Alten méxico is a leading engineering and technology consulting company with a global presence and expertise in a wide range of industries. As a subsidiary of the alten group, we have a proven track record of delivering innovative engineering solutions for our clients. We are currently seeking a talented "as built" documentation control professional to join our team, with a focus on the pharmaceutical industry.
as an "as built" documentation control professional, you will be responsible for managing and controlling the documentation related to the as-built status of pharmaceutical projects. You will work closely with project teams, contractors, and stakeholders to ensure accurate and up-to-date documentation is maintained throughout the project lifecycle.
responsibilities:
* manage and control the documentation related to the as-built status of pharmaceutical projects.
* review and verify documentation for accuracy and completeness.
* collaborate with project teams and contractors to ensure proper documentation practices and processes are followed.
* maintain and update document control systems and databases.
* ensure compliance with industry standards, regulations, and company policies.
* conduct periodic audits of documentation to identify any gaps or discrepancies.
* coordinate with stakeholders to resolve any documentation-related issues.
* provide support and guidance to project teams on documentation control processes and best practices.
* prepare and present reports on documentation status and progress to project managers and stakeholders.
requirements
* bachelor's degree in engineering, technical writing, or a related field.
* previous experience in documentation control, preferably in the pharmaceutical industry.
* strong knowledge of industry standards and regulations related to documentation control in the pharmaceutical industry.
* proficiency in document control systems and software.
* attention to detail and strong organizational skills.
* excellent communication and interpersonal skills.
* ability to work collaboratively in a cross-functional team environment.
* proficiency in english (written and verbal).
* experience with project management methodologies and tools.
* knowledge of good documentation practices (gdp) and good manufacturing practices (gmp).
* understanding of fda regulations and guidelines for documentation control in the pharmaceutical industry.
* experience with electronic document management systems (edms) is a plus.
* knowledge of validation processes and requirements in the pharmaceutical industry is desired.
* previous experience working with engineering teams, contractors, and stakeholders is preferred.
benefits
we offer
* base salary
* major medical expense insurance (includes dental and vision plan)
* 15 days bonus
* 25% vacation bonus
* 12 days of vacation (from the first year)
* social security
* ptu/profit sharing
* biweekly food vouchers
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