Project Qualification Engineer

Posted 6 Days Ago
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Bangalore, Bengaluru, Karnataka
7+ Years Experience
Biotech
The Role
Manage commissioning and qualification of BioPharma equipments, lead factory and site acceptance tests, perform audits, facilitate quality issues, and provide support for product development. Responsible for maintaining complaint and nonconformance processing. Requires 5-8 years of experience in quality and assurance development within the biomedical or pharmaceutical industry, Bachelor's degree in relevant field, professional certification, and fluency in English.
Summary Generated by Built In

Manage commissioning and qualification of BioPharma equipments. Lead and assist with Factory acceptance test and Site acceptance test, IQ/OQ including documentation review and reporting, Manage the completion of FAT and SAT and post tasks, Handling KPI, Root cause analysis pertaining to qualification. High matured handling with customers. Willing to travel both domestic and international- 70% travel profile

The Customer Quality Professional will be responsible for interpreting, building upon, and complying with company service standards. The holder of this position will carefully maintain complaint and nonconformance processing through records and tracking systems, including root cause and corrective actions.

Main Responsibilities & Tasks:

  • Inspect or verify services are compliant with applicable requirements

  • Plan, organize and conduct audits/assessments of supplier's systems, processes and products

  • Work with services to close out any audit findings

  • Document and report audit/assessment results

  • Facilitate quality issues in conjunction with key stakeholders, resolving day to day problems

  • Perform effective containment and problem resolution for all non-conformances

  • Report and assess status of service performance

  • Provide education and coaching on quality systems, regulatory compliance issues and company initiatives

  • Provide support for product development

Qualification & Skills:

  • Bachelor degree in a relevant science, engineering or related subject

  • Minimum 5-8 years' experience in a quality and assurance development ideally within the biomedical or pharmaceutical industry with the ETO project background.

  • Professional Certification — In depth knowledge of Quality auditing, and regulatory standards

  • Good Technical Engineering knowledge, including ability to understand engineering drawing and standards

  • Ability to develop realistic work plans, set personal goals that align with company goals

  • Well-organized and methodical, with a superb attention to detail

  • Ability to prioritize and manage daily assignments

  • Excellent written and verbal communications skills to represent the company professionally

  • Establish and maintain positive working relationships with all in and external interfaces

  • Fluent in English

About Sartorius 

Sartorius is part of the solution in the fight against cancer, dementia, and many other diseases. Our technologies help translate scientific discoveries into real-world medicine faster, so that new therapeutics can reach patients worldwide. 

We look for ambitious team players and creative minds, who want to contribute to this goal and advance their careers in a dynamic global environment.

Join our global team and become part of the solution. We are looking forward to receiving your application. 
www.sartorius.com/careers

The Company
HQ: Göttingen
9,059 Employees
On-site Workplace
Year Founded: 1870

What We Do

Sartorius is a leading international partner of life sciences research and biopharmaceutical manufacturing.

We help our customers #SimplifyProgress from drug discovery to manufacturing so that more people can have access to better medicine. With this, we are #PartOfTheSolution in the fight against diseases worldwide.

With innovative laboratory instruments and consumables, the our Lab Products & Services division focuses on laboratories performing research and quality control at pharmaceutical and biopharmaceutical companies as well as academic research institutes.

The Bioprocess Solutions division, with its broad product portfolio focusing on single-use solutions, helps customers manufacture biotech medications, vaccines, and cell and gene therapies safely, rapidly, and economically.

Based in Göttingen, Germany, Sartorius also has a strong global reach with around 60 production and sales sites worldwide. We regularly expand our portfolio through the acquisition of complementary technologies.

In 2023, Sartorius generated sales revenue of around 3.4 billion euros. Currently, around 14,600 employees from around 110 nations are working for customers around the globe.

Join our team, partner or collaborate with us.

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