Search the 12 jobs at PharmaLex

The Global HR Manager will develop and oversee international HR strategies, implement HR programs and policies, and ensure compliance with employment laws. Responsibilities also include managing HR teams, advising senior leaders, recruiting international candidates, and supporting office operations in Cebu and Makati.

The Dynamics AX/365 Developer will design, develop, customize, and implement solutions on the Microsoft Dynamics AX/365 F&O platform. Responsibilities include developing code, configuring modules, managing security roles, integrating systems, and providing technical support. The role involves collaboration with stakeholders to enhance business processes and ensure compliance with security requirements.

The Quality Engineer I role involves developing and maintaining quality standards for software systems in a regulated environment. Responsibilities include conducting evaluations of software systems, ensuring compliance with documentation, collaborating with engineering teams, and implementing quality assurance tests and procedures.

The Junior Commercial Analyst supports the Senior Commercial Analyst by providing sales and marketing reporting and insights. They utilize CRM systems like Salesforce, PowerBI, and SQL-based systems to develop scalable reports and dashboards, identify performance trends, and maintain accurate data quality.

The Process Engineer I will recommend and implement modifications to equipment and processes to enhance quality and efficiency. Responsibilities include conducting statistical analysis, ensuring compatibility between product designs and manufacturing processes, and developing manufacturing processes compliant with regulations. The role also involves troubleshooting and conducting root cause analysis.

The Sr Engineer at PharmaLex will direct the characterization of optimization strategies and troubleshoot operational issues in various environments. Responsibilities include overseeing engineering techniques, developing policies, supervising a small team, and applying knowledge across engineering disciplines to complete complex assignments and projects.

This role supervises Supply Chain operations, ensuring compliance with cGMP guidelines. Responsibilities include managing personnel involved in material management, coordinating daily activities, liaising with regulatory bodies, and enhancing business systems to optimize supply chain efficiency. The position requires collaboration with internal and external stakeholders to maintain performance targets.

The Specialist QA will perform duties to support the Quality Assurance program, including reviewing and approving product MPs, managing process validation protocols, leading investigations, and conducting site audits, all while ensuring compliance with regulatory standards.

The Sr Associate EH&S will manage Environmental Health & Safety programs, ensure compliance with regulations, interface with regulatory agencies, design training programs, conduct audits, and potentially supervise support staff. Responsibilities include program design, implementation, developing procedures, and assessing long-term EH&S practices.

The Quality Engineer II develops and maintains quality standards and protocols for materials processing, collaborates with engineering and manufacturing to ensure standards are met, designs testing mechanisms, conducts quality tests, performs statistical analysis for product reliability, and ensures documentation compliance.

The Microsoft D365 Functional Consultant will set up and maintain project structures in MS Dynamics 365, manage sales and expense transactions, prepare customer invoices, and liaise with project managers to reconcile project information. They will also support the invoicing team to ensure an effective ERP system.

Seeking experienced Contamination Control Auditors with expertise in Annex 1 projects to conduct gap assessments and report writing. Candidates should possess a Bachelor's degree in Microbiology, over 10 years in pharmaceutical Quality Operations, and strong knowledge of regulatory guidelines and cGMPs. Strong technical writing and communication skills are essential.