Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

• Manufacturing Documentation Specialist

MAJOR DUTIES AND RESPONSIBILITIES

1. Perform review of procedures, batch record and/or forms to assure update with current practice, audits or cGMP and to address requirements of corrective and prevention actions (CAPAs).
2. Perform batch record review for the manufacturing different stages in order to ensure compliance with established procedures and documentation requirements, as well as cGMP regulations.
3. Audit and approve the executed batch records of manufacturing processes for all products manufactured at the site. This involves but not limited to the review of product and components reconciliation, completeness and correctness of information, in-process testing, sampling, expiration date, operation sequence and repeatability of the process.
4. Alert management on trends noted on evaluated process and verify actions taken in order to restate control and participate on the prevention and identification of root causes and internal complaints to pursue permanent corrective measure
5. Evaluate reports and documents the nature of incident and/or deviations at the time of occurrence of during document verification in order to determine immediate corrective actions to be taken and follow up on the investigation cause corrective/ preventive actions and documentation requirements.
6. Categorize and reports documentation errors and deviations in order to aware management of trends and focus on the required corrective measure.
7. Support investigations providing supplemented information related to Sterile Operations events.

KNOWLEDGE / SKILL

• B.S. in Natural Science (Chemistry, Microbiology, Biology) or related fields.
• At least 1-2 years of experience in a regulated environment. Manufacturing or Quality experience, preferable in a documentation function.
• Computer literate (knowledge on Microsoft Word, Microsoft Excel, Microsoft Power Point, QC-Main and SAP).
• Must exercise accurate judgment and be able to evaluate information critically and decide upon appropriate course of action. Must be able to correlate events and determine the action plan required to avoid incidents recurrence and apply them.
• Knowledge of compendia requirement and cGMP, FDA regulations and the ability to interpret and apply them.
• Must possess good verbal and written communication skills in English and Spanish
• Capable to manage multiple priorities.