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Operator II Production

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.  

  

As the Operator II Production you will perform room and equipment cleaning and sanitization, drug product formulation, equipment preparation, and aseptic fill finish batch production, per applicable work instructions, using a variety of equipment in critical cleanroom environments.

  

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 setup, sterilization, formulation, and filling, per work instructions, standard operating procedures, and batch record process steps.
  • Operate, troubleshoot, and maintain advanced aseptic processing equipment, such as isolators, filling machines, lyophilizers, and autoclaves.
  • Conduct equipment checks and validations to ensure precision, functionality, and compliance with aseptic requirements.
  • Collaborate closely with cross-functional teams, including Quality Assurance, Quality Control, and Maintenance to address deviations, resolve issues, and enhance processes.
  • Participate in aseptic process simulations, media fills, and equipment qualifications.
  • Perform in-process inspections and quality checks at a higher complexity level to ensure product integrity.
  • Complete applicable logbook, form, and batch record documentation as required while adhering to strict cGMP and  Good Documentation Practices.
  • Drive continuous improvement initiatives by identifying opportunities to optimize processes, reduce waste, and enhance efficiency.
  • Maintain qualification to wok within controlled critical areas (Grade A/B, C, D or ISO 5,7,8) and follow Standard Operating Procedures (SOPs) for gowning, cleaning, and sanitization.
  •  Comply with policies, guidelines, and regulatory requirements of the Quality System and applicable current Good Manufacturing Practices (cGMPs).
  • Other duties as required and assigned by management.

 

Requirements: 

  • High school diploma or equivalent; additional technical or vocational education is preferred.
  • 2+ years’ experience working in the pharmaceutical/biopharma/biotech industry and within aseptic clean room environments.
  • Knowledge of aseptic techniques, cleanroom protocols, and cGMP.
  • Ability to read and comprehend work instructions and standard operating procedures
  • Ability to troubleshoot minor production equipment issues in collaboration with maintenance team as necessary.
  •  Exceptional attention to detail, accuracy, and documentation skills.
  • Ability to analyze complex process data and troubleshoot deviations.
  • Excellent communication skills and the ability to collaborate effectively with cross-functional teams.
  • Flexibility to work in shifts, including evenings, nights, weekends, and holidays, as dictated 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:

  • Standing for extended periods and performing repetitive tasks.
  • Lifting up to 25 lbs, bending, and reaching to handle equipment and materials.
  • Wearing required personal protective equipment (PPE) such as gowns, gloves, masks, and goggles.

Role will be in Parsippany, NJ. 

 

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 $36,000 to $74,360, 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 primary work location. If hired to work 2nd in this role, the pay differential will be 10%. If hired to work 3rd shift in this role, the pay differential will be 20%. Additional compensation for this role will be provided based on competitive annual incentive compensation targets in the form of an annual bonus - payouts are based on individual and company performance.

  

Benefits for this role include comprehensive healthcare (medical, dental, and vision) with a premium differential, inverse to base salary, to be paid by employees, a 401k plan and company match, short and long-term disability coverage, basic life insurance, wellness benefits, reimbursement for certain tuition expenses, sick time of 1 hour per 30 hours worked, vacation time for full time employees to accrue up to 120 hours in the first four (4) years of employment, and 160 hours in the fifth (5th) year of employment as well as 15 paid holidays per year. We are proud to offer paid parental leave subject to a minimum period of employment at Ferring. 

   

Ferring is an equal opportunity employer. All aspects of employment will be based on merit, competence, performance, and business needs. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local laws.   

  

Join our team and your voice will be heard, and your contributions will be valued. If you love to come up with new ways to make a positive difference and see them through, you will fit right in.    

  

We are proud to be an Affirmative Action/Equal Opportunity Employer (including Disability/Protected Veterans). We maintain a drug-free workplace.    

 

 

Location:

Parsippany, New Jersey

Average salary estimate

$55180 / YEARLY (est.)
min
max
$36000K
$74360K

If an employer mentions a salary or salary range on their job, we display it as an "Employer Estimate". If a job has no salary data, Rise displays an estimate if available.

What You Should Know About Operator II Production, Ferring

Join Ferring as an Operator II Production in Parsippany, New Jersey, where you'll contribute to life-changing biopharmaceutical therapies. With over 70 years of commitment to science, Ferring fosters an entrepreneurial spirit and prioritizes people in everything they do. In this role, you will be immersed in a fast-paced cleanroom environment, where your primary responsibilities include performing room and equipment cleaning, drug product formulation, and aseptic fill finish batch production, all while adhering to strict regulatory standards. You will operate and maintain cutting-edge aseptic processing equipment like isolators and filling machines while collaborating with cross-functional teams to enhance production processes. Ferring is highly regarded as one of the most innovative companies globally, and they value their employees, providing a welcomed atmosphere that stands out for its commitment to growth and excellence. From conducting quality checks and validating equipment functionality to participating in ongoing continuous improvement initiatives, your contributions will directly impact patient health and safety. With a strong focus on training and development, Ferring ensures you're well-prepared for the challenges you might face in your day-to-day activities. With flexible benefits and competitive compensation, this role not only promises professional growth but also aligns with Ferring’s 'People First' philosophy, ensuring that you have the support you need to thrive both personally and professionally.

