Compounding Technician II (M-F 5:30a-2:00p)

Fagron Nederland BV; Canton, Northern (MA, KY); Hybrid; USD 25,000 - 39,000; Full time

Benefits offered by this job

Competitive salary

Comprehensive benefits

International opportunities

Job summary

Fagron US in Canton, MA, is seeking a sterile compounding technician to perform and support aseptic manufacturing in an ISO 7 cleanroom, following cGMPs, GDPs, and SOPs. The role requires keen attention to detail and the ability to work independently with limited supervision.

You will contribute to batch records, maintain gowning qualifications, ensure aseptic technique, and collaborate with a team to meet production goals while upholding safety and quality standards.

Qualifications

• Experience in manufacturing environment preferred.
• Understanding of cGMP and GDP requirements preferred.
• Gowning or cleanroom experience preferred.
• Ability to successfully complete gowning and media fill qualifications.
• Strong attention to detail with multitasking and prioritization abilities.
• Quality-minded with accuracy and accountability.

Responsibilities

• Support daily compounding activities, including staging batches, equipment cleaning and set-up, and completion of batch records and logbooks.
• Independently perform assigned compounding activities per approved procedures and production requirements.
• Meet Right First Time (RFT) by minimizing errors and deviations and completing corrections accurately and promptly.
• Maintain adherence to SOPs, cGMPs, GDP requirements, and manufacturing schedule.
• Assist with inventory control by documenting components and materials used.
• Complete and maintain gowning and media fill qualifications.
• Maintain proper aseptic technique and follow cleanroom procedures.
• Prioritize and manage multiple production activities while ensuring quality and accuracy.
• Identify and communicate process, equipment, or documentation concerns to supervisors or experienced teammates.
• Work independently and as part of a team to meet production requirements.
• Demonstrate initiative by seeking help when needed and supporting teammates.

Skills

Attention to detail

Multitasking

Communication

Reliability

Quality-minded

Punctuality

Follow procedures

Gowning/cleanroom experience

Job description

About the Job

Perform and support sterile compounding activities within classified cleanroom areas. Follow established procedures, cGMPs, SOPs, and aseptic practices while working in an ISO 7 environment for extended periods. This role requires increasing technical proficiency, attention to detail, and the ability to independently perform assigned compounding activities with limited supervision.

Key Responsibilities

• Support daily compounding activities, including staging batches, equipment cleaning and set-up, and completion of batch records and logbooks.
• Independently perform assigned compounding activities in accordance with approved procedures and production requirements.
• Meet Right First Time (RFT) expectations by minimizing errors and deviations and completing required corrections accurately and promptly.
• Maintain adherence to SOPs, cGMPs, GDP requirements, and the manufacturing schedule.
• Assist with inventory control by accurately documenting components and materials used during production.
• Successfully complete and maintain required gowning and media fill qualifications.
• Maintain proper aseptic technique and follow established cleanroom procedures.
• Demonstrate the ability to prioritize and manage multiple production activities while maintaining quality and accuracy.
• Recognize and communicate process, equipment, or documentation concerns to supervisors or experienced team members.
• Work effectively both independently and as part of a team to meet production requirements.
• Demonstrate initiative by asking questions, seeking assistance when needed, and supporting team members.
• Perform additional duties and responsibilities as assigned by management.

Basic Qualifications

• Previous manufacturing or related experience preferred.
• Working understanding of cGMP and GDP requirements in a manufacturing environment preferred.
• Previous gowning or cleanroom experience preferred.
• Ability to successfully complete and maintain required gowning and media fill qualifications.
• Strong attention to detail with the ability to multitask and prioritize work effectively.
• Quality-minded with a strong focus on accuracy and accountability.
• Reliable attendance and punctuality.
• Ability to follow established procedures and perform assigned compounding activities with limited supervision.
• Ability to communicate effectively with team members and management.
• Ability to stand for extended periods, including up to 6 hours per shift.
• Ability to twist, bend, reach, and lift product materials as required during the shift.

What's on Offer?

We offer a dynamic environment where talent and ambition can develop to its fullest. We have an open and informal organization culture, where individuals need to have strong motivation and ability to work independently. Fagron is a widely expanding, international, professional and ambitious pharmaceutical company with multiple growth opportunities. Job opportunity includes competitive salary, comprehensive benefits, performance package, and ability to be part of an international leader in an expanding industry.

Ready for the challenge?

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. Fagron US is proud to be an affirmative action and equal opportunity employer.