Mstg Scientist Ii

**Title**:MSTG Scientist II**:

- Date: Jul 26, 2023- Location: New Brunswick - OHM- Company: Ohm Laboratories Inc, USA**Job Summary**

Scientist II, MSTG, performs process development studies, Exhibit batch and process qualification activities. This position also prepares technical documentation to support development and validation program at Sun Pharma. This position provides technical support to Manufacturing and Quality department.

**Area Of Responsibility**
- Design and execution of DOE’s, process optimization studies, and process qualification batches, Process data compilation and data analysis using statistical tools.
- Develop documentation package, involving from conceptual study to various phases of product development like process study, characterization, process qualification and cleaning validation.
- Comprehensive understanding of manufacturing technology and equipment used in solid oral manufacturing.
- Responsibility for preparation of Master batch records, Exhibit Batch protocols, pre-validation and process validation documentation and reports.
- Provide troubleshooting support to manufacturing operations. Complete the assigned projects with mínimal supervision.
- Champion compliance investigations, commitments (CAPA), and change controls.
- Participate on cross-functional team that address specific problems, facilitate discussion and research, enabling procedures to become more efficient, and to build and enhance interdepartmental relationships.

**Education and Job Qualification**
- Minimum B.S. in relevant science field, Pharmacy, Pharmaceutical Sciences, Chemical Engineering or related disciplines. M.S. preferred.
- Proficient in MS Office (Word, Excel, Projects, PowerPoint).
- Organizational and recordkeeping skills.
- Strong analytical thinking, problem solving skills and decision making skills.
- Strong communication (verbal and written) skills.
- A self-starter with a hands-on approach and a can-do attitude.
- The requirement for English language proficiency for this job role is Intermediate-B1+ (comparable to Global CEFR Independent B1) level based on the Common European Framework of Reference for Languages (CEFR).

**Experience**

Minimum six (6) years of experience. Experience in solid oral dosage development is desirable.