10 jobs found in Hauppauge

Full Time - Great Benefits! Also Part Time position open! Full Time Hours 7:30 a.m.-4:00 p.m. $15.00 per hour 5-day work week M-F Part time hours 7:30 a.m.-12:30 p.m. must work total 20-25 hours per week M-F We're looking for Production Personnel who care about the QUALITY of their work Suffolk County's top Die-cutting manufacturer has full time & part time openings for individuals with mechanical ability, who work well with their hands, are attentive to details and have a positive attitude We'll train the right candidates who meet the following:• able to Lift 70 pounds repeatedly• Math skills including decimals, fractions, measurement calculation• understand written and spoken English• Check-able work references which demonstrate a history of reliability• Successfully pass the pre-employment drug screen and criminal background check. Climate control facility. Production Personnel work independently running Laminating, Slitting and Die-Cutting machines to produce parts from...

Job Brief: The Manufacturing Supervisor position is an individual contributor role and reporting to a Manager or Senior Manager of Manufacturing Operations at the client New York. The job duties for this position include but are not limited to the following: · Plan, organize and oversee all activities related to the manufacturing of tablets and capsules to include delivery, in-process, and finished product samples in a defined schedule. · Review and compile the documents generated during the production of tablets and capsules such as batch manufacturing records and validation protocols. · Ensure and compliance with safety, quality, productivity, and performance expectations and execution of manufacturing operations. · Provide daily supervision and support to the operators in regarding day-to-day production activities such as trouble shooting and other work tasks. · Coordinate with departments such as Quality Assurance (QA), Quality Control (QC), Research & Development (R),...

Ref ID: 02815772 Classification: Office Assistant Compensation: $14.00 to $15.00 hourly Part Time temporary administrative candidate needed for an ongoing office role. Day to day duties include, pulling patient files, data entry of EOB forms and various clerical tasks. Please email your resume to for consideration. Job Requirements: Part Time temporary administrative candidate needed for an ongoing office role. Day to day duties include, pulling patient files, data entry of EOB forms and various clerical tasks. OfficeTeam, a Robert Half Company, matches professionals in the administrative field with remote or on-site jobs on a temporary and temporary-to-full-time basis. Whether you're a seasoned administrative pro or starting your career, we have options for you. Our experienced staffing professionals can promote you to employers and advocate on your behalf. We provide access to top jobs, competitive compensation and benefits, and free online training. For more...

DescriptionPart Time temporary administrative candidate needed for an ongoing office role. Day to day duties include, pulling patient files, data entry of EOB forms and various clerical tasks.Please email your resume to for consideration.RequirementsPart Time temporary administrative candidate needed for an ongoing office role. Day to day duties include, pulling patient files, data entry of EOB forms and various clerical tasks.OfficeTeam, a Robert Half Company, matches professionals in the administrative field with remote or on-site jobs on a temporary and temporary-to-full-time basis. Whether you're a seasoned administrative pro or starting your career, we have options for you.Our experienced staffing professionals can promote you to employers and advocate on your behalf. We provide access to top jobs, competitive compensation and benefits, and free online training. For more opportunities, get the Robert Half app and receive instant notifications when our AI matches your skills and...

My client is a fast growing pharma company looking for QA Manager. QA lead for internal GMP Manufacturing and QC operations. Review and approval of Master Documents (batch records, protocols, reports, etc.) Point person and final approver of deviation and OOS investigations. Executed documentation/record review and approval. Oversee, approve equipment qualifications and process validations. Experience with FDA inspection Min Bachelors degree in Life Sciences or related field. Min 3 years of Quality Assurance experience in a pharmaceutical or biotech company. Experience in development, implementation of Quality Systems is preferred. Experience with FDA submissions a plus Strong knowledge of global regulatory and cGMP compliance standards.

Job ID: 249120 Oldcastle BuildingEnvelope®, a CRH company, is the leading supplier of products specified to close the building envelope. They include: custom-engineered curtain wall and window wall, architectural windows, storefront systems, doors, skylights and architectural glass. Summary Oldcastle BuildingEnvelope®, located in Hauppauge, NY has multiple FULL-TIME, permanent material handler/production worker positions on several shifts. First shift production is: 7:00 AM to 3:30 PM. Second shift production is 3:30 PM to 12 AM. Material handler position is 2:00 PM to 10:30 PM. All shifts have required overtime that can be both or either at the beginning and the end of the shift. The standard shift is Monday thru Friday but may require some Saturdays. We are a union shop. Pre-employment drug test and background screening will be conducted on qualified applicants after acceptance of job offer. Essential Duties and Responsibilities • Move glass and metal...

QUALITY ENGINEERING MANAGER POSITION REPORTS TO THE VP OF GLOBAL QUALITY CONTROL IN THIS ROLE YOU ARE THE PRIMARY SITE LEADER FOR QUALITY AND MANAGEMENT OF THE QUALITY STAFF YOU WILL PARTICIPATE IN DESIGN OF STRATEGIC PLANNING AND IMPLEMENTATION YOU ARE RESPONSIBLE FOR ENSURING THAT ALL PRODUCT SHIPPED FROM THIS SITE IS COMPLIANT WITH ALL INTERNAL PRODUCT SPECIFICATIONS AND MEETS ALL STATED CUSTOMER REQUIREMENTS. YOU WILL NEED : A BS DEGREE IN EE OR ENGINEERING WITH ELECTRONICS ASSEMBLY 10 YEARS OF EXPERIENCE AS A SENIOR PROFESSIONAL / ENGINEERING MANAGER DEMONSTRATED SUCCESS AS A MANAGER OF PEOPLE FDA REGULATORY EXPERIENCE - ISO 13485 IS A PLUS STRONG PRINTED CIRUIT BOARD ASSEMBLY (SMT) EXPERIENCE AND BOX BUILD ASSEMBLY EXPERIENCE IN DOE DFX, DFM, DFA EXPERIENCE NPI EXPERIENCE NO PEOPLE CURRNETLY LIVING OUTSIDE OF THE U.S. WILL BE CONSIDERED

RELIABILITY ENGINEER IS NEEDED FOR A MAJOR INTERNATIONAL COMPANY THAT IS PRODUCING ELECTRONIC COMONENTS FOR THE MEDICAL DEVICE INDUTRY , SECURITY INDUSTRY ETC. THIS IS VERY HIGH END AND VERY SOPHISITCATED EQUIPMENT. This position, while based in NY, IS CONSIDERED A GLOBAL POSITION - IN OTHER WORDS YOU WILL HAVE INTERNATIONAL RESPONSIBILITY. You will report to the VP OF GLOBAL QUALITY CONTROL The company is also establishing a Reliability and Failure Analysis lab in which you would participate You will develop reliability predictions using Windchill / Relex and / or approved prediction methodologies for mechanical and electrical designs and supplied components perform built-in-test (BIT) analysis , implementation and validation review specs , drawings , engineering change notices, support design reviews, production readiness reviews, NPI, translate concepts, ideas, new products, new components into clearly defined quantitative models and process optimization objectives...