Development Scientist Job at Excelgens Consulting Services India Private Limited
Excelgens Consulting Services India Private Limited Greenville, NC 27834
Job Title: Development Scientist
Location: 143 1240 Sugg Parkway Greenville NC 27834 USA
Duration: 01+year (With possible extension)
This position serves as a primary point of contact with the client regarding pharmaceutical development and clinical manufacturing project related activities. This role is responsible for supporting these activities in the areas of supervision, process development, clinical trial batch manufacturing, packing and documentation.
Education: Minimum of bachelor’s degree in pharmaceutical science, chemistry, engineering, or related science with at least 3 years of industrial pharmaceutical experience.
Responsibilities include, but are not limited to:
- Independently design and execute experiments.
- Interpret data and make sound recommendations based on data.
- Solve formulation and process problems.
- Author SOP’s, IQ/OQ/PQ documents, development and technical reports, and CMC sections for regulatory submissions
- Maintain competency and training for relevant processes and equipment.
- Ensure that all work is accurate, precise, properly documented, within GMP requirements.
- Organize multiple project responsibilities to ensure tasks are appropriately prioritized and executed on time.
- Design, coordinate, and execute development and CTM activities, including formulation, data interpretation, equipment selection, generation of batch records and other appropriate documentation, and problem-solving exercises.
- Ongoing communication with clients, internal support groups, resources, vendors, and staff.
Job Type: Contract
Salary: $35.00 - $40.00 per hour
Schedule:
- 8 hour shift
- Day shift
- Monday to Friday
Ability to commute/relocate:
- Greenville, NC 27834: Reliably commute or planning to relocate before starting work (Required)
Education:
- Bachelor's (Required)
Experience:
- Molecular biology: 1 year (Preferred)
- CMC sections: 1 year (Required)
- GMP: 3 years (Required)
- clinical trial: 3 years (Required)
- manufacturing, documentation: 3 years (Required)
Work Location: One location
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