Job Details

Continuious Improvement Technician July 30, 2026

Located in Homewood, AL

Pay: $25-28/hr DOE

Job Full 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 ManufacturingTheory 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

7:00am to 3:00pm

M-F

Pay

$25-28/hr - DOE

Birmingham (South), AL
3348
200 Cahaba Park Circle
Suite 130
Birmingham, AL 35242

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