Sr Engineer

Pinnaql, Inc.; Manatí (PR); On-site; USD 90,000 - 130,000; Full time

Job summary

Validation & Engineering Group, Inc. in Puerto Rico seeks an engineer to lead process optimization and troubleshoot operations in manufacturing and capital projects, applying advanced engineering principles to design and implement major system modifications.

Candidates will develop, organize, analyze and present results, with 4+ years in pharma/biotech, preference for aseptic Fill/Finish, and bilingual English/Spanish. Travel expectations modest; GMP/cGxP knowledge required.

Qualifications

• Masters + 2 years of engineering experience or Bachelor + 4 years in engineering, preferred mechanical/chemical.
• Experience in pharmaceutical/biotech processes and validation documentation.
• Bilingual English/Spanish with strong oral skills.
• Familiarity with GLPs and GMPs; ability to apply engineering concepts to production.

Responsibilities

• Independently characterizes and directs process optimization strategies or troubleshooting in operations, manufacturing, pilot plant or capital projects.
• Applies advanced engineering principles to design/implement major system modifications and capital projects.
• Develops, organizes, analyzes and presents results for complex operational issues or projects.

Skills

Aseptic processing

PQ / validation

Regulatory compliance

Data interpretation

SDLC

GMP / cGxP

Microsoft Office

Lab equipment operation

Education

Masters in Engineering

Bachelors in Engineering

Tools

MS Windows

Microsoft Office

Documentation (URS/DS)

Job description

Current job opportunities are posted here as they become available.

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

Description:

Independently provides and/or directs the characterization of process optimization strategies and/or troubleshooting of operational issues in the operations, manufacturing, pilot plant or capital projects environment. Applies advanced and diverse engineering principles to the design and implementation of major system modifications, experiments, process and/or capital projects. Develops, organizes, analyzes and presents interpretation of results for operational issues or engineering projects of significant scope and complexity.

Qualifications:

• Engineer with years of experience, preferably in aseptic processing environments, including Fill/Finish operations such as vial and syringe filling lines.


• Experience in characterization activities and performance qualification (PQ) for New Product Introductions (NPI).


• Minimum of 4 years of experience in direct pharmaceutical, medical device or biotechnology industries.


• Experience in direct process / manufacturing areas.


• Must be fully bilingual (English / Spanish) with excellent oral skills.


• Must be proficient using MS Windows and Microsoft Office applications.


• Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.


• Experience in Design Documentation (URS, DS), IQ, OQ, PQ protocols development and execution, deviations and reports generation.


• SDLC, Risk Assessment, Data Integrity, Factory Acceptance Test (FAT) & Site Acceptance Test (SAT).


• Available to work extended hours, possibility of weekends and holidays.

Education:

• Masters + 2 years of Engineering experience OR Bachelors in Engineering + 4 years of Engineering experience. Preferred: Mechanical or Chemical Engineering


• Working knowledge of pharmaceutical/biotech processes


• Familiarity with validation processes


• Familiarity with documentation in a highly regulated environment


• Ability to operate specialized laboratory equipment and computers as appropriate.


• Ability to interpret and apply GLPs and GMPs.


• Ability to apply engineering science to production.


• Able to develop solutions to routine technical problems of limited scope


• Comprehensive understanding of validation protocol execution requirements.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.