Validation Engineer

Supporting Technical Operations Leaders to Build High-Performing Biopharma Teams | Recruitment Consultant @ Panda
Leiden, The Netherlands  –  6 Months (Extension Possible)

Job Description
Our client is a well-known Biotech company in the Netherlands currently experiencing a high workload within their Validation team. This role is crucial for supporting the qualification and validation activities necessary to maintain cGMP compliance across their equipment and processes.

You will be responsible for executing and documenting essential equipment qualification and re-qualification activities as defined by the Validation Master Plan. Your focus will be on maintaining the validated state of existing equipment, qualifying newly introduced equipment, and supporting the team in deviation handling and CAPA ownership to ensure continuous compliance and operational readiness.

Qualifications

Education Requirement:  Degree in Engineering or equivalent.

Minimum years of experience:  At least 4-5 years experience in validation, CQV, or Project Engineering positions within a  GMP  environment.

Core technical expertise:  Strong knowledge of  GMP  (Good Manufacturing Practice).

Required hands-on skills:  Experience in writing, executing, and reporting qualification protocols, along with reviewing protocols and reports.

Required scientific/technical knowledge:  

Experience with  Equipment Qualifications  (IQ/OQ/PQ) and  Routine Equipment (Re-)Qualification .

Preferred Requirements

Additional experience:  

Experience with in the  Bio Pharmaceutical  or  Biotech  industry is a significant advantage.

Advanced technical skills:  Experience supporting the introduction of new programs concerning Validation information.

Specific technologies or platforms:  N/A

Industry or domain exposure:  Experience supporting and owning  deviation handling  and  CAPA's .

Soft skills or certifications:  Analytical, self-starter, and proficient in  English  (Dutch is an advantage).

Practicalities

Start Date:

ASAP

Contract Duration:  6 months (Extension possible)

Location:

The Netherlands (Specific location to be confirmed)

Additional:  The interview process is fast: A Teams interview with the Director of Engineering and Validation Manager (max 1 hour), followed immediately by a decision. You may also participate in Practical Process Improvement (PPI) project teams.

Interested?
Interviews and offers can move quickly. Send your CV to  Oluali Titelman  at    today to secure your spot in the process.

Seniority level
Mid-Senior level

Employment type

Contract

Job function

Engineering, Manufacturing, and Science

Industries

Pharmaceutical Manufacturing, Biotechnology Research, and Hospitals and Health Care

Referrals increase your chances of interviewing at Panda International by 2x

#J-18808-Ljbffr