Technical Writing Jobs in Puerto Rico

Specialist Quality Control with experience in the Pharmaceutical Industry Quality Control Laboratory Testing Project Management and Quality processes. Preferable experience as Microbiologist Chemist Biochemistry Molecular Sciences or Chemical Engineering.Skills:Scientific Data AnalysisStrong Technic...

Specialist Quality Control with experience in regulated industry.Skills: Scientific Data AnalysisStrong Technical Writing (English and Spanish) mainly focusesStrong knowledge of Microsoft Excel as a Tool for Data AnalysisGood Communication skillsProject ManagementKnowledge in Computer System and Met...

Scientific Data Analysis Strong Technical Writing (English and Spanish) mainly focuses Strong knowledge in Microsoft Excel as a Tool for Data Analysis Good Communication skills Project Management Knowledge in Computer System and Method Validation (Experience preferable) Strong knowledge and experie...

Scientific Data Analysis Strong Technical Writing (English and Spanish) mainly focuses Strong knowledge in Microsoft Excel as a Tool for Data Analysis Good Communication skills Project Management Knowledge in Computer System and Method Validation (Experience preferable) Strong knowledge and experie...

Preferred: Chemical Engineering background Experience in Biotech/Biopharma companies Drug Substance manufacturing support/technical support experience Statistical/Data Analysis experience Technical Writing SkillsRequirementsMasters degree OR Bachelors degree in Engineering & 2 years of Engineering...

Provide oversight for the development implementation and maintenance of quality programs systems processes and procedures to ensure compliance with internal policies regulatory requirements and industry standards.Ensure the performance and quality of services conform to establishedQuality System sta...

Develop implement administer and certify compliance policies procedures and practices to ensure alignment with corporate legal and ethical standards.Provide compliance guidance and advice to cross-functional teams ensuring adherence to internal and external regulations.Investigate complaints and ver...

Key Responsibilities:Develop review and execute commissioning and qualification protocols (IQ/OQ/PQ) for downstream processing equipment.Coordinate FAT/SAT execution and documentation with vendors and engineering teams.Perform field inspections loop checks and functional verifications during commiss...

SUMMARYUnder general supervision provides characterization of process optimization strategies and/or troubleshooting of operational issues in the operations manufacturing pilot plant or capital projects environment.Applies basic engineering principles to the design and implementation of system modif...

We are seeking a highly skilled and detail-oriented CSV Validation Specialist to lead validation activities for computerized systems related to labeling inspection and vision technologies in a regulated pharmaceutical environment. This role ensures that all systems meet compliance requirements and o...