Environmental Defense Fund Program Overview The food system accounts for around one-third of global climate impacts, and this will only increase as we work to feed a growing global population of 10 billion people. Methane emissions are a major part of these impacts but are mostly an under-realized strategy for climate action. The livestock sector must accelerate methane mitigation if the world is to slow the rate of climate change and avoid disastrous tipping points. Dairy Methane Action Alliance (DMAA) is a global initiative convened by EDF to spur action and accountability to drive down dairy methane emissions. With 8 major companies already signed on, it requires signatories to measure, report, and make a public action plan to reduce methane emissions, while providing the tools, resources and networks to unlock barriers and speed action. Overall Function The Scientist, Livestock Methane will be a critical part of the Livestock Methane Science team,...

Site Name: USA - Pennsylvania - Marietta Posted Date: Sep 9 2024 Are you interested in working with cutting-edge laboratory technology to improve quality and accelerate regulatory compliance? If so, this Quality Control Support Supervisor role could be an exciting opportunity to explore. As Quality Control Support Supervisor, you will have responsibility for p roviding leadership to Lab Support Team in order to manage non-testing processes within QC. This includes: Sample Management, Stability, Compendial Review, QC Master Data/Monograph Creation, Auditing, Equipment Lifecycle, Performance Management. You will ensure tasks are executed within SLA timelines, drive projects to closure in support of site goals, and serve as owner for Lab Support Quality System Events. You will also ensure lab processes are safely executed and are compliant with GMP/regulatory requirements. This role will provide YOU the opportunity to lead key activities to progress YOUR career, these...

Site Name: USA - Massachusetts - Waltham, UK - Hertfordshire - Stevenage, USA - Pennsylvania - Upper Providence Posted Date: Jul 17 2024 The Associate Director of Analytical Development will lead a team of analytical scientists responsible for development, manufacturing, release and stability testing, and characterization of drug substances/API and drug products of Small Molecule and Oligonucleotide therapeutic modalities within the Strategic External Development (SED) organization. The Associate Director will be responsible for people and project management, who would also function as an analytical project lead and technical lead in a broad analytical development role that spans from managing collaboration with appointed CDMOs to overseeing, developing, and executing aligned GSK and CDMO goals for development of small molecules and oligonucleotides. It will further extend to investigation, preparation and reviewing of CMC content for regulatory submissions, as well as...

Site Name: USA - Massachusetts - Waltham, UK - Hertfordshire - Stevenage, USA - Pennsylvania - Upper Providence Posted Date: Jul 17 2024 The Associate Director of Analytical Development will lead a team of analytical scientists responsible for development, manufacturing, release and stability testing, and characterization of drug substances/API and drug products of Small Molecule and Oligonucleotide therapeutic modalities within the Strategic External Development (SED) organization. The Associate Director will be responsible for people and project management, who would also function as an analytical project lead and technical lead in a broad analytical development role that spans from managing collaboration with appointed CDMOs to overseeing, developing, and executing aligned GSK and CDMO goals for development of small molecules and oligonucleotides. It will further extend to investigation, preparation and reviewing of CMC content for regulatory submissions, as well as...

Site Name: USA - Pennsylvania - Upper Providence Posted Date: Sep 5 2024 Are you a scientist in sterile product formulation and injectables eager to lead the development of life-changing drug products? Are you eager to unite science, talent, and technology to get ahead of disease together? This may be the right opportunity for you! This role is Hybrid at our Upper Providence, PA site and does require minimum 2-3 days on-site per week. As a Biopharmaceutical Drug Product, Principal Scientist/ Investigator, you will join the GSK sterile Drug Product Development organization and work on developing late phase drug product formulation, manufacturing process and delivery systems for protein-based therapeutics and NCEs. This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: Member of a team responsible for enabling the progression of new assets from candidate selection to product...

Site Name: USA - Pennsylvania - Upper Providence Posted Date: Sep 4 2024 Are you energized by the challenge of designing innovative ways to use Engineering, Process Analytics Technologies, Automation and Modelling to develop medicines for patients? If so, this opportunity within the Sterile Process Engineering team would be the right fit for you. Our team in the Process Engineering group is passionate about the work we do, and we’d be eager to welcome individuals with a similar interest in using technology to develop medicines. As an Investigator, you will employ knowledge and experience of drug product unit operations, Process Engineering, and modelling to assess, develop and implement new manufacturing platforms and support scale-up, technology transfer and manufacture of Biopharmaceutical drug product through to commercialization. You will work very closely with automation experts and data scientists to enable efficiencies during drug product development. This...

