About Company:
Lucent Biotech Ltd. found its roots in Roorkee (Haridwar) in 2006 and today stands tall and secure amongst the fastest growing pharmaceutical companies of India, under the able guidance of Mr Anil Kumar Bansal, supported and assisted by his two sons, Mr Anirag Bansal & Mr Anmol Bansal. We are a Pharmaceutical company, involved with the preparation of a full spectrum of pharmaceutical formulations, and currently, proud suppliers with a long list of reputed multinational pharmaceutical companies across the globe. Lucent Biotech Ltd. has become a trustworthy name in the Indian Pharma Industry owing to its state-of-the-art infrastructure, standardised practices, quality assurance and, most importantly, a motivated & dedicated workforce. The manufacturing facility is designed by the procedure laid down in the WHO-GMP revised Schedule M, Drugs and Cosmetics Act, 1940, and the company holds GMP & GLP certificates. Our team adheres to the highest standards to prepare world-class formulations across various segments. As a Pharmaceutical manufacturer’s, we have high capacity in all sections to meet the market requirements. The company is dedicated to providing not only quality drugs through a dedicated team and sophisticated equipment but also focus on timely deliveries. Through hard work & perseverance, the organisation has earned the unwavering trust of its clients. Lucent Biotech Ltd. is at the forefront of the fast-growing Pharmaceutical company in India. Since long, large pharmaceutical companies depend on outsourcing of Pharmaceutical products for cost-effectiveness, enhanced production capacity, timely supply, professional expertise or any specific needs. Our clients, the medical fraternity as well as the consumers, have well accepted our products because of consistent quality, cost effectiveness, timely delivery and accessibility.
Website
http://lucentbiotech.com
Vacancy Details:
Job Description:
We are looking for QA Head/QA Manager at ROORKEE.
1.To ensure timely and effective communication with senior management.
2.Investigate the data integrity issues identified along with investigation team, ensuring adequate impact assessment and implement necessary CAPA.
3.Recruitment, retention, supervision, and motivation of personnel.
4.Handling of QMS System and Audit compliance Well competent in handling all critical Quality assurance & Quality control Incidence, Deviation OOS, OOT, change request, GAP Analysis.
5.Co-ordinate in Internal and External Quality Systems Audits and the CAPA implementation.
6.Skilled in coordinating with Internal, External audit and Regulatory authority.
7.Skilled in enhancing organizational competencies by imparting training and developing Quality awareness among manufacturing personnel on global practices.
Leadership Quality:
1.Strong leadership skills including motivation, organization, and constructive mentoring.
2.Strategic planning experience, including resource allocation and personnel management.
3.Strong analytical abilities and strategic planning skills to develop effective QC procedures and efficient solutions to address QC issues, improve operational efficiency, and reduce overall project costs.
4.Excellent communication skills to collaborate with internal managers, QC team members, as well as maintain strong and loyal cross department relationships.
5.Strong ability to work with people with varied background and technical know and ability.
6.Remediation Developed and approved a Remediation Attention Plan outlining strategy, priorities and responses to the consultant observations and recommendations.
7.Provide compliance on the consultant & findings.
8.Worked to improve the quality of investigation and to enhance the knowledge level of investigation.
Contact Mobile: +91-9651117933
Email: -hr.chandini@lucentbiotech.co