PR · On-site
Fluent in Spanish and English (spoken and written). * Proficiency in Microsoft Office 365 (Teams ... Experience working in pharmaceutical manufacturing environments under cGMP and FDA regulations.
Quick apply
PR · On-site
Fluent in Spanish and English (spoken and written). * Proficiency in Microsoft Office 365 (Teams ... Experience working in pharmaceutical manufacturing environments under cGMP and FDA regulations.
Quick apply
PR · On-site
Fluent in Spanish and English (spoken and written). * Proficiency in Microsoft Office 365 (Teams ... Experience working in pharmaceutical manufacturing environments under cGMP and FDA regulations.
PR · On-site
Fluent in Spanish and English (spoken and written). * Proficiency in Microsoft Office 365 (Teams ... Experience working in pharmaceutical manufacturing environments under cGMP and FDA regulations.
Quick apply
PR · On-site
Fluent in Spanish and English (spoken and written). * Proficiency in Microsoft Office 365 (Teams ... Experience working in pharmaceutical manufacturing environments under cGMP and FDA regulations.
PR · On-site
Fluent in Spanish and English (spoken and written). * Proficiency in Microsoft Office 365 (Teams ... Experience working in pharmaceutical manufacturing environments under cGMP and FDA regulations.
Quick apply
PR · On-site
Fluent in Spanish and English (spoken and written). * Proficiency in Microsoft Office 365 (Teams ... Experience working in pharmaceutical manufacturing environments under cGMP and FDA regulations.
San Juan, PR · On-site
$110 - $140/hr
Medical
A valid License and Registration of a Pharmacist & Association of Pharmacists of Puerto Rico is ... Spanish - Advanced (comprehensive, writing and verbal) English - Advanced (comprehensive, writing ...
San Juan, PR · On-site
$110 - $140/hr
Medical
A valid License and Registration of a Pharmacist & Association of Pharmacists of Puerto Rico is ... Spanish - Advanced (comprehensive, writing and verbal) English - Advanced (comprehensive, writing ...
PR · On-site
Fluent in Spanish and English (spoken and written). * Proficiency in Microsoft Office 365 (Teams ... Experience Requirements: * 3+ years C&Q experience in the Pharmaceutical Industry. * In-depth ...
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PR · On-site
Fluent in Spanish and English (spoken and written). * Proficiency in Microsoft Office 365 (Teams ... Experience Requirements: * 3+ years C&Q experience in the Pharmaceutical Industry. * In-depth ...
PR · On-site
Fluent in Spanish and English (spoken and written). * Proficiency in Microsoft Office 365 (Teams ... Experience Requirements: * 3+ years C&Q experience in the Pharmaceutical Industry. * In-depth ...
Quick apply
PR · On-site
Fluent in Spanish and English (spoken and written). * Proficiency in Microsoft Office 365 (Teams ... Experience Requirements: * 3+ years C&Q experience in the Pharmaceutical Industry. * In-depth ...
PR · On-site
Fluent in Spanish and English (spoken and written). * Proficiency in Microsoft Office 365 (Teams ... Experience Requirements: * 3+ years C&Q experience in the Pharmaceutical Industry. * In-depth ...
Quick apply
PR · On-site
Fluent in Spanish and English (spoken and written). * Proficiency in Microsoft Office 365 (Teams ... Experience Requirements: * 3+ years C&Q experience in the Pharmaceutical Industry. * In-depth ...
PR · On-site
Fluent in Spanish and English (spoken and written). * Proficiency in Microsoft Office 365 (Teams ... Experience Requirements: * 3+ years C&Q experience in the Pharmaceutical Industry. * In-depth ...
Quick apply
PR · On-site
Fluent in Spanish and English (spoken and written). * Proficiency in Microsoft Office 365 (Teams ... Experience Requirements: * 3+ years C&Q experience in the Pharmaceutical Industry. * In-depth ...
Guaynabo, PR · On-site
$82.66 - $123.98/hr
Fluent in Spanish and English (spoken and written). * Proficiency in Microsoft Office 365 (Teams ... Experience Requirements * 3+ years C&Q experience in the Pharmaceutical Industry. * In-depth ...
Guaynabo, PR · On-site
$82.66 - $123.98/hr
Fluent in Spanish and English (spoken and written). * Proficiency in Microsoft Office 365 (Teams ... Experience Requirements * 3+ years C&Q experience in the Pharmaceutical Industry. * In-depth ...
... pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in ... Excellent technical writing skills (English/Spanish) 7. Strong leadership skills, time management ...
... pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in ... Excellent technical writing skills (English/Spanish) 7. Strong leadership skills, time management ...
PR · On-site
On Site - Pharmaceutical Manufacturing Site, Puerto Rico (Juncos/ Gurabo/ Las Piedras) We are ... Bilingual (Spanish and English) - written and spoken. * Intermediate to advanced proficiency in ...
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PR · On-site
On Site - Pharmaceutical Manufacturing Site, Puerto Rico (Juncos/ Gurabo/ Las Piedras) We are ... Bilingual (Spanish and English) - written and spoken. * Intermediate to advanced proficiency in ...
PR · On-site
On Site - Pharmaceutical Manufacturing Site, Puerto Rico (Juncos/ Gurabo/ Las Piedras) We are ... Bilingual (Spanish and English) - written and spoken. * Intermediate to advanced proficiency in ...
Quick apply
PR · On-site
On Site - Pharmaceutical Manufacturing Site, Puerto Rico (Juncos/ Gurabo/ Las Piedras) We are ... Bilingual (Spanish and English) - written and spoken. * Intermediate to advanced proficiency in ...
PR · On-site
On Site - Pharmaceutical Manufacturing Site, Puerto Rico (Juncos/ Gurabo/ Las Piedras) We are ... Bilingual (Spanish and English) - written and spoken. * Intermediate to advanced proficiency in ...
Quick apply
PR · On-site
On Site - Pharmaceutical Manufacturing Site, Puerto Rico (Juncos/ Gurabo/ Las Piedras) We are ... Bilingual (Spanish and English) - written and spoken. * Intermediate to advanced proficiency in ...
PR · On-site
Spanish and English * Type of industry: Pharmaceutical * Expected hiring date: August 2026 * Project term: 6-12 months with potential extensions * Amount of openings: 4 * Administrative shift, wiling ...
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PR · On-site
Spanish and English * Type of industry: Pharmaceutical * Expected hiring date: August 2026 * Project term: 6-12 months with potential extensions * Amount of openings: 4 * Administrative shift, wiling ...
San Juan, PR · On-site
... a pharmaceutical manufacturing facility. This role is responsible for managing safety, cost ... Spanish strongly preferred. Desired Skills: * Strong leadership, communication, and stakeholder ...
San Juan, PR · On-site
... a pharmaceutical manufacturing facility. This role is responsible for managing safety, cost ... Spanish strongly preferred. Desired Skills: * Strong leadership, communication, and stakeholder ...
Juncos, PR · On-site
Resources considered for this RFP will support pharmaceutical manufacturing operations and must ... Bilingual proficiency in English and Spanish. Mentor Technical Group es un empleador que ofrece ...
Juncos, PR · On-site
Resources considered for this RFP will support pharmaceutical manufacturing operations and must ... Bilingual proficiency in English and Spanish. Mentor Technical Group es un empleador que ofrece ...
Resources considered for this RFP will support pharmaceutical manufacturing operations and must ... Bilingual proficiency in English and Spanish. Mentor Technical Group es un empleador que ofrece ...
Resources considered for this RFP will support pharmaceutical manufacturing operations and must ... Bilingual proficiency in English and Spanish. Mentor Technical Group es un empleador que ofrece ...
PR · On-site
Bilingual: English and Spanish (written and spoken). * Previous experience supporting pharmaceutical shutdown projects. * OSHA, EHS, or safety-related training/certifications are a plus.
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PR · On-site
Bilingual: English and Spanish (written and spoken). * Previous experience supporting pharmaceutical shutdown projects. * OSHA, EHS, or safety-related training/certifications are a plus.
PR · On-site
Bilingual: English and Spanish (written and spoken). * Previous experience supporting pharmaceutical shutdown projects. * OSHA, EHS, or safety-related training/certifications are a plus.
Quick apply
PR · On-site
Bilingual: English and Spanish (written and spoken). * Previous experience supporting pharmaceutical shutdown projects. * OSHA, EHS, or safety-related training/certifications are a plus.
Spanish strongly preferred. Desired Skills: * Strong leadership, communication, and stakeholder management skills. * Experience serving as an Owner's Representative on pharmaceutical capital projects.
