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Tris Pharma Jobs (NOW HIRING)

Tris Pharma Inc

Packaging Mechanic

Monmouth Junction, NJ

$73K - $85K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Description Tris Pharma, Inc. (www.trispharma.com) is a leading privately-owned U.S. biopharmaceutical company with a focus on development and commercialization of innovative medicines in ADHD ...

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How much do tris pharma jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for tris pharma in the United States is $54.33, according to ZipRecruiter salary data. Most workers in this role earn between $50.48 and $63.70 per hour, depending on experience, location, and employer.

What are some typical challenges faced by employees working in pharmaceutical companies like Tris Pharma, and how can they be addressed?

Employees at pharmaceutical companies such as Tris Pharma often encounter challenges like strict regulatory compliance, fast-paced project timelines, and the need for meticulous attention to detail. Navigating frequent changes in industry regulations and ensuring documentation accuracy can be demanding. To address these challenges, it's important to stay updated on industry standards, participate in ongoing training, and foster effective communication within cross-functional teams. Emphasizing collaboration and proactive problem-solving can help employees thrive in this dynamic environment.

What is Tris Pharma?

Tris Pharma is a pharmaceutical company that specializes in developing, manufacturing, and marketing innovative medicines, particularly in the areas of neurology, psychiatry, and pediatrics. The company is known for its unique drug delivery technologies, which are used to improve the effectiveness and convenience of medications. Tris Pharma produces both branded and generic pharmaceutical products, including liquid and extended-release formulations. The company collaborates with other pharmaceutical firms and healthcare providers to bring new therapies to market and improve patient outcomes.

What is the difference between Tris Pharma vs Pharmaceutical Manufacturing Technician?

AspectTris PharmaPharmaceutical Manufacturing Technician
Required CredentialsHigh school diploma or equivalent; some roles may require GMP trainingHigh school diploma; GMP training often preferred
Work EnvironmentPharmaceutical manufacturing facilities, quality control labsProduction lines, cleanrooms, quality assurance labs
Employer & Industry UsagePharmaceutical companies, including Tris PharmaVarious pharmaceutical manufacturers, including Tris Pharma
Common Search & ComparisonYesYes

Both roles involve working in pharmaceutical manufacturing environments, often requiring GMP training and similar credentials. While Tris Pharma is a specific company, a Pharmaceutical Manufacturing Technician is a broader role found across many pharmaceutical firms. The main difference lies in the employer; Tris Pharma refers to a specific company, whereas the technician role is a general job title in the industry.

What are the key skills and qualifications needed to thrive as a pharmaceutical professional at Tris Pharma?

To thrive as a pharmaceutical professional at Tris Pharma, you need a solid background in pharmaceutical sciences, quality control, and regulatory compliance, often supported by a relevant degree such as pharmacy, chemistry, or a related field. Familiarity with Good Manufacturing Practices (GMP), laboratory information management systems (LIMS), and regulatory documentation tools is typically required. Strong attention to detail, problem-solving abilities, and effective teamwork are critical soft skills for success in this environment. These competencies ensure the development, production, and delivery of safe, effective pharmaceutical products while meeting industry regulations.
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Tris Pharma jobs near you
Infographic showing various Tris Pharma job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 85% Full Time, 2% Part Time, 9% Contract, and 1% Nights. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $113,000 per year, or $54.3 per hour.

IT Manager, Manufacturing Systems

Tris Pharma Inc

Monmouth Junction, NJ

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 8 days ago

Job description

Description

Tris Pharma, Inc. (www.trispharma.com) is a leading privately-owned US biopharmaceutical company focused on development and commercialization of innovative medicines in ADHD, spectrum disorders, anxiety, pain and addiction addressing unmet patient needs. We have >150 US and International patents and market several branded ADHD products in the US. We also license our products in the US and ex-US markets. Our robust pipeline of innovative products employing our proprietary science and technology spans neuroscience and other therapeutic categories.

Our science and technology make us unique, but our team members set us apart; they're the engine fueling Tris' passion and innovation. Our colleagues understand the criticality of operating a successful business and take pride in the company's success. Equally important is how we interact on a daily basis. We believe in each other and in respectful, open and honest communication to help support individual and team success.


We have a position available in our Monmouth Junction facility for an experienced IT Manager, Manufacturing Systems to support our on-site manufacturing operations.  


This position is responsible for leading technology-enabled transformation across pharmaceutical manufacturing, packaging, quality, supply chain, engineering, warehouse and plant operations. The incumbent serves as a key IT partner to the manufacturing organization, with a primary focus on applying automation, data, analytics, AI and agentic AI capabilities to improve operational efficiency, compliance readiness, decision support and user productivity in a highly regulated manufacturing environment. 


