Spark Interview Process Jobs in Usa

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Contract Manufacturing Process Technician **Swing Shift**
Salary not disclosed
San Jose, CA 2 days ago

Company Description

Omega EMS has been at the forefront of developing and delivering cutting-edge solutions in Silicon Valley. Our expertise makes us uniquely equipped to supply unparalleled customer service tailored to each individual need – all within a framework that is firmly rooted in CGMPs (Current Good Manufacturing Practices). With our flexible approach, real world operational experience and commitment to serving customers’ needs with excellence, Omega EMS offers an incomparable “one stop solution” for any EMS project.


Role Description

The Process Technician will be a key contributor to Omega EMS’s SMT line, AXI, and process engineering activities for PCB assembly. This role is responsible for ensuring that every stage of the printed circuit board assembly process meets the highest standards of quality and reliability. The ideal candidate is a resourceful problem solver who can overcome technical challenges and implement practical solutions. As a core member of the manufacturing team, the Process Technician works closely with production operators, engineers, and quality staff to support fast-paced, high-mix builds for Silicon Valley’s most innovative companies, delivering world-class manufacturing systems and processes.


Qualifications


Job Responsibilities:

·        Serve as the first line of technical support for PCB assembly production, troubleshooting and resolving process issues in real time.

·        Set up, inspect, and validate SMT equipment and processes, including stencil printers, reflow ovens, SPI, and X-ray, to ensure high-quality first articles and stable production runs.

·        Contribute to the design and fabrication of stencils, tooling, and fixtures, and manage the tooling log to maintain availability and accuracy.

·        Perform X-ray and visual inspections, identify solderability or void issues, and implement corrective actions where needed.

·        Provide hands-on training and guidance to operators and production staff, improving process understanding and capability across the team.

·        Support and collaborate with SMT, AXI, and Engineering on technical inquiries and escalations; elevate unresolved issues to the Supervisor as necessary.

·        Collect and analyze process data to identify trends, drive systemic improvements, and enhance yield and throughput.

·        Maintain a strong focus on safety, quality, and continuous improvement, while being adaptable and open to learning new tasks as required.


Job Requirement:

·        3+ years of hands-on PCBA experience (5+ years preferred).

·        Strong working knowledge of SMT/PCBA processes, including screen printer programming, solder paste inspection, reflow profiling, and X-ray inspection.

·        Ability to read and interpret wiring diagrams, schematic drawings, and engineering instructions, applying knowledge of electronic theory and components.


What We Offer

Paid Vacation

Paid Holidays

401K/ Roth 401K

Medical, Dental, and Vision


**This is a swing shift hourly role and you will earn between $25 and $27 plus 10% differential.

contract
Senior Process Engineer + CNC
Salary not disclosed
Stow, OH 2 days ago

Job Title: Process Engineer, with 5axis CNC experience - Advanced Manufacturing

Location: Stow, OH

Salary: $80,000-$120,000

About the Role:

Join our dynamic team as a Process Engineer, where you'll be at the forefront of developing and optimizing manufacturing processes for complex product lines. This isn't just an engineering role - it's an opportunity to shape production systems, mentor team members, and drive real innovation on the shop floor. If you're passionate about turning designs into reality and thrive in a hands-on manufacturing environment, we want to hear from you.

What You'll Do:

  • Lead process development and optimization for new product launches and existing manufacturing lines
  • Create and optimize CNC programs using advanced CAM software (Mastercam preferred)
  • Design and validate custom tooling, fixtures, and equipment using 3D modeling (AutoCAD Inventor or similar)
  • Drive continuous improvement initiatives using Lean manufacturing principles
  • Serve as the manufacturing expert for cross-functional teams, providing technical guidance
  • Troubleshoot complex manufacturing challenges in a machining environment
  • Develop and implement process improvements that reduce waste and enhance quality

What You Bring:

  • 5-10 years of hands-on manufacturing engineering experience
  • Expertise in CAD/CAM software and CNC programming (5-axis experience required)
  • Proficiency in 3D modeling and blueprint reading with strong GD&T knowledge
  • Demonstrated experience in tooling selection and fixture design
  • Proven ability to solve complex manufacturing problems using data-driven approaches
  • Strong leadership skills with experience mentoring junior engineers
  • Excellent communication skills and ability to thrive in a collaborative environment

Why Join Us?

