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Integrated Resources, Inc ( IRI )

Integrated Resources, Inc ( IRI )

irionline.com

16 Jobs

723 Employees

About the Company

Integrated Resources Inc. (IRI) is a professional staffing firm specializing in contract, consulting & full time positions in the area of Information Technology, Life Science and Allied Healthcare. Since its inception in 1996, IRI has continued to grow in size, opportunities, service and quality. Our expert team of highly trained counselors work hand in hand with every candidate and client forming a partnership of understanding and commitment.

Listed Jobs

Company background Company brand
Company Name
Integrated Resources, Inc ( IRI )
Job Title
Supply Chain Business Analyst-SAP ERP
Job Description
**Job Title** Supply Chain Business Analyst – SAP ERP **Role Summary** Supports the ERP business processes for external manufacturing networks within the Cell Therapy Vector & External Manufacturing Operations (VEXMO) organization. Converts business needs into clear, testable requirements, drafts UAT scripts, and facilitates SAP S/4 HANA implementations and roll‑outs. **Expectations** - Deliver concise, unambiguous business requirement documents. - Translate requirements into UAT scenarios and execute testing. - Engage stakeholders across IT, Project Management, Supply Chain, Finance, and Operations. - Adapt quickly to fast‑moving cell‑therapy initiatives while maintaining structure. **Key Responsibilities** - Lead requirement gathering workshops and document creation for commercial and clinical assets. - Plan, coordinate, and execute UAT for SAP S/4 HANA Green‑Field implementations. - Manage pre‑/post‑go‑live tasks, including data migration and system validation. - Support SAP ICO supply‑chain functions: planning, procurement, MPS/MRP, purchase requisitions, PO/STO, inventory, logistics execution, inbound/outbound deliveries, 3PL integration, and invoicing. - Use Client ALM for test planning and execution. - Coordinate technology integrations and interface testing (e.g., IDocs). - Maintain master data accuracy and governance. - Communicate status, risks, and resolutions to cross‑functional teams. **Required Skills** - 3+ full life‑cycle SAP S/4 HANA implementations (Green‑Field). - Expertise in SAP IPO/ICO supply‑chain modules and master data. - Strong analytical, problem‑solving, and documentation skills. - Proficiency with UAT planning, execution, and test management tools. - Excellent written and verbal communication; stakeholder‑management capability. - Ability to thrive in a collaborative, fast‑paced environment. **Required Education & Certifications** - Bachelor’s degree in Science, Engineering, Supply Chain Management, or related field. - SAP Certification (e.g., SAP Certified Application Associate – S/4HANA Release 2020/2021 – Supply Chain Planning) preferred.
Lawrence, United states
Hybrid
03-11-2025
Company background Company brand
Company Name
Integrated Resources, Inc ( IRI )
Job Title
MTS Engineer (Tech Transfer)
Job Description
**Job Title:** MTS Engineer (Tech Transfer) **Role Summary:** Supports late‑stage and commercial manufacturing of RNAi therapeutics within the Manufacturing Technical Services team. Focuses on technology transfer, process scale‑up, validation, and continuous improvement to ensure robust, GMP‑compliant production. **Expectations:** - Deliver technology transfer and scale‑up activities at contract manufacturing organizations (CMOs). - Perform deviation assessments, change control, CAPA, and risk evaluations. - Generate and communicate data‑driven reports and process documentation. - Conduct laboratory experiments supporting development and validation. - Travel between client sites as needed and adhere to lab safety standards. **Key Responsibilities:** - Execute technology transfer and process optimization projects at CMOs. - Assist in deviation investigations, change control documentation, and corrective actions. - Collect, analyze, and summarize process data; prepare technical reports and presentations. - Contribute to process validation plans, protocols, and execution. - Author and maintain process control documents; disseminate updates to cross‑functional teams. - Perform lab work to support development and scale‑up activities. **Required Skills:** - Proficiency with Microsoft Office (Word, Excel, PowerPoint); JMP experience preferred. - Strong organizational, written, and verbal communication abilities. - Ability to work independently, manage multiple priorities, and collaborate in teams. - Basic laboratory techniques and familiarity with GMP environments. - Physical ability to lift up to 50 lb and meet lab safety requirements. **Required Education & Certifications:** - Bachelor of Science (B.S.) in a relevant scientific discipline (e.g., biology, chemistry, biochemistry, engineering). - Minimum 2 years of laboratory or GMP manufacturing experience.
Cambridge, United states
