Bangalore, Karnataka, India
11 hours ago
Senior Specialist

 

Work Your Magic with us!  

 

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.  

 


Title: Specialist - Senior Specialist

Location: Bangalore

 

Job Description: We are seeking a highly skilled and motivated Validation and Qualification Owner to join our team. The successful candidate will be responsible for overseeing the validation and qualification processes for our R&D IT systems, ensuring compliance with regulatory requirements and industry standards.

Key Responsibilities:

Develop and implement validation and qualification strategies for new and existing products and systems.Create and maintain validation and qualification documentation, including protocols, reports, and standard operating procedures (SOPs).Coordinate and execute validation and qualification activities, including equipment qualification, process validation, and software validation.Collaborate with cross-functional teams, including engineering, quality assurance, and manufacturing, to ensure validation and qualification requirements are met.Conduct risk assessments and develop mitigation plans to address potential validation and qualification issues.Stay current with industry trends, regulatory requirements, and best practices related to validation and qualification.Provide training and guidance to team members on validation and qualification processes and procedures.Contribute to Audits and Inspections

Qualifications:

Bachelor's degree in Engineering, Life Sciences, or a related field.Minimum of 4 years of experience in validation and qualification within the Pharma sector.Strong knowledge of regulatory requirements and industry standards (e.g. GMP, GAMP, FDA 21 CFR Part 211).Proven experience in developing and executing testing plans and test automationExcellent project management and organizational skills.Strong analytical and problem-solving abilities.Effective communication and interpersonal skills.Exceptional communication and  interpersonal skills.Ability to work independently and as part of a team.

We are an equal opportunity employer that values workforce diversity. We want everyone to be able to bring their best self to work every day which is why equality and inclusion is at the forefront of all our activities. We are dedicated to a policy of non-discrimination in employment on any basis including race, caste, creed, colour, religion, sex, age, disability, marital status, sexual orientation, and gender identity.



What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
 
Apply now and become a part of our diverse team!

 

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