  • Competitive compensation and comprehensive benefits package
  • Opportunity to work with state-of-the-art manufacturing technology
  • Strong focus on professional development and continuous learning
  • Collaborative team environment that values innovation
  • Clear career growth path with opportunities for advancement

Ready to Make an Impact?

If you're ready to take your manufacturing engineering career to the next level, apply now! We're excited to meet passionate engineers who are ready to drive manufacturing excellence.

[Apply Now Button/Link]

#Hiring #ProcessEngineer #ManufacturingEngineer #CNCProgramming #EngineeringJobs #LeanManufacturing #CADCAM #NowHiring #ManufacturingCareers

Not Specified
Manufacturing Process Engineer - Precision Machining
🏢 TekPro
Salary not disclosed
Addison, IL 2 days ago

TekPro is partnered with a precision machining manufacturer in the Chicago area that is looking to add a Process Engineer to their team. Our client offers modern CNC equipment, a clean and organized facility, and the opportunity to work on complex precision machined components.


This role is ideal for someone with experience in a precision machining environment who enjoys developing manufacturing processes, working with engineering and production teams, and supporting the launch of new parts into production.


Key responsibilities include:

  • Developing detailed manufacturing process plans for new parts using SolidWorks for modeling and drafting and Visual Manufacturing (ERP) for documentation
  • Reviewing customer purchase orders, drawings, and specifications to ensure all requirements are incorporated into the manufacturing process plan
  • Ensuring manufacturing process plans comply with all drawing, purchase order, and specification requirements
  • Reviewing existing tooling and gage inventory for use in the manufacturing process
  • Designing and ordering new tooling when necessary
  • Working closely with manufacturing teams to troubleshoot and resolve production issues as they arise
  • Supporting continuous improvement of manufacturing processes and production efficiency



If you have experience in manufacturing engineering or process engineering within a CNC machining environment and are interested, apply now to learn more!

Not Specified
P&ID Designer / Process Engineer
✦ New
Salary not disclosed
Troy, MI 1 day ago

We are seeking a highly skilled and detail-oriented P&ID Designer or Process Engineer to join our engineering team. The ideal candidate will have hands-on experience in creating and revising Piping and Instrumentation Diagrams (P&IDs) using AutoCAD, Revit, and Plant 3D, with a strong understanding of ISO and industry standards. This role is critical to ensuring accurate documentation of process systems for industrial, manufacturing, or energy projects.


Key Responsibilities:

  • Design and revise P&IDs for process systems in compliance with ISO and project-specific standards.
  • Collaborate with mechanical, electrical, and process engineers to ensure accurate system representation.
  • Use AutoCAD Plant 3D and Revit to model piping layouts, instrumentation, and equipment.
  • Maintain and update engineering documentation, including BOMs, datasheets, and control narratives.
  • Conduct quality checks and ensure drawings meet regulatory and safety requirements.
  • Support project teams during design reviews, construction, and commissioning phases.
  • Integrate P&IDs with 3D models and databases for intelligent documentation and asset tracking.



Qualifications:

  • Bachelor’s degree in mechanical, Chemical, or Industrial Engineering (or equivalent experience).
  • 3+ years of experience in P&ID design or process engineering.
  • Proficiency in AutoCAD, Revit, and Plant 3D.
  • Strong knowledge of ISO standards and ANSI/ISA instrumentation symbols.
  • Familiarity with process control systems and industrial equipment.
  • Excellent attention to detail and organizational skills.
  • Strong communication and collaboration abilities.


Preferred Skills:

  • Experience with SmartPlant P&ID or AVEVA Diagrams.
  • Knowledge of BIM workflows and integration.
  • Understanding of process safety and HAZOP documentation.
  • Ability to automate tasks using scripts or macros in CAD environments.
Not Specified
Manufacturing Process Engineer (Circuit Board exp NEEDED) - Gray, ME
✦ New
Salary not disclosed
Gray, ME 8 hours ago

Manufacturing Process Engineer

As a Manufacturing Process Engineer for printed circuit board assemblies (PCBA), your primary role is to develop and document manufacturing processes for electronic assemblies which yield reliable high-quality assemblies at the lowest possible cost.

