Pharma QA Specialist

**Responsibilities**: - Coordinate with suppliers and verify supplier quality standards are in accordance to the requirements - Track and qualify or disqualify suppliers according to standards - Liaise with suppliers or support the senior supplier qual specialist to support documentation compilation and GMP/GDP review per procedural requirements - Monitor...

**Responsibilities**: - Main responsibilities include overseeing batch record review and incoming material quality audit. - Provide quality oversight of GMP manufacturing and manufacturing support, including technical operations, engineering, QC laboratory and supply chain activities. - Review completed incoming material inspection packages, Batch Records,...

Quality Operations Specialists must assist site management to oversight the quality system execution on the manufacturing and production areas at all times. The personnel are required to observe, document, discuss, and report quality adverse events related to the manufacturing of the product and are responsible to ensure highest quality and compliance of...

Quality System Regulatory Compliance Specialist (Pharma MNC/ West)Focus: Ensures site compliance with GMP and regulatory requirements by managing quality systems, supporting audits and inspections, and driving continuous improvement in training, CAPAs, and performance metrics. Working hours: 5 days a week (Mon-Fri), 9am - 6pm Assignment: 6-months contractual...

**Responsibilities**: - Process all Change Plan/Requests for creation or changing of site documents through the company Document Management System following applicable policies, process, and procedures - Perform proofreading of documents and approve submitted to the Documentation Area for further processing in company Document Management System - Notify...

**Responsibilities: - Main responsibilities include overseeing batch record review and incoming material quality audit. - Provide quality oversight of GMP manufacturing and manufacturing support, including technical operations, engineering, QC laboratory and supply chain activities. - Review completed incoming material inspection packages, Batch Records,...

Change Control Specialist (Pharma / Biotech)Location: Islandwide Type: Contract Level: Executive Experience: 2 years Industries: Healthcare / Pharmaceutical, Manufacturing Salary: $4,500 to $6,800 Monthly Posted 21 Oct 2025; Closed on 20 Nov 2025Test Case Generation Quality System GMP Computer System Validation Attention to Detail Change Control Team Player...

Regional Application Specialist – Pharma Quality Control (ASPAC)Regional Application Specialist – Pharma Quality Control (ASPAC) is at the forefront of delivering pharmaceutical accounts a premium support and consultancy. You will be responsible for providing technical support to direct and indirect bioMérieux customers and bioMérieux subsidiaries,...

Our client is a global leader in the pharmaceutical industry, dedicated to improving health and well-being through innovative medicines and healthcare solutions. They seek a Regional QA Specialist to lead regional internal and external audits for their external/contract manufacturers and suppliers, ensuring compliance with regulatory standards and upholding...

**Responsibilities**: - POC and coordinator for data integrity projects, ensure company’s quality requirements and agencies’ requirements are met. - Quality oversight for automation qualifications (Delta V and BAS) and GMP equipment qualifications - Review and approve of qualifications - related documentations (protocols and reports) - Ensure that the...