Documentation Specialist II
6 dagen geleden
Company Overview
">i-Pharm Consulting is a leading biotech company that specializes in quality assurance and GMP documentation.
">Job Summary
">We are seeking a highly skilled Documentation Specialist I to join our team. As a key member of our quality assurance department, you will be responsible for creating and maintaining accurate and compliant documents.
">Key Responsibilities
">- ">
- Develop and implement GMP documentation procedures">
- Ensure compliance with regulatory requirements">
- Maintain accurate records and files">
- Liaise with colleagues at all levels">
Requirements
">To be successful in this role, you will need:
">- ">
- Frequent fluency in English">
- Excellent communication and organizational skills">
- Able to work effectively in a fast-paced environment">
- Ability to expand knowledge of Quality Systems in the biotech sector">
What We Offer
">We offer a competitive salary package, including a base salary of €51,500 - €58,000 per annum, plus shift allowance. You will also have the opportunity to grow your career in quality assurance and GMP documentation.
">Shift Information
">You will work Monday - Friday, 39 hours/week, with one weekend day shift every six weeks. The shift starts at 8:30 am and ends at 5:00 pm.
">About Us
">i-Pharm Consulting is a dynamic and innovative company that values quality, precision, and career growth. We offer a supportive and collaborative work environment that encourages professional development and teamwork.
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