Drug Delivery Device Compliance Manager Msat

Year    KA, IN, India

Job Description

Site Name:

Bengaluru Luxor North Tower

Posted Date:

Jul 15 2025

Basic Qualifications:



Agile and distributed decision-making - using evidence and applying judgement to balance pace, rigour and risk

Managing individual and team performance.

Committed to delivering high quality results, overcoming challenges, focusing on what matters, execution.

Implementing change initiatives and leading change.

Sustaining energy and well-being, building resilience in teams.

Continuously looking for opportunities to learn, build skills and share learning both internally and externally.

Developing people and building a talent pipeline.

Translating strategy into action - a compelling narrative, motivating others, setting objectives and delegation.

Building strong relationships and collaboration, managing trusted stakeholder relationships internally and externally.

Budgeting and forecasting, commercial and financial acumen.

Bachelor's degree or above in engineering, manufacturing technology, pharmaceutical science or equivalent field.

Experience with at least

10-16 years

in drug/device combination (DDC) product and/or medical device development, pharmaceutical development, biotechnology, manufacturing, and/or quality (open to experience in pharmaceutical development experience, or other regulated industry, as an alternative). A minimum of

3-5 years

working in the field of DDC and/or medical device development, DDC and/or medical device manufacturing, and/or lifecycle management of DDCs and/or medical devices is also required.

Technical knowledge and familiarity with product development processes, specifically the evaluation of DDCs and/or medical devices and/or manufacturing processes.

Knowledge of sterile drug product primary pack & devices, qualification process.

Experience with Design History File (DHF) assembly, maintenance, and/or remediation

Strong project management, organizational, and time management skills. Proven ability to manage time effectively, prioritize tasks appropriately, and proactively communicate priorities and efforts with team members and supervisor.

Experience managing documents, databases, and using tracking tools.

Knowledge and understanding of Good Manufacturing Practice (GMP), Pharmacopeia and regulatory standards including EU MDR 2017/745, 21 CFR part 4, 820, 210/211, ISO 13485, ISO 14971, and/or IEC 60601.

Experience supporting regulatory audits.

Design control and risk management experience.

Flexibility to face rapidly changing requirements and reprioritize based on stakeholder input.

Ability to work in a matrix international organization.

Written and oral fluency in English, with strong verbal and written communication skills.

Competence with full MS Office Suite (Word, Excel, Outlook, PowerPoint).


Preferred Qualifications:


Manufacturing Science and Technology (MSAT) is responsible for ensuring that products are produced safely, efficiently, and to the highest quality standards. The GSK MSAT team plays a vital role in ensuring that manufacturing processes are efficient, reliable, and compliant with regulatory standards, ultimately contributing to the successful production of high-quality pharmaceutical and biopharmaceutical products



Why GSK?

Our values and expectations are at the heart of everything we do and form an important part of our culture.

These include Patient focus, Transparency, Respect, Integrity along with Courage, Accountability, Development, and Teamwork. As GSK focuses on our values and expectations and a culture of innovation, performance, and trust, the successful candidate will demonstrate the following capabilities:

Why GSK?



Uniting science, technology and talent to get ahead of disease together.



GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).


Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves - feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.





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Job Detail

  • Job Id
    JD3876195
  • Industry
    Not mentioned
  • Total Positions
    1
  • Job Type:
    Full Time
  • Salary:
    Not mentioned
  • Employment Status
    Permanent
  • Job Location
    KA, IN, India
  • Education
    Not mentioned
  • Experience
    Year