Product Release Specialist (11:00AM-7:30PM)
Cytiva
Wayland, MAHelp us improve access to life-changing therapies that can transform human health
We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.
Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.
We are looking for a Product Release Specialist to work with our expert Quality Assurance team of employees across the world. Do you have a passion for Quality? Then we would love to hear from you.
What you’ll do
- Responsible for quality release of finished good products to packaging for shipment.
- Analyze and review manufacturing and test data in written or electronic form to verify accuracy and completeness necessary for the final release. This also includes subcontractor records when product is processed by a 3rd party (i.e. sterilizer records).
- Create tasks in electronic batch record data collection system to resolve product and process discrepancies.
- Issue Certificate of Quality for final product release when all release requirements have been verified and met.
- Provide consultation and guidance to other groups concerning documentation completeness, accuracy as well as related manufacturing quality management systems and processes.
- Collaborate timely with Cross functional teams to aid effective investigations & problems solving
- Interface with manufacturing to coordinate product release activities to best support production build and shipping schedules.
- Provide input for deviations and product concessions. Support Quality Assurance Engineers with deviation, investigation, and rework documentation review.
- Continually identify, recommend and implement process improvements with a lean and quality focus.
- Comply with EHS regulations & policies.
- Responding to routine quality related queries from other departments.
- Monitoring and aiding the implementation of continuous improvements and process changes to ensure these are implemented in compliance with GMP.
Who you are
- Demonstrated knowledge of Quality Management System Tools and continuous improvement methodologies.
- Demonstrated collaboration, negotiation & conflict resolution skills.
- Effective communication skills (written and oral).
- Ability to multi-task & handle tasks with competing priorities effectively.
- Technical aptitude (i.e. able to read & comprehend technical documentation & execute procedures).
- Experience with generating, tracking and interpreting quality metrics.
- Demonstrate support to a positive quality culture
- 1-year experience in a medical device or pharmaceutical industry.
- 1-year experience with CA/PA systems, including complaint handling.
- Thorough familiarity with cGMPs of sterile product manufacture.
- Knowledge of relevant Electronic Management Systems transactions and familiarity with Excel / Word packages.
Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.
Want to know more? Experience life at Cytiva on our Careers website, Instagram channel and LinkedIn page!
Cytiva is a 3.5 billion USD global life sciences leader with over 7000 associates across 40 countries who are dedicated to our mission to help us improve access to life-changing therapies that transform human health. As a trusted partner to customers that range in scale and scope, Cytiva brings efficiencies to research and manufacturing workflows, ensuring the development, manufacture and delivery of transformative medicines to patients.
Cytiva is part of the Danaher family of companies, a global science and technology innovator committed to helping customers solve complex challenges and improving quality of life around the world.
Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here.
Product Release Specialist (11:00AM-7:30PM)
Cytiva
Sudbury, MAHelp us improve access to life-changing therapies that can transform human health
We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.
Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.
We are looking for a Product Release Specialist to work with our expert Quality Assurance team of employees across the world. Do you have a passion for Quality? Then we would love to hear from you.
What you’ll do
- Responsible for quality release of finished good products to packaging for shipment.
- Analyze and review manufacturing and test data in written or electronic form to verify accuracy and completeness necessary for the final release. This also includes subcontractor records when product is processed by a 3rd party (i.e. sterilizer records).
- Create tasks in electronic batch record data collection system to resolve product and process discrepancies.
- Issue Certificate of Quality for final product release when all release requirements have been verified and met.
- Provide consultation and guidance to other groups concerning documentation completeness, accuracy as well as related manufacturing quality management systems and processes.
- Collaborate timely with Cross functional teams to aid effective investigations & problems solving
- Interface with manufacturing to coordinate product release activities to best support production build and shipping schedules.
- Provide input for deviations and product concessions. Support Quality Assurance Engineers with deviation, investigation, and rework documentation review.
- Continually identify, recommend and implement process improvements with a lean and quality focus.
- Comply with EHS regulations & policies.
- Responding to routine quality related queries from other departments.
- Monitoring and aiding the implementation of continuous improvements and process changes to ensure these are implemented in compliance with GMP.
Who you are
- Demonstrated knowledge of Quality Management System Tools and continuous improvement methodologies.
- Demonstrated collaboration, negotiation & conflict resolution skills.
- Effective communication skills (written and oral).
- Ability to multi-task & handle tasks with competing priorities effectively.
- Technical aptitude (i.e. able to read & comprehend technical documentation & execute procedures).
- Experience with generating, tracking and interpreting quality metrics.
- Demonstrate support to a positive quality culture
- 1-year experience in a medical device or pharmaceutical industry.
- 1-year experience with CA/PA systems, including complaint handling.
- Thorough familiarity with cGMPs of sterile product manufacture.
- Knowledge of relevant Electronic Management Systems transactions and familiarity with Excel / Word packages.
Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.
Want to know more? Experience life at Cytiva on our Careers website, Instagram channel and LinkedIn page!
Cytiva is a 3.5 billion USD global life sciences leader with over 7000 associates across 40 countries who are dedicated to our mission to help us improve access to life-changing therapies that transform human health. As a trusted partner to customers that range in scale and scope, Cytiva brings efficiencies to research and manufacturing workflows, ensuring the development, manufacture and delivery of transformative medicines to patients.
Cytiva is part of the Danaher family of companies, a global science and technology innovator committed to helping customers solve complex challenges and improving quality of life around the world.
Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here.
Product Release Specialist (11:00AM-7:30PM)
Cytiva
Maynard, MAHelp us improve access to life-changing therapies that can transform human health
We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.
Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.
We are looking for a Product Release Specialist to work with our expert Quality Assurance team of employees across the world. Do you have a passion for Quality? Then we would love to hear from you.
What you’ll do
- Responsible for quality release of finished good products to packaging for shipment.
- Analyze and review manufacturing and test data in written or electronic form to verify accuracy and completeness necessary for the final release. This also includes subcontractor records when product is processed by a 3rd party (i.e. sterilizer records).
- Create tasks in electronic batch record data collection system to resolve product and process discrepancies.
- Issue Certificate of Quality for final product release when all release requirements have been verified and met.
- Provide consultation and guidance to other groups concerning documentation completeness, accuracy as well as related manufacturing quality management systems and processes.
- Collaborate timely with Cross functional teams to aid effective investigations & problems solving
- Interface with manufacturing to coordinate product release activities to best support production build and shipping schedules.
- Provide input for deviations and product concessions. Support Quality Assurance Engineers with deviation, investigation, and rework documentation review.
- Continually identify, recommend and implement process improvements with a lean and quality focus.
- Comply with EHS regulations & policies.
- Responding to routine quality related queries from other departments.
- Monitoring and aiding the implementation of continuous improvements and process changes to ensure these are implemented in compliance with GMP.
Who you are
- Demonstrated knowledge of Quality Management System Tools and continuous improvement methodologies.
- Demonstrated collaboration, negotiation & conflict resolution skills.
- Effective communication skills (written and oral).
- Ability to multi-task & handle tasks with competing priorities effectively.
- Technical aptitude (i.e. able to read & comprehend technical documentation & execute procedures).
- Experience with generating, tracking and interpreting quality metrics.
- Demonstrate support to a positive quality culture
- 1-year experience in a medical device or pharmaceutical industry.
- 1-year experience with CA/PA systems, including complaint handling.
- Thorough familiarity with cGMPs of sterile product manufacture.
- Knowledge of relevant Electronic Management Systems transactions and familiarity with Excel / Word packages.
Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.
Want to know more? Experience life at Cytiva on our Careers website, Instagram channel and LinkedIn page!
Cytiva is a 3.5 billion USD global life sciences leader with over 7000 associates across 40 countries who are dedicated to our mission to help us improve access to life-changing therapies that transform human health. As a trusted partner to customers that range in scale and scope, Cytiva brings efficiencies to research and manufacturing workflows, ensuring the development, manufacture and delivery of transformative medicines to patients.
Cytiva is part of the Danaher family of companies, a global science and technology innovator committed to helping customers solve complex challenges and improving quality of life around the world.
Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here.
Senior Mechanical Engineer
Ametek, Inc.
