The Principal Manufacturing Science and Technology (MSAT) Representative is part of a team of experienced pharmaceutical professionals responsible for the technical onboarding and process development of new drug product projects at Sintra BPS. This includes designing the manufacturing process(es) required for drug products. The Principal Technical Transfer Representative 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. This position reports to the Sr. Manager, Technical Transfer.
What you'll be doing:- 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 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, 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 by being visible on the manufacturing floor, resolves issues during manufacturing and leading process improvement activities
- Conduct Non-Conformance Report (NCR) 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
- Participates in new project reviews to determine acceptable fit
- Reviews Master Batch Records of junior colleagues and provides guidance
- Technical representative in regulatory, client and internal audits as product/process Subject Matter Expert (SME), and 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
- Perform filter troubleshooting
- Develops and presents in-depth SME courses on pharmaceutical industry topics
- Mentors new hires in Technical Services and helps with training and on-boarding
What you'll bring:- BS degree required (preferably in a science or engineering related field
- 6+ years pharmaceutical manufacturing experience (preferably in a CDMO)
- 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
- Experience in aseptic processing, sterile filtration, and process validation
- MS Office Suite advanced proficiency
- Experience using Enterprise software (i.e., JDE, BPLM, MiniTab, Trackwise, etc.)
Physical / Safety Requirements:- Require overtime work on occasion, including nights and weekends
- Use of hands and fingers to manipulate office equipment is required
- Position requires sitting for long hours, but may involve walking or standing for periods of time
- Must be able to qualify for Grade A/B area gowning
- Must be able to wear applicable personal protective equipment (PPE)
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