Industrial Engineer with experience in regulated industry to lead lean manufacturing initiatives focused on waste elimination across the site, including but not limited to: Value stream mapping, change-over optimization (SMED) and Time stu...
he EHS Manager is responsible for developing, implementing, maintaining, and continuously improving site Environmental, Health, and Safety programs in support of regulatory compliance, operational excellence, and a strong safety culture. Th...
Specialist Quality Control with experience in: Method Validation Method Transfer Method Qualification Project Managemen Requisitos: Doctorate or Masters + 2 years of directly related experience or Bachelors + 4 years of directly relat...
CSV Specialist to support the installation of several manufacturing solid dosage equipment such as but not limited to: Encapsulator Checkweigher Compression machine Hardness tester Encapsulation machine Auxiliary equipment Main acti...
We are searching for an Sr. Engineer with the ability to fulfill the following responsibilities: Familiar with distribution testing per ASTM D****, International Organization for Standardization (ISO), Technical Association of the Pulp an...
We are seeking a technical resource to support Sterile Manufacturing Operations, with a focus on inspection engineering activities and parenteral inspection technologies, supporting ongoing operations, product transfers, and continuous impr...
We are seeking a Sr. Engineer with experience in C&Q process, Validation, and Packaging equipment. Requisitos: Bilingual (English & Spanish) Experience in C&Q process, Validation and Packaging equipment. Education preferred in engineerin...
The CAPA / Complaints Technical Writer is responsible for authoring, reviewing, and maintaining high-quality documentation associated with Corrective and Preventive Actions (CAPA), customer complaints, investigations, non conformances, and ...
Lugar:
Cayey, PR | 12/06/2026 17:06:42 PM | Salario: S/. No Especificado | Empresa:
QRC GroupQA Specialist / Deviation Investigator to lead investigations of deviations, non conformances, and quality events within a regulated manufacturing environment. Key Responsibilities: Lead end-to-end investigations for deviations and qualit...
The Process Engineer is responsible for ensuring the reliability, compliance, and performance of manufacturing processes, equipment, utilities, and computerized systems within a pharmaceutical or biotechnological environment. This role requ...