To conduct first piece and in-process inspection, final inspection and testing on a variety of parts and products in a manner which will consistently ensure compliance with pre-established customer specifications and quality standards.. Assists in reviewing the calibration status of inspection equipment, ISO Standards, and reports problems as appropriate.. Keeps the Quality Supervisor informed of job related problems and other information related to work activity.. At least 2 years of first piece and in-process mechanical inspection experience in a close tolerance machining job shop environment is preferred.. Work environment: General office and machine shop environment
Our portfolio includes creative solutions geared at helping food industry professionals compete in foodservice, retail, in-store bakery, deli, and prepared foods, among others.. This role supports activities in our LATAM market, and as such, candidates need to be bi-lingual English and Spanish speaking.. Similarly, partner with adjacent process owners (es: IBP (Integrated Business Planning), Sales, Marketing, etc.). Support Organizational Change Management (OCM) activities, in conjunction with Organizational Change Management Lead.. Support localization activities while balancing the goals of simple, standard, global solutions.
We are looking for a research scientist to join our team to train AI models. In this role you will need to hold an expert understanding of chemistry- a completed or in progress Masters/PhD is preferred but not required. Other related fields include, but are not limited to: Research and Development Chemist, Formulation Scientist, Development Chemist, Analytical Chemist, Chemical Engineer, Medicinal Chemist, Biochemist, Process Development Chemist. Note: Payment is made via PayPal. We will never ask for any money from you. PayPal will handle any currency conversions from USD. This job is only available to those in the US, UK, Canada, Australia, or New Zealand.
Quality Assurance Specialist will partner with team members across Quality Assurance, Quality Control, and Technical Operations to ensure effective, efficient, and compliant operations exist at client GxP sites in the Boston area. Responsible for oversight of facilities monitoring programs and data related to the Gene Therapy Manufacturing Facility. Ensure oversight, maintenance, and approval of quality records for change control, deviation, CAPA, supplier quality management, documentation, training, and quality review. 8-10 years of experience in biopharmaceutical or biotechnology based GMP clinical or commercial operations, within the Quality function. Experience with quality systems operations and supplier quality management.
The Scientific Team at Russell Tobin & Associates is seeking a Quality Control Technician for a life-sciences and diagnostics company providing services to the pharmaceutical and biotechnology industries.. Quality Control Technician plays a vital role in maintaining product excellence by performing comprehensive inspection activities to support production operations.. Review and redline SOPs to align with standard work practices and continuous improvement initiatives. Verify test equipment and tools are properly calibrated according to established calibration programs. 3+ years of Quality Control experience in the biomedical industry.
Our portfolio of national and super-regional brands and licensed products includes Hood, Heluva Good, Lactaid, Blue Diamond Almond Breeze, Planet Oat and more.. Minimum of 5 years of experience working with Level 2 (SCADA) and Level 3 (MES) systems is required.. Experience working for a CPG company required (food or beverage company preferred).. Experience with Rockwell Automation Factory Talk View implementations. Experience working with Operations and Engineering staff to build out and document requirements for SCADA and MES applications.
There is an immediate need for a Quality Control Inspector based out of our Andover, MA office.. Working knowledge of measuring instruments such as CNC Video measuring systems, calipers, comparator, DMM, Pin Gage, Force Gage, Drop indicator, Surface Tester, gage blocks, depth gage, Durometer, and thread gages.. We Are Proud Partners With the Chicago Cubs.. We are a Legacy Partner of the Chicago Cubs and we are proud to be the organization's official water efficiency partner!. Through this relationship, which includes the naming rights to Sloan Park, the Cubs' Spring Training facility in Mesa, Arizona, we have had the opportunity to promote our brand and continue our water conservation efforts in the city of Chicago and around the world.
Join a dynamic team as a Supply Chain Project Manager, where you'll play a pivotal role in delivering innovative solutions within the Global Robotics group.. This exciting opportunity involves collaborating with cross-functional teams to ensure timely delivery and operational excellence.. Strong background in supply chain management with a focus on process improvement.. Background in order management within a manufacturing setting.. Once you apply for this position, you may receive a phone call, SMS or email at the time of application from our Virtual AI Recruiter, Alex, to conduct an initial interview.
Implement and manage the records in electronic Quality Systems, such as QMS, EDMS, and LMS, etc. Supervise the QA Documentation department in the creation, issuance, maintenance, archiving, and storage of cGMP and cGXP controlled documentation and records.. Manage electronic document processing, retrieval, and distribution systems (EDMS), electronic learning management system (LMS), electronic Quality Management System (TrackWise), etc. Minimum ten (10) years of related experience in pharmaceutical (manufacturing) environment, biotech industry, Quality Assurance, Quality Control and/or production, or FDA regulated industry. Strong working knowledge of a Quality Management System (QMS) and adherence to 21 CFR Parts 210, 211; aseptic drug manufacturing experience a plus
The Clinical Supply Manager is responsible for forecasting, packaging, labeling and distribution of investigational medicinal product to support Vertex clinical studies.. Working knowledge of regulations relating to clinical labeling, packaging and distribution activities (cGMP, GCP).. At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations.. From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.. Vertex is a global biotechnology company that invests in scientific innovation.
