Job Title : Associate Process Engineer - Biopharma (JP13416)
Location : Holly Springs, NC. 27540
Business Unit : Engineering & Automation
Employment Type : Contract
Duration : 12 months with possible extensions or conversion to FTE
Rate : $30-33 / hr W2 with benefits
Posting Date : 11 / 26 / 2024
Note : 100% onsite - regular working hours - potential on call rotation occasionally.
3Key is hiring! We are looking for Associate Engineer for a consulting engagement with our direct client, a leading global biotechnology company.
Ideal Candidate : B.S. in chemical or mechanical engineering. Some pharma experience in drug substance manufacturing is a plus. Looking for a go getter with some general working experience. (Does not have to be related to this position.)
Key Responsibilities :
- Develop, coordinate, analyze, and present results for operational issues and engineering projects
- Provide technical support to commercial and clinical manufacturing as needed, specific to process control and process equipment.
- Working closely with multiple subject areas, including manufacturing, process engineering, process development, utility operations, maintenance, quality assurance, and validation to implement operational improvements
- Communicating with supervisor and support staff, highlighting issues and proposing solutions.
- Work in a small group of engineers and / or technicians on an ongoing or project basis.
- Complete tasks under the general direction of lead engineers to complete design and engineering within schedule and budget constraints.
- Provide technical support and issue resolution with 24x7 on-call support of process systems on a rotational based frequency.
- Provide system ownership for assigned equipment, and supporting operations at the site.
- Provide engineering support for design, construction, startup, commissioning and qualification.
- Lead or work with teams in design, development and selection of new systems, instruments, calibration capabilities and consumable components.
- Evaluate capabilities of current and potential suppliers, and assess new technologies that could provide cost savings, throughput, or other unique capabilities to Amgen manufacturing.
- Identify, support, and / or lead implementation of engineering-based improvements or upgrades in small to medium scope and complexity.
- Lead the development of calibration / maintenance programs, ensure the availability of spare parts, and coordinate maintenance execution as necessary to ensure systems are in proper working order.
- Ensure systems are installed and operating safely and comply with pertinent environmental health / safety practice, rules and regulations.
- Ensure necessary commissioning and qualification of systems is completed in alignment with site GMP requirements and interact with regulatory inspectors as necessary.
- Apply basic engineering principles and practices in support of daily operation, maintenance, and troubleshooting of plant and process systems.
- Monitor systems to identify performance risks and implement risk reduction strategies.
- Providing troubleshooting support to reduce production downtime. This will involve leading and / or supporting technical root cause analysis and implementation of corrective / preventive action. (Support may be required outside of normal working hours including nights, weekends and holidays)
- Support new product / technology introductions by performing engineering assessments, implementing equipment modifications, and supporting engineering runs.
- Advance the use of condition based and predictive maintenance practices by incorporating advanced data analytics where applicable.
- Own investigations of abnormal conditions through Deviation and business processes.
Basic Qualifications :
Bachelor's degree Or Associate's degree and 4 years of Process Engineer experience OrHigh school diploma / GED and 6 years of Process Engineer experience.
Ability to provide On-Call support coverage nights and weekends, on a rotating basis.Preferred Qualifications :
Bachelor's degree in engineering or related technical fieldPosition requires strong written and verbal skills and the ability to work with minimum direction.Demonstrated interpersonal and facilitation skills and ability to work in a collaborative team-based environment.Ability to apply analytical skills to evaluate and interpret sophisticated problems using multiple sources of information.Ability to function within cross-functional teams and embrace a team-based environment.Experience with Mammalian Cell Culture, Protein Purification, Clean Utilities, CIP, SIP, Production Services, and / or non-GMP Utilities preferredFamiliarity with designing and operating equipment used in biopharmaceutical manufacturing preferredTop Must Have Skill Sets :
Strong working ethicStrong communicationB.S. in chemical or mechanical engineeringPharma experienceEmployee Value Proposition :
Unique industry experience
Career growth
Networking
Interview Process :
Manager screening followed by panel interviews (potential for these to be in person).
We invite qualified candidates to send your resume to recruiting@3keyconsulting.com . If you decide that you're not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com / careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.
Regards,
3KC Talent Acquisition Team