alidation & 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:
- Specialist Tech Engineering
Description:
The Specialist Tech Engineering will provide technical engineering support on all system/equipment optimization strategies, upgrades, replacements, and modifications and ensure that all of the maintenance team operations and activities are maintained in compliance with respect to current corporate policies, industry standards, regulatory standards and FDA standards.
Responsibilities:
- Ensure utility systems, process maintenance, instrumentation/calibration/electrical systems and technical cleaning systems are maintained in compliance with all applicable industry standards, regulatory standards and FDA standards.
- Ensure the maintenance team training program, standard operating procedures and equipment/system operational standards are consistent throughout the team.
- Coordinate technical support to the maintenance team on engineering issues, regulatory issues, compliance issues, calibration issues, quality issues, microbial/environmental issues, technical cleaning issues, validation issues, electrical issues and process maintenance issues.
- Provide technical support for the maintenance team during FDA and other regulatory agency inspections.
- Provide technical support to the maintenance team in response to the FDA and other regulatory agencies.
- Support the maintenance team when responding to high purity water systems and environmental monitoring alert/action notifications.
- Support the investigation on all alert/action notifications. Support the development and maintenance of an audit program for the maintenance team and facilitate routine audits of activities, documentation, operations and related areas to ensure a continued state of compliance.
- Assist plant engineering in the evaluation and implementation of engineering improvements, policy changes, compliance improvements and optimization programs.
- Evaluate sanitization and maintenance procedures.
- Propose changes to the Department Manager.
- Propose modifications for process, utility and clean room systems to the Plant Engineering Group.
Education:
- Master’s degree & 3 years of Engineering experience
- Bachelor’s degree & 5 years of Engineering experience
Skills:
- Leadership and teambuilding,
- Verbal communication.
- Written Communication/Technical Writing
- Comprehensive understanding of validation protocol requirements
- Technical (Equipment Specific)
- Analytical Problem Solving Project Management.
- Vast experience in Maximo and SAP is required.
Qualifications:
- Bachelor's Degree in Science or related field.
- Minimum of 5 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.
- Technical Writing skills and investigations processes.
- Available to work extended hours, possibility of weekends and holidays.
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
- Master's degree with 3 years engineering experience OR Bachelor's degree with 5 years engineering experience
- Minimum of 5 years experience in pharmaceutical, medical device, or biotechnology industries
- Experience in direct process / manufacturing areas
- Vast experience in Maximo and SAP
- Must be fully bilingual (English/Spanish) with excellent oral skills
- Proficient using MS Windows and Microsoft Office applications
- Strong knowledge in cGxP and regulatory guidance and their application to compliance
- Comprehensive understanding of validation protocol requirements
- Technical writing skills and experience with investigations processes
- Leadership and teambuilding skills; verbal and written communication skills
- Available to work extended hours, including possible weekends and holidays
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.
