Process Alliance
Direct message the job poster from Process Alliance.
Company Overview Process Alliance is a leading engineering consultancy firm dedicated to delivering innovative solutions in engineering, automation, manufacturing services, and medical devices. With a commitment to being a better model of problem solving, we have been at the forefront of providing cutting‑edge engineering services to clients across the life science industry. Our team of experts thrives on solving complex challenges and driving technological advancements to meet the evolving needs of our clients.
Job Overview We are seeking a C&Q Engineer to support the successful startup, commissioning, and operational handover of new or upgraded pharmaceutical manufacturing systems. This role is ideal for an engineer with strong project execution skills and hands‑on experience in commissioning, qualification, and operations support in GMP environments.
Key Responsibilities
Support operational readiness planning for new equipment, utilities, and manufacturing areas.
Own or support commissioning & qualification (C&Q) activities including protocol development, execution, and issue resolution.
Assist with manufacturing equipment and process startup, troubleshoot issues during early batches, and improve operational reliability.
Develop and update SOPs, batch records, and operational readiness documentation.
Coordinate operator training, readiness checklists, and manufacturing process walkdowns.
Drive operational improvements and ensure compliance with GMP, safety, and regulatory requirements.
Required Qualifications
Bachelor’s degree in Engineering (Chemical, Mechanical, Biomedical, Industrial, or related discipline).
3–5 years of engineering experience in pharmaceutical, biotech, or other regulated life sciences manufacturing.
Project‑management experience supporting capital projects, equipment installation, or cross‑functional readiness activities.
Hands‑on experience with startups, C&Q activities, FAT/SAT, or equipment installation.
Strong understanding of GMP operations, documentation, and validation principles.
Ability to work collaboratively across engineering, quality, and operations teams.
Company Culture At Process Alliance, we strive to be a better model for how problems are solved, and solutions are delivered. We believe in providing a supportive and inclusive work environment where employees can thrive both personally and professionally. Join our team and be part of a company that is shaping the future of engineering solutions.
Location Indianapolis, IN
Equal Opportunity Employer Process Alliance is an equal‑opportunity employer. We encourage applications from candidates of all backgrounds and experiences.
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Company Overview Process Alliance is a leading engineering consultancy firm dedicated to delivering innovative solutions in engineering, automation, manufacturing services, and medical devices. With a commitment to being a better model of problem solving, we have been at the forefront of providing cutting‑edge engineering services to clients across the life science industry. Our team of experts thrives on solving complex challenges and driving technological advancements to meet the evolving needs of our clients.
Job Overview We are seeking a C&Q Engineer to support the successful startup, commissioning, and operational handover of new or upgraded pharmaceutical manufacturing systems. This role is ideal for an engineer with strong project execution skills and hands‑on experience in commissioning, qualification, and operations support in GMP environments.
Key Responsibilities
Support operational readiness planning for new equipment, utilities, and manufacturing areas.
Own or support commissioning & qualification (C&Q) activities including protocol development, execution, and issue resolution.
Assist with manufacturing equipment and process startup, troubleshoot issues during early batches, and improve operational reliability.
Develop and update SOPs, batch records, and operational readiness documentation.
Coordinate operator training, readiness checklists, and manufacturing process walkdowns.
Drive operational improvements and ensure compliance with GMP, safety, and regulatory requirements.
Required Qualifications
Bachelor’s degree in Engineering (Chemical, Mechanical, Biomedical, Industrial, or related discipline).
3–5 years of engineering experience in pharmaceutical, biotech, or other regulated life sciences manufacturing.
Project‑management experience supporting capital projects, equipment installation, or cross‑functional readiness activities.
Hands‑on experience with startups, C&Q activities, FAT/SAT, or equipment installation.
Strong understanding of GMP operations, documentation, and validation principles.
Ability to work collaboratively across engineering, quality, and operations teams.
Company Culture At Process Alliance, we strive to be a better model for how problems are solved, and solutions are delivered. We believe in providing a supportive and inclusive work environment where employees can thrive both personally and professionally. Join our team and be part of a company that is shaping the future of engineering solutions.
Location Indianapolis, IN
Equal Opportunity Employer Process Alliance is an equal‑opportunity employer. We encourage applications from candidates of all backgrounds and experiences.
#J-18808-Ljbffr