Validation Engineer

Amgen Inc. (IR); Hyderabad; On-site; INR 1,600,000 - 2,500,000; Full time

Benefits offered by this job

Competitive benefits

Professional growth support

Collaborative culture

Job summary

A global biotechnology company is seeking an experienced Validation Engineer in Hyderabad. You will be pivotal in ensuring compliance with regulatory requirements and developing validation documentation for GxP applications. Ideal candidates will possess significant experience in Computer Systems Validations and a thorough understanding of GAMP and FDA regulations. This role offers the opportunity to impact developing treatments while receiving competitive benefits and support for growth.

Qualifications

• 8 - 12 years of experience in validation/regulatory field with Master’s degree, or 10 - 14 years with Bachelor’s degree.
• Experience in the pharmaceutical industry focusing on Computer Systems Validations.
• Fluent knowledge of rules and regulations: GAMP 5, 21 CFR Part 11.

Responsibilities

• Develop validation documentation and standard operating procedures.
• Provide test execution oversight and assist with deviation recommendations.
• Work with client business functions to develop User Requirements Specification.

Skills

Computer Systems Validations

GAMP

Problem solving

Team management

Regulatory knowledge (FDA, EMEA)

Education

Master’s degree in related field

Bachelor’s degree in related field

Tools

Microsoft Office Suite

Salesforce

Tableau

Job description

**Role Description:**Let’s do this. Let’s change the world. In this vital role you will be part of the Benchtop Product Team working on computerized systems validations (CSV) and GAMP (Good Automated Manufacturing Practice). This vital role ensures Amgen systems remain compliant with industry standards and comply with all regulatory requirements.**Roles & Responsibilities:*** Advising clients on how to meet compliance requirements using a risk-based approach.* Develop validation documentation and standard operating procedures for various GxP applications.* Develop test protocols that thoroughly test business requirements.You will play a pivotal role in ensuring compliance across the Process Development and Manufacturing. The Validation Engineer will assist the Benchtop product team with all aspects of the computer validation process across the Operations footprint.Provide test execution oversight and assist with deviation recommendations as required, work with clients to develop validation plans to ensure that, at the end of the project, the system meets GxP requirements.Work with client business functions and subject matter experts to develop User Requirements Specification, Functional Requirements Specification, and/or Design Specifications as required **Basic Qualifications:**Master’s degree with 8 - 12 years of experience in validation/regulatory or related field OR Bachelor’s degree with 10 - 14 years of experience in validation/regulatory or related field ORFunctional Skills: **Must-Have Skills:** Demonstrated experience with minimum of 3 to 5 years in pharmaceutical industry, focusing on Computer Systems Validations / GAMPExperience with regulatory agencies – FDA, EMEA, CFDA, and other regulatory agenciesAbility to understand existing and new business processes and requirements to ensure proper implementation and validation of systems. Fluent knowledge of rules and regulations: GAMP 5, 21 CFR Part 11 Compliance and CFR Part 210, 211 Compliance. **Preferred Skills:** Ability to work independently, excellent problem solving and professional written communications skills. **Soft Skills:*** Excellent leadership and team management skills.* Strong transformation and change management experience.* Ability to work effectively with global, virtual teams.* Excellent analytical and troubleshooting skills.* Ability to manage multiple priorities successfully.* Strong presentation and public speaking skills.* Strong verbal and written communication skills.* High degree of initiative and self-motivation.**What you can expect of us**As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.**Apply now and make a lasting impact with the Amgen team.****careers.amgen.com**As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.Fluent in Microsoft Office suite Including (Excel, Power Point, Visio, Project), Experience with Smartsheets, Salesforce, Tableau a plusFDA Audit experience a plus & working with regulatory agenciesExperience with instrument qualifications (IQ/OQ), validation plans, regulated workflows.