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C Developer Jobs in Puerto Rico (NOW HIRING)

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Partner with QC, validation, IT, and engineering teams to ensure seamless implementation. General ... Experience Requirements: * 3+ years C&Q experience in the Pharmaceutical Industry. * In-depth ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Partner with QC, validation, IT, and engineering teams to ensure seamless implementation. General ... Experience Requirements: * 3+ years C&Q experience in the Pharmaceutical Industry. * In-depth ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Partner with QC, validation, IT, and engineering teams to ensure seamless implementation. General ... Experience Requirements: * 3+ years C&Q experience in the Pharmaceutical Industry. * In-depth ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Partner with QC, validation, IT, and engineering teams to ensure seamless implementation. General ... Experience Requirements: * 3+ years C&Q experience in the Pharmaceutical Industry. * In-depth ...

Pharmpix

PR · On-site

POSITION SUMMARY The Software Developer reports to the Software Engineering Manager and is ... Maintain, enhance, and optimize complex backend systems built primarily in C++. * Design, develop ...

Validation & Engineering Group, Inc

PR · On-site

Commissioning & Qualification (C&Q) Engineer Job Summary: We are seeking a mid-level Commissioning & Qualification (C&Q) professional to support Packaging operations within Process Development (PD)

Validation & Engineering Group, Inc

PR · On-site

Process Engineering Support The scope requires someone who can independently support technical discussions, evaluate equipment solutions, participate in capital projects, understand C&Q expectations ...

Validation & Engineering Group, Inc

PR · On-site

Process Engineering Support The scope requires someone who can independently support technical discussions, evaluate equipment solutions, participate in capital projects, understand C&Q expectations ...

Validation & Engineering Group, Inc

PR · On-site

Process Engineering Support The scope requires someone who can independently support technical discussions, evaluate equipment solutions, participate in capital projects, understand C&Q expectations ...

Validation & Engineering Group, Inc

PR · On-site

Process Engineering Support The scope requires someone who can independently support technical discussions, evaluate equipment solutions, participate in capital projects, understand C&Q expectations ...

Validation & Engineering Group, Inc

PR · On-site

Process Engineering Support The scope requires someone who can independently support technical discussions, evaluate equipment solutions, participate in capital projects, understand C&Q expectations ...

Validation & Engineering Group, Inc

PR · On-site

Process Engineering Support The scope requires someone who can independently support technical discussions, evaluate equipment solutions, participate in capital projects, understand C&Q expectations ...

Validation & Engineering Group, Inc

PR · On-site

Process Engineering Support The scope requires someone who can independently support technical discussions, evaluate equipment solutions, participate in capital projects, understand C&Q expectations ...

Validation & Engineering Group, Inc

PR · On-site

Process Engineering Support The scope requires someone who can independently support technical discussions, evaluate equipment solutions, participate in capital projects, understand C&Q expectations ...

Validation & Engineering Group, Inc

PR · On-site

Process Engineering Support The scope requires someone who can independently support technical discussions, evaluate equipment solutions, participate in capital projects, understand C&Q expectations ...

FITS LLC

C&Q Lead

Gurabo, PR · On-site

$98K - $130K/yr

Bachelor's Degree in Life Science or Engineering, and previous years of exposure in Validation Life Cycle within the Pharmaceutical Industry. * Bilingual (Spanish & English) * Shift: Administrative ...

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Showing results 21-40

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C Developer information

What is a C developer?

C Developers are software engineers who specialize in designing, developing, and maintaining software applications using the C programming language. They work on a variety of projects, including operating systems, embedded systems, and performance-critical applications. C Developers are responsible for writing efficient, reliable, and maintainable code, as well as debugging and optimizing existing software. They often collaborate with other developers, engineers, and stakeholders to deliver robust technical solutions.

What are the key skills and qualifications needed to thrive as a C developer, and why are they important?

To thrive as a C Developer, you need a solid understanding of C programming, data structures, algorithms, and typically a degree in computer science or a related field. Familiarity with development tools such as GCC, GDB, version control systems like Git, and sometimes familiarity with embedded systems or operating system concepts is essential. Strong problem-solving abilities, attention to detail, and effective communication skills set standout developers apart. These skills and qualities are crucial for writing efficient, reliable code and collaborating effectively on complex software projects.

What are some common challenges C developers face when working on large codebases, and how can they address them?

