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Associate Director, Large Molecule Analytical Development

Employer
GSK
Location
King of Prussia, Pennsylvania
Salary
Competitive
Closing date
Sep 21, 2021

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Sector
Pharmaceutical, Laboratory
Jobseeker Type
Professional
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Site Name: USA - Massachusetts - Waltham, USA - Pennsylvania - Upper Providence, USA - Pennsylvania - King of Prussia Posted Date: Jul 30 2021 Are you looking for an opportunity where you will discover and develop chemical compounds or technologies? If so, this Analytical Chemistry Manager could be an ideal opportunity to explore. As part of the Medicinal Science and Technology (MST) response to the new R&D strategy and the acquisition of TESARO, an new enterprise has been created - Strategic External Development. This enterprise is a stand-alone development organization with the primary focus of developing GSK assets through an external network or providers. We are seeking an experienced manager/leader supporting development and registration of GSK's pipeline of preclinical and development-stage candidates. Develop analytical strategies for integrated early and late stage development activities in support of biologics commercialization. Will be a part of a team the person will lead is responsible for the generation of high-quality, on-time, and right-the-first-time data that comprise a critical component of regulatory submissions required to enable the clinical and/or commercial use of GSK products. The analytical data generated by these methods ultimately ensure the safe and effective use of our drug products in healthy volunteers and/or patients and ensure the continuity of supply of these drugs to patients. This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: Leading analytical workstream to develop analytical plans to support clinical product development, product life-cycle management and regulatory submissions, including developing and implementing justifiable strategies and release/stability criteria for various scenarios including accelerated product development. Support all CMC filing activities for various pre-INDs, INDs, IMPDs, CTAs and BLAs and track analytical development /QC commitments. Participate in BLA-enabling activities including product and process characterization, comparability studies, CQA assessment activities; assist in review of regulatory filings in INDs/IMPDs, CTAs and BLAs and ensure that CMC-related changes are reported in accordance with regulatory requirements. Collabrate efficiently with cross functional team members to ensure on-time delivery of major milestones. Manage and oversee analytical activities performed at CROs/CDMOs associated with method development, qualification/validation, transfer and characterization for drug substance, drug product and reference standards. Assure all laboratory documentation and other regulatory compliance systems are maintained according to corporate standards. Participate in CRO/CDMO selection, management and auditing, as needed. Establish and implement processes to enable effective collaboration with CRO/CDMO business partners to ensure efficiency and high quality of results. Partner with GMP/GDP Quality Assurance and Regulatory Affairs-CMC to ensure completion of appropriate documentation and maintenance of high quality standards. Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: BS or MS degree Minimum of 10 years of industry experience Significant experience in the biopharmaceutical industry with relevant experience in late stage product and process characterization for therapeutic proteins/mAbs is highly desirable. Significant experience with methods used for biopharmaceutical characterization is expected, as well as a thorough knowledge of structure-function relationship of therapeutic proteins. Demonstrated experience and knowledge in tech transfer of methods and life cycle management. Approximately 10-15% domestic and international travel is anticipated. Preferred Qualifications: If you have the following characteristics, it would be a plus: Ph.D. or MS in analytical chemistry, biology, biochemistry, or related technical In-depth understanding of bioassay development Extensive experience with biopharmaceutical analytical experience with recombinant biologic modalities and exposure to all stages of biologics drug development. Experience with oligonucleotides, antibody-drug conjugates (ADCs) Why GSK? Our values and expectations are at the heart of everything we do and form an important part of our culture. These include Patient focus, Transparency, Respect, Integrity along with Courage, Accountability, Development, and Teamwork. As GSK focuses on our values and expectations and a culture of innovation, performance, and trust, the successful candidate will demonstrate the following capabilities: Agile and distributed decision-making - using evidence and applying judgement to balance pace, rigour and risk Managing individual and team performance. Committed to delivering high quality results, overcoming challenges, focusing on what matters, execution. Implementing change initiatives and leading change. Sustaining energy and well-being, building resilience in teams. Continuously looking for opportunities to learn, build skills and share learning both internally and externally. Developing people and building a talent pipeline. Translating strategy into action - a compelling narrative, motivating others, setting objectives and delegation. Building strong relationships and collaboration, managing trusted stakeholder relationships internally and externally. Budgeting and forecasting, commercial and financial acumen. *LI-GSK gskbiopharm_development If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US). GSK is an Equal Opportunity Employer and, in the US, we adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class. 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 GSK's Transparency Reporting For the Record site.
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