Job title: documentation strategist
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summary: this role is responsible for overseeing the lifecycle of all documentation, ensuring accuracy and compliance with regulatory requirements.
about the role: major responsibilities include revising existing or creating new standard operating procedures (sops), coordinating updates with cross-functional teams, developing individual training plans, and staying current with industry standards.
key performance indicators: the ideal candidate will have a strong track record of delivering high-quality work, reducing errors, and improving efficiency.
work experience: a minimum of 3-5 years of experience in cgmp/fda regulated industries is required, with a strong knowledge of good manufacturing practices and regulatory requirements.
skills and qualifications: key skills include assembly language, cooperation, efficiency, electronic components, flexibility, general hse knowledge, good documentation practice, installations, international organization for standardization, job description, knowledge of gmp, lean manufacturing, manufacturing, manufacturing process, nuclear medicine, physics, product distribution, production line, scheduler, and languages including english.
benefits: as a valued member of our team, you can expect to receive comprehensive training, ongoing professional development opportunities, and a collaborative work environment that fosters innovation and growth.
other information: we are an equal opportunity employer committed to diversity and inclusion, and we welcome applications from candidates who share our values and commitment to excellence.