In the role of a Manufacturing Process Engineer

  • You will develop and implement manufacturing process technologies, methods, and techniques to assist and promote the building of reliable, high quality PCBA assemblies at the lowest possible cost.
  • You will develop and maintain product assembly procedures for PCBA & cable assemblies.
  • You will provide active consultation to new product development teams regarding manufacturing capabilities, techniques and issues related to design for manufacturability and assembly (DFMA).
  • You will assist in the preparation of new product cost estimates including applicable NRE.
  • You will be responsible for identifying, specifying, validating, documenting, implementing, and training on new equipment and processes.
  • You will design production equipment and fixtures to aid in the assembly of product while improving operator safety/comfort, reducing labor and improving quality.
  • You will provide technical training in PCBA/cable manufacturing techniques, methods, and processes to manufacturing associates.
  • You will maintain reliable and safe manufacturing systems while improving production rates, efficiencies, yields, changeovers, and costs.
  • You will Investigate and diagnose product manufacturing issues and respond to internal and external customer requests for changes and improvements.
  • You will coordinate the implementation of product design changes.
  • You will collect, record, and present data applicable to the status of production projects assigned to you.
  • You will ensure projects are completed on time.


The skills you need to succeed:

  • You must be a self-starter and a strong problem solver.
  • You must have the ability to lead and work as a member of a team.
  • You must be comfortable in a fast paced, dynamic environment.
  • You will have excellent organization and decision-making skills.
  • You must have a high level of energy and enthusiasm.
  • You will have experience with 2d CAD design of electrical assemblies, schematics, and parts, (PCBA design experience highly desirable).
  • You must have experience with validation efforts.
  • You must have experience designing, assembling, and debugging automated or semi-automated electromechanical equipment.
  • You must understand computer and machine programming and I/O logic.
  • You must have strong software abilities: MS Office – proficiency necessary in Word, Excel, Outlook, and PowerPoint.
  • You must have experience with MS Project.


Required Education & experience of a successful candidate:

  • B.S. in Engineering (or equivalent combination of experience and education) in Electrical (EE or EET), Mechanical (ME or MET), or Industrial (IE, IET).
  • 8-10 years of related of work experience.
  • Experience with printed circuit board assembly including through hole and surface mount technology and PCBA test.
  • Experience implementing lean manufacturing and/or six sigma desirable.
Not Specified
Manufacturing Process Engineer - Warehouse
✦ New
Salary not disclosed
Secaucus, NJ 2 hours ago

Manufacturing Process Engineer - Warehouse

Full time/Direct Hire

Secaucus, NJ - Onsite


About The Role

The Manufacturing Process Engineer is responsible for leading the measurement and analysis of warehouse inventory processes, developing standard operating procedures, and implementing continuous improvement projects. The Manufacturing Engineer's scope of responsibility covers the end-to-end warehouse process (material preparation, receiving, storage, inventory, and shipment preparation). This position is set up to highlight and facilitate the skills needed to develop an individual.


What You Will Do

  • Process Development / Support: Design, measure, and support manufacturing process changes; develop standard operating procedures to improve operator efficiency and process consistency.
  • Continuous Improvement: Collect and analyze key performance metrics such as cycle time, storage efficiency and yield to drive process and quality improvements.
  • Participate in Kaizen events to measure, document, and continuously improve warehouse processes.
  • Layout Optimization: Analyze and plan workflow, equipment placement and space requirements to improve warehouse process efficiency.


What You Bring

  • Bachelor's degree in engineering or related field, or advanced degree and equivalent experience.
  • 3+ years of experience in a manufacturing/warehouse environment.
  • Develop detailed layouts for equipment, processes, and workflow.
  • Demonstrate proficiency in applying Lean or Six Sigma principles in a variety of situations.
  • Strong analytical skills, including the ability to mine data to draw meaningful conclusions.
  • Be able to be collaborative, flex and adapt in a warehouse environment.
  • Ability to lead a cross-functional team and work with contractors/vendors to drive projects.
  • Ability to simplify issues/direction and communicate verbally and in writing to all levels of employees.
  • Ability to effectively facilitate projects in a technical, multi-organizational environment
Not Specified
Cable Manufacturing Process Engineer
✦ New
Salary not disclosed
Sunnyvale, CA 2 hours ago

Maxonic maintains a close and long-term relationship with our direct client. In support of their needs, we are looking for a Component Engineer 4.


Job Description:

Job Title: Component Engineer 4

Job Type: Contract

Job Location: Sunnyvale, CA

Work Schedule: On-site

Pay Rate: $94 Based on experience.


DESCRIPTION:


Primary Function of the Position:

  • Responsible for ensuring suppliers meet ISI requirements for quality, service, delivery, and cost. Drive suppliers to continuously improve business and manufacturing processes specifically related to wire harness and cable assembly.
  • Evaluate and select suppliers within copper cables/harness industry. Guide Engineering in choosing suppliers for new products and providing DFM input to new designs. Supports both NPI and on-going production, monitors and works with suppliers to improve supplier performance. Executes detailed projects with suppliers to implement changes and improvements affecting quality, cost, capacity, risk, and sub-supplier management.

