Production Technician Jobs in New Jersey

Job Title: Manufacturing Technician 1 Company: Company Confidential Location: Eatontown, NJ Description: Job Title:  Manufacturing TechnicianGeneral Duties:Responsible for manufacturing medical devices in a lab and preparing / packaging final product. Focus will be on manufacturing operations for small metal parts.  Specific Tasks:Will perform chemical and mechanical surface finishing operations and use microscope inspection tools. Ability to physically handle small, delicate parts is crucial. Read and understand technical drawings, cGMP documentation and design details.  Requirements:Good interpersonal skills and communication skills are important.  Must be able to work to production timelines. Strong professional or academic references are a must.  Experience in chemical lab work, microscope inspection, small parts manufacturing, and process trouble shooting are assets. We provide on-the-job training. We operate a safe, smoke-free, clean, ISO 13485-certified facility and offer competitive benefit packages for full-time employees. Qualified applicants are invited to fax resumes to Register to View .

Job Title: US / Production Associate (NJ, Fair Lawn) Company: Kraft Foods, Inc. Location: Fair Lawn, NJ Description: Kraft Foods/Nabisco a major food manufacturer in Fair Lawn, is seeking highly qualified production associates in our baking and packing departments and in our distribution center/warehouse.The Production Associate position encompasses all aspects of a distribution and manufacturing plant.We offer on the job-training for many of the available positions.Responsibilities may include operating a pallet jack, loading supplies into production machinery, lifting and/or stacking boxes, sanitation of food manufacturing equipment, and operating various types of machinery and equipment (e.g., forklift, high-speed packaging equipment, ovens, palletizers, etc.)

Job Title: Principal Engineer, Manufacturing Tech Support QA QC Company: Sampson Medical Search Location: Summit, NJ Description: If you are interested in this opportunity, please e-mail a resume in a word attachment with your name,  address,  phone number,  cell number and e-mail  to    Register to View      Thank you!  Judie Sampson SUMMARYThis position is responsible for implementing the process validation program for the manufacture of both new and existing biologicals.  Responsibilities include planning, writing and managing the execution of process validation protocols, such as consistency and product comparability protocols.  The authoring of manufacturing and validation sections of regulatory filings will be required.  This position will report to a Sr. Director or 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 products. Knowledge of cell culture, purification and support systems used in the manufacturing of biotech products is essential.DUTIES AND RESPONSIBILITIES NeededEvery 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.  Plan and manage the execution of process validation studies, such as process consistency studies, performed for  products.  The main areas of focus are purification and downstream processing activities. Author the required protocols, reports and regulatory documentation associated with the executed studies.2.  Review and approve protocols and reports authored by other groups.  3.  Author relevant portions of drug substance manufacturing and process validation sections of regulatory filings.4.  Author technical reports supporting technology transfers, deviation/adverse event reporting and process analyses/trending.  This responsibility is shared with the Process Sciences Group.5.  Support the Manufacturing Process Sciences Group, the Statistics and Quantitative Sciences Group and the Clinical Manufacturing Group as required.6.  Consult with other groups to troubleshoot manufacturing process problems.7.  Ensures cGMP compliance.        KNOWLEDGE, SKILLS & EXPERIENCE  Needed1.  BS degree in Chemical Engineering (equivalent non-engineering title for Biochemistry, Chemistry, Microbiology degrees). 2.  Minimum of 12 years experience in a GMP production/development environment.3.  Has previously started-up and/or had a management role in a biotechnology facility.4.  Has detailed process and equipment knowledge of protein purification processes and functions.  Similar knowledge of cell culture processes a plus.5.  Process validation experience required.6.  Has a thorough understanding of cGMP requirements for a large scale manufacturing facility.7.  Experience in successful facility licensure a plus.8.  Excellent communication skills, both oral and written.9.  Demonstrated supervisory skills.

