26 QA Engineering Jobs in São Paulo, Brazil

Role highlights

• What You’ll Do Lead the quality agenda for GEM programs, ensuring safety and key quality risks are clearly framed, owned,…
• You will work closely with the Program Team, Product Development, Manufacturing, Suppliers, and Aftersales to turn data and meeting outputs…

Role highlights

• Partner with Quality, Supply Chain, R&D, and Commercial teams to ensure regulatory compliance throughout the product lifecycle.
• Strong knowledge of regulatory requirements and product lifecycle management for medical devices.

Role highlights

• Minimum Experience/Training Required: At least 10 years in the pharmaceutical industry of which a minimum of 7 years’ quality systems…
• Providing QA oversight on regulatory environment for GCP (pharmaceutical products).

Role highlights

• CTM Company: Thermo Fisher Scientific Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Clinica…
• Clinical Team Manager - Make an Impact at the Forefront of Innovation The Clinical Team Manager / Sr.

Role highlights

• Regulatory Assistant II Job Overview: Responsible for creation/revision/compilation/approval of Specifications/Documents for submission by…
• Summary of Responsibilities: These statements are intended to describe the general nature of the job and are not intended to…

Role highlights

• May routinely conduct Accompanied Field Visits (AFVs) and be accountable for project financials.
• Strong planning and organizational skills to enable effective prioritization of workload and workload of team members Strong interpersonal…

Role highlights

• We are currently seeking a Site Partner ( Study Start Up Associate II / Senior - Regulatory Submissions with clinical…
• Experience in site-facing roles such as Study Start-Up, Regulatory Associate, Site Activation Specialist, Site Activation Coordinator, or s…

Role highlights

• Strong background in cGMP laboratory operations, quality systems, method lifecycle management, equipment qualification, and data integrity…
• Cross-Functional Partnership Partner with Manufacturing, Engineering, Validation, Technical Services, Regulatory Affairs, and Quality Assur…

Role highlights

• We're looking for a CMC Strategy Senior Associate / Consultant who thrives in a dynamic, collaborative environment and is passionate…
• In this role, you'll work within a dedicated client program, partnering closely with a leading organization to drive high-impact submission…

Role highlights

• Bachelor's Degree required, no prior experience required Preferred Fields of Study: Life Sciences, Chemistry, Pharmacy, Engineering, or rel…
• As a valuable member of our Regulatory Affairs team, you'll compile technical documentation, review regulatory requirements, and support pr…

Role highlights

• Regulatory Affairs Specialist to join our diverse and dynamic team.
• Experience ensuring regulatory deliverables are performed in accordance with all relevant regulations, guidelines, policies and procedures…

Role highlights

• Principal Responsibilities Supports global activities related to product, including resolution of regulatory and quality issues.
• SAP ECC Supply Chain Modules, SAP APO.

Role highlights

• Job Overview Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or…
• Provide overall guidance and oversight of multi-regional and multi-protocol programs during initial start-up and maintenance phase as an in…

Role highlights

• Ensures adherence to global quality control and CRA performance metrics.
• AND A minimum of 4/5 years of Clinical Monitoring experience Previous experience working with Oncology projects Based in Sao Paulo/SP…