What are the responsibilities and job description for the AR&D Chemist position at Pii, A Jabil Company?
Job Overview
The Analytical Chemist will be involved in process development, technology transfer, and analytical activities to support the scale-up and optimization of new products.
Responsibilities
The Analytical Chemist will be involved in process development, technology transfer, and analytical activities to support the scale-up and optimization of new products.
Responsibilities
- Perform activities in the development and validation of analytic methods.
- Perform analytical testing of raw material, in-process materials and finished products (includes but not limited to HPLC analysis, GC analysis, dissolution testing, KF testing).
- Perform data analysis and evaluation of test results.
- Assist with the preparation of written test methods, protocols, reports and SOPs.
- Maintain accurate records of test data and test procedures; maintain lab notebooks and logbooks in accordance with company guidelines and GLP.
- Perform other duties as assigned.
- BS in chemistry or related physical/biological science, or equivalent combination of education, training and professional experience that provides the individual with the required knowledge, skills, and abilities.
- 2-3 years of experience gained from a similar role (ideally within pharma) with a working knowledge of process development and manufacturing operations.
- Demonstrate literacy and ability to use data acquisition and processing software.
- Practical experience with chromatographic instruments including HPLC and GC.
- Demonstrate the ability to establish good working relationships with other departments, including vendors, colleagues, and subordinates.
- Demonstrates the appropriate technical knowledge necessary to make sound decisions on development issues with minimal supervision.
- Demonstrate the ability to analyze data and information and assess and resolve complex problems/issues as required.
- Must be able to comprehend and follow all applicable SOPs.
- Demonstrate knowledge and experience with electronic Quality Management Systems such as MasterControl and Trackwise.
- Demonstrate ability to acquire the appropriate knowledge from resources on the current federal, local, and international regulations regarding the production, testing, and release of drug substances and products.
- Good understanding of cGMPs, industry, and regulatory standards and guidelines.
- Demonstrate familiarity with Microsoft programs like Word, Excel, PowerPoint, Project, Teams, Outlook, etc.
- Demonstrate the ability to portray the appropriate level of integrity and professionalism.
- Demonstrate the ability to communicate effectively with management, staff, regulators, and client representatives in written and verbal formats.
- Demonstrate the ability to complete tasks accurately and according to established and shifting timelines.
- Demonstrate the ability to make quality scheduling, resource allocation, and priorities decisions.
- Energetic, execution-focused, self-motivated, and organized individual who is accustomed to working in a deadline-focused, high-pressure entrepreneurial environment.
- Results-oriented and efficient.
- Creative and open-minded who fosters an environment in which sharing of ideas is encouraged.
- Demonstrate the ability to work closely with a diverse customer and employee base (internally and externally).
- Demonstrate the ability to work well in a cross-functional team environment.
- Must communicate fluently in English and have legible handwriting.
- Ability to travel between and within facilities to visit staff, operations, and projects, as needed.
- Ability to sit, stand, climb stairs, and climb ladders to mezzanines (when necessary).
- Ability to lift up to 40 pounds on occasion.
- Ability to use PPE (safety shoes, goggles, respirators, gloves, etc. when necessary).
Salary : $75,000 - $80,000