Wilmington, MAPosition Description:
Ametek Aerospace & Defense is looking for a highly collaborative problem-solver with a natural curiosity about mechanical devices to join us as a Senior Mechanical Engineer in our Wilmington, MA facility. This position will specialize in the development of aerospace components with a specialty in fluid and fuel level sensors and flowmeters. We are seeking a self-starter with mechanical design engineering experience in a manufacturing environment who possesses excellent technical and project management capabilities. This individual will join a global, multi-site business unit that designs and manufactures highly engineered sensors and fluid management systems for aerospace applications.
• Position is for a success-oriented individual with demonstrated experience in the design, manufacture, test & certification of electromechanical devices such as pressure sensors, liquid level sensors, temperature and flow sensors and fuel gauging products.
• Responsible for integrating design for six sigma, reliability & manufacturability into each product design while achieving customer objectives of performance and schedule.
• Will also develop new technologies to sustain competitive advantage, as well as working within a mutli-disciplined team environment.
Position Requirements:
• Must have a strong blend of technical, project & positive customer relationship building experience.
• Requires exceptional written, verbal & interpersonal skills, as well as demonstrated strong use of analytical skills, including FEA.
• Bachelor’s Degree in Mechanical Engineering required
• Master’s Degree in Mechanical, Electrical, or Aerospace Engineering is a plus
• SolidWorks certification is a plus
• 5+ years designing electromechanical sensing devices in a regulated industry, such as aerospace, defense, automotive or medical devices
• Knowledge and understanding of fluid, fuel or flowmeter technology preferred
• Proficiency with geometric dimensioning and tolerancing (GD&T)
• Knowledge and understanding of aerospace components is a plus
• Proficiency in SolidWorks version 2010 or later
• Expertise in designing for a severe vibration and thermal environment
• Knowledge of Finite Element Analysis a plus
• Open to continuous change with the ability to learn new skills
• Proven hands-on capability in the workplace
• Self-motivated, self-starter, strong work ethic, self-advocate
• Able to function (often simultaneously) as an individual contributor, a team member, and a leader supporting various activities
• Organized and analytical, able to eliminate obstacles through creative and adaptive approaches
• Highly collaborative individual with outstanding written and verbal communication skills and team player attitude
• Well-developed problem-solving skills and the demonstrated ability to be self-directed and effectively relate to all levels of an organization
• Ability to work well under pressure, multi task and meet deadlines while remaining flexible on changing work priorities
• Computer skills to include Word, Excel in addition to SmarTeam (or equivalent PDM/PLM system) and SolidWorks
We are an Equal Opportunity Employer and do not discriminate against
any employee or applicant for employment because of race, color, sex,
age, national origin, religion, sexual orientation, gender identity,
status as a veteran, and basis of disability or any other federal,
state or local protected class.
.
Senior Manufacturing Engineer
Ametek, Inc.
Wilmington, MAPosition Description:
• Investigate and effectively resolve critical production issues.
• Represent the operations department on multiple new product development projects.
• Optimize and document manufacturing methods and processes required to meet design objectives on new or improved products/processes.
• Design and coordinate the manufacturing of fixtures and tooling.
• Interface with customer, engineering, and supplier quality contacts during reviews, audits, and on-site visits.
• Participate in Root Cause / Corrective Action projects to address critical quality, design, and process issues.
• Lead PFMEA (Process Failure Mode Effects Analysis) efforts.
• Actively support Material Review Board activities in accordance with AS9100 requirements.
• Ability to layout work areas to optimize product flow.
• Ability to work flexible hours (including some weekends).
• Able to work collaboratively with shop technicians.
• Support lean six sigma initiatives including 5S and continuous improvement projects.
Position Requirements:
• Bachelor’s Degree in Manufacturing, Mechanical or Electrical Engineering, or Engineering Technology is required.
• Additional Training & Certifications in manufacturing related operations are a plus.
• Minimum of 5 years working as a Manufacturing, Production, or Industrial Engineer in an ISO9100 and/or AS9100 compliant manufacturing facility. Aerospace manufacturing experience preferred.
• Direct experience with the design and fabrication of fixtures and tooling using SolidWorks.
• Direct experience with planning assembly operations and writing shop floor Routings and work instructions.
• Demonstrated ability to effectively communicate technical information to internal & external customers.
• Management of multiple simultaneous projects to successful completion in accordance with established schedules and milestones.
• Experience working in a multi-location organization with offsite management is preferred.
