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Engineer Senior

1 month ago

West Greenwich, United States Belcan Full time

Engineer Senior

Job Number: 351030

Category: Manufacturing Engineering

Description: Job Title: Engineer Senior

Pay Rate: $47.82/hr.

Location: West Greenwich, RI

ZIP Code: 02817

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:

Must have engineering degree (mechanical/ chemical engineering)

Will be Single support person, must be self driven and perform independently as will work with cross functional teams outside of ARI campus and they will be supervised remotely

Must have experience with process equipment in pharma background, will be owning processing manufacturing equip (4-6 years of experience, not less than 4)

Not bio pharma need pharma manufacturing background

Must have experience with troubleshooting equipment / reliability background / problem solving

Preference is local but open to seeing job seekers with solid experience to relocating **If they are relocating they will be expected to be onsite within 2 weeks of offer

No gaps of more than 3-4 months in prior work experience

Will not accept PhD w/o industry experience

This engineering position supports manufacturing activities associated with manufacturing process equipment at Client, 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 equipment systems. This may include development of reason 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.

  • 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.

  • Be individually accountable for the verification deliverables on key capital projects.

  • 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.

  • Develop commissioning and function test plan for any equipment modifications and acquisition.

  • Ensure safety during commissioning, validation, maintenance and manufacturing activities.

  • Support Manufacturing and QA with Performance Qualification (PQ) activities if applicable.

  • Act as a liaison between Engineering and Manufacturing during project planning,

execution, and closeout.

  • 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.

  • Support new product/technology introductions by performing engineering assessments,

implementing equipment modifications and supporting engineering runs.

  • Ensure systems are installed and operating safely align with pertinent environmental health/safety practice, rules and regulations.

  • Provide ad hoc technical support and guidance for manufacturing and maintenance.

  • Provide coaching and guidance to project teams and engineers on the CQP process and risk-based approaches to commissioning and verification.

  • Assist in developing and maintaining metrics.

  • Up to 20% domestic travel for cross site training

  • Full time onsite support in required.

  • Work schedule flexibility to support 24/7 operations, requiring occasional after-hours engineering coverage as required from time to time

Preferred Qualifications / Skills / Experience

  • Bachelor"s degree in chemical or other Engineering fields

  • 6+ years' of relevant work experience with 5+ years' experience in Biopharmaceutical

operations/manufacturing environment

  • Experience working in a regulated environment (e.g. cGMP, OSHA, EPA, etc.) and

familiarity with GMP quality systems/processes such as change control, nonconformances,

corrective and preventative actions, and qualifications/validation.

  • 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.

  • Ability to analyze problems, develop and propose engineering solutions in a scientific

manner using data-driven techniques and analyses (e.g., Root Cause Analysis (RCA), Statistical Process Control (SPC), Six Sigma, Predictive Maintenance, etc.)*

  • Experience applying engineering principles to the design and implementation of system modifications, introduction of new processes, and execution of capital projects*

  • Understanding of the execution process of capital projects in a GMP and/or non-GMP

Biopharmaceutical Production facility including procurement, construction, startup, and

validation

  • Understanding of safety requirements working in a Biopharmaceutical Production facility.

  • Independent, self-motivated, organized, able to multi-task in project environments, and

skilled in communication, facilitation, and collaboration*

  • Phenomenal teammate prepared to work in and adopt a team based culture that relies on collaboration for effective decision-making*

  • Strong leadership, technical writing, and communication/presentation skills

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

Location: West Greenwich , RI

Minimum Experience (yrs):

Required Education: Not Specified

Benefits:

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