QA Validation and Systems Specialist

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Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

QA Validation and Systems Specialist

The QA- Validation and Systems Specialist is part of the quality assurance team in Israel and reports to the Systems and equipment Team Leader, Quality Assurance. The QA- Validation specialist is responsible for quality activities related to qualification and maintenance of manufacturing and laboratory equipment and systems whether for research or applied (ISO 13485) products.

KEY TASKS & RESPONSIBILITIES

Validation, qualification and re- qualifications of manufacturing equipment, systems & processes: design, create and approve protocol and field execution of protocols.
Coordinate and support the change controls of new/modification of equipment and packaging material of final products.
Write and support in deviation handling in regard to systems and equipment in the facility.
Initiate, create and review relevant documents in the Documentation system (SOPs, Procedures, Validation Protocols, Manufacturing Protocols)
Internal and external audits performance.
Presenting Sigma-Aldrich Israel Quality system to customers (internal and external) when required
Perform QA shop floor inspections in the production and logistics departments.
Weekly monitoring of temperature and humidity in critical control units.
Perform other duties and responsibilities assigned by Validation and Systems Team Leader, Quality Assurance.

EDUCATION/LANGUAGES
Academic Degree (Bsc.) in Natural Sciences or Engineering (Chemistry, Biochemistry, Biotechnology or Microbiology).
English: Technical (read/written/spoken)

PROFESSIONAL SKILLS & EXPERIENCE

Previous industrial experience in a cGMP-manufacturing environment or ISO 13485 is an advantage.
Previous experience in validation/qualification of processes and equipment.
Proficient Microsoft Office applications including Word, Power Point and Excel.

PERSONAL SKILLS & COMPETENCIES

Good interpersonal skills.
Energetic and able to work in dynamic environments.
Strong problem solving and analytical skills.
Fluency in both written and spoken English.
Excellent communication skills
Good ability to work in teams
Multitasking and time management abilities
Detail oriented, excellent organizational and planning skills.

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of our diverse team!