To Go Specialist Jobs in Puerto Rico

Must Love Dogs!!At Tribe Wellness were more than just a tribe were a movement. Rooted in courage empowerment and integrity weve pioneered solutions that transform the worlds wellness brands into revenue-generating machines. We bridge the gap between brands and revenue by turning our clients custome...

Experienced in Method Validation Method Transfer Method Qualification. Experience in project management good communication skills able to work with multi-functional Teams. Able to communicate effectively in both English and Spanish.RequirementsDoctorate OR Masters 2 years of directly related experi...

Experience of bio-processing unit operationsKnowledge in Root Cause Analysis methodologies (Fishbone Six Boxes Fishbone 5 Whys Kepner Tregoe)Familiar with Lean Manufacturing PracticesAbility to communicate and collaborate with technical and management staff within manufacturing process development a...

We are seeking a Specialist Quality Complaints. The primary responsibilities include:Supporting the product complaint system through:leading and managing product complaint investigationsperforming data analysis and trending of complaint information to detect signals proactively and take appropriate...

Experience in handling deviations/non-conformances investigations.Skills for technical writing and development of reports.Knowledge and experience with root cause analysis tools (e.g. causal factors analysis 5 Whys).Project management skills on identifying/tracking actions and achieving due datesReq...

We are seeking a Specialist Quality Complaints.The primary responsibilities include: Supporting the product complaint system through; leading and managing product complaint investigations performing data analysis and trending of complaint information to detect signals proactively and take appropriat...

Specific responsibilities include but are not limited to: Own change controls for manufacturing process changes Support major/trend deviation investigations throughout the whole lifecycle including Root Cause Analysis investigation determination of Corrective/Preventive Actions authoring process in...

We are seeking a Documentation Specialist for Digital Operations to support manufacturing documentation activities including processes supported by the Tulip platform. This role is responsible for developing reviewing and maintaining controlled documents that support compliance traceability and oper...

Knowledge in: Environmental Monitoring Microbial Identification (Micro ID) Critical Utilities (CU) monitoring Sampling monitoring: equipment and techniques Data trending and evaluation Microbiological testing methods and standards for clean rooms and controlled environments Aseptic behavior in manuf...

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 requires strong expertise in process engineering computer system vali...

Deviations documentation and Change Control Management.RequirementsDoctorate OR Masters 2 years of Manufacturing Operations experience Alternatively Bachelors 4 years of Manufacturing Operations experience Alternatively Associates 8 years of Manufacturing Operations experience Alternatively High...

Support manufacturing operations and EHS team to ensure full compliance with Environmental Health & Safety (EHS) programs.Conduct EHS training and onboarding for new hires including regulatory compliance requirements.Enforce EHS policies procedures and regulatory standards across operations.Support...

Experience in the Manufacturing area specifically writing procedures managing documents in management system (document workflow)RequirementsDoctorate degree OR Masters degree and 3 years of Manufacturing Operations experience Alternatively Bachelors degree and 5 years of Manufacturing Operations exp...

Experience in handling deviations/non-conformances investigations.Skills for technical writing and development of reports.Knowledge and experience with root cause analysis tools (e.g. causal factors analysis 5 Whys).Project management skills on identifying/tracking actions and achieving due datesReq...

Execute Quality disposition (approval or rejection) of bulk drug substances. Provide Quality oversight to ensure that operations for clinical and licensed pharmaceutical Drug Substance (API) are manufactured tested stored and managed according to current Good Manufacturing Practices (cGMP) Good Lab...

Role Description: System Administration and Linux System Administration skills preferably Red Hat Linux Familiarity with Patching in above environments Proven Veritas Cluster skills Experience in Troubleshooting and providing Technical Support Incident Problem Management Network expertise to chec...

Quality Professional with experience in Quality System and addition some knowledge or to be familiar with in PASx/MES application MAXIMO SAP LIMS QMTS and Veeva. Available during weekends and holidays as requested always available to be on site. RequirementsDoctorate OR Masters 2 years of experien...

We are seeking a C&Q Specialist to support a critical shutdown tied to a robotic arm replacement and motion control upgrades (servos/VFDs pneumatic safety interlocks) within a highly automated production system. This role will be responsible for executing and documenting Installation Qualification (...

Knowledge and experience in: Process Safety Pre-Start Up Safety Reviews Process Safety Management (PSM) High Risk Processes Hazardous/Compressed Gases Combustible Dust Risk Assessments and Machine Safeguards.RequirementsMaster degree or Bachelor degree & 2 years of directly related experience Associ...

Deviations documentation and Change Control Management.Requirements-Doctorate OR-Masters 2 years of Manufacturing Operations experience OR-Bachelors 4 years of Manufacturing Operations experience OR-Associates 8 years of Manufacturing Operations experience OR-High school/GED 10 years of Manufact...