Jobs in Juncos

Experience in biotechnology pharmaceutical process support especially on Drug Substance processes and GMP pharmaceutical manufacturing systems. Knowledge in SAP TrackWise electronic batch records (PAS/X) and documents management systems (Veeva).RequirementsDoctorate OR Masters 2 years of Engineeri...

Experience in biotechnology pharmaceutical process support especially on Drug Substance processes and GMP pharmaceutical manufacturing systems. Knowledge in SAP TrackWise electronic batch records (PAS/X) and documents management systems (Veeva).RequirementsDoctorate OR Masters 2 years of Manufactu...

The candidate should bring strong experience in deviation management within a GMP/GxP environment ownership of major and minor deviations and the ability to manage the full investigation lifecycle from initiation through closure.Solid hands-on experience using Veeva QMS to generate designate documen...

-Bachelors in engineering & over 4 years of Engineering experience-Mechanical Electrical or Industrial Maintenance knowledge and experience with automated and manual inspection equipment operation. Technical knowledge of inspection technologies for parenteral and glass containers Apply sophisticated...

Experience with Supplier Engagement Cross-functional leadership and/or Project ManagementRequirementsDoctorate degree OR Masters degree and 2 years of Quality experience Alternatively Bachelors degree and 4 years of Quality experience Alternatively Associates degree and 8 years of Quality experience...

We are seeking a skilled Instrumentation Technician to support production operations. This role is responsible for calibrating and maintaining a wide range of instrumentation PLC and equipment critical to ensuring manufacturing quality and compliance.Key Responsibilities:Calibrate instrumentation lo...

We are looking for motivated and detail-oriented Manufacturing Operators with a background in science or engineering who are looking to build experience in a regulated manufacturing environment (pharmaceutical/medical device).Key ResponsibilitiesOperate and monitor manufacturing equipment following...

We are seeking a highly experienced Principal Engineer to lead and provide technical expertise in Clean Utilities systems GMP investigations and deviation management/documentation. The ideal candidate will combine strong engineering fundamentals with deep knowledge of GMP regulations root cause anal...

Preferred: Experience Clean Utilities And GMP investigation Deviation DocumentationRequirementsDoctorate 2 years Engineering experience ORMasters 4 years of Engineering experience ORBachelors in Engineering 6 years of Engineering experience.Required Skills:Preferred: Experience Clean Utilities An...

Preferred: Experience Clean Utilities And GMP investigation Deviation DocumentationRequirementsDoctorate 2 years Engineering experience ORMasters 4 years of Engineering experience ORBachelors in Engineering 6 years of Engineering experience.Required Skills:Preferred: Experience with Clean Utiliti...

Software Engineering or BA Data Science/AnalyticsProficiency in Python R SQL Power BI Databricks or similar analytics and visualization platforms.Familiarity with enterprise data platforms data warehousing concepts data modeling and data integration solutions (e.g. EDW Databricks SAP MES or equivale...

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 Quality Management System (QMS) remediation activities within a re...

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...

Engineering Experience in Manufacturing Operations Hands-on experience in process engineering manufacturing support or production systems within a regulated environment (biotech pharmaceutical or similar).Technical Knowledge Familiarity with automation systems process equipment and continuous impr...

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...

The Laboratory Investigations Scientist is responsible for conducting documenting and supporting investigations related to deviations out-of-specification (OOS) results and non-conformances associated with the testing and manufacturing of parenteral (sterile injectable) products. This role ensures c...

Sr Engineer with experience in Manufacturing Operations Hands-on experience in process engineering manufacturing support or production systems within a regulated environment (biotech pharmaceutical or similar).Technical Knowledge Familiarity with automation systems process equipment and continuous i...

SummaryThe Senior Supplier Quality Engineer supports the Supplier and Distribution Quality organization by managing supplier quality activities ensuring compliance with quality standards and maintaining approved supplier relationships. This role is responsible for supplier qualification auditing per...

Preferred experience in Packaging Area.Knowledge in equipment characterization/validation Vision system (inspection system analysis).RequirementsDoctorate OR Masters 2 years of Engineering experience Alternatively Bachelors in Engineering 4 years of Engineering experience8hrs shift (Admin) - OT ba...

We are seeking a skilled Instrumentation Technician to support production operations. This role is responsible for calibrating and maintaining a wide range of instrumentation PLC and equipment critical to ensuring manufacturing quality and compliance.Key Responsibilities:Calibrate instrumentation lo...