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Manager Barceloneta Jobs (NOW HIRING)

Fastenal Company

Sales Support

Barceloneta, PR · On-site

$15 - $19.75/hr

Sales Support Road #2 km 56.7, Barceloneta, PR 00617 PR006 In Plant Store Part-time Shift(s): MON ... Duties include, but are not limited to: o Assisting with sales/customer service o Managing ...

AppleOne

Cost Estimation Manager

Barceloneta, PR · On-site

$100K/yr

Barceloneta, PR - Schedule: Monday-Friday, 7:00 AM-4:00 PM Equal Opportunity Employer / Disabled / Protected Veterans The Know Your Rights poster is available here: -06/22- 088_EEOC_KnowYourRights6 ...

Fastenal Company

Sales Support

Barceloneta, PR · On-site

$15 - $19.75/hr

Sales Support Road #2 km 56.7, Barceloneta, PR 00617 PR006 In Plant Store Full-time Shift(s): MON ... Duties include, but are not limited to: o Assisting with sales/customer service o Managing ...

American Cancer Society

Mission Manager

Mayaguez, PR

$32K/yr

Anasco, Arecibo, Aguada, Aguadilla, Barceloneta, Cabo Rojo, Camuy, Ciales, Corozal, Dorado, Hatillo ... Collaborates with the Development Manager and Event Lead to enhance patient and survivor ...

Pharma Bioserv

Be Seen First

Project Scheduler

Barceloneta, PR · On-site

Currently, we are looking for a Project Scheduler for the Pharmaceutical sector in Barceloneta ... Knowledge of resource management principles, including resource planning, allocation, and ...

Abbott

Facilities Engineer

Barceloneta, PR · On-site

This position will support the AVD business and will be based in Barceloneta, Puerto Rico. On-site ... Decisions on contracting, managing, and planning of design, construction, and maintenance services ...

American Cancer Society

Mission Manager

Arecibo, PR

$32K/yr

Anasco, Arecibo, Aguada, Aguadilla, Barceloneta, Cabo Rojo, Camuy, Ciales, Corozal, Dorado, Hatillo ... Collaborates with the Development Manager and Event Lead to enhance patient and survivor ...

Abbott Laboratories

Facilities Engineer

Barceloneta, PR · On-site

$54K - $109K/yr

This position will support the AVD business and will be based in Barceloneta, Puerto Rico. On-site ... Decisions on contracting, managing, and planning of design, construction, and maintenance services ...

AbbVie

PR

$15.75 - $19/hr

Purpose The Site Security Manager serves as the primary point of contact for all security-related issues at AbbVie's manufacturing operations in Barceloneta, Puerto Rico. This role is responsible for ...

Allergan

Manager, Talent Acquisition

Barceloneta, PR · On-site

We are currently recruiting for a Manager, Talent Acquisition (TA) , who will create and implement ... Barceloneta). What will you be responsible for: * Setting the vision, strategy and goals for all ...

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Manager Barceloneta information

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$23K

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How much do manager barceloneta jobs pay per year?

As of Sep 12, 2026, the average yearly pay for manager barceloneta in the United States is $61,351.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,000.00 and $69,000.00 per year, depending on experience, location, and employer.

What are the most commonly searched types of Barceloneta jobs?

The most popular types of Barceloneta jobs are:

Manager Barceloneta jobs near you
Infographic showing various Manager Barceloneta job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $61,351 per year, or $29.5 per hour.

C&Q Specialist | Pharmaceutical

Barceloneta, PR • On-site

LEGAL PROJECT MANAGEMENT PARTNERS LLC
See more jobs at LEGAL PROJECT MANAGEMENT PARTNERS LLCexternal

Contractor

Posted 11 days ago

Job description

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: 

  • Bachelor’s Degree in engineering, life sciences or other related fields.

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