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Upper Merion Township, Pennsylvania, United States
Onsite
This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following:
Design required validation studies and write protocols for the facility and equipment.
Coordinate resources required to complete validation studies in a timely manner.
Execute validation studies per required schedules in a safe, compliant manner (e.g. LOTO).
Analyze test data and report questions/issues. Lead and document investigations of failed validation test results.
Complete validation protocols and validation summary reports with necessary approvals.
Support the review of new systems and modifications to existing systems to ensure designs comply with cGMPs and are able to be validated and maintained in a validated state.
Maintain validation equipment and supplies to enable validation to be completed per schedule requirements.
Support the development of required validation procedures and practices with respect to the facility.
Identify issues and/or improvements to validation procedures, practices, and policies related to validation, equipment and processes.
We are looking for professionals with these required skills to achieve our goals:
Bachelor's degree in a scientific discipline
OR 2+ years of experience working in a regulated GMP environment with an Associated degree
On site role
If you have the following characteristics, it would be a plus:
1+ years of experience in Validation, Automation or Process engineering
Familiar with cGMPs.
Strong interpersonal and organizational skills.
Technical understanding of the industry and validation practices related to the pharmaceutical industry is preferred.
Strong verbal and written communication skills.
Must be able to interact well with peers and senior personnel in multidisciplinary teams involving scientific, engineering, and operational disciplines.
Able to take directions and effective at implementing decisions.
Must have strong technical writing skills
#LI-GSK
Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.
Why GSK?
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.
People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
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