• Prior experience with FAA or other regulated environments.
• Prior experience with soldering, welding, brazing, and other electro-mechanical assembly operations.
• Strong written and verbal communication skills.
• General understanding of GD&T (Geometric Dimensioning and Tolerancing) concepts for manufacturability.
• Excellent multi-tasking skills to work several projects at one time.
• Open to continuous change with the ability to learn new skills.
• Proven hands-on capability in the workplace.
• Self-motivated, self-starter, strong work ethic, self-advocate.
• Ability to work well under pressure, multi-task and meet deadlines.
• Able to function (often simultaneously) as an individual contributor, a team member, and a leader supporting various activities.
• Proven team player who has demonstrated capabilities in the following areas: interpersonal skills, well developed problem-solving skills; solid organizational skills; and the demonstrated ability to be self-directed and effectively relate to all levels of an organization.
• Must be willing to travel up to 10% of the time.
We are an Equal Opportunity Employer and do not discriminate against
any employee or applicant for employment because of race, color, sex,
age, national origin, religion, sexual orientation, gender identity,
status as a veteran, and basis of disability or any other federal,
state or local protected class.
.
Additional Information:
- Travel Percentage: 10%
Principal Quality Engineer
Textron
Wilmington, MADescription
Who We Are
Textron Systems is part of Textron, a $14 billion, multi-industry company employing 35,000 talented makers, thinkers, creators and doers worldwide. We make things that fly, hover, zoom and launch. Things that move people. Protect soldiers. Power industries. We serve customers in industries spanning aerospace and defense, specialized vehicles, turf care and fuel systems.
About This Role
We believe people should love what they do – in this role, you will be responsible for:
The Quality Engineer, reporting to the Manager, Quality Assurance will perform three primary roles within the Quality Engineering function:
Performs Quality Engineering assignments requiring independent evaluation, selection, and application of standard Quality Engineering techniques, procedures, and criteria using judgment and ingenuity in making adaptations and modifications.
Performs Quality Management Systems assignments requiring AS9100 System auditing, root cause and corrective action analysis and Performs Receiving and In-Process Inspection assignments 10% of the time requiring product verification, documentation validation, and associated systems transactions.
Responsibilities:
+ Reviews customer contracts and responsible for requirements analysis, identification and definition.
+ Prepares proposal bid documentation for Quality.
+ Interfaces with Supplier Quality Engineering to provide guidance and support for supplier issues.
+ Works with senior level Engineers on general systems engineering processes.
+ Performs Quality Engineering using defined software tools and applications.
+ Performs inspections using inspection tools and techniques.
+ Performs quality planning activities including development of Quality Plan, and Inspection Plan documents as required by the assigned project(s). Performs design document reviews as appropriate for the assigned project(s).
+ Participates in process improvement activities through monitoring, root cause investigations, auditing, failure analysis etc. Participates in Program Management activities appropriate to the assigned project(s).
+ Participates in Contract Data Requirements List development, review and delivery to the customer as required by the assigned project(s).
+ Utilizes industry and Quality Management System concepts, policies and procedures.
+ Assists in gauging and calibration activities as necessary.
+ Assists in developing fabrication/build processes and standards.
+ Participates in Material Review Board (MRB) disposition activities.
+ Utilizes general understanding of industry and military specifications and standards in performance of the assigned Quality Engineering functions.
+ Utilizes specialized Quality Engineering skills in performance of the assigned tasks.
+ Interfaces with internal organizations and systems in performance of the assigned Quality Engineering functions.
+ Communicates well, both written and verbal, with all the interfacing functions. Maintains good interpersonal skills and demonstrates leadership skills necessary for the position.
+ Conducts internal QMS audits and participates in external registrar or customer audits.
Qualifications
Position Requirements:
Knowledge of Quality Engineering and manufacturing process.
Technical knowledge of inspection and test techniques.
Working knowledge of Microsoft Office software.
Knowledge of statistical techniques and applications
Knowledge of Quality Management Systems (AS9100 and/or ISO9001) and concepts.
Holds or has the ability to obtain a Secret Clearance.
Effective written and oral communication skills.
Technical writing ability.
Ability to analyze specifications, drawings, procedures and schematics.
Ability to apply logical, scientific or analytical thinking to a wide range of intellectual and practical problems.
