Details:
Stefanini Group is hiring!
Stefanini is looking for MS&T Specialist in Davie, FL (Onsite)
For quick Apply, please reach out to Ghanshyam Sharma – call:
2482635646 / email: Ghanshyam.Sharma@stefanini.com
Work Hours: M-F (40 hours)
Work Location: Davie, FL (Onsite)
Shift: 1st Shift (8:00 AM – 5:00 PM)
This position is responsible for performing activities related to critical aspects of products and processes, including process development, pre-validation, and optimization of solid oral dosage forms after Abbreviated New Drug Application (ANDA) filing throughout product launch and commercial lifecycle including process, cleaning, and packaging validation. Executes studies with Research and Development (R & D), Laboratory Technical Services (LTS), manufacturing, and planning.
- Maintains expertise related to formulation, raw material properties, and manufacturing processes. Identifies, analyzes, and suggests corrective actions to optimize procedures, processes, materials, technology, and regulatory compliance issues.
- Digital literacy including basic knowledge of AI (working knowledge of PowerBI, Power Platform, Python, and various presentation tools), JMP, R, etc. is necessary.
Responsibility:
- Adapting Operational Excellence (OpEx) initiatives to improve throughput, reduce waste, and improve safety of the existing commercial products. Coordinate manufacturing of batches if required and prepare technical reports.
- Performing continuous process and cleaning verification, statistical assessments and trend analysis for the development and commercial products.
- Performing investigations to identify the root causes and actively seek remediation approaches and implement Corrective and Preventive Actions (CAPAs).
- Provide Technical assessments/ product impact assessment summaries on time to avoid back-order situation.
- Evaluate the Supplier Material Evaluation team changes (SMET) such as changes to the manufacturing process of Active Pharmaceutical Ingredient (API) or site manufacturing changes for raw materials (API, excipients), cleaning agents and contact surfaces, and packaging components. Coordinate the manufacturing activities and prepare technical reports.
- Execute the experimental and process confirmation studies in coordination with planning, manufacturing, quality, LTS and PM groups.
- Review and analysis of the analytical and statistical data to support the pre-validation work. Analysis of data to ascertain the data meets protocol and product acceptance criteria writes deviation reports and technical assessments as required.
- Supports pre-validation commercial scale report that includes detailed summary of the equipment and qualified equipment parameters (QEPs) assessment, CPPs and CQAs identified during pre-validation work.
- Identify and coordinate the equipment requirements with R & D, Engineering, Employee Health, and Safety (EHS), and PM groups in preparation of Capital Expenditure Request (CER) for the commercial scale pre-validation development/ scale up of the ANDA lots.
- Participation in internal (Corporate and QA audits) and external (FDA, MHRA) audits.
- Remediation of the audit related observations (if any) and timely completion of the action items (if any)
- Maintenance of appropriate documentation of protocols, reports, and laboratory notebooks as required by Standard Operating Procedures (SOPs) and internal policies.
- Actively participate in commercial pre-validation and provide technical support to the manufacturing and quality teams as required.
- Leading multiple new product introduction, site transfer projects, and cleaning validation activities.
- Responsible for completing all training requirements and maintaining 100% compliance with all assignments.
- Responsible for maintaining work areas and performing job functions in a safe and efficient manner in accordance with company policies and procedures, Good Manufacturing Practices (cGMP’s), and Standard Operating Procedures (SOP’s) and Batch Record instructions.
- Responsible for performing additional related duties as assigned.
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