Sr Engineer

Veg Group

Barceloneta (PR)

On-site

USD 70,000 - 90,000

Full time

14 days+

Get more replies from employers

Send a job-specific resume in minutes.

Job summary

A leading engineering firm is seeking a dedicated engineer to work in process optimization and troubleshooting within the pharmaceutical and biotechnology sectors. Candidates should have a Master's or Bachelor's degree in Engineering with relevant experience, particularly in aseptic environments. The ideal applicant is bilingual in English and Spanish, proficient in Microsoft applications, and familiar with regulatory compliance. This role offers an opportunity to impact healthcare and technology positively.

Qualifications

  • Engineer with experience in aseptic processing environments, preferably Fill/Finish operations.
  • Experience in performance qualification for New Product Introductions.
  • Minimum of 4 years in pharmaceutical, medical device, or biotechnology industries.

Responsibilities

  • Direct characterization of process optimization strategies.
  • Design and implement modifications and experiments.
  • Develop and present interpretations of operational results.

Skills

Aseptic processing operations
Bilingual (English/Spanish)
Regulatory compliance knowledge
Project management
Documentation skills

Education

Master's degree in Engineering
Bachelor's degree in Engineering

Tools

MS Windows
Microsoft Office

Job description

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.

Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

Sr Engineer
Sr Engineer

Veg Group • Carolina (PR)

On-site
USD 70,000 - 90,000
Sr Engineer
Sr Engineer

Veg Group • Puerto Rico

On-site
USD 80,000 - 100,000
Sr Engineer
Sr Engineer

Veg Group • Juana Díaz (PR)

On-site
Sr Engineer
Sr Engineer

Veg Group • Humacao (PR)

On-site
USD 75,000 - 100,000
Sr Engineer
Sr Engineer

Veg Group • United States

On-site
USD 75,000 - 100,000
Engineer
Engineer

Veg Group • Juncos (PR)

On-site
USD 55,000 - 75,000
Sr Engineer
Sr Engineer

Veg Group • Juncos (PR)

On-site
USD 70,000 - 90,000
Senior Quality Analyst
Senior Quality Analyst

Validation & Engineering Group, Inc. • Guaynabo (PR)

On-site
USD 70,000 - 110,000
Validation Engineer - Upstream
Validation Engineer - Upstream

Veg Group • Carolina (PR)

On-site
USD 75,000 - 95,000
Project Engineer
Project Engineer

Veg Group • Juncos (PR)

On-site
USD 70,000 - 90,000