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Validation process Engineer
Topsys It Raleigh, NC
$93k-108k (estimate)
Contractor 6 Days Ago
Save

Topsys It is Hiring a Validation process Engineer Near Raleigh, NC

Company Description

TOPSYS IT is a leading provider that offers IT business solutions, consulting, and technology services. Our services aim to provide an accelerated execution path to our clients, helping them reach their information technology objectives quickly and efficiently within their budget. We are a company of senior consultants and IT implementation experts who focus on exceeding expectations and bridging the strategy-execution gap through hands-on, cost-effective, and industry-specific consulting solutions.

Role Description

This is a contract role for a Validation Process Engineer. As a Validation Process Engineer, you will be responsible for the day-to-day tasks associated with process design, process control, analytical skills, process engineering, and chemical engineering. This is an on-site role located in Raleigh, NC.

Role: Validation process Engineer(3-8 experience)

BG: Chemistry or Science or Mechanical Engineering.

Location: Raleigh, NC

Job Duties:

  • Review, develop and execute validation lifecycle documents like FAT, SAT and qualification protocols for new equipment and existing equipment enhancements & upgrades for sterile filling, device assembly, and packaging equipment.
  • Develop aseptic filling, setup, disassembly, cleaning, and sanitization processes to ensure residues from equipment and cleaning chemicals do not cross contaminate into final filled products in accordance with 21 CFR part 211, 810, 811, FDA EMEA, and other regulatory & quality guidelines.
  • The work also involves writing and updating Validation Plans, Change Controls, CAPAs and Risk Assessments through various stages of process validation and product launch activities.
  • Develop, author, and modify Standard Operating Procedures (SOPs), Work Instructions (WIs), Manufacturing batch records (MBRs), and Preventative Maintenance (PM) plans for various sterile filling, device assembly, and packaging equipment.
  • Lead validation activities and write technical reports such as study reports, validation reports, and mechanical shakedown runs, engineering studies, and feasibility development reports. Document and investigate/assist any deviations associated during the executions.
  • Perform instrument and equipment qualification, analytical and microbial swab sampling, visual inspection during validation activities. Interpret and summarize the results obtained from the laboratory testing.
  • Identify and analyze process activities to improve overall equipment efficiency, optimize process to increase batch size & capacity, improve yields, reduce waste, and streamline process flow, and overall process layout.
  • Perform equipment, process setup, and cleaning activities in a team-oriented environment to align with cross functional departments such as production, planning and quality. The duty also involves training/assisting other production team members for timely completion of the projects.

Minimum Education Requirement: This position requires, at a minimum, a bachelor s degree in computer science, computer information systems, information technology, or a combination of education and experience equating to the U.S. equivalent of a Bachelor s degree in one of the aforementioned subjects.

Thanks & Regards

Charithaa

mail: r.charitha@topsysit.com

Phn: 678-899-6853

Job Summary

JOB TYPE

Contractor

SALARY

$93k-108k (estimate)

POST DATE

06/22/2024

EXPIRATION DATE

07/20/2024