Site Name: USA - Pennsylvania - Upper Providence, Belgium-Wavre, Durham Blackwell Street, USA - Massachusetts - Waltham Posted Date: Sep 4 2024 Would you like to be part of GSK’s Vaccine Epidemiology team, with an opportunity to drive Epidemiology strategy and studies across the spectrum of vaccine development? If so, this is an excellent opportunity to explore. Job Purpose To be responsible for Epidemiological studies within a large program or group of related programs (led by a senior epidemiologist) within the context of the GSK Vaccines process in order to ensure the high quality and on-time delivery of all epi data that will allow and support world-wide registration in compliance with the clinical and epi development plan, applicable good practices, and GSK Vaccines standard operating procedures (SOP). Key responsibilities: This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:...

Site Name: USA - Pennsylvania - Upper Providence, Belgium-Wavre, Durham Blackwell Street, USA - Massachusetts - Waltham Posted Date: Sep 4 2024 Would you like to be part of GSK’s Vaccine Epidemiology team, with an opportunity to drive Epidemiology strategy and studies across the spectrum of vaccine development? If so, this is an excellent opportunity to explore. Job Purpose To be responsible for Epidemiological studies within a large program or group of related programs (led by a senior epidemiologist) within the context of the GSK Vaccines process in order to ensure the high quality and on-time delivery of all epi data that will allow and support world-wide registration in compliance with the clinical and epi development plan, applicable good practices, and GSK Vaccines standard operating procedures (SOP). Key responsibilities: This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:...

Site Name: USA - Pennsylvania - Upper Providence, Belgium-Wavre, Durham Blackwell Street, USA - Massachusetts - Waltham Posted Date: Sep 4 2024 Would you like to be part of GSK’s Vaccine Epidemiology team, with an opportunity to drive Epidemiology strategy and studies across the spectrum of vaccine development? If so, this is an excellent opportunity to explore. Job Purpose To be responsible for Epidemiological studies within a large program or group of related programs (led by a senior epidemiologist) within the context of the GSK Vaccines process in order to ensure the high quality and on-time delivery of all epi data that will allow and support world-wide registration in compliance with the clinical and epi development plan, applicable good practices, and GSK Vaccines standard operating procedures (SOP). Key responsibilities: This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:...

Site Name: USA - Pennsylvania - Marietta Posted Date: Aug 27 2024 Are you looking for an opportunity to enhance your engineering compliance expertise within a cutting edge global environment? If so, this Compliance Engineer role could be an ideal opportunity to explore. As Compliance Engineer, you will be responsible for effectively managing change, identifying and mitigating risks, and ensuring critical control parameters are built into the site standard work and quality critical attributes are continuously monitored. This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following: Lead the identification and implementation of projects/initiatives in order to achieve compliance to GSK Engineering standards, EHS standards and Sustainability initiatives . Provide technical support for facilities infrastructure including but not limited to: HVAC, Clean Steam, Compressed Air (GMP and non-GMP),...

Site Name: USA - Pennsylvania - Marietta Posted Date: Aug 27 2024 Are you looking to expand your expertise in project management and drive change in an environment that allows you to design novel approaches and solutions? If so, this Engineering Compliance Project Manager role could be an ideal opportunity to explore. As Engineering Compliance Project Manager, you will be responsible for managing the site’s engineering standard compliance and job safety assessment implementation plan for Technical Services. This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following... Lead department review and response to GSK’s Global Engineering Standards and Policies and EHS Standards per the established plan Lead and manage the development of the technical services department’s job safety assessments Manage site engineering alerts Author, review, revise, or approve Standard Operating Procedures...

Site Name: USA - Pennsylvania - Upper Providence Posted Date: Aug 20 2024 The Senior Finance Partner will support the Vaccines & Global Health business units as finance expert across the complete life cycle of U.S. Government contracts (from initial proposals through contract close out and audit). Acts as a primary point of contact for government auditors and interacts with Contracting Officers on financial matters across multiple government agencies to ensure that all financial & accounting obligations meet or exceed contract requirements and are compliant with all federal acquisition and other government regulations. This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following... Provide full-lifecycle financial management and compliance oversight for the portfolio of GSK government contracts as assigned. Draft, prepare, and execute internal and external correspondence on...

Site Name: USA - Massachusetts - Waltham, USA - Pennsylvania - Upper Providence Posted Date: Aug 19 2024 As a Manager of Analytical Development, you will be joining a team of scientists responsible for managing analytical activities at CDMOs/CROs to ensure generation of high-quality and on-time data for development and registration of pre-clinical and clinical development-stage biologics within the Strategic External Development (SED) organization. The scope of the role spans release and stability indicating method development, qualification and validation, characterization, method trouble shooting, and method transfer. Under guidance, the incumbent will be responsible for executing aligned GSK and CDMO goals for analytical development of biologic therapeutic modalities, including antibodies, antibody-drug conjugates (ADCs), and bi- and multi-specifics . The role could further extend to investigations and preparation of CMC content for regulatory submissions. This role will...

