Validation & Engineering Group, Inc.

MV01-032626 Manufacturing Engineer

Validation & Engineering Group, Inc.  •  Carolina, PR (Onsite)  •  7 days ago
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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:

  • Manufacturing Engineer - Process Development

Manufacturing Engineer will provide support to the Process Development team to efficiently facilitate operations within the production area, optimizing processes, and ensuring production goals are met. Monitors performance of equipment, machines and tools and corrects equipment problems or process parameters that produce non-conforming products, low yields or product quality issues.

Responsibilities:

  • Support manufacturing basic daily activities and/or continuous improvement projects such as; equipment troubleshooting, root cause analysis and non-conforming product evaluation.
  • Completes technical activities leading to new or improved products or process, for current programs, next generation programs and to meet strategic goals and objectives of the company.
  • Prepares reports, publishes, and makes presentations to communicate findings.
  • Analyzes and solves problems from basic engineering principles, theories and concepts through to a wide range of problems which require novel and new innovative approaches.
  • Cultivates internal and external network of resources to complete tasks. Participate in project teams to complete goals and objectives for the projects.
  • Interacts cross functionally and with internal and external customers.
  • Support process and/or equipment validation activities (IQ, OQ, PQ); process performance qualification activities and develop Master validation plans for new processes or products.
  • Work with the Process Development team to efficiently qualify new processes; assist with statistical sampling plans, and other development procedures.
  • Generate manufacturing instructions for new processes being developed.

Qualifications:

  • Bachelor's Degree in Engineering or Science.
  • Three (3) years' experience as Manufacturing Engineer performing Process Development activities.
  • Available to work additional hours and selected weekends as requested
  • Support manufacturing basic daily activities and/or continuous improvement projects
  • Develop new or improved products or process, for current programs.
  • Analyzes and solves problems using basic engineering principles
  • Participate in project teams to complete goals and objectives for the projects.
  • Interacts cross functionally and with internal and external customers.
  • Support process and/or equipment validation activities (IQ, OQ, PQ).
  • Work with the Process Development team to efficiently qualify new processes.
  • Generate manufacturing instructions for new processes being developed.

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.

Validation & Engineering Group, Inc.

About Validation & Engineering Group, Inc.

Validation & Engineering Group, Proudly serving our clients since 1997.

Our Mission states in part: "provide our clients with the best resources to meet their needs". In our search for the best talent, we are inclusive and do not discriminate. V&EG is proud to be an equal opportunity workplace and is an affirmative action employer.

Validation & Engineering Group provides world-class service and expertise to the pharmaceutical, medical device and biotechnology industries. We offer our clients: Validation, Control System Solutions, Instrumentation, Training, Equipment Rentals, and Regulatory Compliance Services to ensure adherence to Federal and European regulatory agencies. Our group had serve in solid dosages, liquids, creams, lyophilizers, and parenteral dosage.

Our agility in responding to our clients’ needs, access to the best pool of talent, and the combined experience and technical expertise of our resources make Validation & Engineering Group a leader in the pharmaceutical, medical devices, and biotechnology industries.

At Validation & Engineering Group we provide professional expertise in the areas of:

•Audit and Assessment

•Automated Process Control System Qualification

•Equipment and Facilities Qualification

•Facilities Start-Up and Commissioning

•GAP Analysis

•Information Systems Computer Validation

•Packaging and Process Analysis

•Process & Cleaning Validation

•Project Management

•Quality Systems

•Risk Based Approach

•Regulatory Compliance

•Standard Operating and Maintenance Procedures

•Training

•Utilities Support and Qualification

In addition we offer Equipment Rentals and training to your workforce such as: Temperature & Relative Humidity, Electrical, Process, Environmental, and. Analytical.

Our Offices:

Puerto Rico:

Centro Internacional de Mercadeo I 100 Carr. 165 Ste 703, Guaynabo, 00968 Puerto Rico

Phone: (787) 622-0996

United States:

2180 Satellite Blvd, Suite 400Duluth, Georgia 30097 United States

Phone: (770) 403-5802

Industry
Architecture & Engineering
Company Size
51-200 employees
Headquarters
Guaynabo, PR
Year Founded
1997
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