Essential Job Duties:

  • Work with NPD to procure custom cables ensuring DFM to achieve quality and cost targets
  • Support NPD with proto builds and track material readiness at Supplier Drive supplier root cause analysis for cable harness failures
  • Mitigate risks and ensure supply continuity by evaluating capacity, lead times and quality issues
  • Develop and maintain harness standards, specifications, and design guidelines.
  • Work with Strategic Sourcing to evaluate new suppliers and new supplier manufacturing sites
  • Complete project/ part qualification deliverables including Supplier pFMEA, Process Validations (IQ/OQ/PQ), Inspection Reports, Gage R&R, and Process Capability AnalysisWork with suppliers to execute cost reductions, capacity improvements, and risk mitigation.
  • Select the right process and supplier for the part, considering long-term fit and total cost of ownership.
  • Manage supplier changes including manufacturing process changes, production optimization, facility changes, new equipment qualification, and new line validations.
  • Drive changes to ISI requirements as necessary by initiating and managing changes to specifications and drawings through the engineering change order process.
  • Own and drive to closure supplier variances from symptom through root cause analysis to corrective action, including careful CAPA documentation.
  • Effectively prioritize and advance multiple concurrent projects and tasks Clearly communicate project status to key stakeholders Build, own, and relentlessly pursue a vision for developing suppliers.
  • Understand proper level of documentation detail for tracking of actions and justification of decisions.
  • Generate key metrics for the team and suppliers and continually drive for timely achievement of those metrics.
  • Drive suppliers to continually improve their business and manufacturing process performance to meet requirements for supplier excellence using a collection of best practices in project management, Six Sigma, Lean, SPC and negotiation. Lead these efforts without managerial guidance at several suppliers simultaneously.
  • Implement corrective and preventive actions for supplier process by driving supplier’s investigations and root cause analysis.
  • Provide effective and timely supply base information and recommendation to management by creating and delivering data-driven supply base information to any level of management at ISI with little or no guidance.
  • Prepare and deliver supplier communications as required by independently working with suppliers on scorecard creation.
  • Work with suppliers and ISI engineering for the new product introduction to: Create product supplier landscapes to determine launch readiness and report to management.
  • Develop supplier ramp readiness plans by judging business risk based on forecast, supplier capacity, quality performance, and process capability.
  • DFM by engaging suppliers early in development cycle to feedback manufacturability improvements in the designs prior to production.
  • Influence and guide Engineering in choosing suppliers by determining selection criteria for preferred suppliers and leading the team effort to evaluate preferred suppliers.
  • Review, analyze and close customer complaints, manufacturing variance requests, and first article inspections by judging risk analyses and justifications.


Required Skills and Experience

  • Minimum 7 years related experience with an BS Engineering degree or 5 years’ experience with MS in Engineering.
  • Excellent written and verbal communication skills including presentations to executive level management.
  • Excellent Interpersonal skills and team building skills.
  • A proven history of implementing Lean/6 Sigma/SPC Programs at suppliers.
  • Excellent Project Management skills.
  • Excellent analytical and problem-solving skills along with good judgment.
  • Demonstrable knowledge in evaluating and challenging supplier technical, quality, and business capabilities.
  • Demonstrable knowledge of a wide range of manufacturing processes including understanding of key input variables for quality, cost, and capacity (Specialization can be in cable assembly, wire cutting, termination, crimping, Soldering, overmold)

Working Conditions

  • Ability to travel to suppliers on an as-needed basis – domestic and international.

Preferred Skills and Experience

  • 4-7 years of engineering experience in cable assembly, wire harness production, or electromechanical manufacturing.
  • The ideal Candidate possesses broad and deep hands-on cable assembly experience along with wire cutting, stripping, crimping, soldering,


About Maxonic:

Since 2002 Maxonic has been at the forefront of connecting candidate strengths to client challenges. Our award winning, dedicated team of recruiting professionals are specialized by technology, are great listeners, and will seek to find a position that meets the long-term career needs of our candidates. We take pride in the over 10,000 candidates that we have placed, and the repeat business that we earn from our satisfied clients.


Interested in Applying?

Please apply with your most current resume. Feel free to contact Manish Rajput ( /(4 for more details.

