Urgent! Validation Engineer Job Opening In King of Prussia – Now Hiring 1925 GlaxoSmithKline LLC
We make and supply medicines and vaccines all around the globe and our teams own every production stage, from creating quality products at our manufacturing sites to designing effective supply forecasting and regulatory inspections; all powered by digital, data and analytics.
We operate at impressive scale, producing over 1.7 billion packs of medicine and 767 vaccine doses in 2021.
We continue to modernize, so we can launch even more new products at speed whilst turbo-charging delivery across our entire portfolio through our relentless focus on quality, safety, and service.
The way we work will change.
For some, the shift in technology and products will be revolutionary.
Our R&D pipeline demands a new kind of supply chain, and we need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of automation and robotics so we can work smarter together.
As a Validation Engineer, you will be responsible for equipment/facility validation projects in a hands-on role including writing validation protocols, scheduling and executing testing, gathering and analyzing data, and writing validation summary reports.
This person will participate as a supporting member representing validation on project teams.
Validation Engineers will lead specific validation projects.
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.
Why you?
Basic Qualifications:
We are looking for professionals with these required skills to achieve our goals:
Associates degree with 2 + years with biotech or pharma experience
OR BS/BA degree with 1+ year of experience with biotech or pharma
Preferred Qualifications:
If you have the following characteristics, it would be a plus:
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.
1+ years of process engineering or validation engineering experience with biotech or pharma
understanding how to read or process P&ID
Working with Kneat
SIP and CIP validation experience
Familiarity with Lock out tag out
Prior experience with Kaye Software in temperature mapping
Please visit 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.
GSK is an Equal Opportunity Employer.
This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.
Important notice to Employment businesses/ Agencies
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site.
All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK.
The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK.
In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK.
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Unlock Your Validation Engineer Potential: Insight & Career Growth Guide
Real-time Validation Engineer Jobs Trends in King of Prussia, United States (Graphical Representation)
Explore profound insights with Expertini's real-time, in-depth analysis, showcased through the graph below. This graph displays the job market trends for Validation Engineer in King of Prussia, United States using a bar chart to represent the number of jobs available and a trend line to illustrate the trend over time. Specifically, the graph shows 172049 jobs in United States and 548 jobs in King of Prussia. This comprehensive analysis highlights market share and opportunities for professionals in Validation Engineer roles. These dynamic trends provide a better understanding of the job market landscape in these regions.
Great news! 1925 GlaxoSmithKline LLC is currently hiring and seeking a Validation Engineer to join their team. Feel free to download the job details.
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An organization's rules and standards set how people should be treated in the office and how different situations should be handled. The work culture at 1925 GlaxoSmithKline LLC adheres to the cultural norms as outlined by Expertini.
The fundamental ethical values are:The average salary range for a Validation Engineer Jobs United States varies, but the pay scale is rated "Standard" in King of Prussia. Salary levels may vary depending on your industry, experience, and skills. It's essential to research and negotiate effectively. We advise reading the full job specification before proceeding with the application to understand the salary package.
Key qualifications for Validation Engineer typically include Engineers and a list of qualifications and expertise as mentioned in the job specification. Be sure to check the specific job listing for detailed requirements and qualifications.
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Before the Interview:To prepare for your Validation Engineer interview at 1925 GlaxoSmithKline LLC, research the company, understand the job requirements, and practice common interview questions.
Highlight your leadership skills, achievements, and strategic thinking abilities. Be prepared to discuss your experience with HR, including your approach to meeting targets as a team player. Additionally, review the 1925 GlaxoSmithKline LLC's products or services and be prepared to discuss how you can contribute to their success.
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