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DO
Field and Regulatory Specialist
Department of Conservation
CA
- $6,488 to $12,215 USD / month
Effective July 1, 2025, the California Department of Human Resources (CalHR) implemented the Personal Leave Program 2025 (PLP 2025) which reduces an employee’s monthly salary by 3% [BU9],…
Added just now
DO
Forensic Documentation Representative
Department of Consumer Affairs
CA
- $5,873 to $8,008 USD / month
Under the general supervision of the Automotive Program (AP) Supervisor I, the Automotive Program Representative (APR) performs a full range of laboratory, office, and field duties related…
Added just now
PE
Personnel Transactions Unit Analyst
Public Employees Retirement System
CA
- $6,031 to $7,547 USD / month
Effective July 1, 2025, The California Department of Human Resources (CalHR) implemented the Personal Leave Program 2025 (PLP 2025). PLP 2025 directs that each employee shall receive a 3…
Added just now
A
Electrical Foreman
Aerotek
Franklin Lakes, NJ
- $27 to $38 USD / hour
Lead and run electrical crews on commercial building projects, ensuring work is completed safely, on time, and to specification.
Added just now
Project Controls Specialist 2
Primoris Renewable Energy
Aurora, CO
Lead establishing project phase codes and budgets in company accounting system
Added just now
Senior Project Controls Specialist (Site Based)
Primoris Renewable Energy
LA · TX
Lead the establishment of project phase codes and budgets in company accounting system
Added just now
Senior Project Controls Specialist
Primoris Renewable Energy
Aurora, CO · Denver, CO
Lead the establishment of project phase codes and budgets in company accounting system
Added just now
Community Based Therapist (MH Professional/Counselor)-Master's Degree Required
Pressley Ridge
Pittsburgh, PA
…justice systems. Individual will work closely as the "Team Lead" with Certified Peer Specialist, Psychiatric Rehabilitation Counselor and the Service Coordinator (Mobile Transition Age…
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AE - Merchandising Team Leader (Assistant Manager)
AEO
Green Bay, WI
You know how to lead and develop teams and have a general understanding of employment law.
Added just now
AE - Selling Team Leader (Assistant Manager)
AEO
Philadelphia, PA
You know how to lead and develop teams and have a general understanding of employment law.
Added just now
PM
Registered Nurse
PrimeCare Medical, Inc.
Glen Burnie, MD
- $42 to $48 USD / hour
Perform twelve (12) lead electrocardiograms and assemble results for interpretation by a provider.
Added just now
IAM Architect
Sapsol Technologies Inc
Taylor, TX
Lead and coordinate IAM modernization program, including six identified sub-projects.
Added 1 min ago
Field Marketing Specialist
Red Bull
Chicago, IL
Ensure a strong sales support program in place to drive distribution, excite the trade, and improve in store visibility in and around university.
Added 1 min ago
PW
Data Analyst 2
People With Developmental Disabilities, Office for
Schenectady, NY
- $90,582 to $114,585 USD / year
…under the direction of the Clinical and Operational Data Team Lead to build high-quality data products that are collaborative, aligned with policy, and proactively inform decision…
Added 1 min ago
MS
Restaurant Shift Supervisor
MOD Super Fast Pizza, LLC
Kirkland, WA
- $19 USD / hour
As a Shift Supervisor, you are building your leadership skills and style. You will lead restaurant operations during scheduled shifts and support training for all new hires, program…
Added 1 min ago
MS
Restaurant Shift Supervisor
MOD Super Fast Pizza, LLC
Prosper, TX
- $13.25 USD / hour
As a Shift Supervisor, you are building your leadership skills and style. You will lead restaurant operations during scheduled shifts and support training for all new hires, program…
Added 1 min ago
Technical Program Manager - VIrtual
Alight
Virtual, TX
Alight is seeking a Technical Program Manager to lead complex technology programs across Engineering, Architecture, Product, Data/AI, Security, Operations and external partners.
Added 1 min ago
Divisional Clinical Manager, Skilled Nursing
BAYADA Home Health Care
Lancaster, PA
Will become SIM trained and certified to assist with our Nurse Residency Program within the offices.
Added 1 min ago
AA
Principal Guest Experience Designer
Alaska Airlines
WA-SeaTac
- $141,250 to $211,900 USD / year
As the lead subject matter expert in guest experience design for an assigned enterprise portfolio, define future-state experience architecture and long-term strategic design direction…
Added 1 min ago
CS
Lead Coach and Program Manager, Scales to Success
Cincinnati Symphony Orchestra
Cincinnati, OH
- $90,000 to $110,000 USD / year
The Lead Coach and Program Manager, Scales to Success (Lead Coach), will play a central role in launching and strengthening the program. Building on the program’s existing foundation and…
Added 1 min ago
Director of Engineering
FourGen Holdings
Oak Brook, IL
Lead, mentor, and develop a team of electrical engineers and designers.
Added 1 min ago
WB
Early Childhood Family Education (5 hours/ week)
White Bear Lake Area Schools #624
White Bear Lake, MN
- $22.66 USD / hour
Performs intermediate human support work providing classroom support for children in the early childhood program, and related work as apparent or assigned. Work is performed under the…
Added 2 mins ago
Technical Analyst, Life Safety
Princeton University
Princeton, NJ
Lead projects related to application onboarding, upgrades, and enhancements.
Added 2 mins ago
Product Management Associate Director - Data Solutions
Sidley Austin LLP (IL LLP)
United States
The Product Management Associate Director - Data Solutions helps shape and lead the execution of the Firm's enterprise data strategy, advancing Sidley toward a unified, governed, and…
Added 2 mins ago
Senior Mechanical Engineer / Project Manager – Industrial
DLZ Corporation
Merrillville, IN
Lead mechanical engineering design for industrial and steel-mill facilities.