Effective ability to organize and prioritize assigned tasks.
Ability to effectively resolve material review actions.
Ability to effectively present information in one-on-one and group situations to customers and other employees of the organization.
Education:
+ Bachelors Degree in Engineering with 5 or more years related experience or Masters Degree in Engineering/with applicable quality experience.
+ Experience in/exposure to quality engineering preferred.
+ Software development experience would be a plus.
This position requires use of information which may be subject to the International Traffic in Arms Regulations (ITAR). All applicants must be U.S. persons within the meaning of ITAR. ITAR defines a U.S. person as a U.S. Citizen, U.S. Permanent Resident (i.e. 'Green Card Holder'), Political Asylee, or Refugee
How We Care
At Textron Systems, our talented people make us successful. We promote an inclusive environment where we value individuality, differences, and unique perspectives.
Our Company is committed to offering employees opportunities to grow and develop. Our benefits and compensation packages are designed to help our talented employees excel and achieve their goals, so they can make a difference every day in and outside of the workplace. Below are just a few examples!
+ Flexible Work Schedule
+ Education Assistance
+ Career Development & Training Opportunities
+ Wellness Program (including Fitness Reimbursement)
+ Medical, Dental, Vision & 401(K) with Company Funding
+ Paid Parental Leave
Are you a Military Veteran?
Textron's products and services are trusted everyday by those who protect our country. We are dedicated to hiring these Veterans and aim to translate their skills to make an impact on our Company.
EEO Statement
Textron is committed to providing Equal Opportunity in Employment, to all applicants and employees regardless of, race, color, religion, gender, age, national origin, military status, veteran status, handicap, physical or mental disability, sexual orientation, gender identity, genetic information or any other characteristic protected by law.
Pay Transparency Policy Statement
The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise, have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.
Job Quality
Primary Location US-Massachusetts-Wilmington
Recruiting Company Textron Systems
Schedule Full-time
Job Level Individual Contributor
Shift First Shift
Req ID: 289791
Director, Operations Engineering
Symbotic
Wilmington, MASymbotic’s talented and diverse workforce develops disruptive robotic solutions for warehouse automation and supply chain transformation, drives results and focuses on customer satisfaction. Our modular and scalable solutions utilize existing space and high-speed robotics combined with proprietary software and technology. Since forming in 2007, Symbotic has grown to over 700 employees in North America and supports an impressive, high-profile customer base. We seek candidates who are passionate about our solution and approach problem solving with a creative mind and a commitment to excellence. If you seek a challenge and want to impact the way the world distributes product from manufacturers to store shelves, we invite you to join our team.
Job DescriptionSymbotic is searching for an innovative, solutions-focused Director of Operations Engineering to be a part of our exciting initiative of scaling the next generation of world-class industrial supply chain and warehouse automation equipment. You will be the connection point between our customers Distribution Centers and our Engineering, Logistics, Manufacturing, Material Planning, Quality and Supply Chain teams.
You will lead and collaborate with talented engineers to support the operational execution of Symbotic’ s warehouse automation systems. This includes collaborating with system integrators and contract manufactures to ensure products are built and tested to design requirements. Hardware Engineering will release designs to Ops Engineering for DFx feedback, manufacturing and supply chain technical execution.
You will build and lead a team of engineers that are responsible for executing on complex cross-functional projects and programs that focus on autonomous robots, robotic work cells, and material handling equipment. This includes being responsible for the Ops Engineering support functions of mechanical engineering, test strategy and development engineering, electrical engineering, and process/industrial engineering.
Successful candidates are self-starters who have demonstrated engineering competencies and experience with industrial automation warehousing equipment including robotics. You must be hands-on, and able to succeed within a high change, scaling environment.
RESPONSIBILITIES:
- In collaboration with supply chain own the technical execution and implementation of new products and product change releases into our internal factories, external suppliers, integrators, and field deployments.
- Partner with Strategic Sourcing team to define sourcing strategies, qualify new suppliers, expand the supply base, and support partner development efforts.
- Manage the full review and approval of vendor documentation required for factory build and configuration management.
- Simultaneously manage multiple high-visibility projects and tasks while effectively influencing, and communicating with internal and external business partners, integrators, contract manufacturing partners and sub-component suppliers and field deployment projects.
