FITS, LLC
Overview
For Process Validation services in the manufacturing area. 3 weeks ago Be among the first 25 applicants The Right Fit
The Technical Part: Bachelor's in Life Science or Engineering with three (3+) years of experience in Process Validation activities within the Pharmaceutical Industry. Excellent written and verbal skills in both English and Spanish. Shift: Administrative and according to business needs. Experience in: Validation protocol execution and generation for manufacturing equipment Strong knowledge of GMP & GDP compliance Documentation and execution of IQ/OQ/PQ protocols The Personality Part: Our Next Piece is someone who’s detail-driven, analytical, and passionate about quality. Being the Piece means you’re the kind of person who spots what others miss, ensures every step is documented, and keeps compliance at the heart of everything. You bring precision, patience, and purpose. Are you ready to Be The Piece? AS A PIECE OF FITS, YOU WILL:
(The day-to-day on the job) Generate technical justification to support and/or document process changes. Design and develop experimental, engineering, or process validation protocols and reports supporting the implementation of operational, process, or raw material changes. Support the execution of experimental, engineering, or process validation runs by providing technical assistance at the shop floor. Maintain up-to-date process documentation (manufacturing directions, batch records, standard operating procedures) and assure they are in compliance. Gather and analyze process data used to monitor process performance and generate product reports. About Us
WHO WE ARE:
We are a Service Provider company different from the rest. We pride ourselves in how we treat the most important piece of our company\'s puzzle: you! We integrate Engineering, Construction, Maintenance, Utilities and Specialized Technical services across the Island (and in the US as well!). Our company is flexible, family-oriented and focused on our resources\' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality talent.
We\'re FITS! Are you the next piece? Seniority level
Mid-Senior level Employment type
Full-time Job function
Sales, General Business, and Education Industries
Wireless Services, Telecommunications, and Communications Equipment Manufacturing Referrals increase your chances of interviewing at FITS, LLC by 2x Get notified about new Validation Specialist jobs in
Guayama, Puerto Rico . Job Listings
LL01-122024 Validation Specialist – Laboratory Systems (QC) Validation Specialist (Upstream Process Equipment) LL04-250822 Validation Specialist (Downstream Process Equipment) LL03-250822 LL02-122024 Validation Specialist – Process Equipment (Syringe Filling Lines) LL03 - 122024 Validation Specialist– Utilities and Facilities LL01-062025 Validation Specialist for Biotech and Aseptic Process LL03-120324 Quality Assurance Specialist LL01-100824 Validation Engineer (1-3 years of experience) MV01-112224 Quality Assurance Specialist [Night Shift] Validation Specialist (Facilities & Utilities) LL01-250822 LL01-250714 Validation Specialist for Packaging Equipment CLEANING VALIDATION ENGINEER OR SPECIALIST LL01-093024 Quality Assurance Specialist ZL01-082724 Specialist QA [Non-Standard Shift] Packaging Validation Specialist (Cognex Vision) We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr
For Process Validation services in the manufacturing area. 3 weeks ago Be among the first 25 applicants The Right Fit
The Technical Part: Bachelor's in Life Science or Engineering with three (3+) years of experience in Process Validation activities within the Pharmaceutical Industry. Excellent written and verbal skills in both English and Spanish. Shift: Administrative and according to business needs. Experience in: Validation protocol execution and generation for manufacturing equipment Strong knowledge of GMP & GDP compliance Documentation and execution of IQ/OQ/PQ protocols The Personality Part: Our Next Piece is someone who’s detail-driven, analytical, and passionate about quality. Being the Piece means you’re the kind of person who spots what others miss, ensures every step is documented, and keeps compliance at the heart of everything. You bring precision, patience, and purpose. Are you ready to Be The Piece? AS A PIECE OF FITS, YOU WILL:
(The day-to-day on the job) Generate technical justification to support and/or document process changes. Design and develop experimental, engineering, or process validation protocols and reports supporting the implementation of operational, process, or raw material changes. Support the execution of experimental, engineering, or process validation runs by providing technical assistance at the shop floor. Maintain up-to-date process documentation (manufacturing directions, batch records, standard operating procedures) and assure they are in compliance. Gather and analyze process data used to monitor process performance and generate product reports. About Us
WHO WE ARE:
We are a Service Provider company different from the rest. We pride ourselves in how we treat the most important piece of our company\'s puzzle: you! We integrate Engineering, Construction, Maintenance, Utilities and Specialized Technical services across the Island (and in the US as well!). Our company is flexible, family-oriented and focused on our resources\' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality talent.
We\'re FITS! Are you the next piece? Seniority level
Mid-Senior level Employment type
Full-time Job function
Sales, General Business, and Education Industries
Wireless Services, Telecommunications, and Communications Equipment Manufacturing Referrals increase your chances of interviewing at FITS, LLC by 2x Get notified about new Validation Specialist jobs in
Guayama, Puerto Rico . Job Listings
LL01-122024 Validation Specialist – Laboratory Systems (QC) Validation Specialist (Upstream Process Equipment) LL04-250822 Validation Specialist (Downstream Process Equipment) LL03-250822 LL02-122024 Validation Specialist – Process Equipment (Syringe Filling Lines) LL03 - 122024 Validation Specialist– Utilities and Facilities LL01-062025 Validation Specialist for Biotech and Aseptic Process LL03-120324 Quality Assurance Specialist LL01-100824 Validation Engineer (1-3 years of experience) MV01-112224 Quality Assurance Specialist [Night Shift] Validation Specialist (Facilities & Utilities) LL01-250822 LL01-250714 Validation Specialist for Packaging Equipment CLEANING VALIDATION ENGINEER OR SPECIALIST LL01-093024 Quality Assurance Specialist ZL01-082724 Specialist QA [Non-Standard Shift] Packaging Validation Specialist (Cognex Vision) We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr