
• Support equipment setup, cleaning, operational checks, and coordination of maintenance activities.
• Collaborate with production leadership and Quality teams to address manufacturing and compliance concerns.
• Assist with daily production coordination, workflow efficiency, and manufacturing schedules.
• Support investigations, inspections, corrective actions, and continuous improvement initiatives.
• Maintain required aseptic qualifications and promote compliance with safety, quality, and contamination prevention standards.

Basic Qualifications

• High school diploma or equivalent.
• Substantial experience in sterile compounding, aseptic processing, or pharmaceutical manufacturing.
• Advanced knowledge of aseptic techniques, cleanroom practices, and contamination prevention.
• Strong understanding of cGMP requirements, batch records, and Good Documentation Practices (GDP).
• Demonstrated ability to independently perform complex manufacturing activities and troubleshoot production issues.
• Strong attention to detail, problem-solving, communication, and organizational skills.
• Ability to mentor and provide technical guidance to other technicians.

PreferredQualifications

• Experience in an FDA-regulated pharmaceutical manufacturing or 503B outsourcing facility.
• Experience with batch record review, employee training, equipment troubleshooting, or process improvements.
• Additional education or technical training in pharmaceutical manufacturing or a related field.

What's on Offer?

Fagron offers its associates competitive salaries and a wide range of benefits including a 401(k) plan with a company matching contribution; medical, vision and dental; health savings account (HSA); holiday/paid time off.

At Fagron, you’ll find plenty of chances to grow - both personally and professionally. We work in an open, dynamic environment where your ideas and talents can shine.

Ready For The Challenge?

We’re proud to be an equal opportunity employer. Diversity makes us stronger, and we’re committed to creating an inclusive workplace where everyone feels welcome.
Fagron US is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race; creed; color; religion; national origin; sex; age; disability; sexual orientation; gender identity or expression; genetic predisposition or carrier status; veteran, marital, or citizenship status; or any other status protected by law.