Manufacturing Engineer Jobs in New Jersey

Job Title: MANUFACTURING ENGINEER - TOOL DESIGNERS Company: Adecco Location: Mahwah, NJ Description: Manufacturing Engineer - Tool DesignersLocation: Mahwah, NJ Continuous Improvement: Manufacturing Engineer - Manufacturing Tool Designers.Support for team to Work on Gage Evaluation and Design Qualifications: HS diploma or equivalent5+ years manufacturing engineer experience Experience working with current Product Models and make detailed drawings using GD & TMust have current PRO E knowledge If you are interested in this opportunity or other opportunities available through Adecco Engineering and Technical, please apply online or email directly to Milly Rivera at Register to View or call Register to View . Adecco Engineering and Technical is an Equal Opportunity Employer.

Job Title: Operations Engineer - Manufacturing Quality Company: Adecco Engineering & Technical Location: Mahwah, NJ Description: REQUIRED:          Must have prior medical device, aerospace, automotive experience.          Process oriented, high tolerancing manufacturing experience.          Work well under pressure.           Excellent communication skills; will be on NCR Board on a daily basis.          2 - 5  years experience in a production/manufacturing environment with emphasis on general machining (milling/turning)          Ability to read blueprints and knowledge of GD&T.          Understanding of general inspection techniques, utilizing optical comparators, calipers, micrometers, height indicators, etc.          Strong communication and written skills, and must possess the ability to concisely convey issues to various levels of the organization.          Demonstrated ability to manage and execute projects to completion          Demonstrated ability to prioritize and accomplish work with little supervision (self starter) with a high level of organization. Responsibilities:Critical: Perform investigations, root cause analysis, and implement corrective actions for internal non-conformance reports (NCR).          Update internal inspection documents to reflect current requirements.          Update internal manufacturing routers          Develop/update inspections techniques to meet current quality requirements          Provide technical support to operators regarding inspection and documentation issues.          Implement Operations portion of Engineering Changes.  APPLY NOW Register to View If you are interested in this opportunity or other opportunities available through Adecco Engineering and Technical, please apply online or email directly to Register to View The Adecco Group is a Fortune Global 500 company and the global leader in HR services. Our group connects over 700,000 associates with our business clients each day through our 6,600 offices in over 70 countries and territories around the world. We offer employment opportunities at any stage in your professional career. Contact us today to discuss available contract and direct hire positions. Adecco Engineering and Technical offers benefits including Holiday, 401(k), Insurance Benefit Plans and Anniversary Bonus opportunities. Adecco Engineering and Technical is an Equal Opportunity Employer.Apply Online About Adecco North America Adecco is a Fortune Global 500 company and the world leader in workforce solutions. Our comprehensive service offering includes temporary and contract staffing, permanent recruitment, outplacement and career services, training and consulting. Adecco is an equal opportunity employer.

