Assignment Details
Our client, a top global Management Consulting firm, is looking to onboard an experienced and qualified Pharmaceutical Quality Consultant to join the team on a one-year contract basis to collaborate with a prominent pharmaceutical company based in Bangalore. The successful candidate will play a pivotal role in ensuring compliance with regulatory standards, driving quality improvement, and overseeing the efficient functioning of quality processes.
Roles & Responsibilities:
- Work on-site within pharmaceutical manufacturing plants, collaborating with multiple stakeholders to ensure quality standards and compliance.
- Effectively manage and lead large teams to achieve quality and operational objectives.
- Rapidly acquire and apply new concepts, including digital and analytics integration within pharmaceutical operations and quality control.
- Drive timely and successful project execution.
Note: This is a project-based role for a duration of 12 months, which requires Full-time on-site support in Bangalore, India.
Skills Required
- Bachelor's degree in a relevant field (Pharmacy, Chemistry, Life Sciences, or related).
- Possess a minimum of 5-10 years of extensive experience within the Pharmaceutical Industry, with a strong focus on Quality.
- Demonstrated expertise in CFR (Code of Federal Regulations) and GMP (Good Manufacturing Practices) compliance.
- Proven track record of driving continuous improvement in operational and quality processes.
- Experience working effectively within large project teams on pharmaceutical projects.
- Strong interpersonal and communication skills.
- Detail-oriented and capable of working in a highly regulated and compliant environment.
Additional Skills Preferred:
- Proficiency in conducting Failure Modes and Effects Analysis (FMEA) to assess and mitigate potential risks within pharmaceutical processes.
- Lean Six Sigma Certification is highly desirable, showcasing expertise in process improvement methodologies.
- Prior experience in conducting internal audits and compliance audits to maintain high-quality standards.
- Diverse experience across operations or quality processes, document management, and SOP (Standard Operating Procedure) simplification within the pharmaceutical industry.
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8 month(s)
10+ years 
Hybrid