She/he helps shape and execute the company's Artificial Intelligence (AI) transformation roadmap for manufacturing systems by identifying high-value use cases, coordinating business and technical requirements, enabling responsible AI tool adoption and helping to build scalable agentic AI solutions.


  • Partners with Manufacturing, Packaging, Quality, Engineering, Supply Chain, Warehouse, Finance, and other business functions to identify opportunities where AI, automation, analytics, workflow and digital tools can reduce manual work, improve decision-making, strengthen compliance controls and increase operational effectiveness


  • Leads discovery, prioritization, design and implementation of AI transformation use cases for manufacturing and related business functions, including agentic AI solutions, knowledge agents, workflow automation, digital assistants, exception monitoring and decision-support capabilities


  • Assists in the building of an agentic AI platform by defining business use cases, data sources, system integrations, security controls, governance requirements, validation considerations, human-in-the-loop review points, support models and scalable implementation patterns


  •  Supports responsible AI adoption in a pharmaceutical manufacturing environment by ensuring solutions are aligned with applicable GxP expectations, data integrity principles, cybersecurity standards, privacy requirements, change control, testing, documentation and appropriate human oversight; Collaborates with IT infrastructure, cybersecurity, data and application teams to ensure manufacturing systems are secure, resilient, integrated, backed up, monitored and aligned with overall enterprise architecture and data governance standards


  • Supports and improves technology used across manufacturing and plant operations (i.e., Enterprise Resource Planning (ERP) integrations, warehouse and inventory systems, barcode scanning, labeling, serialization, manufacturing execution, quality systems, equipment interfaces, data historians, reporting tools and other shop-floor or plant applications, etc.)


  • Builds strong relationships with manufacturing leaders and end users by providing responsive support, clear communication, effective training and practical guidance on system use, process impact and compliance expectations


  • Leads or supports requirements gathering, process mapping, solution design, configuration, testing, user acceptance testing, validation documentation, implementation planning, training and post-go-live support for AI-enabled and manufacturing system enhancements; Establishes adoption practices for AI-enabled tools, including user training, prompt and agent usage guidance, knowledge management, feedback loops, performance measures and continuous improvement of deployed solutions


Requirements

REQUIRED QUALIFICATIONS 

  • Bachelors degree in IT, Computer Science, Engineering, Data Science or related technical field and minimum 7 years progressive IT experience supporting manufacturing systems, digital transformation, automation, analytics, AI-enabled solutions, ERP and/or plant technology in a pharmaceutical, biotechnology, medical device or related regulated manufacturing environment OR a combination of education and experience supporting manufacturing systems, digital transformation, automation, analytics, AI-enabled solutions, ERP and/or plant technology in the above industries REQUIRED
  • Strong practical understanding and working knowledge/ability to use Microsoft AI and analytics stack (i.e., Microsoft 365 Copilot, Copilot Studio, Power Platform, Power Automate, Power Apps, Power BI, Fabric, Azure AI services, Azure OpenAI, Microsoft Graph, Dataverse, SharePoint, etc.) REQUIRED


  • Strong understanding of pharmaceutical manufacturing operations including current Good Manufacturing Practices (cGMP) expectations, computer system validation, data integrity, audit readiness, change control, testing and controlled documentation practices REQUIRED


  • Understanding of Microsoft security, governance, and compliance capabilities relevant to AI adoption, including Microsoft Entra ID, Purview, sensitivity labels, data loss prevention, access controls, etc. REQUIRED


  • Ability to design and support Copilot Studio agents, Power Automate workflows, knowledge-based assistants, retrieval-augmented generation solutions, and human-in-the-loop AI processes that are secure, supportable, auditable, and aligned with business and compliance expectations REQUIRED 


  • Working knowledge and/or experience with ERP systems REQUIRED


Work Arrangements: We are a HYBRID work environment requiring local candidates to be able to work majority of week in our NJ office.  

Anticipated salary range: $ 120 to $ 155K/yr. Base salary offered is contingent on assessment of candidate's education and experience level relative to requirements of the position and a review of related industry standards and internal equity.

Additional benefits: In addition to base salary, full-time employees are also eligible for incentives, including, but not limited to: bonus eligible, medical, dental, vision, Rx insurance, 401K with match, life insurance, paid Company Holidays, PTO, Paid Volunteer Time and Employee Resource Groups.   

Tris Pharma, Inc. offers a highly competitive compensation and benefits package. To build and enhance our diverse workforce, we encourage applications from individuals with disabilities, minorities, veterans, women, LGBTQ, etc. Tris Pharma, Inc. is an Equal Opportunity Employer. #LI-hybrid


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