Site Name: USA - Pennsylvania - King of Prussia Posted Date: May 11 2022 As a Senior Biopharmaceutical Manufacturing Associate you will be a part of a dynamic operations team that brings life changing and life saving medicine to patients around the world. You will demonstrate GSK Values (Patient Focus, Transparency, Respect, & Integrity) and Expectations (Courage, Accountability, Development, & Teamwork) on a daily basis by engaging positively with team members and production support groups. With minimal supervision, the senior biopharmaceutical manufacturing associate performs a variety of large-scale production operations, interacting with automated equipment and monitoring/processing data. You will be responsible for completing daily manufacturing tasks, and achieving full competency in different production areas over time. You will participate in safety and compliance initiatives, investigations, and help solve technical and organizational problems while working with different teams of experts. You work within these teams to continuously improve safety, quality, and schedule/cost performance. You will work on Tech Transfer initiatives. This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: With good documentation and data integrity practices, safely and compliantly completes and documents daily manufacturing tasks per standard operating procedures, batch document instructions, and logbooks • Maintains a high level of mechanical and technical aptitude and training to effectively troubleshoot equipment and processing issues, escalating those that cannot be easily resolved or pose a safety or compliance risk. • Initiates the immediate documentation of investigations that are the result of safety or compliance issues, can independently support root cause analysis, influence full transparency among the team, and engage with EHS and QA on CAPA development. • Supports in cross-functional activities, such as engineering actions, validation actions and Tech Transfer actions, including proactive safety and compliance input prior to execution. Primarily these activities are within the production suite, but sometimes require out of suite or off-site work (i.e. FAT support) • Strives to maintain a high level of competency with current and emerging digital platforms (EBR, AR/VR, etc) • Trains new or less experienced team members • Proposes improvements to standard ways of working or documentation (SOPs, Batch Documents, Logbooks) in order to reduce accidents, defects, and waste, and participates in the endorsed changes • Participates or leads area muster or shift change to ensure the maintenance of the production schedule in their area • Leads the production team as required in the absence of senior staff. Why you? Basic qualifications: High school diploma with 7 years prior cGMP manufacturing experience in the pharmaceutical or biotechnology industry, with the demonstration of a high level of performance OR BS/BA degree with 4 years of cGMP manufacturing experience is required 5:00 am to 5:00pm or 5:00 pm to 5:00 am shift with rotating weekends. Weekend and night shift differential will be applicable depending on the shift. Preferred Qualifications: Strong verbal and written skills The ability to work well in a team environment Must be able to follow detailed processing instructions as well as accurately documenting all necessary documentation Why GSK? At GSK, we have already delivered unprecedented change over the past four years, improving R&D, becoming a leader in Consumer Health, strengthening our leadership, and transforming our commercial execution. Now, we're making the biggest changes we've made to our business in over 20 years. We're on track to separate and create two new companies in 2022: New GSK with a leading portfolio of vaccines and specialty medicines as well as R&D based on immune system and genetics science; and a new world-leading consumer healthcare company of loved and trusted brands. With new ambition comes new purpose. For New GSK, this is to unite science, talent and technology to get ahead of disease together - all with the clear ambition of delivering human health impact; stronger and more sustainable shareholder returns; and as a new GSK where outstanding people thrive. Getting ahead means preventing disease as well as treating it. How we do all this is through our people and our culture. A culture that is ambitious for patients - so we deliver what matters better and faster; accountable for impact - with clear ownership of goals and support to succeed; and where we do the right thing. So, if you're ready to improve the lives of billions, join us at this exciting moment in our journey. Join our challenge to get Ahead Together. *LI-GSK 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. At GSK, the health and safety of our employees are of paramount importance. 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