The position will partner with the Program Management, CMC functional leads and interface directly with CDMOs to manage cross-functional planning and execution of late-stage development program through commercialization.. We are seeking an individual with a Biologics technical background, solid working knowledge of GMPs, experience interacting with external manufacturers/service providers, understanding of the drug substance development pathway through validations, BLA submissions and launch/commercialization, and willingness to pivot as program priorities change.. Partner closely with POVE program management lead, functional area lead and CDMO to lead the planning and execution of late-stage development program through commercialization for assigned Biologics drug substance workstream. At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations.. Vertex is a global biotechnology company that invests in scientific innovation.
Quality Control Technician plays a vital role in maintaining product excellence by performing comprehensive inspection activities to support production operations.. Facilitate Material Review Board (MRB) meetings to ensure timely disposition of non-conforming products or materials. Review and redline SOPs to align with standard work practices and continuous improvement initiatives. Verify test equipment and tools are properly calibrated according to established calibration programs. 3+ years of Quality Control experience in the biomedical industry.
The role involves performing skin and pulmonary function testing for clinic patients, instructing them in medication use, and guiding them through allergy management procedures per established protocols, while also supporting clinical research, scheduling, and maintaining patient records.. Key Responsibilities: Conducting Tests and Instructions: Perform skin testing and pulmonary function testing, and instruct patients in the use of study medications and procedures.. Patient Guidance and Communication: Explain allergy environmental control measures to patients and parents, and communicate issues to other staff as needed.. Experience Pediatric Immunology Technician experience preferred.. Boston Children’s Hospital offers competitive compensation and unmatched benefits including flexible schedules, affordable health, vision and dental insurance, child care and student loan subsidies, generous levels of time off, 403(b) Retirement Savings plan, Pension, Tuition and certain License and Certification Reimbursement, cell phone plan discounts and discounted rates on T-passes.
CVS Health’s Supply Chain Strategy team is transforming the way we serve customers in their path to better health. The Supply Chain Strategy Manager will employ a data-driven approach to create in-depth business cases that support the prioritization of initiatives that improve and modernize our retail and omni-channel supply chain network. This position is eligible for a CVS Health bonus, commission or short-term incentive program in addition to the base pay range listed above. No-cost programs for all colleagues including wellness screenings, tobacco cessation and weight management programs, confidential counseling and financial coaching. Benefit solutions that address the different needs and preferences of our colleagues including paid time off, flexible work schedules, family leave, dependent care resources, colleague assistance programs, tuition assistance, retiree medical access and many other benefits depending on eligibility.
Negotiate with vendor representatives by leveraging benchmark pricing, utilization data, and product research.. MBA or MHA highly desirable. CMRP, Lean/Six Sigma certification preferred. Skilled with Pivot Tables, VLOOKUPs, and IF functions.. Beth Israel Lahey Health requires that all staff be vaccinated against influenza (flu) and COVID-19 as a condition of employment.
Join to apply for the Associate Export Transportation Coordinator role at Mohawk Global. The Associate Export Transportation Coordinator supports Mohawk’s air/ocean export transportation by leveraging Mohawk’s partner relationships as well as their own unique problem solving and analytical skills to assist Mohawk customers.. The Associate Export Transportation Coordinator possesses an inquisitive mindset to investigate and resolve problem shipments and other aspects of freight management, whether they be air, land or sea as necessary.. Sign in to set job alerts for “Transportation Coordinator” roles.. Proposal Coordinator - Transportation (Canada-Northeast US Team) Boston, MA $80,000.00-$90,000.00 3 weeks ago
Two years’ experience in the corrugated box industry preferred with heavy experience in electronics mechanical, hydraulics, pneumatics, and electricity.. Provide training, work direction and guidance while performing work in one or more of the skilled trades.. Assist Plant Manager in scheduling work and determining needs for equipment and supplies.. Report regarding work completed referring unusual technical or personnel issues to the Plant Manager.. Assist in purchase, installation, repair and maintenance of various machines, and plumbing; perform welding and metal fabrication.
Job Title Quality Engineer- Products and Systems Job Description The Quality Engineer-Products and Systems is a key member of our Sleep & Respiratory Care, Quality organization, accountable for ensuring our Sleep & Respiratory Care products are safe and compliant with Internal/External regulations, requirements and standards. Ensures that appropriate Quality, Reliability‐and Post Market Surveillance (PMS) plans are made and include all stages of the product life cycle. ASQ certifications-Certified Quality Engineer (CQE), Certified Quality Auditor (CQA), and/or DfSS Green Belt/Black Belt preferred.. We are a health technology company.. Employees are eligible to participate in our comprehensive Philips Total Rewards benefits program, which includes a generous PTO, 401k (up to 7% match), HSA (with company contribution), stock purchase plan, education reimbursement and much more.
Job Description The GMP Operational Quality Specialist works with a high degree of independence to provide QA Analytical support for release and stability program for commercial products.. The GMP Operational Quality Specialist executes routine tasks and activities in support of QA Analytical function.. Experience in supporting Quality Event Investigations, Root Cause Analysis (RCA) and CAPA implementation.. Experience with electronic document management systems (e.g., Veeva).. Requisition Disclaimer This job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals (“Vertex”).
Vicarious Surgical is seeking a meticulous and detail-oriented Supply Chain Co-op to support our medical device manufacturing operations within a controlled clean room environment. The ideal candidate will be responsible for ensuring the accurate and timely flow of materials, maintaining inventory integrity, and adhering to strict clean room protocols. Store materials in designated locations within the clean room, adhering to strict clean room protocols and material handling procedures. Accurately pick, pack, and stage materials for production, ensuring timely delivery to manufacturing workstations. Knowledge of ERP systems (Netsuite) and inventory management software is highly desirable