Vacancy for M.Pharm, MSc in Quality Functions at Stallion Laboratories

Stallion Laboratories incorporated in 1988 as an integrated private sector Pharmaceutical Formulation Manufacturer, has acquired an unmatched record of managing niche product in formulations with a WHO GMP approved production facility and GLP qualified stringent quality control. The path of success lies in its belief of creativity and no negotiation with the quality of work. Stallion Laboratories Unit-ll a USFDA & UK-MHRA approved facility and proposed to be EU GMP approved plant. With its approval, Stallion aims to enter regulated markets.

Seeking a highly skilled and experienced LEADER (AVP / VP) to lead our Entire QUALITY Functions including QA, QC, 3rd Party Vendor and Audit.

Key Responsibilities
• Responsible for “All Time Readiness” for Audit and Compliance
• Must have Faced and Led minimum 15 US-FDA audit.
• Well versed experience of all GMP systems including facing audits for EU, UK and other Regulated markets. Responsible for Creating, Nurturing, Maintaining and Uplifting Quality Culture across organization.
• Proven track record for Leadership and Team Management skills.
• 100 % adherence to Quality Compliance Practices across organization.
• Proven track record for Automation, Digitalization and Quality Excellence within Quality functions.
• Proven Training and Development skills, providing Organization Level Training on Quality Aspects and updated with all Current Trends.
• Sound Regulatory and Technical Knowledge in all Technical functions with proven Scientific Rationale skills help to manage QMS systems.
• Proven track record for handling various Digitalization, Automation and QMS Software.

Qualifications
• Master's degree or higher in Chemistry, Pharmacy, or a related scientific discipline.
• Extensive experience (typically 20+ years) in a pharmaceutical QA and QC, both domain.