- Collaborate with internal teams and external suppliers to generate high quality, cost effective solutions, and deliver results on-time.
- Develop scalable technical strategies that support product quality, cost, and delivery objectives in collaboration with strategic suppliers and hardware engineering.
- Collaborate with Quality to implement supplier scoring systems to measure critical KPIs and enhance supplier performance, partnering with the supplier to identify quality and reliability goals for key suppliers, and develop risk and status reporting mechanisms for the team.
- Work closely with vendors, suppliers, and other teams to operationally execute on new product designs and product changes, ensuring timely manufacturing, high quality, and on-time delivery.
- Implement continuous and transformational initiatives to drive step change improvements in supplier and factory capacity, product cost, factory and field quality, and field deployment efficiencies.
- Develop and validate test platform and mechanical tools to ensure that product quality metrics are achieved.
- Engage in early product development life cycle, representing operations in design reviews, design for cost, quality, and test. (DFx). The Ops Engineering team will provide technical support for driving root-cause corrective action, hardening of product solution and by serving as a bridge between field operations, product design teams and strategic suppliers.
- Drive Ops Engineering best practices (e.g., operational excellence, safety, quality, performance, etc.) and set standards for project execution results.
BASIC QUALIFICATIONS:
- Bachelor’s degree in mechanical or electrical engineering
- 10 years of experience in a similar field working with the designs of complex automated material handling equipment and robotics encompassing design/innovation, manufacturing/process/test engineering/industrial engineering.
- 10 years of experience managing and leading a team of 5 engineers.
- Experience with industrial and embedded controls used within industrial automation equipment
- Experience with MHE and packaging lines or process design based on Lean Manufacturing techniques
- Demonstrated experience leading engineering/product projects and interacting with cross-functional teams while being highly collaborative.
- Experience scaling supply chain operations and developing high performing teams within a fast growth, high change technology company.
ADDITIONAL QUALIFICATIONS:
- Experience in partnering with global system integrators and contract manufacturers.
- Experience with DFMEA analysis
- Experience with complex automated material handling equipment, packaging technologies, and systems including robotics and high-speed manufacturing.
- Demonstrated experience with Six Sigma or Lean/Kaizen methodologies and tools to facilitate team problem solving and design for Six Sigma input.
- Leadership abilities with proven ability to build a high-performing team.
- Operations Management/ Fulfillment/Distribution Center experience preferred.
- Capital project management skills.
- Design-in-Safety experience.
- Ability to work independently in a fast-paced and rapidly changing environment.
- Ability to manage, influence, negotiate, and communicate with external business partners and internal teams to meet organizational capacity needs.
Additional Information
Symbotic offers competitive compensation and a dynamic, growing company environment. Benefits include very comprehensive coverage for medical, dental, life, disability, flexible spending accounts, and more.
Symbotic is an equal opportunity employer. We do not discriminate based on age, gender, physical or mental disability, nation of origin, veteran status, religious beliefs, sexual identity or expression. Symbotic supports a diverse workforce and we are committed to a work environment free of discrimination and harassment, where all are treated with dignity and respect.
Test Engineer IV
Textron
Wilmington, MADescription
Job Summary:
+ The Textron Team is seeking experienced test engineers to support a major US Air Force Strategic Program. The Test Engineer will perform planning, coordination, and execution of component, subsystem, and full system tests as well as evaluation activities across the program. A strong candidate will possess 10 years of experience in a Test Engineering role. You will have the opportunity to work in a multi-functional team environment and directly support our nation’s war fighters. Whether your desired career path is technical or leadership, Textron is highly diversified with a strong grow-from-within philosophy that offers exceptional opportunities for career progression.
Qualifications
Position Responsibilities:
+ Plan, coordinate, schedule and lead test activities to ensure that test requirements and objectives are met per customer/program requirements and engineering and quality standards
+ Prepare, support and/or review test plans, test requests, test readiness reviews and test reports
+ Lead both in-house and field data collection activities including setup and operation of high speed cameras, telemetry systems, onboard instrumentation, data recorders, and safe handling of explosives
+ Perform preliminary “quick-look” analysis and provide post-test de-brief to engineering team and customers
+ Coordinate with appropriate program, engineering and external organizations during test planning, execution, analysis and reporting phases
+ Must be able to communicate effectively (verbal and in writing) and have good organizational skills
+ Ability to obtain a security clearance is required
Education Requirements:
+ Bachelor’s Degree in Engineering is required. Aeronautical, Aerospace or Mechanical Engineering is preferred.
