Immatics

Senior Director, Payer Accounts

Bachelor's degree with 12+ years in pharmaceutical/biotech market access; 5+ years national payer account management; cell/gene therapy or complex biologics experience; strong strategic, analytical, and cross-functional leadership.

Senior Clinical Sciences Manager

Bachelor’s degree in biology, pharmacy, or related field; 7+ years literature research; clinical trial support; site staff training.

Senior Operational Quality Assurance Specialist

Bachelor's in pharmaceutical/life sciences; 4+ years QA in biotech/pharma; cGMP/gCP; batch release; document control; deviations/CAPA.

Senior Manager Regulatory Affairs*

Senior Manager Regulatory Affairs

Lead Regulatory Intelligence, develop processes, support CTA documentation; 5+ years in Regulatory Affairs; experience with biologics/ATMPs.

Senior Quality Assurance Investigations Specialist - Second Shift

Quality Assurance Investigations Specialist

Bachelor's in pharmaceutical/life sciences or related field; 5+ years QA in cell/gene therapy; 6+ years biotech/pharma; knowledge of regulatory CGMP/GxP; experience with deviations, CAPA, batch release.

Working Student - Sample Management*

Working Student - Sample Management

Enrolled in a Bachelor’s or Master’s program in life sciences or related field; lab/regulated environment experience preferred; strong data skills; English fluency, German preferred.

(Associate) Manager Sample Management*

Manager Sample Management

Master’s or Ph.D. in life sciences; English C1; German preferred; experience in sample management, GxP, and translational research.

Manager Regulatory Affairs - Submission Lead*

Regulatory Affairs Manager

Master’s degree in Life Sciences; 2+ years EU CTIS submissions; English C1; German is a plus.

Director, Facilities, Engineering, and Maintenance

Director of Facilities, Engineering & Maintenance

10+ years in biotech/pharma facilities engineering & maintenance; 5+ years of leadership; BS in Engineering; US work authorization; GMP/regulatory experience.

Quality Control Analyst II

Two+ years in a regulated lab; BA/BS in science; cell culture experience.

Bachelor's in pharma/life sciences; 4+ years QA in cell/gene therapy or biopharma; strong regulatory knowledge; batch release experience; CAPA handling.

Director, Medical Communications

Advanced scientific/medical degree; 10+ years in Medical Communications/Publications; leadership of global publication plans and major congress execution.

Associate Director Regulatory Affairs – CMC Lead*

Associate Director Regulatory Affairs

8+ years Regulatory Affairs CMC experience for biologics/ATMPs; MSc/PhD in natural sciences; EU CMC leadership; GMP/CMC knowledge; Health Authority interactions; English required, German preferred.

Associate Director Regulatory Affairs – Clinical Lead*

Regulatory Affairs Lead

Master’s degree in natural sciences or Regulatory Affairs; 8+ years regulatory affairs in biopharma/ATMPs; EU regulatory strategy leadership; experience with EU Health Authority interactions; CTA lifecycle management in Europe; strong communication; English (German a plus).

Manufacturing Associate

Manufacturing role supporting clinical manufacturing, aseptic cell processing, GMP/GxP compliance, documentation, and collaboration.

Director Clinical Regulatory Affairs (US)

Director of Clinical Regulatory Affairs

Master’s degree; 10+ years in regulatory affairs; proven FDA interaction leadership; complex program regulatory strategy

Associate Director, Team Lead Site Operations

Lead clinical trial site operations in the USA; oversee feasibility, site selection, initiation, monitoring; manage internal staff; ensure SOP/ICH GCP compliance.

SAP S/4HANA Manufacturing Technical and Functional Specialist

5+ years SAP S/4HANA manufacturing experience; ECM and master data; validation in regulated environments; ECC to S/4HANA migrations a plus.

Senior Clinical Research Associate

Senior CRA with 4+ years on-site monitoring; strong knowledge of ICH-GCP, FDA/EMA; site management; trial master files; able to work fully remote.

Clinical Trial Manager

Bachelor's in life sciences; 2+ years on-site monitoring and CTM experience in pharma/biotech; knowledge of ICH-GCP, FDA/EMA; CTMS/eTMF experience; strong communication and project management.

Medical Science Liaison (Southeast)

Medical Science Liaison

Medical Science Liaison with 5+ years in biotech, supporting clinical development and scientific exchange, plus strong communication and travel readiness.

Associate Director of Operational Excellence

Bachelor’s in engineering or life sciences; Lean Six Sigma Black Belt required; 8–10 years OE experience in biotech/pharma or related industries; strong Lean, DMAIC/DFSS, RCA, CAPA, and change leadership.

