What are the responsibilities and job description for the Senior Manager or Associate Director, Analytical Development position at GSK?
Site Name: USA - Pennsylvania - Upper Providence
Posted Date: Jun 2 2026
Senior Manager/Associate Director, Analytical Development
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
As a Senior Manager of Analytical Development, you will join a team of scientists responsible for managing analytical activities throughout development and registration of pre-clinical and development-stage biologic candidates within the DDS Analytical Projects organization. The successful candidate will serve as a project and/or technical lead in a broad analytical area and manage the collaboration with appointed CDMOs & CROs to support GSK’s biologics pipeline.
The scope of the role spans from leading release- and stability-indicating method development and validation to characterization and comparability studies, as well as reference standard qualification. It will further extend to method transfer and troubleshooting, investigations and preparation of CMC content for regulatory submissions. Under minimal guidance, the successful candidate will be responsible for overseeing, developing, and executing aligned GSK goals for biologics analytical development with GSK internal labs and CDMO/CRO.
This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following…
We are looking for professionals with these required skills to achieve our goals:
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/
Posted Date: Jun 2 2026
Senior Manager/Associate Director, Analytical Development
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
As a Senior Manager of Analytical Development, you will join a team of scientists responsible for managing analytical activities throughout development and registration of pre-clinical and development-stage biologic candidates within the DDS Analytical Projects organization. The successful candidate will serve as a project and/or technical lead in a broad analytical area and manage the collaboration with appointed CDMOs & CROs to support GSK’s biologics pipeline.
The scope of the role spans from leading release- and stability-indicating method development and validation to characterization and comparability studies, as well as reference standard qualification. It will further extend to method transfer and troubleshooting, investigations and preparation of CMC content for regulatory submissions. Under minimal guidance, the successful candidate will be responsible for overseeing, developing, and executing aligned GSK goals for biologics analytical development with GSK internal labs and CDMO/CRO.
This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following…
- Lead and manage analytical development activities performed at GSK and CROs/CDMOs associated with method development, qualification/validation, transfer and characterization of drug substance, drug product, in-process testing and reference standards qualification.
- Develop and execute strategies for product and process characterization with a focus on CQA assessment, specification, release, stability, and comparability studies.
- Facilitate tech transfer of methods to GMP testing facility, commercial groups and to CMO's.
- Collaborate with process and quality functions to ensure strong cross functional collaborations and integrated process and product development and characterization.
- Author, review and/or approve key source documents for relevant sections of regulatory filings (IND, IMPD, BLA, etc.).
- Lead and track analytical development commitments to support all CMC filing activities for pre-INDs, INDs, IMPDs, CTAs and BLAs, draft and review of regulatory filings, and address RTQs.
- Assure all documentation and other regulatory compliance systems are maintained according to GSK corporate standards.
- Establish and implement processes, technical concepts, and methodologies to enable effective collaboration with CRO/CDMO business partners to ensure efficiency and high quality of results.
- Partner with Quality Assurance and Regulatory Affairs-CMC to ensure completion of appropriate documentation and maintenance of high-quality standards.
- Provide clear communication to partners and functional line management regarding progress against technical and project objectives/milestones.
We are looking for professionals with these required skills to achieve our goals:
- Ph.D., M.S. or B.S. in chemistry, biochemistry, cell biology, biochemical/bioprocess engineering, or related science/engineering field with extensive biopharmaceutical industry experience.
- 6 years (for Ph.D.) or 8 years (for M.S.) or 10 years (for B.S.) of biopharmaceutical industry experience.
- 5 years of hands-on experience with biochemical, biophysical and/or biological methods used for biopharmaceutical characterization.
- 3 years of CMC analytical development experience, preferably with analytical project leadership experience of biologics.
- Experience in technical transfer of methods and life cycle management.
- Experience with a variety of biologic modalities (ADCs, monoclonal antibodies, bi- and multi-specifics, fusion proteins, co-formulated drug products, etc.), and exposure to all stages of biologics drug development.
- Hands-on experience in biochemical and/or biophysical assay development, qualification/validation,.
- Thorough knowledge of structure-function relationship of therapeutic proteins.
- Proven ability to manage projects and work with cross-functional teams comprised of internal and/or external contacts.
- Ability to work in a fast-paced, multi-disciplinary and dynamic environment with potential for changing priorities, with flexibility to support multiple development programs simultaneously.
- Ability to lead innovation, change, and drive for results.
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/