Not Specified
Process Improvement Specialist
✦ New
Salary not disclosed
Middle River, MD 2 hours ago

Must Haves:

  • Experience with process improvement across multiple different business groups
  • Identifying inefficiencies
  • Investigating and implementing ways to reduce cost
  • Maintaining and developing flowsheets for operations
  • Create accurate time standards for different phases of a job
  • Must be detail oriented
  • Experience in manufacturing, logistics, or warehouse
  • Experience using Excel for data entry
  • Knowledge of data capture
  • Comfortable communicating with the shop floor operators and manager level personnel
  • 80% of your day will be spent on Shop Floor
  • Go getter personality

Nice to Have:

  • Engineering Degree
  • Knowledge of CAD tools – AutoCad, CATIA, or SolidWorks

Day-To-Day:

A client of Insight Global is looking for a Process Improvement Specialist to sit fully onsite in Middle River, MD. They will be joining a team of 3 and working to improve processes across all business units. In this role, you will focus on improving business processes by identifying inefficiencies and implementing cost-reduction strategies. A typical day may involve analyzing workflows, maintaining, and developing operational flowsheets, and establishing accurate time standards for different job phases. You will regularly use Excel for data entry and data capture, ensuring precision in reporting and analysis. Working in a manufacturing environment, you will collaborate with teams to optimize production efficiency and troubleshoot operational challenges. This position requires a keen eye for detail, problem-solving skills, and a proactive approach to continuous improvement. This is a 6 month contract and pays $25-27/hr.


Compensation:


$25/hr to $27/hr.


Exact compensation may vary based on several factors, including skills, experience, and education.


Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.

Not Specified
Process Development Associate I
✦ New
Salary not disclosed
San Diego, CA 2 hours ago

Job Description:

SUMMARY: The Process Development Associate I (PDA I) provides scientific and technical support to the Process Development (PD) team. Working under direct supervision and guidance from senior PD staff, this role is responsible for executing defined laboratory tasks and established protocols to support process characterization and optimization activities. The PDA I contributes to the production of dopaminergic precursor cells (DANPCs) from induced pluripotent stem cells (iPSCs) by performing routine cell culture experiments, maintaining laboratory operations, and assisting with data collection and documentation in accordance with established procedures.


DUTIES AND RESPONSIBILITIES:

• Under supervision, perform routine laboratory experiments following established protocols to support defined unit operations and process characterization studies. • Support PD study execution by assisting designated study leads with protocol preparation, daily cell culture maintenance, sample handling, and preparation for downstream testing activities.

• Perform cell culture activities using established aseptic techniques, including media preparation and routine culture maintenance, in accordance with standard operating procedures.

• Collect experimental data and assist with data organization, review, and documentation; contribute to summaries and reports under guidance.

• Maintain accurate and timely laboratory documentation in compliance with departmental and quality requirements.

• Prepare or help verify cell culture media preparation to support ongoing experiments within the PD team.

• Support cross functional activities by coordinating with teams such as Analytical Development, Manufacturing Operations, MSAT, Device, and Research as directed.

• Assist with tracking and maintaining laboratory inventory, including media, reagents, and consumables, and support material forecasting activities as assigned.


EDUCATION AND EXPERIENCE:

• Bachelor’s degree in Bioengineering, Biomedical Engineering, Molecular Biology, Neuroscience, or a related scientific discipline is required.

• Entry level experience in academic research laboratories or a relevant industry setting is preferred.

• Cell Culture & Aseptic Technique: Foundational experience with mammalian cell culture and aseptic laboratory techniques in an academic or industry setting.

• Protocol Adherence: Ability to follow established methods, procedures, and standard operating protocols with attention to detail and accuracy.

• Data Analysis & Tools: Basic proficiency with data analysis tools or commercially available software used for scientific data evaluation.

• Documentation & Organization: Strong organizational skills with the ability to maintain accurate, timely, and compliant laboratory documentation.

• Collaboration & Teamwork: Ability to work effectively in a collaborative, team-oriented environment and support cross-functional activities as directed.

• Communication Skills: Clear written and verbal communication skills, with the ability to receive direction and provide status updates to senior staff.


