Design and develop application deliverables for new MES implementations.
Provide technical support to factories and troubleshoot MES applications.
Contribute to process improvement and collaborate with cross-functional teams.
A Fortune 100 food and beverage manufacturing company with a global presence. They employ thousands and focus on innovation and efficiency in production.
Provide Level 2 support for Werum PAS-X MES in a global pharmaceutical environment.
Troubleshoot and resolve complex production issues, ensuring system availability.
Collaborate with cross-functional teams to maintain compliant and efficient manufacturing operations.
Our partner is a global pharmaceutical organization operating in the life sciences sector. They maintain a focus on digital manufacturing and compliance, with a collaborative culture.
Establish and maintain the firm's validation strategy and standards, ensuring all deliverables align with cGxP, GAMP 5, and data integrity principles.
Maintain and continuously improve validation toolkits for QAD ERP, NetSuite, QAD EQMS, and ETQ, including URS/FRS templates, risk assessments, and IQ/OQ/PQ scripts.
Lead end-to-end client validation engagements, including validation planning, protocol authoring, execution support, evidence review, and validation summary reporting.
A leading consulting firm specializing in ERP, quality management, and manufacturing solutions for life science manufacturers. They implement various ERP and QMS technologies and have a people-first culture backed by Pine Services Group.
Install and maintain Growth Direct systems to meet customer expectations.
Complete preventative maintenance and emergency repairs on time.
Develop technical and communication skills with guidance from senior FSEs.
Rapid Micro Biosystems develops innovative products for fast, accurate detection of microbial contamination in pharmaceutical manufacturing. The company is a growing global leader in microbiology automation with headquarters in Massachusetts and field offices worldwide.
Drive the strategy and delivery model for Veeva’s Professional Services, acting as a trusted advisor to internal teams and executive leadership.
Own end-to-end engagement design, collaborating across functions, and managing a high-volume pipeline with precision and diplomacy.
Draft and deliver RFx responses, proposals, and statements of work, aligning with internal experts and customer leadership.
Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history with over $3B in revenue, we are a public benefit corporation committed to balancing customer, employee, society, and investor interests.
Collaborate with sales and services teams to guide customers through software evaluation and implementation.
Gather customer requirements, develop business cases, and produce implementation strategies and cost estimates.
Support multiple sales engagements simultaneously while maintaining knowledge of product roadmaps and industry regulations.
Cority helps customers see and prevent risks across their operations in real time using an EHS+ platform. With over 40 years of market leadership, the company employs more than 1,500 people and has a strong, award-winning culture focused on employee well-being.
Serve as a senior expert in computer system validation and computer software assurance, leading validation initiatives and developing reusable frameworks.
Establish and maintain validation strategies, methodologies, and documentation aligned with regulatory standards like cGxP, GAMP 5, and 21 CFR Part 11.
Mentor junior consultants and collaborate with QA, IT, and business stakeholders to ensure effective validation execution across client engagements.
The company is a consulting firm that provides validation and compliance services for life science manufacturers. They have a people-focused culture with opportunities for professional development and growth.
Work closely with cross-functional teams to understand RTSM requirements and code custom solutions in C#, ASP.NET, XML, HTML, CSS, and JavaScript.
Code, test, debug, document, and install modified and new RTSM projects based on customer specifications.
Provide RTSM expertise and guidance, troubleshoot complex system issues, and maintain program integrity and project timelines.
Veeva Systems is a mission-driven pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue and operate as a public benefit corporation focused on balancing customer, employee, society, and investor interests.
Create bioanalytical reports, plans, and submission documents in support of internal projects and regulatory preclinical/clinical studies.
Extract and format data from multiple lab systems for integration into reports using Microsoft Office.
Ensure documentation complies with FDA, GxP, EMA, and other regulatory guidelines.
BioAgilytix provides best-in-class bioanalytical services to support new medicine breakthroughs. They have a team of highly experienced scientists and professionals, are growing, and are committed to being solution-oriented and deadline-driven.
Lead and manage client engagements for the AccessGenius platform, ensuring solutions meet quality and regulatory standards.
Mentor and coach team members while proactively identifying business development opportunities.
Serve as key client contact, managing project delivery from concept to launch and ensuring satisfaction.
Precision Medicine Group is a healthcare consulting and services firm specializing in pharmaceutical cost and coverage solutions. They foster a collaborative culture focused on client delivery and innovation, with a team of consultants and analysts supporting top healthcare leaders.