Interview Data Loading …Urgently Looking for Manager Quality Assurance : Ours is an ISO 45001: 2018, ISO: 14001:2015, ISO 9001-2015 certified leading pharma intermediate and specialty chemical manufacturing company located at Nandesari, Vadodara, serving large Indian and MNC since last 50 years. Candidate must be M.sc with Organic Chemistry and minimum 8-10 years of experience in Quality Assurance with handsome exposure in handing customers audits, IMS audits and documentations, GMP.
Key Responsibilities: [ads id="ads1"] Planning & Co-ordinate Internal/External/Customers audits, To attend External/customer auditsReviewing Internal/External/Customer audits non-conformity reports and ensuring corrective actions are effectively implemented.Select and co-ordinate with the external certification agency.Improvements plans, and other related matters to the Director/Partners office. Overall Responsible for monitoring IMS performance, Operational control. Awareness and implementation of IMS organization’s objectives.[ads id="ads1"] Awareness and implementation of GMP, GLP GDPResponsible for implementation of Integrated Management Systems (Quality, Environmental and Health & Safety) at Sodium Metal Pvt.ltd.Coordinating the management review meetings as per the decided frequency (IMS).Handling customer complaints with root cause and corrective actions.Approving all Specifications, Test methods, and Batch Process and Control Records (BMRs).Approving validation and qualifications protocols and reports.Approving and closing of system documents. Approving stability studies.Approving changes that affect the quality of intermediates.Approving all procedures affecting the quality of products.[ads id="ads1"] To conduct the General Good Manufacturing Practices (GMP) trainings.Approving completed Batch Manufacturing Record (BMR) and Analytical Records for critical process steps before batch release of the finished product for sale.Review and approving closure of deviations.To resolve and close quality related customer complaints properly.Review and approval of Conducting Self-Inspections and closing of it observations.Vendor Qualification and Vendor Audits.Reviewing and approving Annual Product Quality Reviews.[ads id="ads1"] Approving of system proceduresApproving updating different procedures To ensure total quality of dispatch materialArrange training to concerns persons for different quality related subjects To fill customer questionnaire and preparation of customer require documentsTo prepare quality agreement for vendor and customer
Salary is not constrained for right candidate. Interested candidates share cv on hr@smfinechem.in
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Interview Data Loading …
Urgently Looking for Manager Quality Assurance :
Ours is an ISO 45001: 2018, ISO: 14001:2015, ISO 9001-2015 certified leading pharma intermediate and specialty chemical manufacturing company located at Nandesari, Vadodara, serving large Indian and MNC since last 50 years.
Candidate must be M.sc with Organic Chemistry and minimum 8-10 years of experience in Quality Assurance with handsome exposure in handing customers audits, IMS audits and documentations, GMP.
Key Responsibilities:
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Planning & Co-ordinate Internal/External/Customers audits, To attend External/customer audits
Reviewing Internal/External/Customer audits non-conformity reports and ensuring corrective actions are effectively implemented.
Select and co-ordinate with the external certification agency.
Improvements plans, and other related matters to the Director/Partners office.
Overall Responsible for monitoring IMS performance, Operational control.
Awareness and implementation of IMS organization’s objectives.
[ads id="ads1"]
Awareness and implementation of GMP, GLP GDP
Responsible for implementation of Integrated Management Systems (Quality, Environmental and Health & Safety) at Sodium Metal Pvt.ltd.
Coordinating the management review meetings as per the decided frequency (IMS).
Handling customer complaints with root cause and corrective actions.
Approving all Specifications, Test methods, and Batch Process and Control Records (BMRs).
Approving validation and qualifications protocols and reports.
Approving and closing of system documents.
Approving stability studies.
Approving changes that affect the quality of intermediates.
Approving all procedures affecting the quality of products.
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To conduct the General Good Manufacturing Practices (GMP) trainings.
Approving completed Batch Manufacturing Record (BMR) and Analytical Records for critical process steps before batch release of the finished product for sale.
Review and approving closure of deviations.
To resolve and close quality related customer complaints properly.
Review and approval of Conducting Self-Inspections and closing of it observations.
Vendor Qualification and Vendor Audits.
Reviewing and approving Annual Product Quality Reviews.
[ads id="ads1"]
Approving of system procedures
Approving updating different procedures
To ensure total quality of dispatch material
Arrange training to concerns persons for different quality related subjects
To fill customer questionnaire and preparation of customer require documents
To prepare quality agreement for vendor and customer
Salary is not constrained for right candidate.
Interested candidates share cv on hr@smfinechem.in
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