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The Lead, Human Factors Engineering will be serve as a local leader for the Human Factors Engineering Team as it grows. This role will lead human factors work to support the development of devices and combination products for delivery of our wide portfolio of drugs and biologics. This includes leadership in human factors planning, use-related risk management, requirements development and execution of human factors research (user research, formative and summative studies).1. Responsible for....


SENIOR ENGINEER, DELTA V RECIPE LEAD JOB DESCRIPTION Seeking a team player that strives for best-in-class operations amongst a high-performing global team in our Pharmaceutical Operations & Technology IT organization. This lead engineer acts as recipe lead on a DeltaV/Syncade-driven fully integrated facility. This lead creates DeltaV and Syncade design and recipe standards for project that will be used as global standards. The role requires extensive experience and strong knowledge of....


The Senior Manager Clinical Operations is responsible for developing operational strategy for one or more clinical studies, and leading the cross functional Study Management Team to align and deliver on study goals of data quality, timelines, budget and GCP compliance in support of overall program level plans. Responsibilities: The Senior Manager Clinical Operations Lead will independently plan all aspects of the clinical operations for one or more clinical studies and oversee the execution of

- Waltham, MA

TOP TIER PHARMACEUTICAL COMPANY in MASSACHUSETTSglobal biopharmaceutical company developing innovative medicines The company has a diversified commercial product portfolio and a substantial clinical pipeline of product candidates Position SummaryWe have the need for a highly collaborative, experienced Manager of Medical Writing Operations to join our team based in MA. The position reports into our Director of Medical Writing and will lead writing responsibility of documents which ensure....


Two MD contractors needed for Global Pharmaceutical company in Cambridge, MA two roles-Contract Role Only One year contract (renewal up to 4 years), w-2 with benefits offered Has to be office based in Cambridge- we will only consider local candidates at this time. We need PV experience within submissions specifically We have a submission approaching for a product. Need someone with good clinical trial experience. Worked in clinical trial as opposed to post trial setting SPA or European....


High Profile Pharmaceutical company with recent FDA one of a kind approval is hiring a Senior Manager of Regulatory Affairs CMC Reporting to the director technical writing of RA CMC of Regulatory Affairs, the Senior Manager of Regulatory Affairs, CMC will be responsible for the preparation of high quality regulatory submission content focusing on CMC to support global clinical development, registration, and product life cycle management in accordance to regulatory requirements and guidelines.....


Staff Electronic Hardware Engineer Hackettstown, NJ This role is with a global leader in medical technology (imaging, diagnostics, healthcare IT), an organization dedicated to ongoing success by hiring top talent, investing in R&D, and commitment to engineering excellence for over 100+ years. We currently have an opening for an experienced Electronic HW Engineer. The successful candidate has broad experience in electronics design and must be able to work in across functional and across


Sr. Scientist, Process Sciences Summary/Objective: The Senior Scientist plans and conducts experiments to increase the body of scientific knowledge on topics related to the scientific endeavors for our Client. Research may be carried out at a molecular level, using appropriate cell and animal models effects of various factors. Initiates, directs and executes all pre-clinical scientific research and/or development strategies in research and/or development. The senior scientist investigates the....


My client is a dedicated contract development and manufacturing organization (CDMO) focused on development and cGMP manufacturing of biopharmaceutical products derived from mammalian cell culture. They provide a comprehensive range of process development, high quality cGMP clinical and commercial manufacturing services for the biotechnology and biopharmaceutical industries. They have 25 years of experience producing monoclonal antibodies and recombinant proteins in batch, fed-batch and....


This full time, permanent Mechanical Project Engineer career opportunity is at a company that sets the industry quality standard. They design and build all their products in the US. The engineers are known for being highly skilled and innovative. Projects are very diverse so the work here is interesting. Employees leave at 3:00 p.m. on Fridays. The successful candidate's duties and responsibilities will encompass:Analyzing and evaluating assigned projectsAssigning and giving direction to the....


