Project Engineer - King of Prussia, United States - GlaxoSmithKline

GlaxoSmithKline King of Prussia, United States

1 week ago

Description

Site Name:
USA - Pennsylvania - King of Prussia

Posted Date:
Apr
GSK is currently looking for a Project Engineer to join our team in Upper Merion, PA. This role will manage up to $2MM of capital across multiple projects involving commercial-scale process equipment and manufacturing suites.

Responsibilities are inclusive of design, installation, qualification, and improvement of equipment and facilities in an EHS- / Regulatory- / GEP-compliant manner at the Upper Merion GSC Biopharm site.

Key Responsibilities:

Lead and/or participate in the design and installation of new, or modifications to existing, process and/or utility systems, including bioreactors, chromatography skids, depth filtration skids, UFDF skids, etc., to meet technical, budget, and schedule goals.

Develop a project plan and budget, and then implement the approved modifications, following up to ensure the desired result has been achieved.

Document modifications in an appropriate manner. Ensure work is performed to the appropriate GxP standards, policies, and procedures. Generation, completion, & archive of various documents necessary to ensure regulator compliance, e.g. validation protocols / reports, turnover packages, drawings, etc.

Lead discussions and recommend solutions with key customer groups in order to gain a consensus on the repair or modification plans.

Be personally responsible for the coordination of all Engineering activities from implementation to handover to customer for a given project, including management of third party engineering firms and/or trades.

In cooperation with the Validation Group, develop commissioning and validation documentation, including test protocols, and implement validation plans on new process and utility systems and changes to existing systems, in order to maintain the validated status of existing systems.

Stay current with developments in the field of biopharm technology. Support the transfer of technology from development into manufacturing.
Follow up on projects' status and arising issues/changes with all relevant parties (customer, finance, procurement and engineering departments).
Ensure EHS corporate standards, local legislation, and other Regulatory requirements are included while planning and executing all projects.

Also, ensure proper identification and assessment of potential EHS risks that are significant to the business and that can be eliminated or minimized before or during project implementation.

Apply corporate EHS standards related to employee's safety during construction/ demolition processes to achieve zero reportable injury rate, with continuous supervision and control on contractors' activities.

Why you?

Basic Qualifications:
We are looking for professionals with these required skills to achieve our goals:
Bachelor's degree in engineering or equivalent technical discipline
At least 2 years of prior project and/or process engineering experience in the pharmaceutical industry.

Preferred Qualifications:
If you have the following characteristics, it would be a plus:

Prior project experience in the design, construction, start-up and operation of large bulk biopharmaceutical facilities including cell culture and/or microbial fermentation, or protein recovery and purification.

Demonstrated ability to manage projects to completion on time and within budget.
Familiar with cGMPs, GEPs, and NIH Recombinant Guidelines for large scale biological processing. Detailed understanding of Design, Installation, and Commissioning / Qualification / Validation of new pharmaceutical equipment and/or utilities.
Must be able to interact well with peers, subordinates, and senior personnel in scientific, engineering, and operational disciplines.
Demonstrated ability to participate as a leader or member on cross-functional and self-directed work teams
Sense of Urgency / Decision making.
Strong interpersonal skills.
Must be able to work within a multi-disciplinary team environment.
Must be able to generate options to resolve problems, prioritize solutions and implement decisions. Must be competent in handling simultaneously occurring tasks and smaller projects, and have excellent written and oral communication skills.
Good Computer Skills (MS Office, MS Projects).
Project Management Professional Program Certification or Professional Engineer license (Preferable).
#LI-GSK
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GSK US Benefits Summary

t o learn more about the comprehensive benefits program GSK offers US employees.
Why Us?

GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organization where people can thrive.

Getting ahead means preventing disease as well as treating it, and we aim to positively impact the health of 2.5 billion people by the end of 2030.

Our success absolutely depends on our people.

While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive.

We want GSK to be a workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy.

We're committed to being more proactive at all levels so that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce.

If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at US Toll Free) or outside US).
GSK is an Equal Opportunity Employer and, in the US, we adhere to Affirmative Action principles.

This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.

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.

GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment.

This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements.

For more information, please visit GSK's Transparency Reporting

For the Record

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