M-F 1st Shift on-site 5x/week

SRG, the leader in the Life Sciences human capital industry, is looking for a Technical Writer I to join our client's manufacturing team in Houston, TX. This role will be responsible for tracking, management, and completion of Supply Chain Quality Records (such as deviations, material recalls, and CAPA) in partnership with applicable SMEs.

*W2 contract only; we CANNOT accept visa status candidates at this time.

*12 month contract pus extension

MUST HAVES:

• Experience performing root-cause analysis, leading, and completing lab investigations
• Prior experience working in a laboratory setting required
• Responsible for intiation, investigation and completion of Minor/Track and Trend process deviations
• Demonstrates technical writing for the educated but uninformed reader, translate simple to moderate scientific events into a brief and cohesive report as a finished product
• Displays ability to gather data from various sources across the site, performance of Root Cause Analysis (RCA) to determine the most likely cause of the deviation investigation
• Familiarity with cGMP quality systems, and demonstrates ability to read and comprehend GMP documents (i.e. SOPs, logs, Batch Records)
• Proficient in the use of spreadsheets, databases, and word processing software.
• Prior experience with TrackWise preferred

JOB RESPONSIBILITIES:

• Leads error prevention and continuous improvement initiatives based on identified recurring root cause.
• Serves as the Quality Record (PR) Subject Matter Expert (SME), Level I, for the Warehouse / Supply Chain team
• Responsible for the initiation, investigation and completion of Minor process deviations
• Demonstrates technical writing for the educated but uninformed reader, translate simple to moderate scientific events into a brief and cohesive report as a finished product
• Demonstrates ability to capture immediate actions and containment of the event, address comments from stakeholders on the compiled final report
• Displays ability to gather data from various sources across the site, performance of Root Cause Analysis (RCA) to determine the most likely cause of the deviation investigation
• Familiarity with cGMP quality systems, and demonstrates ability to read and comprehend GMP documents (i.e. SOPs, logs, Batch Records)
• Problem solving in a cross-functional setting, and participation and attendance at the deviation review board

* Only candidates selected to be moved forward in the recruitment process will be contacted by SRG's Recruitment Team to schedule a conversation.

Impellam Group and its brands are equal-opportunity employers committed to diversity and inclusion. All qualified applicants will receive consideration without regard to race, color, religion, gender, sexual orientation, pregnancy or maternity, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application, interview process, pre-employment activity, and the performance of crucial job functions.

If you require additional disability considerations, modifications, or adjustments please let us know by contacting HR-InfoImpellamNA@impellam.com or fill out this form to request accommodations.