Level

GSK

Scientist/Sr. Scientist - Bioassay Development, Validation and Tech Transfer

AI in this role

Scientist role focused on the development, validation, and tech transfer of cell-based bioassays in a biopharmaceutical setting.

gmp
bioassay-developmentmethod-validationtech-transferdata-integrity

Scientist/Sr. Scientist – Bioassay Development, Validation and Tech Transfer


At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together.
Find out more:


Our approach to R&D

The Extended Characterization group of the Analytical Development Department within the Drug Development and Supply organization has an exciting opportunity for an enthusiastic and driven Scientist/Senior Scientist to join our Bioassay team. This lab-based position offers an exceptional opportunity to contribute to the development, automation, validation, and tech transfer of cell-based potency methods, which are vital to drug development and manufacturing processes. By joining our team, you will play a key role in delivering new medicines to patients while advancing your career in the biopharmaceutical industry.


Key Responsibilities: 

  • Develop and validate cell-based bioassays used for characterization,
  • Participate in early/late-phase validation and method transfer activities to commercial testing laboratories
  • Provide scientific input on method development with a focus on MOA (Mechanism of Action) functional mechanisms
  • Collaborate with biology SMEs (Subject Matter Experts) to establish cell-based methods suitable for GMP settings
  • Ensure laboratory compliance with regulatory standards, data integrity, safety and quality standards consistent with company policies
  • Identify and address compliance issues in experiments and lab protocols
  • Independently conduct and manage experiments with increasing complexity
  • Design, execute and accurately record experimental data
  • Identify and troubleshoot problems during experiments, proposing solutions based on data and contributing to process improvements
  • Collaborate with data science and automation teams
  • Foster and maintain good relationships both within and outside of Analytical Development department

Basic Qualifications:

  • Ph.D. or Master’s degree in Biology, Biological Science or Molecular Biology with ≥ 2 years of experience, or Bachelor’s degree with ≥ 5 of experience in performing or developing cell-based potency methods in an academic institution, biotechnology, or pharmaceutical industry
  • Two or more years experience in cell biology experience with cell-based method development and troubleshooting
  • Two or more years of experience in cell-culture techniques, including culturing various immortalized adherent and suspension cell lines


Preferred Qualifications:

  • Understanding and experience in GLP (Good Laboratory Practice) or GMP (Good Manufacturing Practice)
  • Experience with cell-based methods for Biologics, oligonucleotide and ADC (antibody-drug conjugate) therapeutics
  • Ability to independently conduct and manage experiments, as well as analyze and interpret data
  • Excellent communication and strong technical writing skills for documentation
  • Experience with liquid handling automation instrument for performing sample preparations and/or cell-based assays (e.g. Hamilton, Tecan, HP D300e) is a plus
  • Experience with cell line creation by gene transfection techniques
  • Experience with Flowcytometry/FACS will be a plus
  • Maintaining and validating GMP compliant instruments
  • Experience with Digital, Data and Analytics tools (e.g. Spotfire, PowerBI)

 

#LI-GSK



Skills

Biopharmaceuticals, Bioprocessing, Cell Line Development, Drug Development, Experimental Methods, Molecular Cell Biology, Pharmaceutical Industry, Pharmaceutical Manufacturing, Quality by Design, Regulatory Submissions, Simulation Models, Technical Writing, 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/

How we rate this

Scientist/Sr. Scientist - Bioassay Development, Validation and Tech Transfer at GSK rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.

Classification

Little AI. AI is not part of the work.

  1. ●●●● Builds AI80 to 100
  2. ●●●○ Works on AI60 to 79
  3. ●●○○ Uses AI40 to 59
  4. ●○○○ Little AI0 to 39

Levels come from how often the tools, models and workflows of the role are named in the posting itself. Open the description and count.

Prepare for this job

A free preview built only from this posting: what it asks for, what you could be asked in an interview, and how to adjust your resume.

Skills and AI tools this role asks for

Bioassay DevelopmentMethod ValidationTech TransferData IntegrityGmp

Questions you could be asked

  1. Tell me about a project where bioassay development was part of your work. What did you do?
  2. Tell me about a project where method validation was part of your work. What did you do?
  3. Tell me about a project where tech transfer was part of your work. What did you do?
  4. Tell me about a project where data integrity was part of your work. What did you do?
  5. Walk me through how you've used Gmp in your day-to-day work.

Adapt your resume

  • List these exact terms on your resume: Bioassay Development, Method Validation, Tech Transfer, Data Integrity, and Gmp. An applicant tracking system matches the wording, not the idea.
  • Attach one line of real, concrete experience to at least one of them — a tool named with nothing behind it rarely survives a human read.

Want an expert to read your CV for this job?

Free. Send your CV and the role you want next. We reply by email within 2 to 4 business days.

Get a free CV review

Get new AI jobs by email

One email a week with the new AI jobs, each rated for how much AI is in the work. No recruiter spam, unsubscribe in one click.

Free. One email a week. Unsubscribe in one click.

Similar roles

Other roles that involve little AI, at other companies.

What kind of AI work fits you?

Answer 12 practical questions in about three minutes. Get a simple profile, the work it points to, and live roles to explore next.

Find my next step

More jobs at GSK

GSK

$136k-$227kUSA - Pennsylvania - Upper ProvidenceRemote2w

Related searches

Same AI level