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Building Automation Project Manager
GPAC
Waukegan, IL
- $85,000 to $115,000 USD / year
A regionally recognized mechanical design, construction, service, operations and facilities management company is seeking a Building Automation Project Manager.
Added just now
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Building Automation Project Manager
GPAC
Schaumburg, IL
- $85,000 to $115,000 USD / year
A regionally recognized mechanical design, construction, service, operations and facilities management company is seeking a Building Automation Project Manager.
Added 6 mins ago
SC
TopStitch - Early Career Development Program
Stitch Consulting Services, Inc.
Indianapolis, IN
- $70,000 USD / year
You default to tools and automation when approaching new problems. It's not a habit - it's how you think. You balance that with knowing when a human critical eye is necessary, and when to…
Added 6 mins ago
Associate Director Technical Producer
Stitch Consulting Services, Inc.
Remote, United States
…custom preference centers, API-triggered messaging, and advanced automation logic that makes Braze…
Added 7 mins ago
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Accountant, Accounts Receivable with SAP S/4HANA
RGP
Loveland, CO
- $40 to $55 USD / hour
Location: Candidate will be onsite in Loveland, CO, five days per week · Availability to be in-office five days per week in Loveland, CO
Added 7 mins ago
Facilities Engineer
University of Colorado Denver
Boulder, CO
Added 7 mins ago
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nCino Salesforce Developer
ManpowerGroup
Boulder, CO
- $70 to $75 USD / hour
We are seeking a Senior nCino Developer to support a large-scale Commercial Lending transformation initiative. This individual will play a key role in designing, developing, and enhancing…
Added 7 mins ago
BAS Construction Technician
Setpoint Systems Corporation
Littleton, CO
System Start-up: Lead the initial start-up phases for building automation systems.
Added 7 mins ago
BAS Construction Technician
Setpoint Systems Corporation
Littleton, CO
System Start-up: Lead the initial start-up phases for building automation systems.
Added 7 mins ago
Operations Manager
Setpoint Systems Corporation
Littleton, CO
…lead our dynamic project teams into the next era of building…
Added 7 mins ago
Engineering Manager
Setpoint Systems Corporation
Littleton, CO
…exceptional results in the design and execution of building automation systems (BAS), including Delta Controls and Tridium. This role demands strong leadership, technical expertise, and the…
Added 7 mins ago
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Warehouse Technician
Setpoint Systems Corporation
Littleton, CO
- $19 to $25 USD / hour
…Setpoint Systems Corporation has been a powerhouse in building automation. As we undergo a period of rapid growth and expansion, we are looking for a motivated, highly reliable individual…
Added 7 mins ago
Operations Manager
Setpoint Systems Corporation
Littleton, CO
…lead our dynamic project teams into the next era of building…
Added 7 mins ago
SS
Warehouse Technician
Setpoint Systems Corporation
Littleton, CO
- $19 to $25 USD / hour
…Setpoint Systems Corporation has been a powerhouse in building automation. As we undergo a period of rapid growth and expansion, we are looking for a motivated, highly reliable individual…
Added 7 mins ago
Engineering Manager
Setpoint Systems Corporation
Littleton, CO
…exceptional results in the design and execution of building automation systems (BAS), including Delta Controls and Tridium. This role demands strong leadership, technical expertise, and the…
Added 8 mins ago
Generative AI / Internal Tools Development
Apogee Engineering
Colorado Springs, CO
Added 8 mins ago
SharePoint & Power Platform Technical Consultant
RSM US LLP
Denver, CO
Added 8 mins ago
Field Ops Engineer II - Phoenix, AZ, Los Angeles, CA, Dallas, TX, Denver, CO
Lumen
Denver, CO
…planning, deployment management, inventory tracking, training, automation initiatives, driving visibility and safety programs, non-storm operational activities, and BCM partnerships focused…
Added 8 mins ago
Senior Growth Intelligence Analyst
Lumen
Denver, CO
Familiarity with CRM, customer data, marketing automation, or Martech platforms.
Added 8 mins ago
Accountant
Gates Co
Denver, CO
…Gates Corporate Accounting (accuracy, timeliness, controls, automation, etc.). - Maintains financial records and ensures that financial transactions are properly recorded. - Ensures the…
Added 8 mins ago
Pipe Mechanical Trades - II Facilities Maintenance Technician Lead (Housing)
University of Colorado Denver
Denver, CO
Added 8 mins ago
Production Network Engineer, Design
Meta
Denver, CO
…and monitoring. Simple, elegant, and scalable network design, automation, and data analytics are the keys to meeting our demands. In this role, you will be part of a team that is…
Added 8 mins ago
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Automated Test Engineer
Eliassen Group
Denver, CO
- $40 to $50 USD / hour
…driving bug resolution across teams. The role focuses on software automation, test reliability, and root-cause analysis in a complex environment spanning Python, C++, and Nix, with…
Added 14 mins ago
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Global Marketing Intern
Prologis Management
Denver, CO
- $25 to $30 USD / hour
Experience working with AI workflows and tools automation or other emerging technology for research, content development, analysis or workflow improvement
Added 14 mins ago
SC
Principal Consultant
Softchoice Corporati
Denver, CO
- $158,720 to $198,400 USD / year

