Posted August 01, 2026
Continuous Improvement Technician
Express Employment
Birmingham, AL, US
Full Time
23USD - 27USD per hour
Job Description
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
- 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
7:00am to 3:00pm
M-F
Pay$25-28/hr - DOE