Job Title: Quality Assurance Engineer - Manufacturing Company: Volt Workforce Solutions Location: Neptune, NJ Description: Job Description:Quality Assurance EngineerManufacturing, Quality Assurance, Regulatory AffairsPAY RATE: $55K-$70K + 10% TARGET BONUSA medical device company is seeking to hire a Quality Assurance Engineer.POSITION OVERVIEW/DESCRIPTION:SUMMARY: The Quality Assurance Professional position is responsible for implementing and maintaining the Quality Systems and its requirements necessary to comply with regulations relevant to the market served. This includes:United States FDA regulations as required by the QS regulations and the CFR part 820 for medical devices.ISO 13485: 2003 and the Canadian Medical Devices Regulations.European Community Medical Device Directives 93/42/EEC of June 14, 1993 (MDD) requirements.PHYSICAL DEMANDS: The physical demands described here 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.Job requires employee to:Stand, walk, talk and, on occasion, provide training to individuals and/or groups. Spend approximately 50% of his/her time working on the computer.WORK ENVIRONMENT: The work environment characteristics described here are representative of those an employee encounters while performing essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.Noise level in the:Office work environment is usually quiet.Manufacturing work environment may become loud on occasion. Employee occasionally works near machinery. Working environment is dynamic and, as a result, can be stressful for some people.ESSENTIAL DUTIES AND RESPONSIBILITIES:The following are included (other duties may be assigned):Primary Responsibilities: Implement internal Quality procedures and systems to comply with regulatory requirements.Support:Management Review process to monitor and evaluate the Quality System's effectiveness.Internal investigations as a result of Customer Complaints, Corrective and Preventive action and/or nonconforming material.Internal facility audits and external vendor audits.Validation activities with respect to compliance with FDA and international requirements when needed.Manufacturing initiatives in order to:Increase manufacturing capacity.Diversify product and customer base.Maintain tracking and trending of various Quality system elements, e.g.:Customer ComplaintChange ControlNonconforming Material ReportCAPADeviationManage sustainable compliance in accordance to USP, ISO, QSR and other applicable regulations.Provide aid to Company’s 510K submissions; register products with foreign Regulatory Agencies.Process Project documents.Receive, index and file both hard and electronic copies.Scan and retrieve documents such as:SOPs (Standard Operating Procedures)ProtocolsDrawingsLabelsOther Regulatory Submission DocumentsAssist users by preparing documentation for routing and approval.Maintain documentation files with both current and prior revisions.Coordinate Training Program when needed.Actively support Product Development initiativesThis is a Direct Hire position, through Volt Workforce Solutions - a division of a Fortune 1000 publicly traded Staffing Industry Leader, based in Woodbridge, NJ. We are among the largest IT staffing companies in the US for contract/temporary and direct hire placements and support most of the top rated IT companies on the East Coast.Job Requirements:QUALIFICATION REQUIREMENTS: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.Required Skills for this Quality Assurance Engineer position include the following:EDUCATION and/or EXPERIENCE:BA/BS in Engineering or Life Sciences requiredA minimum of 4+ years experience in Manufacturing, Quality Assurance and/or Regulatory Affairs a mustLANGUAGE SKILLS: Excellent communication and presentation skills required; Spanish communication skills a plusREASONING ABILITY: Ability to define and analyze problems, collect data, establish facts and draw valid conclusions requiredAbility to interpret an extensive variety of technical instructions necessaryProven independent Project Management skillsCERTIFICATE, LICENSES, REGISTRATIONS: Education documentation required; any other licenses or registrations to Professional Societies such as American Society for Quality, etc. to be provided by the candidate at his/her discretionOTHER SKILLS and ABILITIES: Proven ability to work effectively with various discipline groups to assure conformance to Quality Assurance requirements, internal processes and policiesDemonstrated leadership ability and experienceStrong computer skills are required with proficiency in MS Office applicationsStrong attention to detail Strong interpersonal skillsSpecial Instructions to begin the process:Please email your resume to Volt at: Register to View and it will be expedited to the Recruiter assigned to this position. Our Recruiter will initiate a phone call to you and give you immediate consideration should your resume meet the job requirements.Please reference the following in your subject line to ensure your resume is routed to the correct Recruiter on your behalf: Register to View -17-255711 - Quality Assurance Engineer - Manufacturing, Quality Assurance, Regulatory AffairsIf you are able to include on the subject line the website where you saw this posting, it would be greatly appreciated!Thank you for your attention to these details!For further information regarding this posting, please contact the Recruiter using the email address listed on this posting and again by placing the entire job number in the subject line. Please rest assured that if your resume matches what is reflected in this job posting, you should get a phone call from a Volt Recruiter to discuss this position with you. Volt has a talented and optimistic staffing team focused on the quality of your career. Volt is a world leader in the staffing industry, boasting over 50 years of experience. We work with many of the Fortune 500 and 1000 companies to provide workforce solutions. We offer many contract positions as well as many direct hire full-time positions. Our Contractors receive competitive pay and benefits, as well as educational programs and re-deployment assistance.Volt Information Sciences, Inc. is our parent company and is a publicly owned corporation. Stock is traded over-the-counter and is quoted on the NYSE. To learn more about Volt Information Sciences, please visit: http://www.volt.com and to see more of our job postings, please visit: http://jobs.volt.comVolt is an Equal Opportunity Employer and is dedicated to fostering diversity in the workplace.