On site
Junior
05-11-2025
Company background Company brand
Company Name
Integrated Resources, Inc ( IRI )
Job Title
Manufacturing Technical Services Engineer
Job Description
Job Title: Manufacturing Technical Services Engineer Role Summary: Support late‑stage and commercial drug product manufacturing through technology transfer, process scale‑up, optimization, validation, and continuous improvement to ensure GMP compliance and product quality. Expectations: - Execute technology transfer and scale‑up activities to Contract Manufacturing Organizations (CMOs). - Analyze and present manufacturing data to identify opportunities for process improvement. - Conduct validity documentation and support launch activities, ensuring adherence to cGMP and regulatory standards. Key Responsibilities: - Technology Transfer: Assist in process scale‑up, optimization, and transfer to CMOs; perform due diligence and technical assessments. - Manufacturing Support: Evaluate deviations, contribute to change control, CAPA development, and risk assessments. - Data Analysis: Gather, analyze, trend process data, generate reports and presentations for stakeholders. - Continuous Improvement: Identify and implement process efficiency enhancements. - Validation & Launch Support: Develop and execute validation protocols, sampling plans, and maintain documentation. - Compliance: Apply cGMP principles and regulatory requirements in all manufacturing activities. - Laboratory Support: Perform lab‑scale experiments to support process improvement and technology transfer. Required Skills: - Strong knowledge of cGMP, process validation, and regulatory compliance. - Proficiency with Microsoft Office (Word, Excel, PowerPoint); experience with JMP or equivalent statistical software. - Excellent organizational, analytical, and communication abilities. - Collaborative team player with capacity to manage multiple priorities. Required Education & Certifications: - Bachelor’s degree in Chemical Engineering, Biochemistry, Biotechnology, or related science discipline. - Minimum 2 years’ experience in GMP or biopharmaceutical manufacturing, preferably in process development, technology transfer, or validation. ---
Cambridge, United states
On site
Junior
06-11-2025
Company background Company brand
Company Name
Integrated Resources, Inc ( IRI )
Job Title
Engineer -MTS
Job Description
**Job Title:** Engineer – MTS **Role Summary:** Support end‑to‑end drug product manufacturing and technology transfer for RNAi therapeutics. Responsible for process scale‑up, data analysis, deviation management, and validation activities within a GMP‑compliant environment. **Expectations:** - Ensure commercial product manufacturing readiness for each lot. - Provide timely closure of deviations, investigations, and CAPAs. - Author process control documentation and communicate updates to cross‑functional teams. **Key Responsibilities:** - Assist technology transfer: process scale‑up, optimization, due‑diligence, and technical assessments at CMOs. - Contribute to manufacturing support: deviations, change control, CAPA development, and risk assessments. - Perform data collection, trending, and visualization for internal reviews. - Identify and implement continuous improvement opportunities with regulatory and operational impact assessment. - Support validation: develop protocols, sampling plans, and execute GMP‑compliant activities. - Execute development experiments in the lab as needed. **Required Skills:** - B.S. in applicable science field. - Minimum 2 years’ laboratory experience. - Competent with MS Word, Excel, PowerPoint; data trending (Excel, JMP) is desirable. - Strong written and verbal communication, organization, collaboration, and ability to manage changing priorities. - Experience or exposure to GMP environments. - Ability to travel domestically between client sites; able to lift up to 50 lbs. - Adherence to laboratory safety requirements. **Required Education & Certifications:** - Bachelor’s degree in chemistry, biology, biochemistry, pharmaceutical sciences, or related field. - No mandatory certifications specified; GMP experience preferred.
Cambridge, United states
On site
Junior
05-11-2025