Saltar para o conteúdo

Todas as vagas

GBS Pharma Quality Assurance Officer

SGS · On site, Muntinlupa, PH

Publicada em 9 de nov. de 2026

Candidatar-se a esta vaga com o Jobrona

Crie a sua conta e carregue o CV. Se esta vaga lhe servir, preparamos e enviamos primeiro esta candidatura e mostramos o que foi enviado.

Sobre a vaga

SGS is the world's leading inspection, verification, testing and certification company. SGS is recognized as the global benchmark for quality and integrity. With more than 94,000 employees, SGS operates a network of over 2,600 offices and laboratories around the world. PRIMARY RESPONSIBILITIES - Review and approve Change Control Request and ensure their timely closure by coordinating with owners. - Act as site representative for Trainings and Document Control systems and manage related activities. - Maintain client test methods, specification databases, and coordinate Quality Agreement approvals internally, externally, and with Legal. - Coordinate and support internal, client, and regulatory audits, and prepare responses to audit findings. - Act as backup for QA functions, including release of Certificates of Analysis, vendor evaluations, and other QA management responsibilities. - Follows Training SOP for training and training records. REPORTING LINE Operational direct reporting to Affiliate lab manager or supervisor; administrative accountability to GBS Supervisor. SPECIFIC RESPONSIBILITIES - Review and approve CCRs and coordinate for their timely closure by periodic follow up with associated CR owners. - Be site representative for Trainings and Document control systems and manage all the activities for these programs. - Responsible for keeping track of upcoming periodic reviews of documents and ensure their timely completion. - Set up all the documents in DMS and coordinate for their approvals. - Responsible for keeping track of trainings assigned to all site employees and ensure their timely completion by periodic follow ups. - Evaluate all re-training requirements for the SOPs. - Maintain and update client test methods and specification data bases. - Coordinate approvals of Quality Agreements internally, externally and with SGS legal team. - Follow up with clients for timely approvals of quality agreements. - Coordinate internally for customer and regulatory audits. - Prepare client responses to audit findings, as assigned. - Be backup for QA Associate and release the certificate of analysis. - Work as a backup in some designated areas in the absence of QA management. - As active back up, maintain vendor evaluation program by timely performing the evaluations and follow ups with the vendors. - Review method/specifications assessment form, if provided. - Be part of internal audit team when required and follow up on related corrective actions. - Work on special projects as assigned by the Management. - Ensures the tasks assigned are accomplished in due time. In case of foreseeable delay, the GBS Team Coordinator (or section Lab Manager in their absence) is notified immediately. - Adopts and supports specific operational improvement activities, as communicated by the GBS Supervisor, with focus on the improvement of quality and efficiency. - Performs other related duties as may be assigned either in support of departmental goals or for his/her personal or professional training, education or development as programmed by his/her immediate superior. - At all times, comply with SGS Code of Integrity and Professional Conduct and with all SGS QHSE - For working set up: 3 months onsite, transitioning to a hybrid setup thereafter. PROFILE - Bachelor’s degree related to scientific area is required. - Minimum 3 years working experience in Quality Assurance in Pharma industry is required. - Demonstrated understanding of relevant GMP (Good Manufacturing Practice) regulations is required. Knowledge in compendiums such as USP is preferred. - Proficiency in Microsoft Office applications, including Outlook, Word, and Excel. Ability to learn quickly new technologies. - Excellent written and strong verbal communication skills in English (C1) - Protocol and report writing compliant with regulatory standards. REQUIRED SKILLS - Strong written and verbal communication skills in English (B2+). - Proven ability to manage and coordinate multiple tasks in a fast-paced, professional environment. - Proven time management skills and proficient in effectively prioritizing tasks to meet deadlines set by Supervisors. - Detail-oriented with the ability to identify minor discrepancies.