Lead Manufacturing Associate-LAN

Preparedness today, safer tomorrow. Emergent is a leading public health company that delivers protective and life-saving solutions to communities around the world. Here, you will join passionate professionals where our culture is informed by our values and commitment to protecting and saving lives. Job Summary Execute tasks per CGMP guidelines and Standard Operating Procedures to manufacture, inspect and package Anthrax Vaccine Adsorbed. Complete training and maintain competence per the manufacturing training program. Actively incorporate the Shared Values set out by Emergent BioSolutions while performing day to day activities. Essential Functions Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions. General Complete training and demonstrate competency on Lead Manufacturing Associate qualification blocks in accordance with the training progression pathwayExecute and document procedural steps in compliance with CGMP standards, clean room behavior and Standard Operating ProceduresComply with all applicable rules and regulations of Emergent and the Pharmaceutical / Biotech industry. This includes FDA regulations such as CGMP, GDP, EH&S regulations, and company regulations such as the employee handbookMaintain state of facility environmental control including preparation of defined concentrations of cleaning solutions, daily, monthly, quarterly and annual cleaning of manufacturing areas per StandardOperating Procedures Review all documentation for accuracy and completeness of process signature steps as each step is completed. Perform “real time” review of all documentation (BPRs, forms, logs, etc.) in the area throughout the shiftStock gowning and consumable supplies in the controlled areas maintaining Kanban inventory control of manufacturing materialsPerform bubble point integrity testing of hydrophilic and hydrophobic production filters using defined test programsEnsures that all Batch Production Records are requested and obtained in accordance with the production scheduleVerification of Facilities department execution of preventive maintenance of equipment. Requires thorough understanding of GMP equipment operation and function for intended purpose Leadership Proactively recognize potential issues with manufacturing process equipment and troubleshoot in collaboration with Facilities/MaintenanceMake decisions and escalate manufacturing and quality issues to management in a timely and effective mannerParticipate in self inspections and 6S audits and respond to findingsShow personal commitment and acts to continuously improveBuilds networks and engages in/runs meetingsHolds self-accountable as well as peersDisplays strong core values and cultural responsibilitiesCapable of scheduling and coordinating daily tasks Lean Concepts Contribute to the development and promotion of standard workCollaborate with applicable Integrated Process Teams to drive continuous improvement and learn new Lean conceptsOversee and actively participates in Kanban and 6S systemsIdentify continuous improvement opportunities and collaborates with Integrated Process Teams and Supervisors to drive initiatives through to completion Inspection and Packaging Successfully complete inspector qualification requirements to identify, classify and cull product defects, including those defects which could impact patient safety (inspector qualification)Independently operate labeling equipment with minimal supervision (Qualification)Apply traceability and expiration information to secondary packaging components such as cartons and cases. Confirm suitability of secondary packaging components during printing processes through 100% inspection (carton printing, case creation)Package product in secondary and final packaging components while performing 100% reconciliation of product rejects (Packaging)Complete ambient tracking documentationExecute material issuance and confirmation of process steps using specific SAP modules Building 55 Operations – Prep Execute material issuance and confirmation of process steps using specific SAP modulesPrecisely weigh and hydrate media componentsLoad, run and unload parts washer and sterilization/decontamination using specific validated load configurations per Standard Operating ProceduresAssemble clean process glassware configurations and portable tanks utilizing sanitary connections, quick connects and stainless-steel ancillary partsPerform Cleaning (COP/CIP) and Sterilizing (SOP/SIP) of production vessels through interface with automated control system (DeltaV)Prepare and dispense intermediate materials Building 55 Operations – Upstream Execute detailed manual and high impact process tasks requiring extensive documentation and interface with automated controls. Process operation involves manual orientation of valve configurations and monitoring/adjustment of vessel pressures during execution to maintain the sterile envelope and create differentials to facilitate transfers. Description of specific requirements include:Clean and Sterilize 10L, 120L and 1320L fermenters to defined and validated parameters through interface with automated control systemSterilize media filters and sterile filter seed, intermediate and production mediaPrepare and dispense Saline for Inoculum for 10L fermentation initiationInoculate 10L fermenter through addition of inoculum via peristaltic pump Monitor culture turbidity to verify growth to required process parameters and transfer culture from the 10L to 120L and the 120L to 1320L fermenters upon verification of achievement of these parametersAdjust pH of culture through manual addition of 2N NaOH aliquots to a defined pH