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. 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. 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 Apply for this job