We are actively seeking a Quality Control Chemistry Analyst to join our growing team. The QC Chemistry Analyst position supports the Quality Control group to maintain process optimization and manufacturing activities. The Analyst is charged with being a highly motivated member of the Quality Control (QC) Lab at the manufacturing facility, reporting to the QC Manager. Primary responsibilities for this position will be: perform QC analysis in compliance to cGMP in line with standards prescribed....


We are actively seeking a Quality Assurance Validation Manager to join our growing team. The Quality Assurance Validation Manager is responsible for providing leadership and strategic direction to the establishment of the validation/qualification programs (including the Qualification/PM/Calibration of instruments, equipment, and facilities) and ensuring alignment with corporate standards and regulatory guidance. This position will be responsible for ensuring successful implementation of....


We are actively seeking a Quality Control Manager to join our growing team. The Quality Control Manager is a highly organized member of Lab at manufacturing facility, reporting to the Senior Manager of QC. They are charged with maintaining compliance to cGMP in line with standards prescribed by USFDA. Ensuring compliance to data integrity and cGMP in QC lab in line with standards prescribed by USFDA. Contributing and managing the set up of the QC lab at with guidance of CQA. Assisting in the....

- Lancaster, SC

Overview: A leading manufacturer of animal nutritional supplements is expanding domestically and internationally. This Demand Planning Manager role is a new position within the supply chain group and will report to the Supply Chain Director. Job Duties:Assemble the demand plan for the entire organization.Partner with sales, product managers, senior leadership, and external customers to create, measure, and drive forecast accuracy improvement at the customer and SKU level.Lead cross functional....


We are looking for a Retail Marketing Veterinary Manager to be responsible for maximizing growth of Veterinary Retail customers by leveraging core brand objectives to build, manage, and customize programs to achieve profitable incremental sales and share. This role is accountable for the continued success of the retail marketing team, including articulating the strategy and vision for the Veterinary channel, measuring and developing talent, and ensuring successful planning and ongoing....


The Supply Chain Analyst - Contract Manufacturing position is a ground floor opportunity for a supply chain professional to assist in the development of sound supply chain practices as they related to the contract manufacturing arena. The analyst will provide support in the areas of demand planning, supply planning, warehousing and distribution, and transportation for all contract manufacturing in the domestic U.S. and the international markets. Job Duties:Analyze and create projections....


We are in search of a FULL TIME Family Practice/ Primary Care Physician to provide direct medical care to company employees and their family members.Unlike more traditional healthcare settings, our client's team members have the freedom to spend more time with their patients, while working alongside them every day. It’s a forward-thinking approach that allows them to provide best-in-class services, fostering stronger patient engagement and delivering higher-value programs that have a profound....

- Edgewood, MD

We are looking for a Production Supervisor who will be responsible for supervising all aspects of production on a daily basis and closely monitoring all manufacturing raw material and finished inventories. Responsibilities include:- Interacting on a daily basis with with Sales, Marketing, QC, QA, and Warehouse personnel, and any other internal customers to accurately plan the short-range schedule - Meeting all production commitments, working independently and making effective decisions while....

- Chicago, IL

Our client is a leading global manufacturer of Specialty Chemicals used in industrial and consumer products. Due to their continued growth we are on a search to recruit a Maintenance Supervisor for their Chicago, IL area operation. The Maintenance Supervisor will be responsible for: Mechanical activities of the Industrial Maintenance Mechanics at the site including safety, training, scheduling of all work, quality and efficiency of work activities.Management of MP2 work orders and shutdown....

- Lancaster, SC

We are looking for a Desktop Support Technician to be the central point of contact for IT related incidents and service requests. The role of the Desktop Support Technician will be to provide 1st level support for all employees. The Desktop Support Technician is responsible for resolving support requests as well as meeting customer satisfaction and continuous service delivery demands. The position requires one to be able to work in a fast-paced environment which provides services via the....

141-160 of 162 results
Unless noted above, applicants MUST be authorized to work in the US without Visa Sponsorship. US citizens and Green Card holders ONLY. We do not provide relocation assistance for those living outside the continental US. Please only click apply if you meet the specific requirements of the job listing, you are able to work in the location listed, and are comfortable with the salary range indicated above. Thanks for your interest. We look forward to working with you.