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Simtra BioPharma Solutions (Simtra) is a world-class Contract Development Manufacturing Organization, partnering with pharmaceutical and biotech companies to bring their sterile injectable products to market. With facilities in Bloomington, Indiana, US and Halle/Westfalen, Germany, we offer a wide range of delivery systems including pre-filled syringes, liquid/lyophilized vials, diluents for reconstitution, powder-filled vials and sterile crystallization.   Our product types include biologics and small molecules, cytotoxics, highly potent compounds, diluents for reconstitution and vaccines – which are all directly injected into patients worldwide.  As such, there is a strong emphasis on quality and continuous improvement at Simtra.  We hold ourselves to the highest quality and regulatory standards. While our primary focus is cGMP manufacturing, we offer many support services including formulation and development, lyophilization optimization, global regulatory support and secondary packaging.   Our teams are driven to help clients scale, innovate and bring life-changing medicines to patients worldwide.   Why join Team Simtra? Because we: Make it HAPPEN – We bring a growth mindset to every opportunity, developing new skillsets and exceeding our expectations and those of our customers. Make it TOGETHER – We work as one, respecting each voice and tapping into our unique strengths across teams—so we can solve problems in new ways. Make it RIGHT – We hold ourselves to a high standard of excellence, fulfilling our commitments to the customer, their patients, and our team members. Make it COUNT – We take pride in our day-to-day work, knowing the impact we make – taking on challenges big and small to improve patient health.     This role: The Sterility Assurance Validation Associate I is responsible for the management and the execution of project and system qualifications, and validation confirmations including equipment and processes. The Validation Associate I ensures compliance that meets worldwide regulatory agency requirements, internal company standards/best practices and current industry practices. This position is 100% onsite at the Bloomington facility and reports to the Sr. Technical Services Validation Manager.   The responsibilities: Document (protocols, SOPs, summary reports) new processes and update existing processes where vital that will be reviewed by clients, corporate and regulatory auditors Conduct development studies on critical equipment Owns and onboards new client projects, including the relevant validations on syringe lines Serve as line owner, conducting gap assessments and determining validation approaches when onboarding new projects Collaborates directly with client representatives Owns non-conformance investigations (NCR) Owns corrective and preventive actions (CAPA) Owns change control management tasks (CCM) Participates in client audits and provides rationale / justification for practices with aid from senior team member / management Responds to audit observations and owns deliverables Subject matter expert for up to 3 processes, technologies or process equipment Owns, plans interventions and leads syringe line media fills and has full ownership through closure of the summary Owns & drives value improvement projects (VIP) to realize savings Become trained and perform semi-annual HEPA filter certification testing (integrity testing, velocity testing, visible smoke testing)   Required qualifications: BS degree in science related field with laboratory experience or High School diploma/GED with a minimum of 6 years related experience within a pharmaceutical, biotechnology or related industry including responsibilities comparable to this position (e.g., technical writing, audit experience, project lead, authoring and performing studies, etc.) Mi