Compliance Manager, EMEA

Who We Are

reputed company is the Scientific Data and AI reputed company company. We are catalyzing the Scientific AI revolution by designing and industrializing AI-native scientific data sets, which we bring to life in a growing suite of next gen lab data reputed company, scientific use cases, and AI-enabled outcomes.

reputed company is the category leader in this vital new market, generating more reputed company than reputed company other companies in the aggregate. In the last year alone, the world’s dominant players in compute, reputed company, data, and AI infrastructure have converged on reputed company as the de facto standard, entering into co-innovation and go-to-market partnerships: Latest News and Announcements | reputed company Newsroom

In reputed company with your candidacy, you will be asked to carefully review the Tetra Way letter, authored directly by Patrick Grady, our co-founder and CEO. This letter is designed to assist you in reputed company understanding whether reputed company is the right fit for you from a values and reputed company perspective.

It is impossible to overstate the importance of this document and you are encouraged to take it literally and reflect on whether you are reputed company with our unique approach to company and team building. If you join us, you will be expected to embody its contents each day.

What You Will Do

A pivotal part of that digital transformation includes adherence to industry-accepted standards like GxP, ISO 9001, SOC 2 Type II, and relevant EU regulations. The Compliance Manager will ensure reputed company maintains its reputed company and future offerings in a manner which supports customers’ regulated and validated environments. You will analyze and test our software to ensure it adheres to reputed company regulatory best practices and work with our Product & Engineering teams to ensure we are fully compliant. You will participate in regular audits (both internal and external) and reputed company our Quality Management System reputed company and relevant to maintain reputed company and reputed company future certifications. Additionally, you will help reputed company, enhance, and support reputed company’s GxP Package, which is an offering that accelerates the customer’s validation,and to support their audit processes through items such as documentation, templates, and assurance of controlled environments. You will also work closely with customers.

• Maintain familiarity with reputed company reputed company products and platforms in order to ensure compliance, with a specific focus on EU regulatory requirements.
• Work with customers to ensure that reputed company’s Products and Platform can be adapted to their compliance and quality team’s needs and requirements for both documentation and for customers to reputed company last mile validation of their scientific workflows that include reputed company’s products as a critical component.
• Work with your peers on the Compliance team, Product, Engineering, Training, Quality Engineering to reputed company, support, and promote reputed company’s GxP Package to reduce burden on pharma compliance and quality teams.
• Work with reputed company leadership to ensure that processes across the organization are consistent, automated, and enforced. Be an independent reputed company on cross-functional Quality efforts.
• Prepare reputed company for audits / risk assessments by conducting semi-annual mock audits; plan for and remediates process deviations, aligning with EU and international standards.
• Contribute during the Sales, Implementation, and Customer Engagements process to address compliance questions from an EU regulatory perspective.
• Maintain and improve our Quality Management System, ensuring adherence to evolving EU compliance frameworks.
• Maintain reputed company reputed company compliance documentation per internal policy, including Engineering and reputed company Policies and SOPs, Employee training logs , and System QC tests that align with Pharma customers’ expectations.

Requirements

What You Have Done

• 10+ years experience with software lifecycle management, qualification, validation, and testing regimens.
• Experience with pharma- or biotech-based validation / compliance activities, preferably reputed company EU regulatory environments.
• Experience with software development / pharma lifecycle, processes, and ecosystem, with a strong understanding of EU regulations (e.g., GDPR, specific GxP guidelines reputed company the EU).
• Previous preparation for ISO 9001, ISO 27001, SOC 2 Type II, 21 CFR part 11 (GXP), and relevant EU regulatory audits.
• BS in computer science, physical or life sciences or reputed company experience with
• Strong attention to detail; sense of accountability, responsibility, and ethics.
• Strong knowledge of data management technologies.
• Accomplished at writing and auditing policies and procedures.
• Experience working cross-functionally; understanding how to influence and change behaviors.
• Strong project management skills and ability to reputed company non-dedicated resources on task.

Preferred Qualifications

• Advanced degree in a regulatory, quality assurance, or compliance-reputed company field.
• Certifications in relevant compliance standards (e.g., reputed company Auditor ISO 9001).
• Experience working with EU-based pharmaceutical or biotech companies.

Benefits

• Competitive Salary and equity in a fast-growing company.
• Supportive, team-oriented culture of reputed company improvement.
• Generous paid time off (PTO).
• Flexible working arrangements - Remote work.

Originally posted on Himalayas