Pennington, NJ8 days ago
- $25–$25 Per Hour
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This role owns end-to-end site performance, acting as the senior leader across operations, production, quality, and support functions. Requirements Bachelor's degree in engineering or related discipline, or equivalent manufacturing experience Extensive experience leading manufacturing plant operations
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p>Join Ecolab as a Senior Corporate Account Manager, Personal Care Manufacturing - Industrial Hygiene Solutions within our Life Sciences sector, delivering comprehensive programs and solutions to meet the needs of customers across the Personal Care market segment.
Job Types: Assembly, Distribution, Equipment Operator, Food Production, Forklift Operator, General Labor, General Production, General Warehouse, Machine Operator, Machine Packaging, Manufacturing, Material Handler, Picker/Packer, Production, Shipping and Receiving, Warehouse, Heavy Equipment Operator. More details about benefits can be found at https://flimp.live/trueblueassociates#home. Staff
Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
Is required to perform Cell Therapy manufacturing to maintain hands on expert knowledge of each Unit Operation, demonstrate what good execution looks like to new WCT members and when necessary, back fills for absent team members or makes up the execution resource requirements to meet the production schedule. Is responsible to provide the Production Scheduling team with information (daily, weekly monthly) on the availability of their WCT production resources and tracks/maintain records of all team members actual availability vs planned or unplanned absence due to holidays, sickness or other reasons.
From the smartphones in our pockets that access the world's collective knowledge, to the cloud-based services where all that information lives, to high-speed wireless communication and computing power needed to drive artificial intelligence, augmented and virtual reality, gaming and so much more, our technology is all around us. The candidate must exemplify true leadership in developing their team through leading by example, coaching and employee development and will direct production activities of in-house manufacturing resources on second shift while meeting safety, quality, on time delivery and cost objectives.
p>3+ years of experience in biopharmaceutical GMP production, including at least 1 year in a team leadership or supervisory role (e.g., team lead, group leader, acting supervisor). Work Location - Years 1-2 (Rooting Phase): Shanghai / Wuxi / Suzhou, China (Deep immersion in WuXi system) Years 3+ (Assignment Phase): USA / Singapore (Based on business needs and individual preferences).
Specialized Knowledge: Must possess a working knowledge of techniques and equipment related to pharmaceutical manufacturing of solid oral dosage forms, such as granulators, blenders, tablet presses, fluid bed and coating equipment. At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs.
Job Summary:Our client, a global leader in the life sciences and diagnostics industry, is seeking a Buyer to support procurement and purchasing operations at their Philadelphia-area facility. The ideal candidate will have strong negotiation skills, attention to detail, and experience working in a regulated manufacturing environment.
p>Additional Requirements: Day Shift - 12-hour per day, rotating schedule (6:00am-6:30pm) 3 days on week 1 and 4 days on week 2 of pay cycle (This includes working every other weekend). At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs.
At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. In addition, the Group Leader will perform and demonstrate the actual methods and procedures to produce the products utilizing state of the art processing systems.
To help spot these scams, remember that during our formal recruitment process, L3Harris will NOT (1) ask you for money; (2) offer to send you a check before doing any work; (3) require you to provide sensitive personal information early in the process or sensitive information about your previous employer; (4) send you emails from free commercial services (e.g.
p>Oversee the day-to-day operation of the GMP production, training, communications, assignment and prioritization of work, delivery of objectives, and performance management. Extensive experience in leading teams, supporting the continued development of employees, motivating and engaging them to achieve their potential.
Seeking experienced Manufacturing Associates to support production operations in a fast-paced, high-visibility manufacturing environment. IMPORTANT – READ BEFORE SUBMITTING Candidates must be willing to work a 12-hour 2-2-3 schedule (2 days on, 2 days off, 3 days on rotation).
li>Familiarity with various fabrication manufacturing processes and equipment, including MIG Welding, Plasma/Waterjet cutting, Press Brakes, Saws, Power Rollers, Lathes, and other essential shop tools. MAIN RESPONSIBILITIES
Marketing Message: Join an innovative leader in cold chain and temperature-controlled packaging solutions serving pharmaceutical, biotech, and food industries. Required Skills & Experience: Bachelor"s degree in Mechanical/Industrial Engineering (or equivalent experience) with 5+ years in manufacturing operations leadership.
The OPM will also participate in Capacity Planning for the site by providing details on future forecasted work to the Plant's Master Scheduling Team and by collaborating with Master Scheduling to maintain manufacturing & test schedules for active projects. The OPM will have responsibility for L3Harris Maritime Power and Energy Solutions (MPES) Philadelphia site programs that include production of complex electronic and power conversion equipment used in U.S. Navy sea vessel application.
