Validations Engineer

Werfenlife SA.; España; On-site; PHP 2,411,091 - 3,616,636; Full time

Job summary

Werfenlife SA. is seeking a Quality Manager to ensure compliance with quality standards in manufacturing processes. The role involves reviewing procedures, managing changes, and providing training in quality practices.

The ideal candidate will have a Bachelor's degree in Biotechnology or a related field and at least 3 years of experience in a similar position. Fluency in Spanish or Catalan, along with advanced English skills, is essential.

Qualifications

• Minimum of 3 years of experience in a similar position.
• Fluency in Spanish or Catalan, advanced knowledge of English required.
• Knowledge of Quality standards.

Responsibilities

• Review and approval of manufacturing procedures.
• Change Management and risk assessment.
• Provide training in validation and risk management.

Skills

Management of decisions under pressure

Methodical and well-organized

Teamwork

Ability to express information clearly

Systematic approach and control

Collaboration and coordination

Education

Bachelor's degree in Biotechnology or related field

Tools

Office Tools (Excel & Word)

SAP

Job description

Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong.

Overview

Assure that all products manufactured at OEM are designed, manufactured and released according to established procedures and validated processes. Assure that all facilities, utilities and equipment involved in the production of all products manufactured at OEM complies with defined standards.

Assure the proper implementation of good quality practices in all processes at OEM and be able to identify improvement opportunities necessary to contribute to the robustness of the OEM Quality System.

Responsibilities

Key Accountabilities

• Review and approval of manufacturing procedures, general procedures or instructions.
• Change Management: evaluate the impact of the proposed changes, approve action plan proposal and its implementation.
• Validation/ Qualification:
• Review of qualifications for facilities, equipment and utilities, including qualification strategy, execution and management of potential deviations detected.
• Factory acceptance Test (FAT) / Site acceptance test (SAT) execution / approval.
• Review of process validations, including validation strategy, execution and management of potential deviations detected.
• Be able to establish a strategy to validate changes. Review validation strategies and the corresponding documentation (protocol and report)
• Carry out, review and approve the risk assessment performed at OEM to evaluate the impact of changes in the final product.
• Provide training in validation & risk management to OEM staff to ensure that the organisation is both skilled in implementation and is utilising best in class methodologies.
• Participate in Internal and External Audits as needed.
• Perform Quality Training to all personnel at OEM.
• Management of Non-conformances and CAPA.
• Ensure that validation lots are appropriately tested, reviewed and released.
• Implement new procedures and instructions as a result of the observed practices on site to contribute to the Quality System robustness.
• Be proactive regarding the continuous improvement in Quality processes and procedures.

Internal Networking

To be determined based on department needs, to include interactions such as:

• Operations Area
• R&D Area

Qualifications

Minimum Knowledge & Experience required for the position

• Required: Bachelor's degree (Licenciatura) in any related area Biotechnology, other Sciences, or related field.
• Degree may be substituted by relevant skills and work experience.
• Valuable: Any additional degree higher than that required previously.
• Years of experience
  • Minimun of 3 years in a similar position.
• Min knowledge
  • Software: Fluency in Office Tools (Excel & Word), Valuable Basic knowledge in SAP.
  • Language: Fluency in Spanish or Catalan. Advanced knowledge of English (reading and speaking).
  • Standards: Knowledge of Quality standards.

Management has the discretion of substituting relevant work experience for a degree and/or making exceptions to the years of experience requirements.

Skills & Capabilities

The ideal candidate for this position will exhibit the following skills and capabilities:

• Management of decisions under pressure.
• Methodical and well-organized person
• Teamwork
• Ability to express information clearly and concisely to the staff, ensuring their understanding.
• Ability to apply a systematic approach and constant control, follow-up and verification of the results.
• Ability to collaborate, participate and coordinate actively with working group.
• Reflects values of Werfen in the quality of work and working relationship

Travel Requirements

Not required

Werfen appreciates and values diversity. We are an Equal Opportunity/Affirmative Action Employer M/F/D/V.