Spanish strongly preferred. Desired Skills: * Strong leadership, communication, and stakeholder management skills. * Experience serving as an Owner's Representative on pharmaceutical capital projects.
| Aspect | Spanish Pharmacist | Italian Pharmacist |
|---|---|---|
| Required Credentials | Licencia de Farmacéutico, degree in Pharmacy, national licensing exam | Laurea in Farmacia, state registration, professional license |
| Work Environment | Community pharmacies, hospitals, healthcare facilities in Spain | Community pharmacies, hospitals, healthcare settings in Italy |
| Employer & Industry Usage | Pharmacies, hospitals, pharmaceutical companies in Spain | Pharmacies, hospitals, pharmaceutical industry in Italy |
Spanish Pharmacists and Italian Pharmacists share similar educational requirements, work environments, and industry usage. Both roles involve dispensing medications, patient counseling, and working within healthcare settings in their respective countries. The main differences lie in specific licensing processes and local regulations, but overall, they perform comparable functions in their healthcare systems.
For Spanish Pharmacist jobs in Puerto Rico, the most frequently searched job titles are:
The top searched job categories for Spanish Pharmacist jobs in Puerto Rico are:
Cities in Puerto Rico with the most Spanish Pharmacist job openings:

Contractor
Re-posted 18 days ago
LOCATION: Barceloneta / Manatí, Puerto Rico
We are seeking a Commissioning & Qualification (C&Q) Specialist to support pharmaceutical manufacturing facilities located in the North Area of Puerto Rico (Barceloneta / Manatí). The specialist will be responsible for supporting commissioning, qualification, validation, and implementation activities for pharmaceutical equipment, utilities, systems, and manufacturing areas while ensuring compliance with regulatory requirements and company standards.
This is a contract-based opportunity for an independent professional willing to work at client site.
Main Responsibilities:
Develop and execute qualification protocols including Commissioning, Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) for pharmaceutical equipment, utilities, facilities, and manufacturing systems.
Ensure qualification and validation activities are performed in compliance with company procedures and regulatory requirements.
Manage Change Controls by initiating, reviewing, supporting execution activities, tracking associated tasks, and ensuring closure in accordance with FDA regulations, cGMP requirements, and company quality systems.
Execute installation and operational verification activities for pharmaceutical equipment and systems.
Support commissioning and startup activities across manufacturing and facility environments.
Identify and resolve technical issues encountered during qualification and validation execution.
Develop and maintain protocols, reports, test documentation, SOPs, and qualification packages ensuring complete traceability.
Ensure compliance with applicable global regulatory requirements (FDA, cGMP, ICH, and internal quality standards).
Support periodic reviews, requalification activities, and lifecycle management of systems and equipment.
Coordinate system modifications, upgrades, decommissioning activities, and troubleshooting efforts.
Collaborate with Quality, Validation, Manufacturing, Engineering, Automation, and cross-functional teams to ensure successful project execution.
General Requirements:
Fluent in Spanish and English (spoken and written).
Proficiency in Microsoft Office 365 (Teams, SharePoint, Outlook, Excel, Word, PowerPoint).
Strong documentation and technical writing skills.
Excellent attention to detail and quality mindset.
Effective communication skills and ability to interact with cross-functional teams.
Strong analytical and problem-solving capabilities.
Ability to manage multiple priorities and work in fast-paced environments.
Education Requirements:
Experience Requirements:
Minimum of 3 years of experience in Commissioning & Qualification (C&Q), Validation, Engineering Support, Manufacturing Support, or related pharmaceutical functions.
Experience working in pharmaceutical manufacturing environments under cGMP and FDA regulations.
Strong understanding of equipment qualification, facility qualification, validation lifecycle activities, and risk assessment principles.
Experience supporting investigations, deviations, CAPA, and change control processes.
Experience in qualification of equipment, utilities, facilities, cleanrooms, or manufacturing systems is preferred.
Prior experience supporting sterile manufacturing or injectable pharmaceutical operations is highly preferred.
Experience supporting project execution and cross-functional implementation activities is preferred.
Physical Requirements:
Ability to sit for extended periods.
Light physical activity may be required occasionally.
Must be able to visit field locations as needed.
Must be able to wear personal protective equipment (PPE) when required.
Ability to work in a variety of industrial and manufacturing environments