EEO Statement
Textron is committed to providing Equal Opportunity in Employment, to all applicants and employees regardless of, race, color, religion, gender, age, national origin, military status, veteran status, handicap, physical or mental disability, sexual orientation, gender identity, genetic information or any other characteristic protected by law.
Pay Transparency Policy Statement
The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise, have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.
Job Engineering
Primary Location US-Massachusetts-Wilmington
Recruiting Company Textron Systems
Schedule Full-time
Job Level Individual Contributor
Shift First Shift
Req ID: 289682
Principal Systems Engineer - Surgical Robotic Innovations
Medtronic
Massachusetts, MA- Reporting to the Manager of Software Systems Engineering, you will contribute to system level documentation including: Defining software behavior from user workflows, allocating performance budgets between subsystems, and defining interfaces and capturing system functional breakdown.
- Develop a detailed set of use cases and requirements through documenting and deriving capabilities that are needed from a cybersecurity perspective for a safe and effective surgical robotic system.
- Identifying cyber threats and help the product team architect, design and deliver secure systems.
- Perform threat and risk analysis and define mitigations in line with risk acceptance criteria.
- Employ best practices when implementing security controls within a system including software engineering methodologies; system and security engineering principles; secure design, secure architecture, and secure coding techniques
- Excellent communication and collaboration skills is a must.
Qualifications
- Bachelors degree requiredand minimum of 7 years of relevant experience, or advanced degree with a minimum of 5 years of relevant experience
- A minimum of a Bachelors in Engineering or Computer Science, or equivalent
- Minimum of 5 years experience as a contributing member of engineering projects
- Strong organization acumen with the ability to communicate effectively to non-technical audiences
- Strong knowledge of the technical aspects of software engineering (C++, C#, Matlab, Simulink, python, Qt) is a plus
- Experience with risk management process e.g. FMEA
- Advanced knowledge of system-level hardware and software design and development, requirements definition, analysis, and risk mitigation
- Proven track record contributing to products of high complexity in a regulated environment
- Experience working with multiple teams on concurrent, interdependent projects
- Solid understanding of structured product development (requirements-driven engineering, documentation, rigorous verification, etc)
- Demonstrated skills in self managing priorities
- Fluency in English required
- Experience or knowledge of Enterprise Architect.
- Experience or knowledge of JIRA.
- Experience or knowledge with JAMA.
- Remote work from home and standard office setting
- Based in Boston, MA
- Infrequent travel may be required
R&D Materials Engineer I
Medtronic
Massachusetts, MACareers that Change Lives
Medtronic’s Coronary and Structural Heart (CSH) business – Danvers, Ma location, is looking for an R&D Materials Engineer Ithat will provide Extrusion, Braiding and Injection Molding support for Danvers Shared Technology Center group in a flexible environment. Medtronic is intensely focused on creating a workplace environment which reflects our standing as the world’s top medical device company. The person that takes this role will be expected to play an active role in development of tubing, braided shafts, molding components used to support all Medtronic sites with their development and validation needs.
The ideal candidate will have a passion for the patients we serve and an unrelenting desire to improve our business. The candidate will be motivated and must have exceptional soft skills that will be used to work with a team.
We value what makes you unique. Be a part of a company that thinks differently to solve problems, make progress, and deliver meaningful innovations.
Position Description
This R&D Materials Engineer position will have an emphasis in the development of tubing and braided shafts using extrusion polymer processing skills used to support all Medtronic sites with their development and validation needs.
A Day in the Life
• This position will have an emphasis in technical support in extrusion development, prototyping, validation and production activities. You will work with various engineers and on your own to manage projects and tasks such as:
• Communicating progress toward project objectives to senior engineers, project team members, and project manager.
• Participate with R&D in other sites in the prototype development and clinical phases of new product introduction.
• Focus on the technology and processes of medical extrusion including free extrusion, composite multi-layer extrusion, multi-lumen tubing and extrusion over a core.
