Director / Head of India Operations

MMR Consulting; Bengaluru; Hybride; INR 4 000 000 - 7 000 000; Plein temps

Résumé du poste

MMR Consulting is seeking a leader to run MMR India, accountable for full P&L, growth, and high-quality CQV delivery for local and offshore projects. You will drive business development, staffing and ensure regulatory and GMP compliance across engagements.

Ideal candidate has 12+ years in pharma/biotech engineering, 5+ years leadership, and strong CQV/validation expertise. Hybrid work in Bengaluru/Hyderabad is preferred, with global clients and cross-region opportunities.

Qualifications

• B.Tech/BE in an engineering discipline (Chemical/Mechanical/Biotech/Instrumentation).
• 12-15+ years in pharmaceutical/biotechnology engineering with deep CQV exposure (commissioning, qualification, validation).
• 5+ years leading teams with direct hiring and performance responsibilities.
• Demonstrated command of CQV across processes, utilities, facilities and automation.
• Experience delivering to USFDA/EMA or equivalent and working with GMP/data integrity requirements.

Responsabilités

• Own P&L for MMR India including revenue, margins, utilization and cost.
• Lead business development and propose CQV engagements from India.
• Oversee CQV technical delivery and approve validation strategies, protocols and reports.
• Develop and mentor CQV engineers and client-facing consultants; build succession plans.

Connaissances

Leadership

CQV knowledge

GMP/GAMP 5 know-how

Regulatory familiarity

Proposal writing

Formation

B.Tech / BE in Chemical, Mechanical, Biotechnology, Instrumentation

12-15+ years in pharma/biotech engineering

Outils

CQV methods

Process equipment & automation knowledge

Description du poste

Location Bengaluru or Hyderabad preferred. Hybrid could be possible for the right candidate.

Reports to President, MMR Consulting

Experience 12-15+ years, including 5+ in a leadership role

Type Full time, permanent

About MMR Consulting

MMR Consulting is a life sciences engineering and CQV consultancy. We work with pharmaceutical, biotechnology and CDMO clients across North America, Europe and Asia on capital projects, from design and engineering through commissioning, qualification and validation.

Our teams support facility builds, process equipment, clean utilities, automation and regulatory readiness for clients operating under USFDA, EMA and other major agencies. Our India operation delivers into these global programs and is now positioned to grow, both as a delivery capability and as a business in its own right.

The role

MMR CONSULTING is looking for a leader to run the MMR India business, where the major responsibilities include P&L ownership, business development, technical delivery of services, and growing the team. The team will support local India projects, in addition to off-shore projects globally.

Job Description

Business and P&L

• Full P&L accountability for MMR India, covering revenue, margin, utilization and cost
• The annual operating plan and budget, and delivery against it
• Pricing and commercial structuring on engagements originating in India
• Statutory, tax and compliance obligations for the entity, working with our finance team and local advisors

Business development

• Build and convert a pipeline with pharmaceutical, biotechnology and CDMO clients in India
• Write and own CQV proposals end to end: scope, technical approach, staffing plan and price
• Represent MMR at industry forums, ISPE chapters and on client sites
• Grow existing accounts, and work with global leadership on opportunities that span regions

Technical and CQV oversight

• Act as the senior technical authority for CQV work produced in India
• Review and approve validation strategy, protocols and reports before they reach the client
• Hold the quality bar on GMP, data integrity and regulatory expectation
• Embed our methodology into new hires and raise the technical capability of the team

People and capability

• Hire, develop and retain CQV engineers and project staff
• Build the training path that takes a graduate engineer to a client-facing consultant
• Set objectives, run performance reviews and plan succession for key roles
• Build a culture that good engineers want to stay in

What you bring

Required

• E. or B.Tech in Chemical, Mechanical, Biotechnology, Instrumentation or a related engineering discipline
• 12-15+ years in pharmaceutical or biotechnology engineering, with substantial depth in commissioning, qualification and validation
• 5+ years leading teams, with direct responsibility for hiring and performance
• Demonstrable command of C&Q across process equipment, clean utilities, facilities and automation
• Working knowledge of some of these guidelines; GMP, GAMP 5, ASTM E2500, ISPE C&Q baseline guide, 21 CFR Part 11 and current data integrity expectations
• Experience delivering into, or being inspected by, USFDA, EMA or an equivalent agency
• Ability to attend occasional meetings with meaningful overlap into North American business hours

Preferred

• Consulting background. Candidates from a CQV or life sciences engineering consultancy will be prioritized
• An established network among pharmaceutical, and biotechnology manufacturers in India
• A track record of writing and winning CQV proposals

We will seriously consider strong candidates from industry, currently in-house at a pharmaceutical or biotechnology manufacturer, who can demonstrate commercial instinct and the appetite to build a business rather than run a function.

MMR Consulting is an equal opportunity employer. We consider all applicants on merit, without regard to gender, religion, caste, age, disability, marital status or any other protected characteristic.