rangeInstall sterilizing grade filters, perform integrity testing and execute sterilization of filter skidMonitor culture turbidity to verify growth to required process parameters and filter culture from 1320L fermenter to Harvest Tank Building 55 Downstream Operations Add ALOH to Harvest tank.Draw samples and submit them through LIMS.Clean and sterilize Harvest TanksClean and sterilize centrifuge as well as run the centrifugation processesDispense and sterilize ALOHCPG additionFinal Filtration Quality Systems Initiate Non-Conforming Events and perform/document all necessary containment activities. Accurately complete triage assessment tool and proactively assist NCE author with investigationEscalates non-conforming events to Manufacturing leadership in real-time to ensure appropriate containment and immediate corrections are completedInitiate changes in the change control system regarding periodic review document revisionsRevise existing procedures in the document management systemAssist author with investigation of root cause, impact assessment and identification of durable corrective and preventive actions Training Train all levels of associates - Complete and maintain Qualified Trainer training qualification. Qualification includes strategies for trainee motivation and competence development, adult learning principles, step by step training guide and proper documentation of all activities to ensure crediting of qualification status Behavior/Cultural Responsibilities Standing Shoulder to Shoulder (no matter what):working collaboratively with others, communicating, and managing conflict effectivelyBreak Through Thinking:cultivating innovation and nimble learningOwn It Always:ensuring accountability, and making good and timely decisionsCompete Where It Counts:demonstrating courage and focusing on customersIntegrity and Instills Trust:gaining the confidence and trust of others through honesty, integrity and authenticityManages Complexity:making sense of complex, high quantity, and sometimes contradictory information to effectively solve problemPlans and Aligns:plan and prioritize work to meet commitments aligned with organizational goalsDrives Engagement:creating a climate where people are motivated to do their best to help the organization achieve its objectives The above statements are intended to describe the nature of work performed by those in this job and are not an exhaustive list of all duties. Nothing in this job description restricts managements right to assign or reassign duties and responsibilities to this job at any time which reflects management’s assignment of essential functions. Minimum Education, Experience, Skills HS DiplomaMinimum of 4 years of experience working in a cGMP environment Knowledge and understanding of cGMP and CFR requirementsPersonal Competencies: Self-awareness, Integrity, Team Player, Creative, and Culturally awareAble to work independently with limited supervisionStrong mechanical aptitude as determined by trainer assessment U.S. Base Pay Ranges and Benefits Information The estimated annual base salary as a new hire for this position ranges from $61,000 to $73,900. Individual base pay depends on various factors such as applicant’s education, experience, skills, and abilities, as well as internal equity and alignment with market data. The salary may also be adjusted based on applicant’s geographic location. Certain roles are eligible for additional incentive compensation, including merit increases, annual bonus, [and/or long-term incentives in the form of stock options.] Additionally, Emergent offers a comprehensive benefits package*. Information regarding additional benefits can be found here: https://www.emergentbiosolutions.com/careers/life-at-emergent (*Eligibility for benefits is governed by the applicable plan documents and policies). If you are selected for an interview, please feel welcome to speak to a Human Resources Partner about our compensation philosophy and available benefits. There are physical/mental demands and work environment characteristics that must be met by an individual to successfully perform the essential functions of the job. This information is available upon request from the candidate. Reasonable accommodations may be made to enable individuals with disabilities to perform all essential functions. Emergent BioSolutions is an Equal Opportunity/Affirmative Action Employer and values the diversity of our workforce. Emergent does not discriminate on the basis of race, color, creed, religion, sex or gender (including pregnancy, childbirth, and related medical conditions), gender identity or gender expression (including transgender status), sexual orientation, age, national origin, ancestry, citizenship status, marital status, physical or mental disability, military service or veteran status, genetic information or any other characteristics protected by applicable federal, state or local law. Information submitted will be used by Emergent BioSolutions for activities related to your prospective employment. Emergent BioSolutions respects your privacy and any use of the information submitted will be subject to the terms of our Privacy Policy . Emergent BioSolutions does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on Emergent BioSolutions’ approved agency list. Unsolicited resumes or candidate information submitted to Emergent BioSolutions by search/recruiting agencies not already on Emergent BioSolutions’ approved agency list shall become the property of Emergent BioSolutions and if the candidate is subsequently hired by Emergent BioSolutions, Emergent BioSolutions shall not owe any fee to the submitting agency.