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Position Overview Provide analytical expertise and leadership in the development of drug substances and pharmaceutical products from early development through commercialization. Plan analytical research and development activities, devise strategies for achieving project goals and independently manage CMC timelines. Make pivotal contributions to drug product development strategy at project team level. Independently manage multiple projects and ensure timely delivery of all deliverables to meet....


Associate Director, Process Development Position Summary: This position will support the development of novel active compounds within the company pipeline. Specifically, this position will provide strategic leadership for drug substance unit operations, scale-up and optimization in development from R&D to cGMP Phase 3 manufacture to process validation. Specific areas of focus include reaction engineering, crystallization and process modeling. The individual is expected to integrate QbD....


Associate Director, Biologics Development Position Overview The Associate Director, Up-stream , will be an instrumental team member of the Biologics Development Process Sciences Department, based in Irvine, CA. The primary roles of this position are to independently plan, design, and execute the experiments and develop processes to support protein expression, fermentation, and purification process development of natural and recombinant proteins (including neurotoxin and antibodies) from....


Principal Engineer is a technical leader who is a member of the Commercial Device Engineering team accountable for leading the technical aspects of combination products that are on-market device products. These products enhance patient and medical professional experiences with drugs via delivery devices. In particular, this technical leader needs to have the medical device manufacturing experience including polymer / plastics processing and assembly methods, working with outside vendors and....

- Bluffton, OH

General Position SummaryThis position is responsible for supporting new model program to start smooth production of new model parts’ orders. Duties for this position include support role for contract review, forecast and production capacity management, order processing, sales planning activity, Sales Department required reports and asset management. Essential Job Functions Support the reviewing of contracts.Support collecting all necessary information for contract reviews.Support in arranging....

- Lewiston Woodville, NC

The overall purpose of a Maintenance Supervisor/Team Lead is to oversee the day-to-day supervision of maintenance associates and provide leadership and management in the work environment. The Maintenance Supervisor/Team Lead will employ the Team Management Concept within the Maintenance Department to meet and exceed production requirements and goals; and provide training to lower level maintenance associates, to assist and develop their knowledge, skills, and abilities. Specific areas of....

- Gratiot, OH

TITLE: Medical Technologist, MLT(ASCP) or MT(ASCP) LOCATION: Ohio Are you considering a career change? Looking for a smaller community, that offers a low cost of living and has plenty of activities in the area but is within an hour of a large city. If so, an opportunity to work with an integrated health care system based in east central Ohio is looking for someone to join their team. This facility is part of a not-for-profit system and has over 300 physicians and multiple outpatient care....

- Cambridge, OH

TITLE: Medical Technologist, MLT(ASCP) or MT(ASCP) LOCATION: Cambridge, Ohio Are you considering a career change? Looking for a smaller community(25K population), that offers a low cost of living(18% lower than US average) and plenty of activities in the area but is within an hour of a large city. If so, an opportunity to work with an integrated health care system based in east central Ohio is looking for someone to join their team. The system is a not-for-profit and has over 300 physicians....


TITLE: Respiratory Therapist(RRT or CRT) LOCATION: Cambridge, Ohio Are you considering a career change? Looking for a smaller community(25K population), that offers a low cost of living(18% lower than US average) and plenty of activities in the area but is within an hour of a large city. If so, an opportunity to work with an integrated health care system based in east central Ohio is looking for someone to join their team. The system is a not-for-profit and has over 300 physicians and multiple


TITLE: Director of Quality, Risk and Safety Management LOCATION: Northern, NV Would you like to work in a facility that will allow you to have work/life balance? This area is not like Las Vegas or Reno. It offers the mountains, skiing, scenic bikeways, lakes and rivers. It also offers a vibrant community that has theatre, galleries and some cowboy country all in a town of 35,000 population. Summary: The Director of Quality, Risk and Safety Management is responsible for but not limited to:....

- Danville, VA

TITLE: RN- ICU Director Location: South Central, Virginia Are you interested in making a difference in patient care? Are you looking for a facility that is interested in candidates that want to grow professionally but have not been given the opportunity? Would you like to work in a facility that is midsized(250 beds) and can offer small town living with all the amenities within an hour of 2 larger cities? Then this could be an opportunity for you. Description: The ICU Director is responsible....


Job descriptionUnder indirect supervision, performs variety of non-professional patient care duties for Health Plan members in inpatient skilled nursing facility (SNF); is responsible and accountable for assigned tasks. Essential Responsibilities:Gives input to RN for development and revision of patient care plan.Assists with ongoing data collection; identifies changes in patient status and reports changes to RN/LPN.Implements care plan; sets priorities of care with licensed staff.Assists with


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.....


Industrial Engineer-Distribution Maintain the Labor management & Engineered Standards Program for the Distribution centers -Develops standards for new operations -Monitors accuracy of installed standards on continuous basis -Collect data, hold meetings with supervisors and employees, update labor management systems to new standards, maintain all records of time studies or other data to change studies, -Knowledge of Warehouse Management Systems -Labor Management Systems, required knowledge....


SUMMARY OF RESPONSIBILITIES: The person in this position supports new product launch to ensure Supplier Quality Assurance/Control Management documents meet customer expectations, including developing related documents. Also will manage ECI (engineering management implementation) by communicating all department schedules and expectations. MUST have: automotive manufacturing QC/QE experience (minimum 3 years), product launch AND welding. JOB DETAILS:. Review new product design, and coordinate....


Directs Team Leaders and other Team Members in assigned manufacturing area(s) in the execution of the group’s responsibilities. Support the manufacturing areas and maintain the overall production area with a focus on minimizing down time, increasing productivity, and coordinating preventative maintenance activities. Manages group of team members, and responsible to accomplish company goals and targets in accordance with all company policies, maintenance standards and methods, and standards for


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....


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....

- Gorman, NC

This is a permanent, full-time position offering a great salary, a benefits package, and a fun and friendly work environment! Responsibilities: - Oversee all field labor, quality control, labor coordination, ensure safety on the job and make sure project is completed under budget and on time. - Completely responsible for quality installation of the project. - Coordinate weekly safely meetings, on-site functions, and equipment deliveries with the general contractors. - Schedule periodic....

321-340 of 388 results