• Work with technicians on the set-up, running and breakdown of extrusion equipment.
• Carry out Process Development efforts with an end goal of successfully completing Process Ranging, Characterization and Validation in support of achieving commercialization objectives and timelines.
• Generate and manage project documentation according to prescribed policies and guidelines.
• Attend and Contribute to Team meetings and Design Reviews in conjunction with assigned projects.
• Provide engineering support in product line transfers from outside facilities to Danvers.
• Work with various engineers or independently with various extrusion projects and tasks
• Develop product and process specifications.
• Provide detailed project plans and updates as required. Carry out tasks within projects to meet agreed upon timelines.
• Maintain good lab documentation practices
• Ensure Danvers Shared Technology Center strategic objectives are met. Ensures Quality, Service, Cost and Technology expectations are realized for our customers
Qualifications
Must Have:
• Bachelor’s degree with 0+ years of experience
Desired/Preferred Qualifications
• Bachelor’s degree in Engineering or Science
• Ability to travel 20-40%
• Ability to work well with others and teams
• Technical Writing Skills
• Strong Interpersonal Skills
• Good verbal and written communication skills
• Extrusion, Molding and Polymer processing background
• Knowledge of Plastics Processing (free extrusion, composite multi-layer extrusion, multi-lumen tubing and extrusion over a core)
• Knowledge of polymer materials
• Medical device experience
About Medtronic
Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.
We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let’s work together to address universal healthcare needs and improve patients’ lives. Help us shape the future.
Physical Job Requirements
The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. (ADA-United States of America)
Posted
18 days ago
Description
Help us improve access to life-changing therapies that can transform human health
We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.
Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.
We are looking for a Product Release Specialist to work with our expert Quality Assurance team of employees across the world. Do you have a passion for Quality? Then we would love to hear from you.
What you’ll do
- Responsible for quality release of finished good products to packaging for shipment.
- Analyze and review manufacturing and test data in written or electronic form to verify accuracy and completeness necessary for the final release. This also includes subcontractor records when product is processed by a 3rd party (i.e. sterilizer records).
- Create tasks in electronic batch record data collection system to resolve product and process discrepancies.
- Issue Certificate of Quality for final product release when all release requirements have been verified and met.
- Provide consultation and guidance to other groups concerning documentation completeness, accuracy as well as related manufacturing quality management systems and processes.
- Collaborate timely with Cross functional teams to aid effective investigations & problems solving
- Interface with manufacturing to coordinate product release activities to best support production build and shipping schedules.
- Provide input for deviations and product concessions. Support Quality Assurance Engineers with deviation, investigation, and rework documentation review.
- Continually identify, recommend and implement process improvements with a lean and quality focus.
- Comply with EHS regulations & policies.
- Responding to routine quality related queries from other departments.
- Monitoring and aiding the implementation of continuous improvements and process changes to ensure these are implemented in compliance with GMP.
Who you are
- Demonstrated knowledge of Quality Management System Tools and continuous improvement methodologies.
- Demonstrated collaboration, negotiation & conflict resolution skills.
- Effective communication skills (written and oral).
- Ability to multi-task & handle tasks with competing priorities effectively.
- Technical aptitude (i.e. able to read & comprehend technical documentation & execute procedures).
- Experience with generating, tracking and interpreting quality metrics.
- Demonstrate support to a positive quality culture
- 1-year experience in a medical device or pharmaceutical industry.
- 1-year experience with CA/PA systems, including complaint handling.
- Thorough familiarity with cGMPs of sterile product manufacture.
- Knowledge of relevant Electronic Management Systems transactions and familiarity with Excel / Word packages.
Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here. If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.
Want to know more? Experience life at Cytiva on our Careers website, Instagram channel and LinkedIn page!
Cytiva is a 3.5 billion USD global life sciences leader with over 7000 associates across 40 countries who are dedicated to our mission to help us improve access to life-changing therapies that transform human health. As a trusted partner to customers that range in scale and scope, Cytiva brings efficiencies to research and manufacturing workflows, ensuring the development, manufacture and delivery of transformative medicines to patients.
Cytiva is part of the Danaher family of companies, a global science and technology innovator committed to helping customers solve complex challenges and improving quality of life around the world.
Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here.