MSAT Scientist III - 1966256
Lakewood, NJ, 08701, US
Salary: 90000k/year - 102000k/year
Reference ID: 1966256
Date Posted: 04/29/2024
Shortcut: http://shurig-solutions-inc.jobs.mrinetwork.com/9fpwxJ
Job Title: MS&T Scientist III
Location: US-NJ
Overview:
The purpose of this position is to support the Company in the development and optimization of manufacturing processes, improving them and increasing the scale. The ultimate goal is to develop processes that optimize the product yield and minimize the cost of production. These products include injectables and nasal/sublingual sprays
Responsibilities:
- Utilize and apply knowledge of basic scientific principles, theories, and concepts to develop solutions to problems of moderate complexity.
- Design and conduct experiments at small and medium scales in coordination with the R&D group.
- Collect and analyze data from development batches and provide process development reports and tech transfer reports.
- Provide input in developing robust process validation programs.
- Perform risk assessment and present ideas for modifying existing procedures and suggest alternative methods to improve results.
- Understand, keep current, and apply current technology to include cGMP, and sterile manufacturing techniques.
- Collaborate with Engineering, Operations, OpEx, and QA groups and prepare robust manufacturing records, technical reports, and SOPs. Prepare, analyze, and organize data for training, and meetings.
- Use statistical process control and other statistical tools for comparison and hypothesis testing. Apply engineering, pharmaceutical sciences, or materials sciences fundamentals to model the product and process to solve complex technical problems.
- Provide technical expertise to resolve challenges that are associated with full-scale commercial production.
- Work in the aseptic compounding and filling processes and assist in maintaining the equipment used for production.
- Train and mentor new employees within the department. This includes but is not limited to processes and procedures in compliance with established protocols and regulatory guidelines.
- Work closely with internal and external departments to ensure the efficient progress of projects.
- Understand and comply with all Company safety, environmental, and quality practices and procedures as outlined in organizational/departmental guidelines and SOPs, as well as, applicable federal, state, and local regulations.
- Represent the department in interactions with other departments, as well as, internal and external clients in various settings such as meetings, teleconferences, e-mails, printed reports, etc.
- Strengthen inter-departmentmental relationships at the Individual Contributor level.
Qualifications:
Bachelor’s Degree (BS) in Engineering or Natural Sciences required with a minimum of 3 years of relevant experience in the pharmaceutical industry or an equivalent combination of education and experience.
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