QMS Specialist

Vadodara, India (hybrid role: 3 days office, 2 days home per week)

Salary: Competitive + Benefits + Bonus

If you are an agile, committed and detail-oriented Quality Specialist, with experience gained in specifically in pharmaceutical Quality Management Systems and Computerized Systems, then we want to hear from you.

Join us to help improve peoples' lives and make healthcare better for everyone!

Why Pharmanovia?

Pharmanovia is a dynamic, fast-growing international pharmaceutical company with a portfolio of over 20 brands across more than 160 markets. Our mission is to improve patient health globally through the revitalisation of niche, tried-and-trusted medicines.

Our core behaviours are:

We act decisively but we never compromise on quality.
We keep our promises and do as we say.
We value our heritage and foster an entrepreneurial spirit.
We reinvest in our future – in our products, our brands and our people.
We give back to our communities.

Since its inception in 2013, Pharmanovia has grown consistently year on year, focusing on delivering high-quality branded prescription medicines to patients, prescribers, and healthcare providers across the world. Our growth has enabled the company to reinvest in its products, brands, people, and to give back to its communities. A people business with a strong, supportive culture that encourages innovation and entrepreneurial spirit, our team comprises over 300 employees and 29 nationalities, operating from offices in the UK, Denmark, Netherlands, Switzerland, Italy, Spain, Germany, U.A.E., India, Australia and Singapore.

We are an agile, committed, and innovative global specialty pharma business and a preferred partner for innovator pharma companies, instigating a paradigm shift in the life cycle management of iconic medicines. We seek to extensively engage with clinical communities to communicate product improvements and prioritise environmental, social, and governance considerations across the business and workforce.

Pharmanovia’s therapeutic areas include Cardiovascular, Oncology, Endocrinology and Neurology.

About the role:

As our QMS Specialist, you’ll play a key role in shaping, running, and continuously improving our global Quality Management System within a dynamic, multi-entity, virtual pharmaceutical organisation. This is more than maintaining systems — it’s about driving quality excellence across all GxP activities and partnering with teams to ensure compliance is embedded into everything we do.

You’ll contribute to the design, implementation, and optimisation of quality systems, monitor critical quality processes, and provide hands-on quality support and oversight across the business. Your work will have real impact, ensuring our operations meet the highest regulatory and quality standards worldwide.

Reporting directly to the Associate Director, Internal Quality System, you’ll bring a solid understanding of QMS requirements in GMP and GDP environments, along with practical experience implementing and managing Computerised Systems (CS). As the go-to expert for CS compliance and lifecycle management, you’ll work closely with internal stakeholders and external partners, acting as a trusted advisor on quality and compliance matters.

We’re looking for someone who is organised, detail-driven, and proactive, with the confidence to communicate clearly and effectively at all levels. You’ll enjoy problem-solving, asking the right questions, and continuously building your technical expertise — thriving in an environment where quality, collaboration, and continuous improvement are at the heart of the business.

Main responsibilities & duties:

Maintain and update controlled quality documents, including SOPs, policies, and templates
Support and oversee deviation investigations and CAPA lifecycle management, ensuring timely closure and regulatory compliance
Review and oversee change control records, supporting impact assessments and coordinating stakeholder input reviews
Ensure that the GxP computerized systems meet the regulatory requirements (Annex 11) – a key deliverable of the role
Act as system administrator for TrackWise Digital EQMS software to support the effective operation of the QMS
Administrate and monitor the GxP training system, maintaining training compliance and records
Participate in internal audits and support audit readiness for external audits and regulatory inspections
Coordinate document and data archiving processes in alignment with data integrity and retention standards
Compile and analyse quality metrics for reporting in QA and Management Reviews
Assist with cross-functional quality risk assessments
Contribute to continuous improvement initiatives and support harmonisation efforts across affiliates
Liaise with cross-functional teams (Regulatory, PV, Supply Chain, Medical Affairs) to support QMS compliance
Maintain awareness of relevant GxP requirements (e.g., EU GMP, GDP, ICH, MHRA, Swissmedic) and emerging regulatory expectations
Coordinate and maintain oversight of Product Quality Complaint investigations
Other QA related activities as required to support the department or business

About you:

We’re looking for candidates who bring at least two years’ hands-on experience in a GxP-regulated Quality role, with a strong track record of working with QMS elements and Computerised System (CS) implementation within a pharmaceutical MAH or virtual organisation. If you enjoy working in regulated environments where quality really matters — and where your expertise can make a visible impact — this could be a great next step.

In addition, you’ll bring:

Bachelor's degree in life sciences or related degree, or equivalent relevant experience
Proven experience in Computerized System implementation
Practical experience with QMS elements: document control, deviations/CAPA, change control, training, complaints, audit support
Familiarity with EU/UK GMP, GDP, Annex 11, and ideally some exposure to Swiss or ICH frameworks
Experience in a multi-entity or virtual operating model
Exposure to TrackWise, Veeva, or other electronic QMS platforms
Experience supporting inspections (MHRA, EMA, Swissmedic, etc.)
Involvement in quality metrics and management review reporting
Strong attention to detail and organisation skills
Able to work independently and manage competing priorities remotely
Problem-solving mindset with ability to interpret regulations pragmatically
Excellent verbal and written communication
Excellent IT skills across all MS packages including Excel, Word, PowerPoint, Outlook, Teams
Team player, comfortable in a global, cross-functional environment

What we offer:

We offer a competitive salary plus bonus and rewards package including holiday, health & wellbeing program, employee recognition awards, social events, pension scheme and hybrid working.

By applying for this role, your details will be sent to Ortolan People, who are engaged to provide recruitment support in processing applications. We will endeavour to respond to all applicants within three working days. Occasionally for roles with a very high volume of applicants, this may not be possible.

Pharmanovia

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