MSAT Senior Associate (Tech Transfer)

Simtra BioPharma Solutions•Bloomington, IN

1d•Onsite

About The Position

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. This role: The MSAT Senior Associate is part of a team of experienced pharmaceutical professionals responsible for the technical onboarding and process development of new drug product projects at BPS. This includes designing the process(es) required for the new project. The MSAT Senior Associate will work closely with a cross-functional group consisting of Program Management, Sales, Supply Chain, Process Validation, Research and Development (R&D), and others, during development and transfer of new projects to Simtra. This position reports to the Sr. Manager, Technical Transfer.

Requirements

Bachelor’s degree required, preferably in a science or engineering related field.
Requires in depth knowledge of systems and equipment, including: scales, mixing systems and mixing monitoring methods, aseptic formulations, fill volume limit setting, disposable formulation technology, homogeneity testing, control charting, identification and response to trends.
In-depth expertise in aseptic processing, sterile filtration, and clinical manufacturing and/or Process Validation
Five (5) years pharmaceutical manufacturing experience, with a minimum of 3 years of applicable MSAT/Tech Transfer/Process Development experience.
Computer proficiency in Microsoft Word, Excel, and Outlook and the ability to use enterprise software (examples include: JDE, BPLM, MiniTab, Trackwise, etc.)

Responsibilities

Lead the onboarding and process development activities & tasks for the manufacture of new drug products, including the supporting development studies.
Serve as the lead technical expert among a cross functional team
Lead the cross functional team through technical activities, development studies and clinical and/or PPQ batches
Create Technical Transfer documents supporting this goal (Tech. Transfer Plan, Process development studies (i.e. mixing studies, filtration studies, purge studies, etc.), Demonstration batch records, GMP clinical/PPQ master batch record)
Heavy participation / co-lead with Process Validation representative on PPQ strategy and protocol development
Lead during hand-off to the commercial team following PPQ batches
Provides technical support to daily Manufacturing operations. The position is visible on the Manufacturing floor, resolves issues during manufacturing and leads process improvement activities.
Conduct deviation (DEV) investigations without assistance, as well as creation, ownership and implementation of Corrective Actions/Preventive Actions (CAPA)
Change Control Management (CCM) owner and impact assessment
Ownership of fill volume dosing qualifications (FVOQ)
Critical evaluation of product impact and responsible for advising if product meets release criteria and regulatory requirements
Grade A/B gowning qualification. Will enter Grade B areas for Batch support
Participates in new project reviews to determine acceptable fit at Simtra
Reviews Master Batch Records of junior colleagues and provides guidance
Independently represents Simtra in regulatory, client and internal audits as product/process Subject Matter Expert (SME). Ownership of audit responses and related CAPAs.
Participates independently in client calls and on-site visits to discuss and set strategy for projects and issue resolutions
SOP owner & process SME
Trained and will perform filter troubleshooting
Develops and presents in-depth SME courses on pharmaceutical industry topics
Mentors new hires in MSAT/Technical Services and helps with training and on-boarding