Engineer

Posted 13 Days Ago
Be an Early Applicant
Juncos, PRI
In-Office
Junior
Biotech • Consulting • Pharmaceutical • Manufacturing
The Role
Provide engineering support for process optimization, troubleshooting, and minor design projects in manufacturing/pilot plant environments. Apply standard engineering techniques, audit equipment performance and regulatory compliance, collaborate with cross-functional teams, assist project managers with design and cost estimates, and complete routine technical tasks under general supervision.
Summary Generated by Built In

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:

  • Engineer

Summary:

  • Under general supervision, provides characterization of process optimization strategies and/or troubleshooting of operational issues in the operations, manufacturing, pilot plant or capital projects environment.
  • Applies basic engineering principles to the design and implementation of system modifications, experiments and/or capital projects.
  • Organizes, analyzes and presents interpretation of results for operational issues or engineering projects of minor scope and complexity.

Functions:

  • Provide solutions to a variety of technical problems of moderate scope and complexity.
  • Under general supervision will evaluate, select and apply standard engineering techniques and procedures. Assistance given for unusual problems.
  • Perform assignments that have clear and specific objectives and require investigation of limited number of variables.
  • Initiate and complete routine technical tasks.

Operations Engineering:

  • Function as a technical expert to equipment or systems regarding troubleshooting operations. Frequently become actively involved in daily operations when required to meet schedules or to resolve complex problems.
  • Routinely audit the operational performance and regulatory compliance of a moderate number of equipment items or systems of significant complexity.
  • Work with research, manufacturing, maintenance, process development, utilities, facilities, quality assurance and/or validation departments in developing requirements and recommendations for system modifications.

Design Engineering:

  • Work under the direct supervision of project managers to complete design, engineering, and construction projects within schedule and budget constraints.
  • Work with consultants, architects and engineering firms on development of standard design documents.
  • Obtain and critique quotes for equipment modifications or installations.
  • Generate rudimentary project cost estimates and schedules.
  • Other functions may be assigned

Education:

  • Bachelor's degree in Engineering & 2 years of Engineering experience

Preferred Qualifications

  • Experience with equipment and/or process troubleshooting in a regulated environment.
  • Knowledge of pharmaceutical/biotech processes and GMP production operations.
  • Organizational & technical writing skills.
  • Proficient presentation & communication skills in English and Spanish

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.

Skills Required

  • Bachelor's degree in Engineering
  • 2 years of engineering experience
  • Experience with equipment and/or process troubleshooting in a regulated environment
  • Knowledge of pharmaceutical/biotech processes and GMP production operations
  • Organizational and technical writing skills
  • Proficient presentation and communication skills in English and Spanish
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The Company
154 Employees
Year Founded: 2019

What We Do

Pinnaql, Inc. is a professional services consulting firm providing quality, regulatory, and operational excellence solutions to biopharmaceutical, medical device, and CDMO companies worldwide. The company specializes in laboratory validation, engineering, and compliance, helping regulated life sciences organizations navigate manufacturing challenges, reduce execution risks, and accelerate the transition from lab innovation to commercial market readiness.

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