Skip to main content
Tallo logoTallo logo

Find Jobs

Find Jobs Near You – Available Work in Your Location

Skip to job details

Back to Results

Apply for this opportunity

To apply for this job, you'll continue to an external website or email application.

Meet Life Sciences

Senior Process Engineer

Career Insights for Pharmaceutical Manufacturing Process Engineer

See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.

Scorecard

Based on South Carolina data

Review key factors to help you decide if this role fits your goals. How is this calculated?

Were these scores useful?

What they do

A Pharmaceutical Manufacturing Process Engineer designs and maintains manufacturing equipment, facilities and processes for a pharmaceutical company. Maintains process controls for the specific sterile processing requirements of pharmaceutical manufacturing.

$111,597 / year median in South Carolina

+12% projected growth

Explore Career

Job Description

Senior Process Engineer at Meet Life Sciences Senior Process Engineer at Meet Life Sciences in Charleston, South Carolina Posted in about 13 hours ago.
Type:
full-time
Job Description:
Job Summary The Senior Process Engineer provides technical support for clinical and commercial sterile/parenteral drug product manufacturing. The role focuses on process tech transfer, validation, troubleshooting, investigations, and manufacturing documentation in a cGMP-regulated environment. Responsibilities Support process tech transfers, validation activities, and manufacturing projects. Author Master Batch Records and process validation documentation. Provide technical troubleshooting support during manufacturing operations. Lead manufacturing investigations and CAPA activities. Develop CQA assessments, pFMEA risk assessments, validation protocols, and sampling plans. Coordinate laboratory studies with formulation development teams. Partner with internal stakeholders and clients on project activities. Ensure compliance with cGMP, FDA, EU, SOP, and batch record requirements. Qualifications Bachelor's degree in Engineering, Pharmacy, Chemistry, or related field. 5+ years of technical support experience in sterile pharmaceutical manufacturing. Experience with parenteral drug product tech transfers preferred. Strong knowledge of cGMP requirements and sterile manufacturing processes. Strong technical writing, troubleshooting, analytical, and communication skills. Proficiency with Microsoft Office. Willingness to work fully on-site and travel up to 5% domestically.