CODEX Validation Group is an Engineering and Validation services provider with operation in Puerto Rico and USA. We are looking for Project/Validation Engineers with strong background in the Medical Device and Pharmaceutical industries.
Responsibilities:
- Served as the equipment owner during the transfer of manufacturing lines.
- Lead and support new equipment installation.
- Provide project and validation support to Manufacturing and Engineering areas for the Medical Device and Pharmaceutical industry.
- Work along project managers and other site resources to comply with established milestones and deadlines. Report results to management as required.
- Troubleshoot equipment and software problems related to medical device manufacturing lines.
- Be able to evaluate equipment related interface software’s and provide solutions as required.
- Participate on the evaluation and generation of customer requirements for new equipment’s.
- Work in the validation documentation generation like IQ, OQ, PQ for manufacturing equipment’s, assembly lines and packaging.
- CSV documentation generation and execution.
- Follow-up actions to ensure the completion of activities assigned.
- Develop periodic meetings to report projects progress and implementation strategies in order to meet deadlines.
Requirements:
- Engineering degree (Mechanical preferred)
- Strong GMP knowledge and excellent documentation skills.
- Experience in technology transfer and/or new equipment installation support.
- Experience with validation documentation generation like IQ, OQ, PQ for manufacturing equipment’s, assembly lines and packaging.
- Experience with CSV documentation generation and execution.
- Technical writing and problem solving skills.
- Good communication and interpersonal skills at all levels.
- Able to work with minimum supervision.
- Ability to handle multiple tasks at the same time and ability to prioritize.
- Willing to work extra hours, any shift or Holidays (e.g. shutdowns, extraordinary events).
- Team work oriented, active participation in project teams when required.
- Ability to interface with other site groups when required.
EDUCATION and/or EXPERIENCE:
BS in Engineering (Mechanical preferred) with 3 to 5 years of experience in the Medical Device and Pharmaceutical industry. (it’s important: Please send your resumes if you understand that you fulfill all the minimum requirements for the position).
Job Type: Contract
Salary: $0.00 per hour
Schedule:
- 8 hour shift
- Day shift
- Monday to Friday
- Overtime
Contract Length:
Work Location:
- One location
Company’s website:
- www.codexvalidationgroup.com
Company’s Facebook page:
- https://www.facebook.com/CodexValidationGroup
Work Remotely:
Source: Indeed.com
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