WORKING CONDITIONS

Office and Lab environment. While performing the duties of this Job, the employee is frequently exposed to some toxic or caustic chemicals. This is an indoor position requiring the ability to perform experiments in the laboratory and use a computer. Some Cleanroom access is required


PHYSICAL DEMANDS While performing the duties of this Job, the employee is Regularly required to stand; walk; sit; use hands to finger, handle, or feel; reach with hands and arms and talk or hear. The employee must occasionally lift and/or move up to 20 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. These work environmental characteristics are representative of the environment the job holder will encounter. Reasonable accommodation may be made to enable people with disabilities to perform the essential functions of the job.

Not Specified
Process Engineering Manager, Oral Dosage Forms
🏢 Kelly
Salary not disclosed

Kelly® Science & Clinical is seeking a Process Engineering Manager for a direct hire opportunity with one of our clients, a leading small molecule CDMO at their Colorado Springs, CO facility. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.


Workplace: Onsite in Colorado Springs, CO


Position Title: Process Engineering Manager, Oral Dosage Forms


Position Type: Direct hire


Salary: $125,000-140,000


Are you ready to drive innovation and success in pharmaceutical manufacturing? We are seeking a dynamic Principal Investigator to serve as a technical authority in process development, scale-up, and technology transfer. If you thrive in collaborative, fast-paced environments and are passionate about advancing life-changing therapies, this is your opportunity to make a significant impact.


Responsibilities


Strategic Process Development & Scale-Up

  • Spearhead the development and scale-up of robust, scalable manufacturing processes across a wide spectrum of drug products
  • Design and lead process characterization and optimization studies, defining critical process parameters and proven acceptable ranges
  • Champion Quality by Design (QbD) strategies and advanced statistical methodologies, ensuring seamless progression from laboratory concepts to pilot-scale execution


Technology Transfer Leadership

  • Serve as the technical lead for all technology transfer activities, bridging R&D, global manufacturing sites, and client partners
  • Develop and implement comprehensive transfer protocols and process equivalence strategies to ensure flawless execution
  • Lead high-performing, cross-functional teams through knowledge transfer, process mapping, and documentation best practices


Pilot Plant & cGMP Operations Management

  • Oversee cGMP-compliant pilot plant operations, supporting clinical and commercial production, validation, and process improvement
  • Drive continuous improvement projects—maximizing efficiency, quality, and yield
  • Provide expert troubleshooting and manage deviations, ensuring on-time project delivery


Capital Projects & Facility Optimization

  • Lead equipment qualification and validation for cutting-edge process installations
  • Direct facility expansion and modification projects to support innovation and new technology implementation
  • Optimize facility workflows to enhance operational excellence and scalability


Quality Assurance & Regulatory Compliance

  • Ensure strict adherence to cGMP (21 CFR 210/211) and data integrity (21 CFR 11) regulations
  • Develop and execute robust process validation strategies in accordance with global regulatory standards
  • Lead investigations, implement corrective/preventive actions, and maintain perpetual audit readiness


Project Management & Client Engagement

  • Manage multiple, high-profile client technology transfer programs—delivering on time and within budget
  • Serve as the primary technical liaison for clients, providing strategic insight and technical guidance
  • Develop detailed project plans, risk assessments, and contingency strategies to de-risk tech transfer activities
  • Mentor cross-functional teams, fostering a culture of excellence and innovation


Qualifications


Education:

  • Bachelor’s degree in Engineering, Pharmaceutical Sciences, or related field; advanced degree (MS/PhD) preferred


Experience:


  • 8+ years’ experience (Bachelor’s), 5+ years (MS), or 3+ years (PhD) in pharmaceutical process development, technology transfer, and scale-up within a CDMO or CRO environment
  • Demonstrated success managing complex, cross-functional projects in a regulated setting


Technical Mastery

  • Deep expertise in pharmaceutical process engineering, manufacturing technologies, process validation, and equipment qualification
  • Comprehensive understanding of cGMP, quality systems, and regulatory compliance
  • Proven skills in process automation, risk management, and project execution


Leadership & Collaboration

  • Recognized leadership in guiding technical teams and cross-functional project groups
  • Outstanding client relationship management and communication abilities
  • Strategic thinker with a results-driven mentality, adept at navigating complex challenges and inspiring teams


Why Join Us?

  • Work alongside industry leaders and innovators
  • Participate in high-impact projects accelerating life-saving therapies to market
  • Competitive salary, comprehensive benefits, and opportunities for continued professional growth


What happens next:

Once you apply, you’ll proceed to the next steps if your skills and experience look like a good fit. But don’t worry – even if this position doesn’t work out, you’re still in our network. That means our team of expert Science & Clinical recruiters will have access to your profile, making your opportunities limitless.

Not Specified
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