Primary responsibilities include: Generation of user specification documents based on input from project leads, stakeholders, and SMEs for use in new equipment procurement process and overall CAPEX execution process. Explore new technical solutions with potential for Taste Ops by attending technical expos, shows, and reaching out to various relevant systems suppliers.
Each individual's pay is based on a variety of factors, including their role and the associated pay range for that role, their geographic location (i.e., country, state, metropolitan area), as well as their skills, experience, education and certifications, and performance. Whether it's providing clean water to more than a billion people on the planet, producing materials that are essential in everyday technology devices from smartphones to electric vehicles, or protecting workers around the world.
Each individual's pay is based on a variety of factors, including their role and the associated pay range for that role, their geographic location (i.e., country, state, metropolitan area), as well as their skills, experience, education and certifications, and performance. Whether it's providing clean water to more than a billion people on the planet, producing materials that are essential in everyday technology devices from smartphones to electric vehicles, or protecting workers around the world.
p>The Manager; Manufacturing Optimization Analytics will partner with stakeholders from the member functions and Business Insights and Technology stakeholders to establish core capabilities within the team, namely:
p>PwC does not intend to hire experienced or entry level job seekers who will need, now or in the future, PwC sponsorship through the H-1B lottery, except as set forth within the following policy: https://pwc.to/H-1B-Lottery-Policy. As a SAP Manufacturing Senior Manager, you will specialize in providing consulting services for SAP supply chain and operations applications, enabling clients to optimize their supply chain processes and improve operational efficiency.
Responsible for the conceptual design engineering of new products, special products and contribute to the improvement of existing products and manufacturing methods to meet customer demands. Provide technical support in the areas of bearing design, design improvements, customer support, production support and review of new applications.
p>The Manufacturing Excellence Manager is responsible for leading and sustaining world-class manufacturing performance through the Barry Callebaut Operating System (BCOS), which is fully grounded in Integrated Work Systems (IWS) principles.
li>Coordinate with matrixed personnel including System Engineering, Control Account Managers, Quality Control and Assurance Officers, Procurement Officers, Team Leads, Design & Analysis Engineers, and Subject Matter Experts within US ITER. The purpose of this role is to ensure the successful manufacture, testing, and delivery of complex engineered components and assemblies through strong technical leadership and coordinated oversight of external suppliers.
h4 style="margin:0px 0px 15px;padding:0px;border:0px;font-style:normal;font-weight:400;font-size:14px;line-height:inherit;font-family:'untitled sans' , sans-serif;color:rgb( 34 , 34 , 34 );letter-spacing:normal;word-spacing:0px;white-space:normal">Founded in 2002 in New Jersey, GenScript Biotech Corporation accelerates innovation in biotech and healthcare by providing researchers and companies with the building blocks needed to develop groundbreaking treatments and products. This individual will support sales of GMP-grade nucleic acid reagents (including guide RNAs, ssODNs, long ssDNA, dsDNA HDR templates, and custom endonucleases) as well as GMP peptide and recombinant protein manufacturing services supporting vaccines, protein therapeutics, and advanced cell and gene therapy programs.
p>Century Therapeutics (NASDAQ: IPSC) is a biotechnology company advancing a pipeline of induced pluripotent stem cell (iPSC)-derived cell therapies with the potential to meaningfully address autoimmune diseases, including type 1 diabetes, and cancer. The Senior Engineering Associate/ Associate Engineer, Manufacturing Science and Technology will be responsible for developing/ implementing and executing manufacturing processes for Century's cellular therapy programs.
p>Required Skills: Automation, Business Process Improvements, Change Controls, Data Management, Edge Computing, Escalation Management, Incident Management, Information Technology (IT) Infrastructure, Manufacturing Engineering, Manufacturing Environments, Operations Management, Pharmaceutical Manufacturing, Problem Management, Product Management, Real-Time Programming, Relational Database, Software Development Life Cycle (SDLC), Stakeholder Management. Your leadership will ensure that critical production data is consistently and reliably connected to these platforms, enabling trusted insights that improve throughput, quality, visibility, and decision making across our global manufacturing network, ultimately supporting the delivery of life changing therapies to patients.
p>For additional information and details regarding Grainger's benefits, please click on the link below: https://experience100.ehr.com/grainger/Home/Tools-Resources/Key-Resources/New-Hire. Rewards and Benefits: With benefits starting on day one, our programs provide choice and flexibility to meet team members individual needs, including:
Quva BrightStream partners with health systems to aggregate, normalize, and analyze large amounts of complex data across their sites of care, and through proprietary machine learning, transforms data into actionable insights supporting revenue optimization, script capture, inventory management, drug shortage control, and more. The primary function is to oversee all operations, and personnel, of Inspection, Labeling and Packaging Operations where multiple requirements and challenges will exist requiring a good knowledge base and ability to apply operational, quality, and regulatory skill sets.
