Continuous Improvement Technician

Continuous Improvement Technician Express Employment

• 3.5 Birmingham, AL Job Details Full-time $23
• $27 an hour 13 hours ago Qualifications Safety data sheet (SDS) reading Laboratory equipment performance testing and validation Document control within pharmaceutical industry Pharmaceutical regulatory compliance Safety regulations Laboratory instrument validation Technical writing within manufacturing Employee relationship building Microsoft Office Manufacturing standard operating procedures Records management Laboratory standard operating procedures Compliance documentation Relationship management Laboratory information systems (LIS) Test validation method Industrial chemical handling Standard operating procedures (SOPs) Cross-functional communication Chemical safety protocols Full Job Description Key Responsibilities Author and submit revisions to controlled documents such as SOPs and controlled forms in support of GMP Operations.

Support and perform equipment validation and qualification activities. Prepare, review, and/or audit technical documentation supporting GMP Operations. Lead, manage, and implement large cross-functional projects, evaluate current business processes, systems, and workflows. Analyze current processes to determine opportunities to optimize and improve processes and workflows. Implement Lean Six Sigma tools to optimize cost and improve efficiency. Develop a good collaborative working relationship with the Management team to help achieve department goals. Assist Site Managers with collecting and evaluating data. May also be required to support production activities on an occasional basis Skills and Abilities Must be trained and understand continuous improvement principles like Lean Manufacturing , Theory of Constraints , etc.

• Beginner Must be able to execute compendial procedures involving complexity.
• Intermediate Must be familiar with cGMP and OSHA regulations.
• Beginner Must be able to effectively communicate results, problems, or issues, verbally as well as in writing.
• Intermediate Must be computer literate and savvy with MS Office applications, software programs related to LIMS .
• Intermediate Must be able to work in a team environment and be flexible to easily adapt to changes in assignments.
• Intermediate Must follow safe practices as identified in the appropriate MSDS during working with chemicals, and must follow applicable state and federal regulations.
• Beginner Must be capable of maintaining clear and concise laboratory records and communicating clearly both within and between departments.
• Intermediate Must be thoroughly familiar with cGMP applicable to laboratories in pharmaceutical settings and with method verification/validation concepts. Must be able to review laboratory records to ascertain compliance with applicable specifications, methods, and SOPs.
• Beginner Schedule M-F Pay $23-27/hr
• DOE