Analytical Project Coordinator, Quality Control

Advancing medicine to save lives. Together. Thanks to many decades of experience and our passion for what we do, we make an essential contribution to the global availability of biopharmaceuticals, especially for patients with rare and serious diseases. Rentschler Biopharma SE is a leading contract development and manufacturing organization (CDMO) focused exclusively on client projects. We offer customized full-service solutions for bioprocess development and the production of complex biopharmaceuticals. As a German family-owned company with an international footprint and global reach, we combine experts, expertise and years of experience to develop best-in-class solutions - together with our clients.Rentschler Biopharma has approximately 1,400 employees and is headquartered in Laupheim, Germany, with a site in Milford, MA, USA. In 2024, we joined the United Nations Global Compact, underlining our commitment to sustainability. As an independent family-owned company, we live by the motto: Many hands, many minds - ONE TEAM! Open, respectful cooperation characterizes our working environment, where quality awareness, diligence and responsibility are our top priorities. With all the diversity of our talents in the Rentschler team, we pursue one vision together: advancing medicine to save lives. Duties and ResponsibilitiesPrimary QC contact for the complete analytical methods portfolio and link between project team, international customers as well as internal and external laboratoriesRepresentative of the QC labs as well as Rentschler quality standards in assigned client projects; working in collaboration with all QC departments (AD, Microbiology, Raw Materials, and Release) and potentially Process Development Analytics to gather information to present to client and providing client feedback and requests back to the appropriate departmentsDetermines client needs for requested work packages and collaborate internally to assess capabilities/capacityPrepare for client facing meetings by consulting SMEs, reviewing work package data, and generating presentations as appropriateProject planning of analytical work packages including method developments, qualifications, validations, specification development, sampling plansAssess new projects as it relates to QC activities and capabilitiesCoordination of analytical support and timelines between development, production, and QC departmentsOrganizational and technical support of analytical method developments in the context of projects Initiate and own change controls related to client request for SOPs, Specification Documents, Scope of Analytical MethodsInter-laboratory compilation, evaluation and documentation of various analytical data as well as collaboration in the lifecycle management of analytical methods as it relates to assigned projectsProvide collaboration and potential authoring SOP's, lab investigations, OOS Investigations, and deviations as it relates to assigned projectsEscalation of quality critical issues in customer projects within the Rentschler Quality UnitReview/Collaboration of development, validation, and Qualification of analytical methods per ICH USP guidelinesContinuous research for new methods/techniques as well as initiation and organization of laboratory testingEnsure department readiness for audits by both internal and external authorities; potential contact person for analytical laboratories during both internal and external inspectionsQualificationsMasters Degree in field of biochemistry, biotechnology or comparable field with at least 5+ years of experience in Analytical Process Sciences, Analytical Development, and/or project management in a Pharmaceutical, Biotechnology, CDMO, or other healthcare related field.ORBachelors Degree with 7+ years of experience in Analytical Process Sciences, Analytical Development, and/or project management in a Pharmaceutical, Biotechnology, CDMO, or other healthcare related fieldSolid experience in common biological and protein chemical analytical methodsKnowledge of GMP-compliant analyticsStrong Understanding of GMP's with expectations of a commercial GMP environmentMust communicate effectively (verbal and written) with director and peers; written communicate skills require full competence in following detailed written instructions, creating/revising SOP's and reportsAdvanced knowledge development, approval, manufacturing and testing of biopharmaceuticals Proficient in Microsoft Office - Outlook, Word, Excel, PowerPoint and ProjectWorking ConditionsMay require working in laboratory environment including using chemical reagents and analytical equipmentPersonal Protective Equipment must be worn as requiredNormal office working conditions: computer, phone, files, fax, copierWill interact with other people and clientsPace may be fast and job completion demands may be highPhysical RequirementsFrequent lifting up to 10 lbsFrequent standing/walking to work in lab environment for extended periodsFrequent sitting for extended periods to use computer