
Process Engineer Chemical Manufacturing
Overview
You will own process tech transfer, equipment qualification, validation, and scale-up in a regulated life sciences manufacturing environment. You will work with cross-functional teams to optimize chemical processes and drive efficiency. This contract role requires 10+ years of process engineering experience and hands-on validation work.
What You'll Do7
- 1Lead process tech transfer from R&D to manufacturing, ensuring smooth scale-up.
- 2Design and execute equipment qualification and validation protocols including IQ, OQ, PQ.
- 3Optimize chemical manufacturing processes for yield, quality, and safety.
- 4Troubleshoot process deviations and implement corrective actions.
- 5Collaborate with cross-functional teams to support production schedules.
- 6Drive continuous improvement initiatives using Lean and Six Sigma methodologies.
- 7Document all activities in compliance with regulatory standards.
Requirements6
- 1Bachelors degree or higher in Chemical Engineering or related field.
- 210+ years of process engineering experience in chemical manufacturing.
- 3Hands-on experience with process validation and IQ/OQ/PQ protocols.
- 4Strong understanding of GMP regulations and environmental health and safety standards.
- 5Proven ability to lead cross-functional teams and manage multiple priorities.
- 6Excellent problem-solving skills with a root cause analysis mindset.
Salary Insight
$64k per year
Location
Required Skills
Similar open positions
Explore active roles that match your skills and interests.
CRB
VerifiedSenior Process Engineer Small Molecule Manufacturing
CRB seeks a skilled Process Engineer III/IV/V to lead small molecule API process development scale-up and manufacturing optimization. This role combines technical leadership with strategic client engagement supporting design scope management budget and schedule while mentoring junior staff and aligning projects with cGMP FDA EMA and ICH guidelines. The ideal candidate drives improvements and delivers high-quality outcomes.
Interact Engineering LLC
VerifiedProcess Engineer Pharmaceutical Manufacturing Temp-to-Hire
Seeking a hands-on Process Engineer for a temporary position supporting oral solid dosage and sterile operations. The role involves driving process robustness compliance and continuous improvement in a dynamic pharmaceutical environment. This opportunity focuses on equipment qualification technology transfer and cross-functional collaboration.
Actalent
VerifiedProcess Engineer (Contract) Hudson WI
We seek an experienced Process Engineer to lead technical development and scaling of aseptic manufacturing processes for innovative pharmaceutical and combination-device products. This consulting engagement involves defining future-state aseptic operations by translating feasibility findings into robust process designs equipment requirements and contamination-control strategies. The role requires collaboration with technical stakeholders equipment vendors and project teams to ensure scalable compliant manufacturing aligned with industry best practices. Ideal for seasoned aseptic professionals who enjoy solving complex technical challenges and influencing critical design decisions.
RAPS PROFESSIONAL SERVICES PRIVATE LIMITED
VerifiedProcess Engineer RAPS Professional Services Private Limited
Lead ownership of manufacturing processes to ensure quality stability and efficiency. Optimize operations through structured problem solving. Drive continuous improvement in safety quality yield productivity and cost reduction. Analyze production data to identify improvements and reduce variation. Develop and maintain documentation SOPs and control plans. Support new product introductions equipment validation and industrialization. Collaborate with cross functional teams to achieve production goals. Provide technical guidance and coaching to technicians. This role offers hybrid remote work in Pinellas Park FL 33782.
Sterling Engineering Inc.
VerifiedSenior Systems Engineer – Pharmaceutical Automation
You will own complete technical integration of complex pharmaceutical manufacturing equipment, from installation through qualification. This role centers on system-level engineering for two aseptic filling systems at a major pharmaceutical customer. You will lead IQ/OQ qualification activities, coordinate mechanical, controls, automation, and validation teams, and translate regulatory requirements into system specs. With direct exposure to customers and engineering leadership, you will influence system architecture and technical strategy for GMP-regulated environments. This position offers a clear path to Principal Engineer or Technical Leadership roles, supporting life-saving products.
1525 JuN - Seattle Dexter
VerifiedSenior Engineer I Validation
Lead validation efforts at a BMS facility to ensure GMP compliance and operational excellence. Drive validation projects and mentor team members to achieve high-quality outcomes. Shape the future of patient care through innovative solutions.