usa-technical writer ii (manufacturing/quality).

Octal Corporation is a U.S based company that specializes in the engineering, manufacturing, and assembly of various conversion kits, components and systems for both retrofit and upgrades, as well as maintenance of military tracked and wheeled vehicles.  Octal Corp is looking for Quality Control Inspector to join it's growing team. This position includes Quality Control functions, as well as Quality Assurance functions as necessary, of CNC machined parts, weldments and assemblies produced in house as well as inspection of incoming parts materials and\or services from outside vendors. Please feel free to apply and discuss the position. salary: $25 - $25 per yearshift: Firstwork hours: 8 AM - 4 PMeducation: No Degree RequiredResponsibilitiesWORK PERFORMED / RESPONSIBILITIES:  To perform visual and dimensional quality inspections, such as first piece inspections, in process inspections, and final inspections, in accordance to the Quality Management System. Operate CMM, optical comparators, and all other inspection tools as needed to generate accurate inspection reports. Review CoC and other documentation as needed to ensure quality of parts, materials and\or services received from outside vendors. Generate reports and data entry. Analysis and completion of final inspection reports Ensure accuracy and organize documentation of the inspections performed. Raise flags to the appropriate personnel whenever a nonconformance is suspected. Set up & Monitor the QC room – cleanliness, organization, humidity, temp, etc. SkillsPart inspectionOperating CNC CMMoptical comparatorsProcess InspectionsFinal InspectionsRead Mechanical BlueprintsAttention to DetailsTime ManagementInspectionQualificationsYears of experience: 0 yearsExperience level: ExperiencedRandstad 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 you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.

job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. With therapeutic areas that include Oncology, Vaccines, and Rare Diseases, our partner aims to make treatments streamlined, easily accessible, and globally produced. If you share their goal of approaching healthcare in a novel way, look no further - apply for your dream job now! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Parsippany, New Jersey job type: Contract salary: $40.00 - 42.19 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Ensure SLS quality systems are maintained consistent with cGMPs, company policies, site procedures and regulatory guidance. The quality systems to be maintained include, but not limited to, laboratory investigations, instrument/facility qualifications, analytical method validation and transfers, deviation management, notification to management, corrective and preventive actions (CAPAs), site quality review team (SQRT) and change management.Ensure testing/administration is conducted in a manner consistent with cGMPs, company policies, site procedures and regulatory guidance. Position Responsibilities:Review/approve various types of laboratory documentation ensuring that strong scientific justification, adequate impact assessments and appropriate definition of root cause and corrective actions are identified. These documents would include (but not limited to) stability study change control, equipment change control, corrective and preventive actions, quality notification reports, testing notes, instrument/facility qualifications, analytical method validation and transfers and laboratory investigation reports.Ensure site quality systems are consistent with cGMPs, company policies, site procedures and regulatory guidance.Able to interpret quality requirements, both internal and external, and apply them to real life situations in the pharmaceutical industry.Experience with the principles and application of quality risk management.Work together with the SLS management to assure that objectives and metrics are met.Contribute to quality assurance management team initiatives and objectives.Create, track and approve corrective/preventive action items to help ensure they are completed within the agreed timeframes.Ensure testing/administration are conducted in a manner consistent with cGMPs, company policies, site procedures and regulatory guidance.  qualifications: Bachelor's degree or higher in Chemistry/Biology or related discipline.Experience: 2-5 Years of related analytical chemistry/microbiology experience with a Bachelor's degree or 2-5 years working in a Quality Assurance position in the pharmaceutical industry. This experience should include authoring/approving analytical investigations and deviations.Experience with electronic laboratory support systems (gQTS, gLIMS, PDOCS) preferred.Experience with Human Performance and Risk Management principles is highly desirable.QC/QA experience in a drug product or API manufacturing environment is desirable.Excellent written and oral communication skills with the ability to summarize complex situations in an easily understandable narrative.Must be comfortable interacting with all levels of management in the organization  skills: CAPA, Biology, Chemistry Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.

For over 65 years, Glebar has been designing and manufacturing precision centerless, micro, OD and Double Disc grinders and gauging equipment.  Glebar is looking for an experienced Quality Assurance Technician.  This position is responsible for the inspection and testing of manufacturing processes and products to ensure the product quality.  In support of the production and supply chain team, the quality assurance technician will work with a variety of inspection and test equipment and document inspection procedures to ensure and maintain product quality and records traceability. The quality assurance technician will also assist to appropriately identify nonconforming products and remove non-conformance's from the production flow until such product can be dispositioned. Cross-functional collaboration with the engineering and production and supply chain team is required  salary: $66,560 - $72,800 per yearshift: Firstwork hours: 8 AM - 4 PMeducation: No Degree RequiredResponsibilities Programming and operation of CMM for in house and supplier manufactured products Experience in quality assurance / quality control role in precision manufacturing environment or equivalent Deep knowledge of quality lab inspection equipment such as optical comparator, micrometers, calipers, gage blocks, bore gages etc.. strong ability to work with minimum to no supervision Advanced blue print reading and GD&T interpretation skills Basic shop math Ability to follow verbal work instructions and adhere to written procedures Microsoft Excel, Word strong Computer Skills Knowledge of milling, turning, grinding, EDM, and precision manufacturing processes Basic reading skills. Must be able to follow directions Regularly lift 30-50 pounds Regularly perform repetitive tasks Regularly possess manual dexterity to put parts or pieces together quickly and accurately Must be willing to work on their feet for the majority of the shift Follow company procedures and directives. The essential functions of this role include:manual lifting up to 50lbsSkillsQuality AssuranceInspectionBlueprintsMicrosoft WordMicrosoft ExcelBlueprint ReadingProduct InspectionQualificationsYears of experience: 3 yearsExperience level: ExperiencedRandstad 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 you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.