What are the responsibilities and job description for the Chemical Engineering Intern position at Piramal Pharma Solutions?
POSITION SUMMARY: Piramal Pharma Solutions’ Riverview facility (Ash Stevens, LLC) is seeking a qualified Chemical Engineer Intern to join our Engineering team. The incumbent will be providing an internship to gain hands-on experience. 0-2 years of cGMP manufacturing experience is desired or equivalent in work experience or education. Applicants should have proven experience working on teams where combined contribution, collaboration, and results were expected. Demonstrated proficiency in common computer tools such as word processing, spreadsheet, and web-based applications. Experience where attention to detail and personal accountability were critical to success. Demonstrates good interpersonal skills, is attentive and approachable. Maintains a professional and productive relationship with area management and co-workers.
To perform this position successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required:
Shall adhere to all applicable regulatory requirements, including FDA, EPA, OSHA, and related safety, health and environmental procedures, policies and practices.
Consistent support and practice of all Piramal Pharma Solutions mission, vision, and values.
Identify and protect the original technical information as part of the company property.
KEY RESPONSIBILITIES
- Design and execute experiments with supervision to assess impact and feasibility of new processing technologies.
- Critically analyze and interpret data using statistical methods.
- Organize, record, and maintain experimental data sets.
- Communicate study findings across multiple departments.
- Apply mathematical and scientific concepts to support technical troubleshooting
- Maintain a safe work environment in accordance with policies/procedures/regulations.
EDUCATION/EXPERIENCE.
- Works on routine manufacturing assignments per written procedures, where ability to recognize deviation from accepted practice is required.
- Analyzes data to determine correlations and cause and effect
- Adheres to Good Manufacturing Practices and standard operating procedures.
- Weighs and checks raw materials. Assembles, cleans and sanitizes process equipment, monitors processes.
- Completes work instructions and maintains clean room environment to comply with regulatory requirements.
- Trains for proficiency in the operation of primary production equipment within the assigned functional area.
- Trains for proficiency in process systems (i.e. SAP, Trackwise, Microsoft Office) and some supporting business systems (i.e. SAP.).
- Support procedural protocol activities in the Manufacturing Sciences Laboratory.
- Supports troubleshooting in production, working with an interdisciplinary team and providing analytical summaries to the Engineering and Tech Transfer Teams.
- Assists in maintaining material and components inventory level.
- Supports safe work environment.
- Work in teams and have continual interaction with members of his/her team as well as other manufacturing teams throughout the production process in order to exchange information regarding the batch(s) in process.
- Works on assignments that are routine in nature where judgment is required in resolving problems and making routine recommendations.
JOB COMPETENCIES
- Excellent written and oral communication skills.
- Knowledge of applicable data privacy practices and laws.
- Practice using data analysis to inform next steps
- Hands-on and advanced troubleshooting and problem-solving skills.
- Self-motivated and directed; strict attention to detail.
- Able to multi-task and meet demands of customers; meet deadlines in a high-pressure environment.
- Follow GMP and 21 CFR Part 11 regulations.
- Willing to work off-shift times, as necessary, to complete projects.
- Willing to work on-call rotation
