Spclst , Technology Compliance

Job Description

The Opportunity

• Based in Hyderabad join a global healthcare biopharma company and be part of a 130- year legacy of success backed by ethical integrity forward momentum and an inspiring mission to achieve new milestones in global healthcare.
  Be part of an organisation driven by digital technology and data-backed approaches that support a diversified portfolio of prescription medicines vaccines and animal health products.
  Drive innovation and execution excellence. Be a part of a team with passion for using data analytics and insights to drive decision-making and which creates custom software allowing us to tackle some of the worlds greatest health threats.
  Our Technology Centers focus on creating a space where teams can come together to deliver business solutions that save and improve lives. An integral part of our companys IT operating model Tech Centers are globally distributed locations where each IT division has employees to enable our digital transformation journey and drive business outcomes. These locations in addition to the other sites are essential to supporting our business and strategy.
  A focused group of leaders in each Tech Center helps to ensure we can manage and improve each location from investing in growth success and well-being of our people to making sure colleagues from each IT division feel a sense of belonging to managing critical emergencies. And together we must leverage the strength of our team to collaborate globally to optimize connections and share best practices across the Tech Centers.

Role Overview

We are seeking a mid-level specialist to lead and sustain GMP-compliant SDLC activities for the DataLynx platform and support future validation efforts for SEEQ. This role is critical to ensuring regulatory alignment and operational continuity across quarterly release cycles and long-term system lifecycle management.

What we look for:
Imagine getting up in the morning for a job as important as helping to save and improve lives around the world. Here you have that opportunity. You can put your empathy creativity digital mastery or scientific genius to work in collaboration with a diverse group of colleagues who pursue and bring hope to countless people who are battling some of the most challenging diseases of our time. Our team is constantly evolving so if you are among the intellectually curious join usand start making your impact today.

About Us

The Manufacturing Value Team is a strategic arm of the Digital Manufacturing Division focused on delivering digital solutions that drive operational excellence compliance and innovation across global manufacturing sites. We combine deep business process knowledge with cutting-edge technology to support factory automation data analytics and system lifecycle management. Our mission is to enable smarter faster and more compliant manufacturing through digital transformation.

Key Responsibilities

• Own and execute GMP SDLC deliverables for DataLynx including validation documentation testing protocols and release planning.

• Collaborate with cross-functional teams (Quality IT Product) to ensure compliance with SDLC-SOP-09 and CSA methodology.

• Support periodic validation cycles and change control processes for DataLynx and SEEQ platforms.

• Maintain system documentation and configuration profiles in alignment with GMP standards.

• Participate in workshops and stakeholder sessions to define validation scope and resource needs.

• Contribute to SOP development and lifecycle sustainment for IT system administration and validation packages

Qualifications

• Bachelors degree in Computer Science Engineering Life Sciences or related field.

• 35 years of experience in GMP validation SDLC execution or CSV/CSA methodologies.

• Familiarity with tools such as Jira Confluence and Digital SDLC platforms

• Strong understanding of regulatory frameworks (FDA EMA ICH) and risk-based validation approaches.

• Excellent documentation communication and stakeholder engagement skills.

Preferred Skills

• Experience supporting validation efforts for manufacturing intelligence platforms.

• Knowledge of SDIRA IT Supplier Management and automated compliance tools.

• Prior exposure to SOP authorship and lifecycle sustainment in a GMP environment.

Why Join Us

This is a strategic role with long-term impact on our digital manufacturing platforms. Youll be part of a high-performing team driving compliance innovation and operational excellence across global systems.

#HYDIT2025

Required Skills:

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully
Merck & Co. Inc. Rahway NJ USA also known as Merck Sharp & Dohme LLC Rahway NJ USA does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place introductions are position specific. Please no phone calls or emails.

Employee Status:

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.