GSK
Overview
Join to apply for the
Director of Large Scale Manufacturing
role at
GSK . This role is on-site in Rockville, MD and is part of the Site Leadership Team with accountability for production in a designated Value Stream at the Rockville site. The role supports developing and driving the Site business strategy in line with GSK and B&D Strategy objectives, focusing on safety, quality, and compliance while delivering business targets. Technology and smart manufacturing are central to increasing speed, quality, and scale of product supply. This position offers the opportunity to lead a team, foster inclusion, and contribute to GSK’s mission of getting ahead of disease together. Responsibilities
Accountable for product quality, employee safety, cGMP compliance, OSHA compliance, and consistently achieving performance goals to meet current and future market demand. Develop a diverse and inclusive culture that improves safety and quality while delivering service and cost improvements. Collaborate with the Site Leadership Team to align resources and set priorities to deliver a balanced scorecard. Set courageous goals to achieve and maintain top quartile performance in pharmaceutical manufacturing. Coordinate with GSK and GSC central functions to align business objectives with GSK strategic priorities and ensure teams are set up to succeed. Develop GPS capability within the Value Stream to accelerate delivery of performance goals. Work with GSC strategy and regulatory/commercial partners to develop targeted product cost of goods with accountability for achieving COGs targets. Develop and mentor team members to build a robust succession pipeline for the Value Stream, Site, and GSK. Align ways of working across GSC to standardize systems, processes, and equipment to maximize performance and compliance. Accountable for the P&L of the Value Stream for short to mid-term budget setting and delivery, optimizing flow through the value stream to maximize efficiency and minimize working capital and lead time. Basic Qualifications
Bachelor of Science – biological/chemical science or any discipline of engineering 10+ years of experience in biopharma/pharmaceutical manufacturing (clinical and/or commercial) Experience leading teams at a GMP drug substance biopharma facility/site with experience in fermentation/cell culture, purification, buffer/media prep, supply chain, manufacturing strategy, equipment commissioning/validation, change management, process validation, product registration, and/or product lifecycle management Preferred Qualifications
Master’s degree in engineering, science, or business administration Experience in large-scale manufacturing environments Strong quality, compliance, and safety orientation with regulatory agency interfacing experience Excellent leadership, cross-functional collaboration, and influencing skills with a focus on teamwork and results Problem solving, continuous improvement mindset, strategic agility, and business acumen Location and Employment Type
On-site role based in Rockville, MD. Full-time employment. Salary and Benefits
The US annual base salary for new hires in this position ranges from $161,700 to $269,500. This range considers location, skills, experience, education, and market rate. In addition, the role offers an annual bonus and eligibility for a share-based long-term incentive program. Available benefits include health care and other insurance, retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave. If salary ranges are not displayed for a specific country, compensation will be discussed during recruitment. More details are available in the GSK US Benefits Summary. Why GSK?
GSK is a global biopharma company focused on uniting science, technology and talent to get ahead of disease together. We aim to positively impact health at scale across key therapeutic areas and empower our people to thrive in a culture that values ambition, accountability and integrity. If you require accommodations to apply, please contact the GSK Service Centre at 1-877-694-7547 or +1 801 567 5155. GSK is an Equal Opportunity Employer. All qualified applicants will receive 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, military service, or any basis prohibited by law. Important notice to Employment businesses/Agencies: GSK does not accept referrals from employment businesses/agencies without prior written authorization. See posting for further details. GSK is committed to accessibility and inclusion. If you are a US Licensed Healthcare Professional or Healthcare Professional, certain transparency requirements may apply.
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Join to apply for the
Director of Large Scale Manufacturing
role at
GSK . This role is on-site in Rockville, MD and is part of the Site Leadership Team with accountability for production in a designated Value Stream at the Rockville site. The role supports developing and driving the Site business strategy in line with GSK and B&D Strategy objectives, focusing on safety, quality, and compliance while delivering business targets. Technology and smart manufacturing are central to increasing speed, quality, and scale of product supply. This position offers the opportunity to lead a team, foster inclusion, and contribute to GSK’s mission of getting ahead of disease together. Responsibilities
Accountable for product quality, employee safety, cGMP compliance, OSHA compliance, and consistently achieving performance goals to meet current and future market demand. Develop a diverse and inclusive culture that improves safety and quality while delivering service and cost improvements. Collaborate with the Site Leadership Team to align resources and set priorities to deliver a balanced scorecard. Set courageous goals to achieve and maintain top quartile performance in pharmaceutical manufacturing. Coordinate with GSK and GSC central functions to align business objectives with GSK strategic priorities and ensure teams are set up to succeed. Develop GPS capability within the Value Stream to accelerate delivery of performance goals. Work with GSC strategy and regulatory/commercial partners to develop targeted product cost of goods with accountability for achieving COGs targets. Develop and mentor team members to build a robust succession pipeline for the Value Stream, Site, and GSK. Align ways of working across GSC to standardize systems, processes, and equipment to maximize performance and compliance. Accountable for the P&L of the Value Stream for short to mid-term budget setting and delivery, optimizing flow through the value stream to maximize efficiency and minimize working capital and lead time. Basic Qualifications
Bachelor of Science – biological/chemical science or any discipline of engineering 10+ years of experience in biopharma/pharmaceutical manufacturing (clinical and/or commercial) Experience leading teams at a GMP drug substance biopharma facility/site with experience in fermentation/cell culture, purification, buffer/media prep, supply chain, manufacturing strategy, equipment commissioning/validation, change management, process validation, product registration, and/or product lifecycle management Preferred Qualifications
Master’s degree in engineering, science, or business administration Experience in large-scale manufacturing environments Strong quality, compliance, and safety orientation with regulatory agency interfacing experience Excellent leadership, cross-functional collaboration, and influencing skills with a focus on teamwork and results Problem solving, continuous improvement mindset, strategic agility, and business acumen Location and Employment Type
On-site role based in Rockville, MD. Full-time employment. Salary and Benefits
The US annual base salary for new hires in this position ranges from $161,700 to $269,500. This range considers location, skills, experience, education, and market rate. In addition, the role offers an annual bonus and eligibility for a share-based long-term incentive program. Available benefits include health care and other insurance, retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave. If salary ranges are not displayed for a specific country, compensation will be discussed during recruitment. More details are available in the GSK US Benefits Summary. Why GSK?
GSK is a global biopharma company focused on uniting science, technology and talent to get ahead of disease together. We aim to positively impact health at scale across key therapeutic areas and empower our people to thrive in a culture that values ambition, accountability and integrity. If you require accommodations to apply, please contact the GSK Service Centre at 1-877-694-7547 or +1 801 567 5155. GSK is an Equal Opportunity Employer. All qualified applicants will receive 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, military service, or any basis prohibited by law. Important notice to Employment businesses/Agencies: GSK does not accept referrals from employment businesses/agencies without prior written authorization. See posting for further details. GSK is committed to accessibility and inclusion. If you are a US Licensed Healthcare Professional or Healthcare Professional, certain transparency requirements may apply.
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