Bryden pi - Temporary Quality Assurance Manager at The Brydens Group

Tunapuna, Tunapuna-Piarco, Trinidad and Tobago -

Full Time

Start Date

Immediate

Expiry Date

10 Jul, 26

Salary

0.0

Posted On

11 Apr, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Management Systems, ISO 9001:2015, Good Distribution Practice, Pharmaceutical Safety, Food Safety, Internal Auditing, Risk Management, Corrective Action Plans, Product Recall, Regulatory Compliance, Statistical Analysis, Pharmacovigilance, Technovigilance, Budget Management, Team Leadership, Process Improvement

Industry

Description

Bryden pi Limited is seeking to recruit a suitable candidate for the following position in the Operations Division: Temporary Quality Assurance Manager The incumbent to implement, maintain and monitor the quality management system and ensure consistent adherence to the Company’s established procedures, standards and specifications for quality, food and pharmaceutical product safety for the Company’s processes, products and services, as well as to ensure that process analysis, compliance and corrective action processes are established for continuous improvement at our various locations Some Main Responsibilities include: Implement and continuously monitor quality management standards throughout the organization in accordance with ISO 9001:2015 and EU guidelines on good distribution practice of medicinal products for human use and WHO guidelines for good distribution/storage practices for pharmaceutical products, local regulatory and customer requirements. Review statistical studies, technological advances, regulatory standards and trends to stay abreast of issues in the field of quality assurance, pharmaceutical and food safety to ensure the effectiveness of the QMS. Lead identified quality improvement initiatives, activities and projects throughout the organization, using relevant Quality methodologies. Lead Management Review with SLT, ensuring quality issues are highlighted and adequately addressed, utilizing risk management principles to ensure the QMS is maintained and continuously improved. Lead and participate in internal and external quality audits and ensure that all necessary documents and follow up actions are completed on a timely basis. Review non-conformances and corrective action plans. Evaluate root causes, conduct analysis and report product and process recurring deficiencies. Lead the product recall process and assist with the review and disposition of non-conforming products in adherence to Bpi and supplier procedures. Collaborate with management on quality assurance standards and best practices according to their departmental (Quality) KPI’s and objectives. Submit monthly and quarterly reports to the Operations Manager on quality performance of processes and systems inclusive of non-conformances, quality audits, supplier quality notifications and product complaints. Confer with Marketing and Sales Departments to define customer quality requirements, expectations and address matters related to product quality. Participate in and support all customer service improvement initiatives. Co-ordinate with Regulatory and other relevant departments for Pharmacovigilance and techno vigilance matters. Prepare budget and manage departmental expenditure. Monitor and trend performance of all temperature controlled spaces during storage and distribution of time and temperature sensitive pharmaceutical & medical products Supervise daily activities of the quality assurance system at the various sites within the organization, inclusive of customer service activities. Perform other duties that may be required to enhance the operations of the Company Qualification, Experience and Requirement: Minimum of BSc. in Business Management or related field. Professional certification in quality assurance/Lead Auditing/TQM, knowledge of ISO 9001:2015 and/or cGMP/HACCP guidelines A minimum of five (5) years’ experience in a similar capacity. Experience in a manufacturing, warehousing & distribution environment would be an asset. Experience in Quality Assurance and Auditing/ ISO Internal Auditor Training Or relevant combination of training and experience A valid Police Certificate of Good Character Key Competencies: Strong interpersonal, communication, negotiating, organizational and analytical skills Excellent knowledge in quality management standards Proactive with process improvement and efficiency Ability to prioritize work load to meet deadlines and expectations Location Macoya Department Quality - Bpi Employment Type Temporary Minimum Experience Manager/Supervisor

Responsibilities

The incumbent will implement and monitor quality management systems in accordance with ISO 9001:2015 and pharmaceutical safety guidelines. They are responsible for leading quality improvement initiatives, conducting audits, and managing corrective action plans across the organization.