Closed listing

GSK

Biomanufacturing Associate II

King of Prussia, PA, United States

This opening has closed.

The original listing is kept below for reference.

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About employer

Job details

Experience: OR High School degree, 1+ years of cGMP manufacturing experience.
Posting language: English
Posted: Nov 10, 2026

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Original job description

Archived listing. The details below describe a past opening.

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 Biopharm Manufacturing Associate II, you will perform production operations including fermentation or cell culture operations, preparation of solutions, chromatographic separation, filtration and concentration operations, autoclave and parts washing of process assemblies, and area cleaning/upkeep. Will be responsible for completing daily manufacturing tasks, and increasing competency in different production areas over time. Will participate in safety and compliance initiatives, as well as investigations. Will engage in the GSK Production System to continuously improve safety, quality, and schedule/cost performance.

The purpose of this role is to be a part of a dynamic, multi-tiered operations team that brings life changing and life saving medicine to patients around the world. They will demonstrate GSK Values (Patient Focus, Transparency, Respect, & Integrity) and Expectations (Courage, Accountability, Development, & Teamwork) on a daily basis by engaging positively with team members and production support groups. Under the direction of senior personnel, the biopharmaceutical manufacturing associate II performs a variety of largescale production operations, interacting with automated equipment and monitoring/processing data. Will be responsible for completing daily manufacturing tasks, and increasing competency in different production areas over time. They will participate in safety and compliance initiatives, investigations, and help solve technical and organizational problems while working with different teams of experts. Will work within these teams to continuously improve safety, quality, and schedule/cost performance.

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

Demonstrate GSK Values – Patient Focus, Transparency, Respect, and Integrity – in every interaction, in every work task, and with every responsibility of the job role. Live GSK’s Expectations of Courage, Accountability, Development, and Teamwork to achieve high performing behaviors in the workplace.
With good documentation and data integrity practices, safely and compliantly completes and documents daily manufacturing tasks per standard operating procedures, batch document instructions, and logbooks
Proactively works with senior staff to achieve competency in production operations
Supports in cross-functional activities, such as engineering actions, validation actions and Tech Transfer actions, including proactive safety and compliance input prior to execution. Primarily these activities are within the production suite, but sometimes require out of suite or off-site work (i.e. FAT support)
Monitors equipment and critical process parameters, and escalates any issues or abnormalities and participating the resulting troubleshooting activities
Strives to maintain a high level of competency with current and emerging digital platforms (SAP, EBR, AR/VR, etc)
By learning the production schedule and assessing it daily, proactively ensures all processing equipment and necessary materials are adequate and available to set the team up for success
Transparently participates in investigations that are the result of safety or compliance issues.

Why you?

Basic qualifications:

BS/BA degree, with cGMP manufacturing experience
OR an Associate’s degree from Montgomery county community college in Biotechnology or related technical field with cGMP manufacturing experience
OR High School degree, 1+ years of cGMP manufacturing experience.

Preferred Qualifications:

Demonstrated level of high performance
Strong verbal and written skills
The ability to work well in a team environment
Must be able to follow detailed processing instructions as well as accurately documenting all necessary documentation

#earlycareers

Skills Biopharmaceuticals, Bioprocessing, Cell Line Development, Experimental Methods, Technology Transfer

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.

If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - usrecruitment.adjustments@gsk.com

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. 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 the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

About employer

More about this job

Skills

Supply chain management
Cleaning
Regulatory compliance
Teamwork
Documentation
Troubleshooting
SAP
Biotechnology
Communicable diseases

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Jobs in the United States