Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas.

Due to continuous growth currently we are looking for a Senor Consultant / SME - Watson LIMS

who can be available for full time Freelancing contract role with a Remote setup.

Responsibilities:

• Responsible for validating Laboratory Information Management Systems (LIMS), particularly Watson LIMS, including URS preparation, functional testing, IQ/OQ/PQ execution, and 21 CFR Part 11 compliance.
• Functional and Administration experience on Waston LIMS is an added advantage
• Strong understanding of GMP, GDP, GAMP, ICH, USFDA, MHRA, and other regulatory requirements.
• Familiarity with digital tools like HPALM, JIRA, Trackwise
• Sound experience in Risk Assessment and Mitigation in Pharmaceutical domain

Requirements:

• At least 5+ years of experience in Thermo Scientific Watson LIMS Validation or Administration activities.
• Excellent communication skills
• Ability to work as a team player in a consulting environment
• Able to manage direct relation with stakeholders and project team members
• Proactive approach
• Results driven oriented
• Good problem-solving skills.
• Full availability to travel domestically and abroad: up to 50-75%

Location: PAN India (Remote)

As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation. PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world.

If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you.

Apply now and take the first step towards an amazing future with us.