Job Title: Manufacturing Technician Company: Burpee Materials Technology Location: Eatontown, NJ Description: Job Title:  Manufacturing TechnicianGeneral Duties:Responsible for manufacturing medical devices in a lab / manufacturing environment.   Focus will be on manufacturing operations for small metal parts.  Specific Tasks:Will perform medical device manufacturing and assembly operations in an ISO13485 facility. Will perform mechanical surface finishing operations and use microscope inspection tools. Ability to physically handle small, delicate parts is crucial. Read and understand technical drawings, cGMP documentation and design details.  Requirements:Good interpersonal skills and communication skills are important.  Must be able to work to production timelines. Strong professional or academic references are a must.  Experience in microscope inspection, small parts manufacturing, and process trouble shooting are assets. We provide on-the-job training. We operate a safe, smoke-free, clean, ISO 13485-certified facility and offer competitive benefit packages for full-time employees. Qualified applicants are invited to submit resumes via fax to Register to View .

Job Title: Manufacturing Technician Company: Collagen Matrix Location: Franklin Lakes, NJ Description: Assembler / Fabricator of Medical Devices Collagen Matrix, Inc., located in Franklin Lakes, NJ, is a growing company whose collagen technology is at the forefront of tissue engineering. Our mission is to develop, manufacture and market innovative collagen-based medical devices for tissue and organ repair and regeneration. We are currently searching for candidates with the right stuff to join our clean room production team. The positions require a minimum HS diploma or GED, but we would prefer individuals who have completed some college level biology or chemistry courses. A thorough understanding of written and spoken English is essential. You must have reliable transportation; our location is not serviced by public transportation. We currently operate on one shift, M-F. Our products are implantable devices that are usually surgically implanted and left in the body where they are naturally absorbed. We do not manufacture electronics or computer parts. These are permanent, full-time positions. No previous experience is required. All successful candidates will be fully trained. Job responsibilities include: Purification of raw material Product fabrication Packaging Maintenance and calibration of equipment Washing and sanitizing laboratory such as: equipment, glassware and plastic ware. Completion of batch records Collagen Matrix, Inc. offers a benefits package including health and dental coverage and 401(k) along with an excellent work environment. Please submit resume via e-mail or fax. Only candidates considered for a position will be contacted. http://www.collagenmatrix.com

Job Title: Production Technician Company: Florida Power & Light Company Location: Sayreville, NJ Description: Performs multi-functional responsibilities, both operating and maintaining a gas fired power plant with experience on 4160v higher. Also experience with switchgears, transformers, and MCCs (Motor Control Centers) desirable. Conduct preventive, minor and major maintenance tasks on plant electrical equipment and systems. Read, interpret and work from electrical diagrams and blue prints.Use wide variety of electrical instruments, test equipment, hand and power tools. Maintain stock and records of plant electrical materials, supplies, tools and spare parts. Performs associated responsibilities as prescribed by safe work practices. Experienced in performing electrical maintenance on plant equipment including 480 volt, 3 phase motors and controls, DC batteries and control circuits motors. Previous experience working with high voltage equipment > 1000 Vacand transmission switching trained/certified highly desirable.Position may be filled at a lower level based on the skills and experience of the most qualified candidate.

Job Title: Electronics Production Associates Needed! Company: Randstad Location: Vineland, NJ Description: One of our clients in the Vineland area is looking for production associates with experience in soldering electronics. Our client is a large producer of power generators, and they have a great need for people that have electronics assembly experience. This is a first shift (7AM to 330PM) temp to perm full time position with our client. You have the opportunity to gain full time employment with a very respectable local employer in less than three months! The position is paying $11.50 to start, but then increases to $13.50 when you convert into the company.Working hours: 7AM to 330PMQualified candidates should have a proven track record of stable employment in the production of electronics. They should know how to use a tin based soldering pen. "At home" experience does not qualify you for this position. Only people that can provide two positive work references from reputable employers will be considered for this position. Qualified candidates must also be able to pass a background check and drug screen. You must also have a reliable form of transportation to make it to and from work each day. Interested candidates should submit resumes to this posting, and follow up with a call to Kyle at Register to View .Randstad is a world leader in matching great people with great companies.  Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company.  Whether youre looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.Contact information If you would like more information on this job, please contact Agent  Custer,Kyle Robert Agent Email  Register to View Address  510 HERON DRIVE SWEDESBORO, NJ 08085 Phone Number  Register to View Please refer to job code onAssociatesNeeded21 when responding to this ad.

