Documentation Specialist Opportunity
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We are seeking a skilled Documentation Specialist to join our team. As a key member of the team, you will play a critical role in creating and updating high-quality documentation for our Biologics CoE.
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Main Responsibilities:
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* Create and update various documents, including SOPs, BPDs, Protocols, Reports, and WI, in compliance with regulatory requirements.
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* Put SOPs through the VEEVA system for approval and validation.
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* Collaborate with relevant teams, labs, and quality assurance to ensure seamless documentation processes.
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Required Skills and Qualifications:
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* Previous experience with VEEVA is essential.
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* Proven track record of updating SOPs and technical writing.
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* Ability to work independently with strong attention to detail.
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* Strong technical background, either engineering or scientific.
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Benefits:
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A dynamic and innovative work environment with opportunities for growth and development. Contribute to the creation of life-changing treatments for individuals suffering from rare diseases.