Operator I, Production

USA LE; Parsippany-Troy Hills (NJ); On-site; USD 55,000 - 70,000; Full time

Job summary

Ferring is seeking an entry-level aseptic processing technician to support cGMP manufacturing in a cleanroom environment in Parsippany, NJ. The role requires 1 year of pharmaceutical exposure and attention to detail in documenting processes and maintaining equipment.

The candidate will operate isolators, autoclaves, and filling machines, participate in validations and process simulations, and support continuous improvement initiatives while complying with regulatory requirements and gowning

Qualifications

• High school diploma or equivalent; additional technical or vocational education is a plus.
• Minimum 1 year experience in pharmaceutical/biopharma/biotech and aseptic clean room environments.
• Knowledge of aseptic gowning/techniques, cleanroom protocols, and cGMP.
• Ability to read and comprehend work instructions and standard operating procedures.
• Ability to understand equipment alarms and escalate as necessary.
• Exceptional attention to detail, accuracy, and documentation skills.
• Ability to work in a controlled aseptic environment, following gowning and hygiene protocols.
• Good communication skills and the ability to work collaboratively in a team.

Responsibilities

• Perform aseptic processing tasks, including cleaning cGMP Areas, Parts Preparation Filter Integrity Testing sterilization, operating parts washers and autoclaves, perform tray loading and unloading, per wok instructions, standard operating procedures. Perform general material handling.
• Set up, calibrate, and operate aseptic processing equipment such as isolators, filling machines, and autoclaves.
• Assist with initial/subsequent validation of a new area, including manufacturing equipment and processes.
• Collaborate with cross-functional teams, including Quality Assurance, Quality Control, and Maintenance to troubleshoot issues and resolve deviations.
• Participate in aseptic process simulations, media fills, and equipment qualifications.
• Participate in in-process inspections and quality control checks to verify the integrity of product quality.
• Complete applicable logbook, form, and batch record documentation as required while adhering to strict cGMP and Good Documentation Practices.
• Contribute to continuous improvement initiatives by identifying opportunities to enhance processes, reduce waste, and increase efficiency.
• Complete initial aseptic gowning and process qualification and maintain qualification to work within Grade A and Grade B cleaning environment.
• Comply with policies, guidelines, and regulatory requirements of the Quality System and applicable current Good Manufacturing Practices (cGMPs).
• Flexibility to work weekends and holidays, as required by production schedules.
• Other duties as required and assigned by management.

Skills

Aseptic processing

cGMP knowledge

Documentation

Team collaboration

Education

High school diploma or equivalent

Tools

Autoclaves

Filling machines

Isolators

Job description

As a privately-owned, biopharmaceutical company, Ferring pioneers and delivers life-changing therapies that help people build families and live better lives. Our independence helps us cultivate an entrepreneurial spirit and long‑term perspective that enables us to achieve growth and scale, while remaining agile and true to our 'people first' philosophy. Built on a 70-year plus commitment to science and research, Ferring is relentless in its pursuit of science that drives powerful discoveries and therapies to help people build families, stay healthy, and stand up to the world's oldest enemy: disease.

With Ferring, you will be joining a recognized leader, identified as one of "The World's Most Innovative Companies" by Fast Company , and honored by Fortune with inclusion on its "Change the World List," for addressing society's unmet needs. Ferring US is also Great Places to Work® Certified, distinguishing it as one of the best companies to work for in the country.

Responsibilities:

• Perform aseptic processing tasks, including cleaning cGMP Areas, Parts Preparation Filter Integrity Testing sterilization, operating parts washers and autoclaves, perform tray loading and unloading, per wok instructions, standard operating procedures. Perform general material handling.
• Set up, calibrate, and operate aseptic processing equipment such as isolators, filling machines, and autoclaves.
• Assist with initial/subsequent validation of a new area, including manufacturing equipment and processes.
• Collaborate with cross-functional teams, including Quality Assurance, Quality Control, and Maintenance to troubleshoot issues and resolve deviations.
• Participate in aseptic process simulations, media fills, and equipment qualifications.
• Participate in in-process inspections and quality control checks to verify the integrity of product quality.
• Complete applicable logbook, form, and batch record documentation as required while adhering to strict cGMP and Good Documentation Practices.
• Contribute to continuous improvement initiatives by identifying opportunities to enhance processes, reduce waste, and increase efficiency.
• Complete initial aseptic gowning and process qualification and maintain qualification to work within Grade A and Grade B cleaning environment.
• Comply with policies, guidelines, and regulatory requirements of the Quality System and applicable current Good Manufacturing Practices (cGMPs).
• Flexibility to work weekends and holidays, as required by production schedules.
• Other duties as required and assigned by management.

Requirements:

• High school diploma or equivalent; additional technical or vocational education is a plus.
• Minimum 1 year experience working in the pharmaceutical/biopharma/biotech industry and within aseptic clean room environments.
• Knowledge of aseptic gowning/ techniques, cleanroom protocols, and cGMP.
• Ability to read and comprehend work instructions and standard operating procedures.
• Ability to understand equipment alarms and elevate as necessary.
• Exceptional attention to detail, accuracy, and documentation skills.
• Ability to work in a controlled aseptic environment, following gowning and hygiene protocols.
• Good communication skills and the ability to work collaboratively in a team-oriented environment.
• Flexibility to work weekends and holidays, as required by production schedules.
• Meet minimal visual acuity requirements necessary for quality assessments in a production or packaging environment.
• Be able to be medically cleared to wear full-face tight-fitting respirator based on OSHA Respiratory Protection Standard.

Physical Requirements:

• Ability to stand for extended periods and perform repetitive tasks.
• Lifting, bending, and reaching to handle equipment and materials.
• Wearing appropriate personal protective equipment (PPE) such as gowns, gloves, and masks.

Ferring + you

At Ferring, we offer competitive total compensation along with an exceptional range of flexible benefits, personal support and tailored learning and development opportunities all designed to help you realize your full potential both in life and at work. From working hours that respect your lifestyle, a culture that is welcoming and equitable, and the chance to work with the industry's most impressive people, these are just some of the ways we live our "People First" philosophy.

Our Compensation and Benefits

At Ferring, base salary is one part of our competitive total compensation and benefits package and is determined using a salary range. The base salary range for this role is $ [000,000] to $ [000,000] , which is the reasonable estimate of the base compensation for this role. The actual amount paid may differ based on non‑discriminatory factors such as experience, knowledge, skills, abilities, education and