Cadila Pharmaceutical Ltd Released Job Openings On 14-09-2021.Zydus Cadila is a fully integrated, global healthcare provider, with strengths all along the pharmaceutical value chain.
Vacancy Details:
Cadila Pharmaceutical Ltd Recruiting B.pharma,M.sc Candidates with 20 to 25 yrs of Experience for Head/VP/GM-Quality Assurance/Quality Control Position.Complete Details for the Head/VP/GM-Quality Assurance/Quality Control as follows.
Important Details :
- Location :Jammu
- No of Vacancies:Not Disclosed by Recruiter
- Details of Salary: Not Disclosed by Recruiter
- Opening date for online Application: 14/09/2021
- Mode of application :Online
- Email id:mamta.pitale@cadilapharma.co.in
Job Description/Skills Required
Overall responsible for site quality/GMP compliance and Quality management System, at Samba Unit.Managing all aspects of Quality Strategy Development, Implementation and Communicating directly with Global Regulatory Agencies on all regulatory matters.Responsible for quality system of P2P / LL operation, business development /people development and support.
Principal Tasks:-
- Quality activities at samba plant.
- Overall responsibilities of GMP/GLP/ regulatory compliance.
- To meet the regulatory 24X7 compliance.
- Training of QA/QC employee within departments.
- FDA/ Licensing related activity monitoring.
- To ensure and accurate reliable efficient and timely testing of finished products, Raw material, Packing materials, in process and process validation sample and release and reject of the same.
Responsibilities :
- To ensure the compliance of GMP/GLP related activities of products manufacturing at Samba location.
- Develop and Implement efficient and effective Quality strategies to bring products to market (Domestic & International).
- Ensure the company is in full compliance with regulatory agencies.
- Serve as the key contact for regulatory agency, notified body and customer / regulatory audits of the facilities.
- Develop and Implement efficient and effective Quality strategies to bring products to market (Domestic & International).
- Identify relevant quality standards for product development, manufacturing and defining design requirement for domestic and international markets.
- Ensure the company is in full compliance with regulatory agencies.
- To ensure CGLP compliance and ensure all SOP related to Quality system (QA/QC) prepared, reviewed and implemented properly.
- Promote the development of a facility wide understanding of the key elements related to quality system and regulatory compliance requirements.
- To ensure timely qualification of equipments, instruments, preventive maintenance, Annual maintenance and calibration of the instruments.
- Effectively lead and manage department Quality personnel.
- As a member of the senior management team, provide sound advice and guidance regarding the impact of regulatory and quality issues on overall corporate strategy and operations.
- Determining the root cause of problems that involves compliance with Regulatory/ Domestic requirements.
- Overseeing the corrective and preventive actions for the problems
- Conducting Recall
- Handling preparation and follow up for GMP Inspections.
- Keep a regulatory watch and inform the departments concerned of any regulatory changes.
- Identify ways to continuously improve quality and compliance with regulations and company standards, policies and procedures.
- Training of SOP as per the Training schedule.
- Arranging the training and troubleshooting session of the instrumentation for the instruments application engineer for related instruments.
- To train the analyst for GLP aspects in laboratory.
- Any other responsibility assigned by management.
- To provide safe environment in quality department and support EHS policy of the company.
