Site Name: USA - Maryland - Rockville Posted Date: Feb 13 2025 GSK is currently looking for a Processing Engineering Manager to join our team in Rockville, MD. In this role you will be the Manager for the Process Engineering function to support a Process Value Stream (VS) or Production Area at the Rockville Biopharm site. This role will act as the point of contact for all process engineering support for the Value Stream or Production Area and will organize, prioritize, and direct the activities of the dedicated process engineers. Key Responsibilities: Act as the engineering manager for the assigned value stream or production area by collaborating with other functional groups, proposing and driving value stream objectives, owning and reporting metrics, managing planned and unplanned work, and supporting investigations and RCAs. Assign and prioritize all work requests and oversee project execution to ensure requirements are met, timelines are met, client’s needs are addressed, and projects aligns with GSK values and expectations. Mentor and assist in skills development of the process engineers within the department Demonstrates a proficient understanding of equipment, instrumentation, and materials of construction to specify, design, procure, construct, start-up, fully commission and troubleshoot equipment and systems including a general understand of other functions including automation and validation. Lead in the evaluation, selection, and implementation of new equipment or modifications to existing systems with consideration to new processing technologies or strategies. This may include assessing an economic, environmental, quality, or productivity impact. Coordinate the schedules and supervise the activities of contractors, vendors, and engineering teams including maintenance of equipment Prepare or review operation, safety, and maintenance procedures to ensure accuracy and completeness Own process systems as a subject matter expert to assist in regulatory audits and investigations Provide support during off hours for complex issues that may arise to support ongoing VS operations Lead investigations and discussions and recommend solutions with key customer groups in order to gain a consensus on the preventive and corrective actions Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: BS degree in Engineering 5+ years of experience as a process engineer in the pharmaceutical/biopharmaceutical industry Preferred Qualifications: If you have the following characteristics, it would be a plus: 8+ years of experience as a process engineer in the pharmaceutical/biopharmaceutical industry preferred Demonstrated ability to participate as a leader or member on cross-functional and self-directed work teams Must exhibit the behaviors to interact with direct reports, peers, and site internal customers. Experience working in a regulated GMP environment. Demonstrable experience working to standards required for regulatory compliance of aseptic processing facilities. Engineering and process knowledge associated with various sterilization technologies, GXP utilities and associated pharmaceutical processes. In-depth understanding and knowledge of cell culture and/or purification, including but not limited to bioreactor systems, centrifuges, CIP skids, chromatography system operation, column performance and UF skid operation. Project execution experience, including the ability to PM a project by delivering scope, cost and schedule. Previous experience leading technical groups preferred Experience supporting batch and continuous industrial control systems GMP experience, change and deviation management experience required Must be proficient with business s/w – MERP (plant maintenance), Veeva, MS Office #LI-GSK The annual base salary for new hires in this position ranges from $113,025 to $188,375 taking into account a number of factors including work location within the US market, the candidate’s skills, experience, education level and the market rate for the role. In addition, this position offers an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. Available benefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave. Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees. Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology). Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together. 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). 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