Operator

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Irving, TX
In-Office
Biotech
The Role
The Opportunity:
The Manufacturing Operator works independently and in coordination with the Lead Operator and/or Supervisor. He/she will be responsible for the accurate and compliant manufacturing of various silicone products, utilizing a variety of automated and semi-automated equipment and processes.  Will operate mixing, coating, cutting, and packaging machines in accordance with SOPs and GMP guidelines. Will perform basic troubleshooting and maintain equipment cleanliness. Interfaces and works with engineering and senior manufacturing personnel in identifying and implementing process improvements and process validations.
The schedule is: 10 PM start time, with 6:30 am finish time, Monday night through Saturday morning.

What we’re looking for 

  • Education: High school diploma or general education degree (GED) preferred; minimum two years related experience and/or training; or equivalent combination of education and experience.
  • Experience – Previous experience in a manufacturing environment preferred.

Collaboration Tool: Microsoft Office Suite (Outlook, Excel, Word).

Preferred Qualifications: 

  • Experience in a chemical plant. 
  • MFG experience preferred.
  • Understanding/familiarity with cGMP and RCRA training. 

How you will thrive and create an impact 

  • Adheres to the company's strict safety regulations. 
  • Maintains a safe, clean, and organized work area, ensuring that others do the same. 
  • Learns and adheres to safety rules for the work area regarding the management of chemicals and equipment. 
  • Responsible for learning the safety hazards of processes, equipment, and materials and applying that knowledge during routine operations. 
  • Monitors and performs daily activities within the production area (processing/ packaging/ testing/ sampling) to ensure safety practices are being followed.
  • Identifies and corrects potential hazards, ensuring compliance with safety regulations. 
  • May assist with hazardous waste disposal activities, including properly identifying and classifying waste streams, ensuring segregation, and adhering to applicable regulations. 
  • May be responsible for devising and implementing safety improvements. 
  • Performs routine tasks such as cleaning, weighing, and set-up of systems for operation, packaging, and in-process testing. 
  • Will be trained on applicable manufacturing procedures. 
  • Performs routine maintenance and cleaning of production equipment to ensure its optimal operation.
  • Corrects routine and non-routine problems by analyzing, troubleshooting, and correcting equipment/process problems. 
  • Monitor and record critical process parameters.
  • Communicates with management on product testing results, trends, and deviations. Recommend process adjustments. 
  • Performs a wide variety of skilled duties in the preparation and operation of process equipment.
  • Understand the mechanism of production machines and demonstrate the ability to identify areas of the operations process. 
  • Ensures packaging of finished goods meets all NuSil packaging specifications to meet customer requirements. 
  • Accurately uses computerized operating systems to run and monitor manufacturing equipment, if required. 
  • Is responsible for accurately completing and reviewing manufacturing and quality documentation, including all calculations and notes.
  • May optimize and evaluate formulation levels for product workup. 
  • May collaborate with the Research & Development group when necessary. 
  • May be required to wear special garments in controlled manufacturing environments, including synthetic-material coveralls, beard covers, bouffant caps, booties, and/or powder-free vinyl gloves.
  • May assist various departments with the proper collection and disposal of hazardous waste. 
  • May assist with the inspection/operation, and maintenance of various safety equipment and laboratory ware. 
  • May be required to wear special garments in controlled manufacturing environments, including synthetic-material coveralls, beard covers, bouffant caps, booties, and/or powder-free vinyl gloves.
  • All employees are expected to maintain a safe work environment, obey safety rules, and exercise caution in all work activities. 

Disclaimer:
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer.

Why Avantor?

Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science.
 
The work we do changes people's lives for the better. It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor.
 
We are committed to helping you on this journey through our diverse, equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor, dare to go further and see how the impact of your contributions set science in motion to create a better world. Apply today!

EEO Statement:

We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law.

If you need a reasonable accommodation for any part of the employment process, please contact us by email at [email protected] and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address.

For more information about equal employment opportunity protections, please view the Know Your Rights poster.

3rd Party Non-Solicitation Policy:

By submitting candidates without having been formally assigned on and contracted for a specific job requisition by Avantor, or by failing to comply with the Avantor recruitment process, you forfeit any fee on the submitted candidates, regardless of your usual terms and conditions. Avantor works with a preferred supplier list and will take the initiative to engage with recruitment agencies based on its needs and will not be accepting any form of solicitation.

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The Company
HQ: Radnor Township, PA
9,968 Employees
Year Founded: 1904

What We Do

Avantor®, a Fortune 500 company, is a leading global provider of mission-critical products and services to customers in the biopharma, healthcare, education & government, and advanced technologies & applied materials industries.

Our portfolio is used in virtually every stage of the most important research, development and production activities in the industries we serve.

Our global footprint enables us to serve more than 225,000 customer locations and gives us extensive access to research laboratories and scientists in more than 180 countries. We set science in motion to create a better world.

More than 13,500 strong, our associates are passionate about our mission to set science in motion to create a better world. We share enthusiasm for innovation, excellence, and achievement. Whether we are collaborating with our customers to advance science or solve multifaceted problems, we help them reach their goals more efficiently and effectively.

Visit our website to learn more about Avantor.


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