p>The GMP Manufacturing Technician II is responsible for executing and supporting manufacturing, dispensing, and packaging operations for solid dose products (e.g., tablets, capsules, powders) in a current Good Manufacturing Practice (cGMP) environment. Pace® Life Sciences delivers a comprehensive suite of contract CMC development, CTM manufacturing, regulatory compliance, consulting, and facility support services to the pharmaceutical, biopharmaceutical, and gene therapy industries.
p>The GMP Manufacturing Technician is responsible for executing and supporting manufacturing, dispensing, and packaging operations for solid dose products (e.g., tablets, capsules, powders) in a current Good Manufacturing Practice (cGMP) environment. Pace® Life Sciences delivers a comprehensive suite of contract CMC development, CTM manufacturing, regulatory compliance, consulting, and facility support services to the pharmaceutical, biopharmaceutical, and gene therapy industries.
Quva BrightStream partners with health systems to aggregate, normalize, and analyze large amounts of complex data across their sites of care, and through proprietary machine learning, transforms data into actionable insights supporting revenue optimization, script capture, inventory management, drug shortage control, and more. About Quva: Quva provides industry-leading health-system pharmacy services and solutions, including 503B sterile injectable outsourcing services and AI-based data software solutions that help power the business of pharmacy.
p>Experience, Qualifications, Knowledge & Skills: Strong expertise in life sciences manufacturing, ideally spanning areas such as manufacturing science and technology, technology transfer, process development, digital manufacturing, operational excellence, or quality/manufacturing transformation. Celebrating over 25 years of ground-breaking technological innovation across more than 38,000 trials and 12 million patients, Medidata offers industry-leading expertise, analytics-powered insights, and one of the largest clinical trial data sets in the industry.
The role sits at the intersection of manufacturing, engineering, capital projects, and supply chain, and is responsible for shaping, selling, and delivering large scale greenfield programs across industries including life sciences, industrials, automotive, high tech, and process manufacturing. Champion digital manufacturing and Industry 4.0 solutions, including MES, digital twins, automation, data platforms, and advanced analytics, embedded into greenfield designs.
The candidate will leverage TCS's entire portfolio of services for targeted firms while working collaboratively with other market development, solutions teams and industry SMEs to create demand and capture qualified opportunities. Introduction: The Business Development Director position is a key growth and transformation role within TCS' Market Unit responsible for driving and executing Business Development strategies to acquire target clients in the manufacturing industry.
li>Judgment - Displays willingness to make decisions; Exhibits sound and accurate judgment; Supports and explains reasoning for decisions; Includes appropriatepeople in decision-making process; Makes timely decisions.
li>Manage all aspects of DP Manufacturing from authoring and revision of manufacturing documents (MBRs, Protocols, QRAs, etc), oversight of manufacturing operation, managing deviations, investigations, and relevant change actions, supporting product release, and ensuring the finished product arrives in warehouse for distribution. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs.
We're also the partner of choice when OEMs need highly reliable and innovative dip molding and dip coating equipment for demanding applications including medical, electronics, industrial, automotive, energy and agriculture. The Dip Operator is responsible for operating and monitoring dipping equipment used in the production of medical devices, industrial parts or coated products.
Facilitates the application of Global Manufacturing Excellence principles and tools (work instructions and procedures for safety, quality, Daily Direction Setting (DDS), cleaning, inspection, lubrication (CIL) maintenance, center lining (CL).
Required Skills: Audit Management, Biopharmaceutical Industry, Business Process Improvements, Data Management, Design, Digital Manufacturing, Global Compliance, GMP Compliance, Good Manufacturing Practices (GMP), Manufacturing Support, Pharmaceutical Manufacturing, Problem Management, Quality Management, Real-Time Programming, Regulatory Requirements, Software Development Life Cycle (SDLC), Technical Issues, TIBCO Spotfire. Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities.
Working experience in "ServiceNow" and knowledge on Incident, Problem, Change, SLM and Knowledge Management processes. Coordinate communications between suppliers, OEM, and business stakeholders for their particular area.
In this highly visible, hands-on role, you work closely with design engineering, quality, supply chain, and operations to ensure new tools are manufacturable, reliable, serviceable, and ready for smooth transition into sustained production. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service.
Production Associate Roles: Must have visual acuity of 20/20 (corrected or uncorrected) and normal color vision to safely perform critical tasks such as visual inspection of materials, equipment, and labeling, including distinguishing color-coded components in a GMP environment. This role is responsible for life cycle management of clinical and commercial products including process monitoring and troubleshooting, implementation and validation of process improvements and changes, and supporting investigations and corrective/preventive actions.
p>You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.