Senior Process Engineer – Technical Operations-1
| Company | Inventing for Life |
|---|---|
| Location | Elkton, VA, USA |
| Salary | $Not Provided – $Not Provided |
| Type | Full-Time |
| Degrees | Bachelor’s, Master’s, PhD |
| Experience Level | Senior |
Requirements
- Bachelor of Science (B.S.) degree in chemical engineering, biochemical engineering, biological systems engineering, biology, biochemistry, chemistry or related life science or engineering discipline and a minimum of five (5) years of relevant industrial experience
- OR Master of Science (M.S.) degree in chemical engineering, biochemical engineering, biological systems engineering, biology, biochemistry, chemistry or related life science or engineering discipline and a minimum of three (3) years of relevant industrial experience
- OR PhD in chemical engineering, biochemical engineering, biological systems engineering, biology, biochemistry, chemistry or related life science or engineering discipline with no experience required
- Experience working in a pharmaceutical or cGMP environment
- Technical writing and presentation experience
- Strong leadership skills
- Strong personal character, ethics, and integrity
- Strong verbal and written communication skills; interpersonal and team skills; and collaborative skills
- Excellent organizational skills
- Robust problem-solving skills and a hands-on approach to troubleshooting and investigation, with a bias towards going to see problems for oneself in the field.
- Strong desire to succeed and to help others to do the same.
- The ability to examine an issue from diverse perspectives (e.g. safety, compliance, maintenance, automation, equipment, process, and people) in order to best understand and resolve it.
- Enthusiasm, confidence, and initiative-taking ability needed for continuous learning and application of knowledge.
- Ability to manage projects and assignments, working towards deadlines within a schedule.
Responsibilities
- Achieving safety, quality, and environmental compliance excellence in all assignments
- Providing technical leadership and support for a sterile manufacturing facility, including data analysis, troubleshooting, problem solving, coaching/teaching, and report writing
- Collaborating with cross-functional teams across levels, including leading teams or groups
- Initiating, supporting, or leading change control implementation
- Learning new processes and procedures
- Leading and conducting technical investigations and analyses to determine the root cause of problems
- Recommending and implementing corrective and preventative actions
- Executing continuous improvement projects
- Recommending, creating, writing, reviewing, and approving procedures, instructions, protocols, and other GMP documentation
- Coaching and teaching others
- Contributing to or leading safety reviews and improvements
- Performing shift work as needed (expected to be minimal)
- Provide support, including leadership support, during inspections.
Preferred Qualifications
- Experience managing, coaching, and developing others
- Experience managing and executing projects or change controls
- Experience with SAP and DeltaV