Kelly® Science & Clinical is seeking Manufacturing Documentation Specialist for a 6 month contract position at a Global Pharmaceutical client in Manati, Puerto Rico.  If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.

Salary: $19.60  per/hour

Overview

This client is Global Biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.

In this role you’ll be responsible to 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).

This role will give you an opportunity to transform patients’ lives through science by contribute with a global leading biopharma company powered by talented individuals who drive scientific innovation.

Responsibilities:

• 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.
  

• 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.
  

• 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
  

• 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.
  

• Categorize and reports documentation errors and deviations in order to aware management of trends and focus on the required corrective measure.

Qualifications:

• 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.
  

• Fully bilingual (Spanish/English) communication skills, both written and verbal.
  

• What happens next:
  

• Once you apply, you’ll proceed to next steps if your skills and experience look like a good fit. But don’t worry – even if this position doesn’t work out, you’re still in our network. That means our team of expert Science & Clinical recruiters will have access to your profile, making your opportunities limitless.

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