Job Title: Engineer - Manufacturing Engineer - Pharmaceutical Engineer - Process Engineer - Validation - Company: CyberCoders Location: Edison, NJ Description: Engineer - Manufacturing Engineer - Pharmaceutical Engineer - Process Engineer - Validation - .body .body h4 .body .section tr.oddRow a, a:link, a:visited Engineer - Manufacturing Engineer - Pharmaceutical Engineer - Process Engineer - Validation - near Raritan, NJ This job is open as of 2/20/2010. Apply Now! Not a fit for this job? Search other Engineer jobs! Are you an employer? Visit us for more info! Email this job to a friend - $1000 Location Raritan, NJ; Edison, NJ Salary $90,000 - $120,000 Education Bachelor of Science Category Engineering Experience Required At least 2 Years Short Description Engineer - Manufacturing Engineer - Pharmaceutical Engineer - Process Engineer - Validation - Required Skills Manufacturing Engineer, Pharmaceutical Engineer, Engineer, Validation, GMP, Biotechnology, Management, Process Validation, cGMP, chemical engineering Recruiter Erin Beagle Date Updated 2/20/2010 Skills Required Manufacturing Engineer, Pharmaceutical Engineer, Engineer, Validation, GMP, Biotechnology, Management, Process Validation, cGMP, chemical engineering Job Description Engineer - Manufacturing Engineer - Pharmaceutical Engineer - Process Engineer - ValidationA specialty biotechnology company in New Jersey needs a Principal Engineer for Manufacturing Technology support! This is a growth opportunity and an excellent multi-national company.If you are an Engineer in the Biotechnology industry, with at least 12 years of experience in GMP Production/development, who has a BS degree in Chemical Engineering , please read on!What you need for this position:-BS degree12 + years in the Biotechnology industry-EXELLENT writing skills - previous experience writing sections of Regulatory Filings-Understanding of cGMP requirements for a large manufacturing facility- Excellent communication skills, writing skills and ability to liaise with other departments-Knowledge of Cell Culture, purification and support systems is a MUSTWhat you'll be doing:-Implementing Process Validation program-Planning, Writing and Managing the execution of process validation protocols-Writing Manufacturing and Validation sections of Regulatory Filings.-Support process validation for manufacture of new and existing biologicalsWhat's in it for you:-Extremely competitive compensation package-Excellent company work environment-Room to grow and expand as the company doesSo, if you are an Engineer in the Biotechnology industry, with at least 12 years of experience in GMP Production/development, who has a BS degree in Chemical Engineering , please apply today!Must be authorized to work in the United States on a full-time basis for any employer. Are you a fit for this position? Please Click Here to Apply! (your information will be kept strictly confidential!) Not a fit for this position? Click Here to Search Other CyberCoders Jobs! Looking forward to receiving your resume through our website and going over the position with you. Clicking apply is the best way to apply, or you may also: Email your resume in Word to: Register to View **Please do NOT change the email subject line in any way. You must keep the JobID: CC HotJobAp : EB-PrinEngineer -- in the email subject line for your application to be considered.*** Erin Beagle - Executive Recruiter - CyberCoders Other Jobs

Job Title: Manufacturing Engineer - Rubber Extrusion Company: FF & C Management Location: Elizabeth, NJ Description: Seeking 3 + years rubber extrusion and splicing experience to expand and improve EPDM extrusion process lines. Compensation to $85,000, plus bonus and full company benefits.For complete details contact Bernard Borges submit resume online at:http://dmc9.com/bxb/app.asp Or email to Register to View Register to View ARE AN EQUAL OPPORTUNITY EMPLOYER and our employment decisions are made without regard to race, color, religion, age, sex, national origin, handicap, disability or marital status. We reasonably accommodate individuals with handicaps, disabilities and bona fide religious beliefs. Jobs Career Position Hiring. We will make every effort to consider applications for all available positions and shall use one or more of the contact methods and addresses indicated in resume or online application. Indicated location may be proximate or may be desirable point of embarkation for paid relocation to another venue.  CONSIDERED EXPERIENCE INCLUDES:  Rubber Processing Extrusion Plastic Process Engineer Chemical Engineer Manufacturing Engineer Chemist R & D Chemical Engineer Plastic Packaging Materials Rubber Manager Director FDA Scale-up ManufacturingIf you submit an application or resume, which contains your email address, we will use that email address to communicate with you about this and other positions. We use an email quality control service to maintain security and a remove and dead address filter. To cancel receiving email communications, simply send an email from your address with the word "remove" in the subject line to Register to View If you have further concern regarding email received from us, call Register to View . We will be glad to have a real human being contact you upon request.Please refer to job code 2256 when responding to this ad.

Job Title: Engineer - Manufacturing Engineer - Pharmaceutical Engineer Company: CyberCoders Location: Raritan, NJ Description: Engineer - Manufacturing Engineer - Pharmaceutical Engineer - Process Engineer - ValidationA specialty biotechnology company in New Jersey needs a Principal Engineer for Manufacturing Technology support! This is a growth opportunity and an excellent multi-national company.If you are an Engineer in the Biotechnology industry, with at least 12 years of experience in GMP Production/development, who has a BS degree in Chemical Engineering , please read on!What you need for this position:-BS degree12 + years in the Biotechnology industry-EXELLENT writing skills - previous experience writing sections of Regulatory Filings-Understanding of cGMP requirements for a large manufacturing facility- Excellent communication skills, writing skills and ability to liaise with other departments-Knowledge of Cell Culture, purification and support systems is a MUSTWhat you'll be doing:-Implementing Process Validation program-Planning, Writing and Managing the execution of process validation protocols-Writing Manufacturing and Validation sections of Regulatory Filings.-Support process validation for manufacture of new and existing biologicalsWhat's in it for you:-Extremely competitive compensation package-Excellent company work environment-Room to grow and expand as the company doesSo, if you are an Engineer in the Biotechnology industry, with at least 12 years of experience in GMP Production/development, who has a BS degree in Chemical Engineering , please apply today!Must be authorized to work in the United States on a full-time basis for any employer.

Job Title: Manufacturing Engineer Company: Masco Location: Saddle Brook, NJ Description: Arrow Fastener Co., Inc. a division of Masco Corporation, a Fortune 300 diversified home products manufacturer, has an immediate opportunity for an experienced Manufacturing Engineer. Located in northeast New Jersey, the selected candidate will perform specific duties that ensure a smooth operating, highly integrated manufacturing environment. The Manufacturing Engineer will perform a wide variety of tasks, relying on experience and good judgment to accomplish all manufacturing goals. The candidate is expected to use a wide degree of creativity and advanced problem solving skills to support and promote continuous improvement efforts. The following are essential functions of the position: ·         Manage multiple projects to improve manufacturing methods in all departments ·         Understand all processes in manufacturing and collaborate with team leaders to maximize performance efficiencies  ·         Recommend and facilitate quality initiatives that improve product performance and reduce the total cost of quality  ·         Provide product and quality related technical support to sales and customer service  ·         Interface with internal and external resources to assist in improving and troubleshooting equipment and machinery ·         Interact with production personnel to address issues and ensure consistent product flow  ·         Design tooling and fixtures to support new products and determine fit to current manufacturing processes ·         Perform time studies, determine standard rates, and develop standard operating procedures ·         Maintain accurate product routings, bills of material, and ECOs for revision control  Requirements include but are not limited to: ·         Bachelor’s Degree (BSME, BSIE) required. ·         Five or more years experience with significant manufacturing exposure ·         Knowledge of current industry manufacturing concepts, practices and procedures ·         Ability to apply various problem-solving techniques to achieve positive results ·         Strong PC skills, including Office and CAD ·         Appropriate oral and written communication skills  Preferred requirements include:  ·         Experience working in a Lean Manufacturing environment  ·         Die stamping, heat treating, plating, and/or assembly experience ·         Familiar with quality systems and methods

Job Title: Sr. Manufacturing Engineer Company: ImClone Systems Incorporated Location: Branchburg, NJ Description: ImClone Systems, a wholly-owned subsidiary of Eli Lilly and Company (NYSE:LLY), is committed to advancing oncology care by developing a portfolio of targeted biologic treatments designed to address the medical needs of patients with a variety of cancers. Founded in 1984, ImClone has a rich culture of discovery and deep expertise in oncology. Beyond its marketed product ERBITUX®, ImClone has several additional investigational monoclonal antibodies in various stages of clinical development. ImClone's research and clinical development capabilities are augmented by its expertise in the scale-up and manufacturing of biologics. The company's state-of-the-art FDA-approved manufacturing facilities provide it with one of the largest biologic manufacturing capacities in the world.GENERAL SUMMARYThis position is responsible for the technical support of the manufacturing operations. This position will report to the Director or Associate Director in Manufacturing Technology and will interact with engineering, manufacturing, validation, quality assurance, quality control and regulatory departments. Interaction may be required with contract producers of ImClone’s products. Knowledge of cell culture, purification and support systems used in the manufacturing of biotech products is essential. Database experience a plus.ESSENTIAL DUTIES AND RESPONSIBILITIESEvery effort has been made to identify the essential functions of this position. However, it in no way states or implies that these are the only duties you will be required to perform, nor is it intended to be such a listing of the skills and abilities required to do the job.The omission of specific statements of duties does not exclude them from the position if the work is similar, related, or is an essential function of the position.Responsible for supporting manufacturing operations through the performance of the following duties:1.Trends and analyses production data.2.Troubleshoots issues in conjunction with manufacturing staff. Communicate issues in a timely manner.3.Assists in the transfer of processes and process improvements from process development to the production facility and from one production facility to another.4.Authors technical reports supporting technology transfers, deviation/adverse event reporting and process analysis/trending.5.Ensures cGMP compliance.6.Works with validation to support the start-up of new facilities and validation of existing facilities.7.As required, assists in the planning and execution of process validation activities. May be asked to support additional projects in Manufacturing Support & Process Validation group.ESSENTIAL KNOWLEDGE, SKILLS, EXPERIENCE1.BS degree in Chemical Engineering, Microbiology, Biochemistry or Chemistry.2.A minimum of 7 years relevant experience in a GMP production/development environment.3.Demonstration of superior performance as a Manufacturing Engineer III or an equivalent position.4.Previous supervisory experience of 1-2 years.5.Experience in fermentation and/or protein purification manufacturing.6.Process and equipment knowledge of cell culture and purification functions.7.Thorough understanding of GMP requirements for a large scale manufacturing facility.8.Process validation experience a plus.9.Excellent communication skills, both oral and written. REQUIREMENTS - QUALIFICATIONS: Sr. Manufacturing Engineer See information above

