Job Title: Manufacturing Engineer
Location: Thousand Oaks, CA
Pay Rate: $41.06/hr.
ZIP Code: 91320
Start Date: Right Away
Keywords: #Engineering
Benefits:
* Medical / Health Benefits with multiple plan options, Flexible Spending Accounts, Dental and Vision / glasses / prescription contact lens and eye test options available.
* On the job training / cross-training to develop and expand skills, creating opportunity for advancement and personal development. Tuition reimbursement available for relevant development opportunities.
* Life Insurance, disability insurance, and voluntary life insurance for family members available. Accident and critical illness insurance optional.
* Scheduled performance reviews create opportunities for advancement and pay increases.
* We have many success stories from individuals who took advantage of the training, cross-training, and personal development opportunities for advancement. We also have success stories of individuals who desired a reliable, scheduled and consistent career with appropriate work-life balance, health benefits and good job security. Whichever way you define success, this work culture cares about team members and treats each individual with dignity, inclusion, respect and recognition.
* A Referral Program compensates active employees for referring friends and former colleagues when the referral results in hiring the person. Our team has grown with referrals and internal promotions.
Responsibilities:
Fully onsite at ATO - no opportunity for remote, Full time onsite support in required.
Standard business hours, some possibility for OVT
Looking for industry experience as a manufacturing engineer
This engineering position supports manufacturing activities associated with manufacturing process equipment at Client Thousand Oaks (ATO). The engineer works in partnership with the maintenance, Project Management, Engineering Technical Lead, and manufacturing to develop, improve and oversee the operation and reliability of equipment. The Engineer role will provide direct engineering technical support as follows:
- Identify, support, and/or lead implementation of engineering based improvements or
upgrades to the process equipment. This may include development of rationale for
improvement and identification of design requirements and then translation of requirements
into process equipment/system design, specification and supporting the construction,
startup, and validation of equipment.
- Be individually accountable for the verification deliverables.
- Assist in the identification of critical quality parameters and process attributes for new equipment.
- Advising and coordinating equipment maintenance as vital to ensure systems are in proper working order.
- Provide oversight for verification deliverables developed by outsourced/contract verification staff.
- Assist in development and review of User Requirements Specifications (URS).
- Suggest design modifications to address risks and design in quality and safety.
- Develop or oversee development of commissioning and function test plan for any equipment modifications and acquisition in line with CQP, Automation Systems, SOPs, and standards.
- Act as a liaison between Engineering and Manufacturing during project planning, execution, and closeout.
- Ensure safety during commissioning, validation, maintenance and manufacturing activities.
- Monitor systems to identify performance risks and implement risk reduction strategies.
- Providing problem solving support to reduce production downtime. This will involve leading and/or supporting technical root cause analysis involving multidisciplinary site teams and implementation of corrective/preventive action.
- Ensure systems are installed and operating safely align with pertinent environmental health/safety practice, rules and regulations.
- Lead and provide ad hoc technical support and guidance in a timely manner for manufacturing and maintenance on equipment troubleshooting.
- Support Manufacturing and QA with Performance Qualification (PQ) activities if applicable.
- Identifying reliability improvements for assigned equipment to improve equipment uptime.
- Support Lean Transformation and Excellence in Operations process improvement by leading, supporting, and documenting improvement opportunities to reduce cost, improve safety/quality, or improve speed.
- Work schedule flexibility to support 24/7 operations, requiring occasional after-hours engineering coverage as required from time to time.
- Provide concise and clear documentation for actions taken on systems.
Full time onsite support in required.
Public Information
Internal Use Only General and Administrative
Demonstrated skills in the following areas:
* Basic technical report writing and presentations
* Verbal communication
* Personal Organization
* Dealing with and managing change
* Technical (Equipment Specific)
* Analytical Problem Solving
* Computer Literacy (Maximo, Track wise, E-Builder, PCS, BMS and QEMS)
* Specialized equipment/process expertise
* Ability to handle multiple projects/troubleshooting at the same time
* Schedule development, facilitation and collaboration
* Basic project management, project completion and follow-up
* Problem solving skills requiring the application of scientific and engineering theory and calculations and
creative skills in the development of hypotheses and approach.
* Project Cost development
* Conflict Resolution
* Customer service in a technical setting
* Management of contractors and vendors.
* Experience in developing SOPs and delivering training
* Individual must be a team player prepared to work in and embrace a team-based culture that relies on
collaboration for effective decision-making
Preferred Qualifications / Skills / Experience
* Bachelor's degree in engineering-related field
* 5 years of relevant work experience with 3 years" experience in operations/manufacturing
environment
* Direct experience with regulated environments (FDA, OSHA, EPA, etc.)
* Working knowledge and experience with cGMP procedures and engineering practices on
pharmaceutical/biotech production processes, clean utilities, facilities, instruments and equipment
* Direct knowledge of design and troubleshooting with GMP Biopharmaceutical Production
* facility equipment/systems such as cell culture reactors, chromatography, filtration, as well as other
equipment needed to support these processes such as autoclaves, clean in place (CIP) systems,
washers, clean steam, etc.
* Process automation knowledge - understanding of automation infrastructure, current technologies,
and automation project execution / verification.
If you are interested in this role, please apply via the apply now link provided. Our overriding goal is to provide quality staffing solutions that help people, organizations, and communities succeed. Belcan is a leading provider of qualified personnel to many of the world's most respected enterprises. We offer excellent opportunities for contract, temporary, temp-to-hire, and direct assignments. We are the employer of choice for thousands worldwide. For more information, please visit our website at Belcan.com
EOE/F/M/D/V