Validation Engineer
We are seeking a skilled Validation Engineer to join our team on an initial 12-month contract. This role involves ensuring the ongoing validation and compliance of equipment, systems, and processes in a highly regulated environment.
Key Responsibilities:
* Executing FAT/SAT/IOQ protocols including generation of protocols and reports.
* Designing, executing and reporting on validation studies for equipment, systems and processes.
* Ensuring validation studies are managed in conjunction with all required standards and legal requirements.
* Providing technical interpretation and guidance of current FDA and EU validation requirements.
* Ensuring that the validation status of equipment and systems are in compliance with cGMP at all times.
* Maintaining validation documentation through the validation lifecycle.
* Participation in external regulatory inspections.
Requirements:
* 3-5 years of experience in a healthcare manufacturing environment (preferably pharmaceutical).
* Degree in Science (Chemistry, Microbiology, or Pharmacy) or Engineering (Chemical, Mechanical, or Electrical).
* Strong knowledge of validation regulations, GAMP, ISPE, and quality systems.
* Technical understanding of pharmaceutical equipment and processes.
* Excellent communication, project execution, and problem-solving abilities.
* Proficient with MS Project and SPC tools (advantageous).
Benefits:
This is an excellent opportunity for you to develop your skills and contribute to the success of our organization. We offer a competitive compensation package and opportunities for professional growth.
About Us:
We are a global company committed to delivering high-quality products and services to our customers. Our values include integrity, innovation, and teamwork.