Job Title: Manufacturing Engineer Company: American Van Equipment Location: Lakewood, NJ Description: Job Purpose:Develops and improves manufacturing processes by studying product and manufacturing methods.Duties:* Evaluates manufacturing processes by designing and conducting research programs; applying knowledge of product design, fabrication, assembly, tooling, and materials; conferring with equipment vendors; soliciting observations from operators.* Develops manufacturing processes by studying product requirements; researching, designing, modifying, and testing manufacturing methods and equipment; conferring with equipment vendors.* Improves manufacturing efficiency by analyzing and planning work flow, space requirements, and equipment layout.* Assures product and process quality by designing testing methods; testing finished- product and process capabilities; establishing standards; confirming manufacturing processes.* Provides manufacturing decision-making information by calculating production, labor, and material costs; reviewing production schedules; estimating future requirements.* Prepares product and process reports by collecting, analyzing, and summarizing information and trends. .* Provides manufacturing engineering information by answering questions and requests.* Maintains product and company reputation by complying with government regulations.* Keeps equipment operational by coordinating maintenance and repair services; following manufacturer's instructions and established procedures; requesting special service.* Maintains product and process data base by writing computer programs; entering data.* Completes design and development projects by training and guiding technicians.* Maintains professional and technical knowledge by attending educational workshops; reviewing professional publications; establishing personal networks; participating in professional societies.* Contributes to team effort by accomplishing related results as needed.Skills/Qualifications:Dealing with Complexity, Informing Others, Leadership, Supervision, Hardware Specifications, Manufacturing Methods and Procedures, Manufacturing Quality, Product Development, Presenting Technical Information, CAD, CAD/CAM Circuit Design

Job Title: Manufacturing Engineer - Medical Products (60-68k) Company: Engineering Resource Group, Inc. Location: Burlington, NJ Description: The primary function of this position is to support the day to day manufacturing operations to achieve performance objectives in the areas of quality , production volume, and cost efficiency. This position will also participate on and lead project teams involving, but no limited to, process improvement, validation studies of processes, and capital projects. The position will also have responsibility to cover as supervior of manufacturing operations on an as needed basis. Principal responsbilities: 1. Provide technical services and support to the manufacturing operations to achieve improved manufacturing performance including but not limited to improving product quality, reducing scrap rates, improving productivity, increasing plant capacity and improving profitability.    2.          Supervisor Manufacturing shift production as needed 3. Work individually and along with corporate and outside resources to develop and conduct process validations, analyze data, and write reports including IQ, OQ and PQ reports. 4. Oversee as Project manager small to mid size capital projects from conception through design development, installation, and startup including IQ, PQ and OQ preparation and oversight. 5. Consult with engineers, technicians, drafts people, and manufacturing personnel regarding product design and production problems. 6. Interact with outside vendors to investigate/procure quotations and equipment. 7. Assist set-up persons and toolmakers; troubleshoot machinery tooling. 8. Implement and maintain Statistical Process Control (SPC). 9. Conduct cost analyses to optimize expenditures. 10. Document processes according to Quality System requirements. 11. Participate and lead committees related to continuous improvement, CAPA, NCB, and customer complaints investigation and the Quality System. 12. Co-ordinate new product/ new process activity via NPX manufacturing orders, including develop, refine, improve processes and train manufacturing operators. 13. Adheres to and ensures the compliance of Teleflex's Code of Conduct, all company policies, rules, procedures, and housekeeping standards.