Job description
Validation & Engineering Group, Inc. (V&EG) 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:
- Associate Engineer
Summary:
Under close supervision, assists with or directly provides technical engineering support in process optimization strategies, upgrades, replacements, and modifications in the operations, manufacturing or pilot plant environment. Ensures that all operations are accomplished in a compliant manner consistent with current corporate policies, industry standards, and applicable regulatory requirements.
Functions:
- Perform standard engineering work requiring application of standard techniques and procedures.
- Complete routine technical tasks.
- Prompt and regular attendance to workplace.
- Other functions may be assigned.
Operations Engineering:
- On a daily basis, monitor operations of a unit operation or system and actively assist operations, maintenance or project personnel as required.
- Routinely audit the operational performance and regulatory compliance of a limited number of equipment items or systems of minor to moderate complexity.
- Routinely troubleshoot operational issues with individual equipment or skids.
- Assist with the proposal, initiation, testing and implementation of proposed changes to process, utility and/or facility systems
- Assist more senior engineers in the evaluation and implementation of engineering improvements, policy changes, compliance improvements and optimization programs.
**Other functions may be assigned.
Education:
- Bachelor's Degree in Science or Engineering.
Relevant Experience:
- 2 minimal years of experience in operations/manufacturing environment preferred.
- Exposure to or direct experience with regulated environments (i.e. cGMP, OSHA, EPA) preferred.
Preferred Qualifications:
- 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.
- Available to work extended hours, possibility of weekends and holidays.
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