The Role
The Field Support Specialist provides technical support for Growth Direct™ systems, managing customer complaints, documentation, and ensuring compliance with quality standards in US pharmaceutical environments.
Summary Generated by Built In
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 primarily the US 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.
Primary Responsibilities
- Provide first-line remote technical support for Growth Direct™ system robotic, software, imaging, and microbial related issues
- Manage customer complaints per SLAs, Escalation Processes, and with Technical 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
- Perform backup coverage for Order Management as needed
- Support customers by participating in the weekend and holiday coverage rotation, ensuring new issues are acknowledged and urgent cases addressed promptly.
Skills
- 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
- Strong team player with a collaborative mindset
- Computer/Microsoft Office proficiency
- Experience with remote support tools, CRMs, and virtual collaboration platforms
- Regularly makes decisions autonomously with limited guidance/supervision required
Knowledge
- 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 and US 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
Education
- Minimum of technical degree in Life Sciences, Microbiology, Computer Science, Engineering or equivalent experience; bachelor's degree preferred
Environmental Factors
- Remote position primarily supporting US based customers during Eastern business hours.
- Candidates residing near our Lowell or Lexington, Massachusetts offices may elect to work on-site.
- Occasional travel to US - HQ for training and/or customer sites within US required (5% travel)
- Working outside of business hours may occur for critical customer issues
- Must have valid driver's license and passport
Rapid Micro Biosystems is proud to offer a competitive total compensation package designed to attract, inspire and retain the best talent in our industry. In addition to base pay, our full-time regular employees are eligible for an attractive benefits package, cash incentive opportunities, and an equity grant.
The base salary hiring range for this position is $64,500-85,900
Starting salaries are determined based on skills, experience, budget and other job-related factors. More information about our total compensation package will be shared with candidates during the recruitment process.
ABOUT RAPID MICRO BIOSYSTEMS:
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.
Equal Opportunity:
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.
Top Skills
Customer Relation Management (Crm)
Lims
MS Office
Qms
SQL
Am I A Good Fit?
Get Personalized Job Insights.
Our AI-powered fit analysis compares your resume with a job listing so you know if your skills & experience align.
Success! Refresh the page to see how your skills align with this role.
The Company
What We Do
Rapid Micro Biosystems is an innovative life sciences technology company providing mission-critical automation solutions to facilitate the efficient manufacturing and fast, safe release of healthcare products such as biologics, vaccines, cell and gene therapies, and sterile injectables. We are the trusted partner in quality control microbiology automation, enabling our customers to improve and save lives.
This vision has been realized with the development of the Growth Direct® System.
Our Growth Direct® platform automates and modernizes the antiquated, manual quality control microbiology testing workflows used in the largest and most complex pharmaceutical manufacturing operations across the globe. The Growth Direct® platform brings the quality control lab to the manufacturing floor, unlocking the power of in-line/at-the-line QC automation to deliver faster results, greater accuracy, increased operational efficiency, better compliance with data integrity regulations, and quicker decision making that customers rely on to ensure safe and consistent supply of important healthcare products.
Our company values guide us in our vision:
Customer Driven – We are committed to providing our customers with the highest quality products and services
Respect – We welcome and embrace our differences to create a trusting environment
Grit – We are determined to turn challenges into successes.
One RMB – We operate as one team, committed to our shared purpose.
The company is headquartered and has U.S. manufacturing in Lowell, Massachusetts, and global locations in Switzerland, Germany, and the Netherlands
