Job Openings CQV Engineer

About the job CQV Engineer

Job Title: CQV Engineer

Job Location: Bengaluru, Karnataka, India

Job Location Type: Hybrid

Job Contract Type: Full-time

Job Seniority Level:

Overview

We are hiring for a number of CQV roles across the [XXX] area. We have both short and long term contracts and all are with biotech client project (site based). Some roles may introduce a shift scenario - that will all be an option discussed when you apply.

We are looking for Intermediate to Senior Engineers who will bring their expertise with them and drive our projects to completion. All roles are with Biotech clients.

Ideally candidates should have an emphasis on CIP/downstream CQV execution experience, a GMP/GDP background and a degree in a science and or Engineering based discipline.

Responsibilities

  • Performs work in compliance with PM Group’s Service Delivery Platforms and Quality Management System
  • Inputs into Departmental Improvements, as appropriate Plans activities thoroughly for self
  • Demonstrates effective verbal and written communication Skills
  • Demonstrates an understanding of commercial aspects (hours and capital cost) of their work
  • Interacts and communicates with own department, other departments, project team members, clients and other

external parties to ensure co-ordination of activities

  • Delivers scope of work within budgeted hours
  • Liaises with clients as appropriate, to ensure CQV requirements are addressed
  • Keeps abreast of current technology, regulatory and industry standards
  • Represents PM Group positively when interacting with external parties
  • Has the ability to come up with a variety of approaches to

problem solving and learn

  • Takes proactive steps to improve technical knowledge
  • Demonstrates a willingness to implement innovation and Knowledge Management principles and practices
  • Identifies own professional limitations and seeks out ways to strengthen them
  • Uses initiative in problem solving and can make decisions independently
  • Completes necessary professional Institute reports
  • Demonstrates knowledge of PM Group and / industry standard methodologies and tools for CQV and GMP
  • Prepares technical documents in accordance with agreed schedules and report progress in a timely fashion to avoid any undue delays
  • Aware of and identifies changes to project scope
  • Liaises with senior colleagues and mentors as appropriate

Qualifications

  • Minimum of 2 years’ experience
  • Computer literate with good experience of MS Word and

Excel

  • Relevant experience (e.g. summer work etc.) in related

Industry

Why PM Group?

As an employee-owned company, we are inclusive, committed and driven. Corporate Responsibility and Sustainability are the heart of our new 2025 business strategy. Click here to read more in our Corporate Responsibility and Heath, Safety & Wellbeing Report 2022.



Inclusion and Diversity are core to our culture and values. Wherever we work, we commit to a culture of mutual respect and belonging by building a truly inclusive workplace rich in diverse people, talents and ideas. Valuing the contributions of all our people and respecting individual differences will sustain our growth into the future.



PM Group is committed to ensuring our hiring process is fair and accessible to all and will provide candidates with disabilities with reasonable accommodations required to participate in the recruitment process. If you require any assistance in this regard, please let us know.


Lifelancer ( https://lifelancer.com ) is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains.

For more details and to find similar roles, please check out the below Lifelancer link.

https://lifelancer.com/jobs/view/b267b6bb03ffcd8abc5b2784f2c27d7f