GSK

Senior Scientist, Upstream Processing

King of Prussia, PA, United States

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Job details

Experience: A minimum of 3 years of direct GMP manufacturing experience or upstream processing experience in a biotechnology manufacturing facility or Pilot Plant.
Posting language: English
Posted: Nov 9, 2026

Original job description

We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programs, pension plan membership, and shares and savings programme. We embrace modern work practices; our Performance with Choice programme offers a remote or hybrid working model, empowering you to find the optimal balance between remote and in-office work.

Discover more about our company-wide benefits and life at GSK on our webpage Life at GSK | GSK

Find out more about GSK and R&D: Our approach to R&D

Senior Scientist, Upstream Processing

Join us as a Senior Scientist, Upstream Processing and play a key role in advancing scientific research that makes a real difference. You will work closely with diverse teams to design, carry out, and analyze experiments. Your insights will help shape innovative solutions that align with our mission to unite science, technology, and talent to get ahead of disease together. We value curiosity, teamwork, and a hands-on approach to solving important challenges. This role offers meaningful growth and impact as you develop your career in a supportive environment.

We value curious, motivated scientists who take ownership, communicate clearly, and thrive in a collaborative environment. This role offers you a chance to grow your skills, make a meaningful impact, and contribute to GSK’s mission of uniting science, technology, and talent to get ahead of disease together.

This role is located in Upper Merion, PA and requires working on-site. Hybrid or remote work options are not available for this position.

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

Leads the manufacture of clinical supply of investigational biopharmaceutical molecules. Specifically: hands-on cGMP large scale cell culture for use in early phase clinical trials
Leads or works on projects and assignments where independent action and a high degree of initiative and knowledge are required for execution or to provide recommendations
Supports the technology transfer process through active participation in ensuring that new processes fit and execute consistently
Troubleshoots problems in the execution of processing activities; proactively assesses options and impact and takes action to rectify or communicate to appropriate decision makers
Identifies process improvement opportunities with impact on safety, compliance, and efficiency/cost
Maintains and performs compliance checks for documentation in logs, media forms, batch records, and electronic systems in accordance with company policy and legal requirements
Strives for Right First Time in the manufacture of investigational material through attention, focus, planning, and adherence to procedural and regulatory expectations

Basic Qualifications We are looking for professionals with these required skills to achieve our goals:

BS, MS, or PhD in Chemical Engineering, Biology, Chemistry, or other engineering or scientific field.
A minimum of 3 years of direct GMP manufacturing experience or upstream processing experience in a biotechnology manufacturing facility or Pilot Plant.

Preferred Qualifications:

Please note the following skills are not necessary, just preferred, if you do not have them, please still apply:

Thorough knowledge of Good Manufacturing Practices (GMP) regulations.
Demonstrates good interpersonal skills and communicates well both verbally and through written communications.
Maintains a professional and productive relationship with area management and co-workers.
Thorough knowledge of routine laboratory/plant equipment and demonstrates high level of technical expertise with working familiarity with several methods, techniques, laboratory procedures and processes.
Possess in-depth knowledge of how to analyze and interpret experimental/process data.

Join us in making a difference in patients’ lives around the world. We value your unique perspective and invite all interested candidates to submit their application.

Skills Data Integrity, Detail-Oriented, Digital Fluency, Emergency Response, Financial Acumen, GxP Regulations, Lean Management, Manufacturing Processes, Problem Solving, Production Management, Project Coordination, Quality Compliance, Regulatory Compliance, Risk Awareness, Site Operations

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/

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More about this job

Skills

Clinical trials
Process improvement
Regulatory compliance
Documentation
Media formats
Electronics
Chemical engineering
Good manufacturing practices
Biotechnology
Interpersonal skills
Manage quantitative data
Emergency response
Financial capability
Manufacturing processes
Problem solving
Communicable diseases

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