Validations Specialist

Rapid Micro Biosystems • St. David's, MA

1d • $70,000 - $85,000

About The Position

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 your skills. You’ll do more, learn more, and have the ability to make a profound impact on our business.

As a part of the RMB Global Customer Support Team, the Validation Specialist is responsible for execution of validation protocols for a cutting edge, automated system, including Installation/Operation Qualifications, Performance Qualifications, and support throughout the Method Qualification process. Additional responsibilities include writing/revising SOPs and validation documents, documenting customer feedback, and contribute as the technical expert during the Sales process.

This role requires up to 80% travel across North America, Europe, and Asia. Typical trips last approximately one week, with occasional longer assignments.

The anticipated start date for this role is Monday, July 6.

Requirements

• Bachelor's Degree is Life Sciences Discipline
• 2+ years of experience in the pharmaceutical industry in either Microbiology QC Labs or Validation

Nice To Haves

• Strong technical writing, verbal communication, and presentation skills
• Excellent problem solving and troubleshooting skills
• Experience and competence in a range of microbiological methods
• Knowledge of GxPs
• Knowledge of 21 CFR Part 11 and Annex 11
• Enthusiastic, detail oriented, and capable of working independently as well as working within a cross-functional team
• Proficient in Microsoft Office including Word, Excel, and PowerPoint
• Ability to form dependable and professional relationships with customers
• Project Management experience is a plus

Responsibilities

• execution of validation protocols for a cutting edge, automated system, including Installation/Operation Qualifications, Performance Qualifications, and support throughout the Method Qualification process
• writing/revising SOPs and validation documents
• documenting customer feedback
• contribute as the technical expert during the Sales process

Benefits

• competitive total compensation package
• attractive benefits package
• cash incentive opportunities
• equity grant

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level