Frequently Asked Questions (FAQs) for Operator II Production Role at Ferring
What are the main responsibilities of an Operator II Production at Ferring?

As an Operator II Production at Ferring, your primary responsibilities will include performing various aseptic processing tasks such as setup, sterilization, formulation, and filling. You will operate advanced equipment, conduct inspections, collaborate with cross-functional teams, and ensure compliance with Good Manufacturing Practices (cGMP). Monitoring product integrity and participating in continuous improvement initiatives are also key elements of this role.

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What qualifications do I need to apply for the Operator II Production position at Ferring?

To qualify for the Operator II Production position at Ferring, you should have a high school diploma or equivalent, with additional technical or vocational education preferred. You will need at least 2 years of experience in the pharmaceutical or biopharma industry, specifically in aseptic cleanroom environments. Familiarity with cGMP regulations and excellent attention to detail are essential for success in this role.

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How does Ferring support career development for Operator II Production employees?

Ferring is committed to investing in their employees’ growth and development. As an Operator II Production, you will have access to tailored learning opportunities that promote your professional advancement. Through ongoing training programs and participation in processes such as equipment qualifications and aseptic process simulations, you will develop the skills necessary to excel in your role and potentially advance within the company.

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What is the work environment like for an Operator II Production at Ferring?

The work environment for an Operator II Production at Ferring is dynamic and collaborative, set in state-of-the-art cleanroom facilities. You will be working alongside dedicated professionals in a space that values safety and compliance. The company promotes a culture that embraces flexibility, encouraging employees to maintain a healthy work-life balance while actively contributing to the success of the team.

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What kind of benefits does Ferring offer to Operator II Production employees?

Ferring offers a comprehensive benefits package for Operator II Production employees, including competitive healthcare options, a 401k plan with company match, short and long-term disability coverage, paid parental leave, and generous vacation time. Additionally, there are wellness benefits and reimbursement for certain educational expenses, all reflecting Ferring's commitment to supporting their team members both personally and professionally.

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Common Interview Questions for Operator II Production
What experience do you have with aseptic processing techniques?

When answering this question, detail your previous experience in aseptic environments, focusing on specific techniques you've used. Mention your familiarity with standard operating procedures and any relevant equipment you have operated, highlighting successful outcomes from your work in those situations.

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How do you handle deviations from standard operating procedures?

In your response, stress the importance of adherence to SOPs and explain your methodical approach to addressing deviations. Share any specific experiences where you identified issues and worked collaboratively with your team to resolve them, demonstrating your problem-solving skills and ability to communicate effectively.

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Can you describe a time when you implemented a process improvement?

Here, focus on a situation where you identified an inefficiency within a process and take the time to explain your thought process. Highlight the action steps you took to implement improvements and the positive impact it had on overall production or quality.

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What safety protocols do you follow when working in a cleanroom environment?

Discuss specific safety protocols related to gowning, sanitation, and equipment handling. Emphasize your commitment to maintaining a safe working environment and share any relevant training you've had to reinforce these practices.

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How do you ensure quality during production processes?

Articulate the multifaceted measures you take to ensure product quality, such as conducting in-process inspections and rigorous documentation. Share how you collaborate with Quality Assurance and other departments to uphold compliance standards.

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What would you do if you found discrepancies in documentation?

Explain the importance of accurate documentation in a regulated industry. Describe your approach to handling discrepancies, including how you would investigate the issue and ensure that corrections are made in a timely and compliant manner.

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Describe your experience working with cross-functional teams.

Here, illustrate your collaboration skills by providing examples of how you have effectively communicated and worked alongside teams from Quality Control, Maintenance, or other functions in past roles. Highlight the outcomes of successful teamwork.

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What motivates you to work in the biopharmaceutical industry?

In your response, convey your passion for contributing to healthcare and improving patient outcomes. Share personal experiences or influences that have inspired your career choice, showing your commitment to the industry’s mission.

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How do you stay updated with industry regulations and best practices?

Discuss your methods for keeping current with industry regulations, such as attending seminars, participating in training sessions, or engaging with professional organizations. This demonstrates your proactive approach to professional development and compliance.

Join Rise to see the full answer
What are your long-term career goals as an Operator II Production?

In your answer, reflect on your aspirations within the company and the industry at large. Talk about your willingness to grow in your role, share your interest in pursuing further education or certifications, and express enthusiasm for contributing to Ferring's success.

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DATE POSTED
March 28, 2025

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