C Developers working with large codebases often encounter challenges such as maintaining readability, managing dependencies, and identifying bugs related to memory management. To address these issues, developers typically use modular programming techniques, adhere to consistent coding standards, and leverage version control tools for collaboration. Regular code reviews and comprehensive documentation also help teams maintain code quality and ensure that knowledge is shared across developers, making it easier to onboard new team members and reduce technical debt.

What is the difference between C Developer vs C++ Developer?

AspectC DeveloperC++ Developer
Required CredentialsTypically a bachelor's in computer science or related field; certifications are optionalSimilar credentials; often includes certifications in C++ or software development
Work EnvironmentEmbedded systems, operating systems, or low-level programmingApplication development, game development, or software engineering
Industry UsageEmbedded devices, firmware, OS kernelsDesktop applications, game engines, high-performance software

The main difference between a C Developer and a C++ Developer lies in their focus areas. C Developers primarily work on low-level programming and embedded systems, while C++ Developers often handle more complex applications that leverage object-oriented features. Both roles require similar foundational skills, but their application domains and project types differ significantly.

Are C developers still in demand?

C developers are still in demand, especially in industries like embedded systems, operating systems, and hardware programming. Proficiency in C remains valuable due to its performance and low-level capabilities, and knowledge of related tools like compilers and debugging is often required.

What job categories do people searching C Developer jobs in Puerto Rico look for?

The top searched job categories for C Developer jobs in Puerto Rico are:

What are popular job titles related to C Developer jobs in PR?

For C Developer jobs in PR, the most frequently searched job titles are:

C Developer jobs near you
Infographic showing various C Developer job openings in Puerto Rico as of August 2026, with employment types broken down into 78% Full Time, and 22% Contract. Highlights an 95% In-person, and 5% Remote job distribution.

C&Q Specialist | Pharmaceutical

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR • On-site

Contractor

Re-posted 20 days ago

Job description

LOCATION: Las Piedras / Gurabo / Juncos

We are seeking a Commissioning & Qualification Specialist to support a pharmaceutical manufacturing facilities in Juncos/Gurabo area. The specialist will be responsible for conducting commissioning and qualification activities of Class D facilities and equipment to ensure they comply with requirements and regulatory standards. This is a 9 month+ contract-based opportunity for an independent professional willing to work at client site.

Main Responsibilities:

  • Develop and execute qualification protocols (Commissioning, IQ, OQ, PQ) for pharmaceutical equipment and facilities. 
  • Ensure qualification and validation activities meet company procedures and regulatory requirements.
  • Manage Change Controls by initiating or reviewing for approval prior to execution, tracking associated tasks to ensure timely completion, and documenting closure in full compliance with FDA regulations, cGMP requirements, and company quality system procedures.
  • Perform installation and operational checks for pharmaceutical equipment and systems.
  • Develop commissioning protocols and execute commissioning activities for Class D rooms.
  • Identify and resolve technical issues during qualification activities.
  • Create and maintain accurate and complete documentation, including protocols, test scripts, reports, and SOPs. Ensure traceability of all qualification and validation activities.
  • Ensure compliance with global regulatory standards (e.g., FDA, ICH, etc.) and industry guidelines.
  • Support the periodic review and requalification of pharmaceutical systems.
  • Coordinate system upgrades, decommissioning, and troubleshooting.
  • Partner with QC, validation, IT, and engineering teams to ensure seamless implementation.

General Requirements:

  • Fluent in Spanish and English (spoken and written).
  • Proficiency in Microsoft Office 365 (Teams, SharePoint, Outlook, Excel, Word, PowerPoint) and project management tools.
  • Proficiency in documentation practices and attention to detail.
  • Effective communication skills and ability to present complex technical information to diverse audiences.
  • Excellent problem-solving skills and ability to work collaboratively in a cross-functional team environment.
  • Excellent communication skills.

Education Requirements:

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

Experience Requirements:

  • 3+ years C&Q experience in the Pharmaceutical Industry.
  • In-depth knowledge of regulatory requirements (e.g., cGMP, FDA) related to commissioning, qualification, and validation activities.
  • Strong understanding of equipment and facility qualification, risk assessments, and validation principles.
  • Experience in conducting investigations, particularly related to deviations, and familiarity with Corrective and Preventive Action (CAPA) processes.
  • Prior experience in the commissioning and qualification (C&Q) of Grade D cleanroom environments is highly preferred.

Physical Requirements:

  • Ability to sit for long periods.
  • Light physical activity may be required occasionally.
  • Must be able to visit field locations as needed.
  • Must be able to use personal protective equipment (PPE) when required.
  • Ability to perform in a variety of industrial environments.