Remote Technical Support Specialist en Rapid Micro Biosystems

Winning the race to bring new healthcare products safely to a waiting world drives Rapid Micro Biosystems (RMB) to combine today’s innovative technologies as never before. Your career at RMB puts you at the center of diverse global teams that span robotics, AI, Machine Learning, imaging, microbiology, and more, re-shaping how urgently needed pharmaceuticals are made, tested, and released for decades to come. The sky’s the limit.

Careers at RMB are fast-moving, with the high growth you’d expect from a world leader in microbiology automation. Advancement at RMB affords an opportunity to achieve your personal goals and develop your passions, in an inclusive environment where every employee has the resources and opportunities to hone their skills. You’ll do more, learn more, and have the ability to make a profound impact on our business.

The Technical Support Specialist is responsible for providing remote technical support for Growth Direct™ systems to meet or exceed customer expectations across the European market. This position requires advanced problem-solving skills, both technically and in handling customer situations in pharmaceutical quality control environments. The Technical Support Specialist is an experienced professional with well-developed communication skills who has a full understanding of GxP practices, LIMS/QMS systems, and company policies. As a trusted resource, the Technical Support Specialist works autonomously to troubleshoot complex issues while maintaining Service Level Agreements and documenting cases in Customer Relation Management (CRM) database.

·          Provide first-line remote technical support for Growth Direct™ system robotic, software, imaging, and microbial related issues

·          Process customer complaints per SLAs, Escalation Processes, and with Field Service Engineer coordination as needed

·          Case management within the Customer Relation Database, inputting pertinent information that includes date stamps, symptoms, investigation details and the resolution

·          Provide support for issues encountered during validation activities (IQ/OQ/PQ) and LIMS software platform integrations

·          Initiating and recommending product design change/improvement from customer data collected

·          Develop and maintain technical documentation

·          Complete all necessary training on time to meet Quality requirements

·          Demonstrated ability to read, comprehend, and interpret technical documentation, including organizational and instrument procedures, and those from customer/regulatory agencies

·          Strength in defining problems, collecting data, establishing facts, and drawing valid conclusions

·          Experience with SQL queries and data analysis preferred

·          Well-developed and professional output of written and spoken communications in English

·          Strong customer service soft skills with ability to handle challenging situations professionally

·          Computer/Microsoft Office proficiency

·          Experience with remote support tools, CRMs, and virtual collaboration platforms

·          Professional email etiquette and remote communication skills

·          Regularly makes decisions autonomously with limited guidance/supervision required

 

·          Experience working directly on software-controlled laboratory instruments

·          Previous experience in technical support with well-developed professional customer handling skills

·          Knowledge of computer networking, internet protocols, and system administration

·          Demonstrated experience working in ISO or GMP controlled environments

·          Understanding of pharmaceutical QC applications: environmental monitoring, water testing, bioburden, sterility preferred

·          Understanding of 21 CFR Part 11, EU GMP, and ALCOA+ data integrity principles preferred

·          Experience working with LIMS platforms (LabWare, Sample Manager LIMS, MODA, or similar) preferred

·          Knowledge of Pharmaceutical Microbiology a plus

·          Additional EU language skills (German, French) preferred

 

Minimum of technical degree in Life Sciences, Microbiology, Computer Science, Engineering or equivalent experience; bachelor's degree preferred

·          Remote position supporting EU customers during CET business hours

·          Occasional travel to US for training and/or customer sites within EU may be required (5% travel)

·          Working outside of business hours may occur for critical customer issues

Rapid Micro Biosystems creates, sells, validates, and services innovative products for fast, accurate, and efficient detection of microbial contamination in the manufacture of pharmaceuticals, biologics, biotechnology products, medical devices, and personal care products.

The company’s Growth Direct™—the first and only growth-based system to automate rapid compendial QC Micro testing—ensures data integrity, compliance, and operational efficiencies driven by rapid methods and automation.

Rapid Micro Biosystems is dedicated to providing groundbreaking technology and products to support companies in their journey to achieve greater reliability, efficiency, and better predictability, ultimately providing higher quality products for improved patient outcomes.

Rapid Micro Biosystems is headquartered in Lexington, Massachusetts. Our research & development, and manufacturing operations are located in Lowell, Massachusetts. Additionally, we maintain field offices in Freising, Germany; Switzerland, and Singapore.

Rapid Micro Biosystems is committed to the principle of equal employment opportunity. Applicants for employment and employees are reviewed on their individual qualifications for a position. Under no circumstances will Rapid Micro Biosystems discriminate against qualified persons on the basis of race, color, religious creed, retaliation, national origin, ancestry, sexual orientation, gender identity, disability, mental illness, genetics, choice of health insurance, marital status, age, veteran status, or any other basis prohibited under applicable law.