Vice President of Quality

Confidential; Haryana; Hybrid; INR 4.500.000 - 6.500.000; Vollzeit

Zusammenfassung

Confidential is seeking an experienced Senior Quality Leader to oversee sterile pharmaceutical manufacturing quality across multiple sites in India. The role focuses on QA/QC, regulatory compliance, and readiness for USFDA and European inspections.

Strong leadership of cross-functional quality teams is required. The candidate should have deep expertise in sterile manufacturing, oncology injectables, vaccines, or biologics, with a track record of global regulatory alignment and corporate quality

Qualifikationen

• Strong experience in sterile pharmaceutical manufacturing, preferably oncology injectables, vaccines or biologics.
• Proven expertise in QA/QC and regulatory compliance with hands-on exposure to USFDA and European GMP.
• Experience managing quality across multiple manufacturing sites or corporate leadership experience preferred.

Aufgaben

• Lead quality operations across multiple manufacturing sites, ensuring quality and regulatory compliance.
• Oversee QA, QC, audits, inspections, and corrective actions.
• Strengthen quality systems and readiness for USFDA and European inspections.
• Lead quality teams and drive continuous improvement across business units.

Kenntnisse

Sterile manufacturing

QA/QC expertise

USFDA GMP knowledge

Regulatory compliance

People leadership

Ausbildung

B.Pharm / M.Pharm / Biotechnology

Jobbeschreibung

Location

Can be based anywhere in Punjab, Himachal or Haryana

Reporting to: Chairman & Managing Director

Company Overview

An established pharmaceutical and biotechnology organization with business interests in medicines, vaccines, nutrition products, and in-house R&D.

Key Responsibilities

• Lead quality operations across multiple manufacturing sites, ensuring consistent quality standards and compliance with regulatory requirements.
• Oversee Quality Assurance (QA), Quality Control (QC), audits, inspections, and corrective actions across the organization.
• Strengthen quality systems and ensure readiness for USFDA and European regulatory inspections.
• Lead quality teams, resolve critical manufacturing quality issues, and drive continuous improvement across all business verticals.

Must-Have Candidate Profile

• Strong experience in sterile pharmaceutical manufacturing, preferably in oncology injectables, vaccines, or biologics.
• Proven expertise in QA, QC, and regulatory compliance, with hands‑on exposure to USFDA and European GMP requirements.
• Experience managing quality across multiple manufacturing sites or business units; Corporate / Group Quality leadership experience preferred.
• B.Pharm, M.Pharm, or Biotechnology background, with strong technical and people leadership skills.
• Senior Quality Leaders / VP Quality / Senior GM Quality ready to step into a corporate leadership role may also apply