Our Automaton Technician plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, your responsibilities will include improving QuVa’s production efficiency through implementing, reviewing, testing, repairing, and maintaining critical equipment. The person will be required to maintain and repair manufacturing equipment in both Controlled Non-Classified areas, and in Classified clean room environments within the pharmaceutical manufacturing facility. The Automation Technician will be capable of following procedures, documenting work as/when performed and maintaining a clean/organized workplace supporting site compliance and upholding quality standards. The position operates within legal and regulatory compliance, ensuring systems are maintained and operating according to site and regulatory requirements. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US.

This is a full-time role for our 3rd shift, working Monday through Friday from 10PM to 6:30AM. This is a set, consistent schedule with minimum overtime requirements and based on site in our Bloomsbury, NJ location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws.

What the Automation Technician Does Each Day:

• Provides technical skills and expertise in supporting automated manufacturing equipment, ensuring it operates efficiently
• Supports operations by troubleshooting equipment, monitoring PLC issues, performing root cause analysis on complex issues, executing improvements, and documenting corrective actions
• Maintain a log of activities carried out on equipment, hours worked, spare parts used, etc. using the site Work Order management system. Works with Quality to review and address critical activities that impact classified production environments
• Efficient use of different software tools and computer applications including but not limited to Microsoft Office, PLC programming software, HMI programming software, Fanuc Teach Pendant, SCADA systems and industrial networks
• Effectively and accurately handles most technical questions for assigned products
• Understands and adheres to policies and procedures

Our Most Successful Automation Technicians:

• Have strong problem-solving skills including training in the scientific method
• Demonstrate interpersonal communication skills
• Motivate cross functional teams to meet aggressive timelines
• Are proficient in technical writing and current computer usage (Word, Excel, PowerPoint, )
• Have good working knowledge of regulatory guidance as it pertains to APIs and injectable drug products

Minimum Requirements for this Role:

• Technical degree or equivalent with 2 years’ experience in GMP manufacturing in an operation, maintenance or troubleshooting capacity OR
• High School Diploma or equivalent with 4 years’ experience in GMP manufacturing in an operation, maintenance or troubleshooting capacity
• Understanding of Good Documentation Practices
• Knowledgeable in ISO 7/5 environment cleanroom gowning and behaviors
• Proven ability to adapt and manage effectively in fast paced, changing environment
• Must be currently authorized to work in the United States on a full-time basis; QuVa is not able to sponsor applicants for work visas

Any of the Following Will Give You an Edge:

• Experience in aseptic processing
• Experience with FDA, GMP, and ISO standards
• Experience working with PLCs, HMIs, Robotics, and SCADA systems, preferably Rockwell or Siemens platforms

Benefits of Working at QuVa:

• Set, full-time, consistent work schedule
• Comprehensive health and wellness benefits including medical, dental and vision
• 401k retirement program with company match
• 17 paid days off plus 8 paid holidays per year
• National, industry-leading high growth company with future career advancement opportunities

About QuVa:

QuVa Pharma is a national, industry-leading, FDA registered 503B outsourcing services company that provides hospitals with essential medications in ready-to-administer injectable formats that are critical for effective patient care. We are leading the way with unmatched expertise in current Good Manufacturing Practices and sterile pharmaceutical manufacturing, and the highest quality and safety standards so hospitals can more confidently and reliably focus on patient care nationwide. As a leader in sterile compounding, we continue to invest in automation and integrated technologies to improve our production processes, safety, consistency, and product quality.

As part of our team, you'll experience being at the forefront of groundbreaking solutions, collaborating with brilliant minds, and making a tangible impact in healthcare delivery.

QuVa is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. QuVa's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with QuVa is “at will.”