Job summary
Job post source
This job is directly from PACIV
Job overview
The Validation Engineer at PACIV will manage commissioning, qualification, and validation activities for biotechnology and pharmaceutical clients, ensuring compliance and quality standards.
Responsibilities and impact
The role involves executing system lifecycle deliverables, participating in cross-functional teams, supporting product launches, capital projects, and process improvements within client manufacturing and laboratory systems.
Compensation and benefits
The position offers a competitive salary with benefits including PTO, health insurance with 90% premium paid by PACIV, a $25,000 basic life insurance plan, 401(k) with company match, and project performance bonuses.
Experience and skills
Candidates need a Bachelor's or Master's in Engineering or a technical field, 3+ years of pharmaceutical validation experience, strong communication, computer skills, and familiarity with validation principles and CSV, with project management experience preferred.
Work environment and culture
The job requires working in a 24/7 manufacturing environment, emphasizing teamwork, accountability, and handling high-pressure situations.
Company information
PACIV is an international control systems integration and regulatory compliance engineering firm serving Bio-Pharmaceutical, Medical Device, F&B, and Water/Wastewater sectors.
Job location and travel
The position is based in Indianapolis with up to 20% travel to suppliers, collaborators, and client sites.
Unique job features
The role offers involvement in diverse validation projects across biotechnology and pharmaceutical sites with opportunities to work on large product launches and process improvements.
Company overview
PACIV is a global leader in industrial automation and control systems, specializing in providing comprehensive solutions for the life sciences, pharmaceutical, and biotechnology industries. They generate revenue by offering services such as process automation, instrumentation, and control systems integration, ensuring compliance with regulatory standards and optimizing operational efficiency. Founded in 1997, PACIV has a rich history of innovation and excellence, with a strong commitment to quality and customer satisfaction, making them a trusted partner for major industry players worldwide.
How to land this job
Tailor your resume to highlight your experience with system lifecycle management, including commissioning, qualification, and validation deliverables, especially in Biotechnology and Pharmaceutical environments.
Emphasize your ability to work effectively within cross-functional teams, your project management skills, and your familiarity with Computer System Validation, Data Integrity, and CFR Part 11 compliance.
Apply through multiple channels such as PACIV's corporate career site and LinkedIn to maximize your chances of being noticed for the Validation Engineer role.
Connect with current PACIV employees in the Indianapolis office or within the validation and engineering teams on LinkedIn; start conversations by referencing recent PACIV projects or asking about team culture and expectations for this role.
Optimize your resume for ATS by incorporating keywords from the job description like 'validation engineer,' 'commissioning and qualification,' 'CSV,' 'Data Integrity,' 'CFR Part 11,' and 'project management' to pass automated screenings.
Use Jennie Johnson's Power Apply feature to automate tailored applications, identify the best application portals, and find relevant LinkedIn connections, allowing you to focus your energy on preparing for interviews and networking.
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