Site Name: USA - Massachusetts - Waltham, USA - Pennsylvania - Upper Providence Posted Date: Aug 19 2024 As a Manager of Analytical Development, you will be joining a team of scientists responsible for managing analytical activities at CDMOs/CROs to ensure generation of high-quality and on-time data for development and registration of pre-clinical and clinical development-stage biologics within the Strategic External Development (SED) organization. The scope of the role spans release and stability indicating method development, qualification and validation, characterization, method trouble shooting, and method transfer. Under guidance, the incumbent will be responsible for executing aligned GSK and CDMO goals for analytical development of biologic therapeutic modalities, including antibodies, antibody-drug conjugates (ADCs), and bi- and multi-specifics . The role could further extend to investigations and preparation of CMC content for regulatory submissions. This role will...

Site Name: USA - Maryland - Rockville Posted Date: Aug 14 2024 GSK is currently looking for an Operational Quality Manager to join our team in Rockville, MD. OQ Manager will be responsible for Operational Quality’s day to day activities at LSM/SSM site including batch record review and day to day Quality Operations. The OQ Manager will manage a team of Quality professionals accountable for batch record reviews confirmation of GMP operations in production and support groups i.e. laboratory and engineering. The job holder will be the main liaison with production management team and will participate in daily planning meetings, approve deviations to processes, to support LSM/SSM activities Key Responsibilities: Manage team of Operational Quality professionals (24/7) to support production activities and shop floor presence Ensure Operational Quality schedules and activities support batch record review and batch disposition needs Review and approve deviation reports,...

Site Name: USA - Pennsylvania - Marietta Posted Date: Aug 12 2024 Are you looking for an opportunity to enhance your project management expertise within a cutting edge global environment? If so, this Project Engineer role could be an ideal opportunity to explore. As Project Engineer, you will be responsible for the support of a variety of site process equipment and facility infrastructure systems. This position will be responsible for project management, budgeting, scheduling, change control, commissioning and qualification of site CAPEX projects, energy conservation projects and plant shutdown modifications. This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following: Lead the design, installation, or modification of the facility infrastructure, support equipment, or primary process equipment and associated control systems which are aligned with GSK Biological global standards. Provide...

Site Name: Cambridge 300 Technology Square Posted Date: Aug 9 2024 Provides medical/scientific expertise in the safety evaluation and risk management of key GSK assets in clinical development and/or the post-marketing setting. Ensures scientifically sound review and interpretation of data and management of safety issues and escalates safety issues identified through the safety review process to senior management and safety governance as appropriate. Makes recommendations for the further characterization, management, and communication of safety risks. Focus on efficiency and effectiveness to meet the needs of our Patients and HCPs. Supporting the pharmacovigilance and benefit-risk management of the assigned portfolio of GSK global assets to ensure Patient Safety globally. If appointed as a manager (i.e., Team/Group Leader) is responsible for leadership of a team of individual contributors. Line Management (including functional matrix reports) leadership competencies...

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. R&D is committed to discovering and delivering transformational vaccines and medicines to prevent and change the course of disease. We believe the Greater Boston area is an important hub for the biotech and pharma industry, which is why we’ve invested in growing our footprint and expanding our R&D space in Cambridge, with a primary focus on additional state-of-the-art lab space. Here, we will bring together talent and expertise, building upon GSK’s long history of vaccine development, to create globally leading viral capabilities and cutting-edge vaccines technologies, as we add to our robust portfolio targeting infectious diseases at every stage of life. In the plan to create a new hub for mRNA-based vaccine discovery in Cambridge, we are building new laboratories that will be focused on the development of state-of-the-art methods that will...

Site Name: USA - Pennsylvania - Upper Providence Posted Date: Aug 8 2024 Are you a scientist in sterile product formulation and injectables eager to lead the development of life-changing drug products? Are you eager to unite science, talent, and technology to get ahead of disease together? This may be the right opportunity for you! As a Scientific Leader/Associate Director, you will be responsible for taking a leading role in the development of GSK’s sterile products. You will lead international drug product development teams to define and implement formulation and development strategies to best support the future positioning of the organization. This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: Member of a team responsible for enabling the progression of NCEs from candidate selection to product commercialization. Leading drug product development matrix teams supporting product...

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 . R&D is committed to discovering and delivering transformational vaccines and medicines to prevent and change the course of disease. We believe the Greater Boston area is an important hub for the biotech and pharma industry, which is why we’ve invested in growing our footprint and expanding our R&D space in Cambridge, with a primary focus on additional state-of-the-art lab space. Here, we will bring together talent and expertise, building upon GSK’s long history of vaccine development, to create globally leading viral capabilities and cutting-edge vaccines technologies, as we add to our robust portfolio targeting infectious diseases at every stage of life. In the plan to create a new hub for mRNA-based vaccine discovery in Cambridge, we are building new laboratories that will be focus on the development of state-of-the-art methods that will...