Job Title: Principal Engineer, Manufacturing Tech Support Company: ImClone Systems Incorporated Location: Branchburg, NJ Description: ImClone Systems is dedicated to developing and commercializing novel therapeutic products in the field of oncology. Our efforts have resulted in a commercially available novel therapy, ERBITUX (cetuximab), as well as a broad spectrum of innovative product candidates with potential application in multiple tumor types. As a member of the oncology community, we are committed to providing treatments to meet the unmet needs of cancer patients. To fulfill this commitment, ImClone Systems fosters integration of the principles of teamwork and scientific integrity into all facets of the Company's activities. We believe that these values will benefit patients, physicians, and our employees while creating value for our shareholders.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 implementing the process validation program for the manufacture of both new and existing biologicals. Responsibilities include planning, writing and managing the execution of process validation protocols, such as consistency and product comparability protocols. The authoring of manufacturing and validation sections of regulatory filings will be required. This position will report to a Sr. Director or 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.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.Plan and manage the execution of process validation studies, such as process consistency studies, performed for ImClone's products.The main areas of focus are purification and downstream processing activities. Author the required protocols, reports and regulatory documentation associated with the executed studies.2.Review and approve protocols and reports authored by other groups.3.Author relevant portions of drug substance manufacturing and process validation sections of regulatory filings.4.Author technical reports supporting technology transfers, deviation/adverse event reporting and process analyses/trending. This responsibility is shared with the Process Sciences Group.5.Support the Manufacturing Process Sciences Group, the Statistics and Quantitative Sciences Group and the Clinical Manufacturing Group as required.6.Consult with other groups to troubleshoot manufacturing process problems.7.Ensures cGMP compliance.ESSENTIAL KNOWLEDGE, SKILLS, EXPERIENCE1.BS degree in Chemical Engineering (equivalent non-engineering title for Biochemistry, Chemistry, Microbiology degrees).2.Minimum of 12 years experience in a GMP production/development environment.3.Has previously started-up and/or had a management role in a biotechnology facility.4.Has detailed process and equipment knowledge of protein purification processes and functions. Similar knowledge of cell culture processes a plus.5.Process validation experience required.6.Has a thorough understanding of cGMP requirements for a large scale manufacturing facility.7.Experience in successful facility licensure a plus.8.Excellent communication skills, both oral and written.9.Demonstrated supervisory skills.

Job Title: Production Technician Company: Aerotek Commercial Location: New Brunswick, NJ Description: A world-leading designer and manufacturer of diagnostic equipment and software for the ophthalmic community has an opening for an experienced Production Technician.This individual will interact with other technicians and managers to complete assignment. The position is anticipated to last four months with an opportunity for permanent employment after that time.Major job duties include:* Unpacking, assembling, and configuring operating systems to specification* Installing imaging boards and application software* Performing optical alignment of instrumentation* Troubleshooting hardware and software problems* Formatting hard drives and maintaining customer recordsJob requirements and qualifications:* Associates degree in computer science, information technology or related field* 2 years experience with general computer assembly, maintenance, or repair to configure turnkey computer systemsStandard work week is M-F 7:30am-5:00pm. Overtime is expected.Join Aerotek Commercial Staffing(SM). We employ people in light industrial, light technical and office support positions across the nation. If you are looking for a competitive wage, solid opportunity, and a career path to success, contact us now! We offer comprehensive benefits to include medical, dental, optical, and optional 401k. Don't put your career in the hands of just anyone, put it in the hands of a specialist. Join the Aerotek Commercial Staffing team! Allegis Group and its subsidiaries are equal opportunity employers and will consider all applications without regard to race, marital status, sex, age, color, religion, national origin, veteran status, disability or any other characteristic protected by law.