MES​/LIMS Integration Expert; Quality

Company Description ACR Pharma Inc. is a boutique consulting firm dedicated exclusively to the pharmaceutical industry, with deep experience in oral solid dose (OSD), biologics, and dermatological manufacturing. The firm is known for understanding the specialized technical and compliance requirements needed for successful pharmaceutical consulting engagements. ACR Pharma Inc. operates with a lean structure and a strong emphasis on quality over quantity, providing highly qualified experts at competitive rates.

This approach offers team members access to impactful projects and a focused, professional environment.

Role Description The MES / LIMS Integration Expert is a full-time, on-site role based in NH. This position is responsible for designing, configuring, and implementing integrations between Manufacturing Execution Systems (MES
-Syncade) and Laboratory Information Management Systems (gLIMS) within pharmaceutical operations. Day-to-day tasks include gathering and analyzing user requirements, mapping data flows, configuring interfaces, troubleshooting integration issues, and ensuring that system changes align with regulatory and quality standards. The role will collaborate closely with manufacturing, quality, IT, and validation teams to streamline data exchange, support batch release processes, and optimize end-to-end workflows.

The expert will also document configurations, develop user guidelines, support training, and participate in continuous improvement initiatives for digital manufacturing and lab systems.

• Proficiency in using MES / LIMS or similar systems and familiarity with quality standards and regulatory requirements
• Extensive experience in validation processes.
• Strong understanding of Lonza’s CSV validation guidelines, templates, and SOPs.
• Excellent project management skills to lead and coordinate MES validation activities.
• Effective communication and collaboration skills to work with various stakeholders.

• Advanced technical knowledge of Quality control and manufacturing operations.
• Working knowledge and experience with Quality Systems including deviations, change controls, CAPAs, OTNs, deviations; both the system (Track Wise) and the practical applications in operations
• Knowledgeable in process, equipment, cleaning, and computer system validations to the extent of being able to effectively review and approve protocols and reports and support implementation of new equipment.
• Demonstrated ability to manage medium to large sized projects within required time frames.
• Demonstrate ability for effective Planning, Organizing and Controlling competency
• Demonstrate sound decision making.
• Ability to work inter-departmentally and with customers.
• Demonstrates role model behaviors for GMP and Safety behaviors
• Strong written and verbal communication skills
• Ability to work in MS Project, Word, Excel, Power Point

This position is not eligible for visa Sponsorship