Title	Location	Date
Senior Director, Payer Accounts Full Time · $260K-$285K · 12+ YOE Houston or United States · Remote	Houston or United States Remote	Apr 29, 2026
Senior Clinical Sciences Manager Full Time · 7+ YOE United States or Houston · Remote	United States or Houston Remote	Apr 28, 2026
Senior Operational Quality Assurance Specialist Full Time · 4+ YOE Houston, Texas, United States · Onsite	Houston, Texas, United States Onsite	Apr 28, 2026
Senior Manager Regulatory Affairs* Full Time · 5+ YOE Munich or Tübingen · Hybrid	Munich or Tübingen Hybrid	Apr 24, 2026
Senior Quality Assurance Investigations Specialist - Second Shift Full Time · 5+ YOE Stafford, Texas, United States · Onsite	Stafford, Texas, United States Onsite	Apr 17, 2026
Working Student - Sample Management* Part Time, Full Time, Contract, Internship, Temporary, Seasonal, Volunteer Tuebingen, Baden-Württemberg, Germany · Onsite	Tuebingen, Baden-Württemberg, Germany Onsite	Apr 16, 2026
(Associate) Manager Sample Management* Full Time Tuebingen, Baden-Württemberg, Germany · Onsite	Tuebingen, Baden-Württemberg, Germany Onsite	Apr 14, 2026
Manager Regulatory Affairs - Submission Lead* Full Time · 2+ YOE Munich or Tübingen or Germany · Hybrid	Munich or Tübingen or Germany Hybrid	Apr 13, 2026
Director, Facilities, Engineering, and Maintenance Full Time · 10+ YOE Stafford, Texas, United States · Onsite	Stafford, Texas, United States Onsite	Apr 10, 2026
Quality Control Analyst II Full Time · 2+ YOE Houston or Stafford · Onsite	Houston or Stafford Onsite	Apr 8, 2026
Senior Operational Quality Assurance Specialist Full Time · 4+ YOE Houston, Texas, United States · Onsite	Houston, Texas, United States Onsite	Mar 26, 2026
Director, Medical Communications Full Time · 10+ YOE Houston or United States · Remote	Houston or United States Remote	Mar 26, 2026
Associate Director Regulatory Affairs – CMC Lead* Full Time · 8+ YOE Munich or Tübingen or Germany · Hybrid	Munich or Tübingen or Germany Hybrid	Mar 23, 2026
Associate Director Regulatory Affairs – Clinical Lead* Full Time · 8+ YOE Munich or Tübingen or Munich · Hybrid	Munich or Tübingen or Munich Hybrid	Mar 9, 2026
Manufacturing Associate Full Time · 0+ YOE Houston, Texas, United States · Onsite	Houston, Texas, United States Onsite	Mar 3, 2026
Director Clinical Regulatory Affairs (US) Full Time · $221K-$254K · 10+ YOE Houston or United States · Hybrid	Houston or United States Hybrid	Feb 17, 2026
Associate Director, Team Lead Site Operations Full Time · 4+ YOE United States · Remote	United States Remote	Feb 16, 2026
SAP S/4HANA Manufacturing Technical and Functional Specialist Full Time · 5+ YOE Stafford or Texas · Onsite	Stafford or Texas Onsite	Feb 16, 2026
Senior Clinical Research Associate Full Time · $120K-$125K · 4+ YOE United States · Remote	United States Remote	Feb 9, 2026
Clinical Trial Manager Full Time · 4+ YOE United States · Remote	United States Remote	Feb 9, 2026
Medical Science Liaison (Southeast) Full Time · $200K-$230K · 5+ YOE United States or Texas · Remote	United States or Texas Remote	Jan 15, 2026
Associate Director of Operational Excellence Full Time · 8+ YOE Houston or Stafford · Onsite	Houston or Stafford Onsite	Jan 9, 2026

Activities	Biotechnology researchDrug discoveryClinical researchImmunotherapy developmentPharmaceutical manufacturing
Headquarters	DE
Industries	BiotechnologyPharmaceuticals
Name	Immatics
Employees	645
Type	Public
Subsidiaries	Immatics Biotechnologies GmbHImmatics US, Inc.
Tagline	Develops T-cell redirecting immunotherapies for cancer treatment.
Founded	2,000
Website	immatics.com
Stock Exchange	NASDAQ
Stock Symbol	IMTX

Immatics

About Immatics