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Senior Manager – Late-Stage Process Transfer & Validation

Barrington James

Burgos

Híbrido

EUR 60.000 - 90.000

Jornada completa

Hace 3 días
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Descripción de la vacante

A leading CDMO in Spain is searching for a Senior Manager of Late-Stage Process Transfer & Validation to oversee the tech transfer and validation activities for pharmaceutical products. In this key leadership role, you will ensure seamless scale-up and GMP readiness while collaborating with cross-functional teams and client stakeholders. Candidates should possess a strong educational background combined with extensive experience in pharmaceutical manufacturing. Attractive hybrid work options and competitive benefits await you.

Servicios

Autonomy and ownership in high-impact programs
Direct access to senior leadership
Relocation support (if applicable)
Beautiful location in Spain

Formación

  • 7+ years of experience in pharmaceutical manufacturing or process development.
  • Demonstrated expertise in late-stage development, tech transfer, and process validation.
  • Strong knowledge of EU GMP, ICH, EMA / FDA guidelines.

Responsabilidades

  • Lead late-stage technology transfer of drug product manufacturing processes.
  • Oversee process validation, including PPQ campaign planning and execution.
  • Develop project plans, risk assessments, and validation master plans.

Conocimientos

Project Management
Communication
Risk Assessment

Educación

Degree in Pharmacy, Chemical Engineering, Biotechnology or related field
MSc or PhD preferred

Descripción del empleo

Senior Manager – Late-Stage Process Transfer & Validation

Location : Spain (Hybrid / Flexible Options Available)

Company : Confidential – Mid-Size CDMO Specializing in Drug Product Development & Manufacturing

About Us

We are a dynamic, mid-sized Contract Development and Manufacturing Organization (CDMO) located in Spain, supporting global pharmaceutical and biotech clients from clinical development through commercial supply. With a strong focus on injectables, aseptic fill-finish, and complex drug products, we blend scientific excellence with operational agility.

As we continue to grow our late-stage and commercial manufacturing capabilities, we're seeking a passionate and experienced Senior Manager of Process Transfer & Validation to lead key tech transfer and validation programs, ensuring seamless scale-up and GMP readiness.

Your Role

As Senior Manager, Late-Stage Process Transfer & Validation, you will be the technical lead for process scale-up, technology transfer, and validation activities for late-phase and commercial drug products. You’ll collaborate cross-functionally with internal teams and client stakeholders to ensure robust, compliant, and timely execution of tech transfer and validation strategies.

Key Responsibilities

  • Lead late-stage technology transfer of drug product manufacturing processes (e.g., aseptic fill-finish, lyophilization, complex formulations)
  • Oversee process validation, including PPQ campaign planning and execution
  • Develop and manage project plans, risk assessments, and validation master plans
  • Act as primary technical interface with clients during late-phase development and transfer
  • Work closely with MSAT, Quality, Regulatory, and Operations to ensure GMP-compliant implementation
  • Author and review protocols, reports, and regulatory documentation (e.g., BLA / MAA sections)
  • Support continuous improvement and troubleshooting of existing processes post-validation

Qualifications

  • Degree in Pharmacy, Chemical Engineering, Biotechnology or related field (MSc or PhD preferred)
  • 7+ years of experience in pharmaceutical manufacturing or process development, ideally in a CDMO or multi-product GMP environment
  • Demonstrated expertise in late-stage development, tech transfer, and process validation
  • Strong knowledge of EU GMP, ICH, EMA / FDA guidelines
  • Excellent communication and project management skills

Spanish is a strong plus.

What We Offer

  • A key leadership role in a growing international CDMO
  • Autonomy, ownership, and visibility in high-impact programs
  • Collaborative, agile culture with direct access to senior leadership
  • Competitive salary, bonus, and relocation support (if applicable)
  • Beautiful location in Spain with hybrid working options

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