Responsibilities may include:
- Create & maintain highly detailed spreadsheets
• Providing technical support for vaccine, biologic, and sterile manufacturing processes in the form of data analysis, troubleshooting, problem-solving, report writing
• Supporting change control implementation
• Learning new processes and procedures
• Recommending, creating, writing process control and automation instructions
• Performing shift work as needed
• Conducting technical investigations and analyses
• Recommending and implementing corrective and preventative actions, and helping lead reduction of atypical events
• Writing, reviewing, and improving procedures for operation of equipment and processes
• Contributing to process and equipment safety reviews
Qualifications
Preferred Experiences:
• Experience working in a cGMP environment
• Work, co-op, or internship experience in industry
Qualifications:
The successful candidate must have:
• Excellent academic record
• Strong verbal and written communication skills, team skills, personal character, and ethics
• Strong problem solving skills and a hands-on approach to problem solving, with a bias towards going to see problems for oneself in the field.
• Ability to examine an issue from diverse perspectives (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 its applications.
• Strong desire to succeed and to help others to do the same.
o Technical/analytical data comprehension;
o Leadership, judgment, organization and project management abilities - Create & maintain highly detailed spreadsheets
o Independent decision making and coordination of activities;
o Attention to detail and follow-up skills.
Additional Information
All your information will be kept confidential according to EEO guidelines.
About the Company
LanceSoft - Pharmaceutical Client
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