Job Information
Insight Global QA Data Associate in West Point, Pennsylvania
Job Description
One of our large pharmaceutical clients is actively hiring a QA Data Associate for a year long project. This team supports manufacturing for specialty products and services. They currently have a manual batch record system so one of their main responsibilities will be gathering batch records, making copies & scanning the data into a digital form. These batch records contain data related to batch production, and more specifically culture media batch record. It could include details such as numbers of starting materials, weighing protocols, temperatures, PH levels, etc. Eventually, this role will turn into more of a data analytics role where you will be creating platforms & dashboards so you can run trends and make analysis.
Other responsibilities may include:
Authors, supports, updates, and/or leads documentation updates such as SOPs, batch records, change control documents, technical protocols, validation documents and other GMP documentation
Supports deviations, including assessment of product impact and determination of root cause and corrective/preventative actions, assists in writing of investigations as well as quality incidents.
Supports equipment, and facility projects for the Culture Media and Weigh and Dispense Operations, and Black Widow Spider areas.
This role is hybrid, 3 days onsite & 2 days WFH.
We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com .
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Skills and Requirements
2+ years experience working in a GMP Manufacturing environment, preferred pharmaceutical
Strong Data Entry & Data Analytics experience
Batch Record Entry experience
Highly developed communication Pharmaceutical industry experience
Power BI experience null
We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal employment opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment without regard to race, color, ethnicity, religion,sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military oruniformed service member status, or any other status or characteristic protected by applicable laws, regulations, andordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to HR@insightglobal.com.