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- Philadelphia, PA
new job!

Refinery Analytical Chemist Near Philadelphia PA Assists with Lab Technical activities related to all of the refinery processes and products including test methodology, equipment purchases, and equipment calibration and repair. Assists in managing daily laboratory operations insuring: quality of test results, efficient inventory management, and the proper storage/ handling of samples for regulatory compliance purposes.Perform technical work in analytical or physical chemistry involving a....

- MI
new job!

REQUIREMENTS: Looking for advancement opportunities in a small industry leader organization where you can wear lots of hats, make an impact and still maintain work life balance? Do you have the following?Minimum of a BS in Chemistry or Chemical Engineering, advanced degree preferredAt least 7 years of related experience in direct glazing, adhesives, sound damping or polymer/water-based coatingsExperience must include: 3 years of developing and testing adhesives or other bonding material.....


Process Development Engineer – Solids Processing Location: Suburban NY close to NYC and North NJ Here's an opportunity to make a big impact with zero “corporate red tape”. Get in near the ground floor in this established and well-funded startup company. They are working to develop a “Green” source of traditional petrochemicals used to make plastics! Your success in this position is a key step in the overall company’s success. In this role, you will be a big-fish in the small pond. Let’s start....

- Hopkinsville, KY
new job!

Our Food Safety Manager is responsible for managing our in-house Micro-Lab and implementing and managing process control systems and preventative actions in the food safety area. You will manage all HACCP and Regulatory compliance issues at this processing site. Client company cannot sponsor or transfer Visa's at this time. Qualifications:Bachelor’s degree in Food Science, Microbiology, Chemistry, Biology. An advanced degree is preferred.A minimum of two years’ experience in Food Safety....


Job DescriptionSummary of the Position:Keeps Regulatory Affairs Director appraised weekly of all tasks and projects. Gather documentation and compile materials required for international product registrations. Coordinate with International Product Manager and the International Business Unit a viable timeline for registration approvals with the Regulatory Affairs Supervisor or Director of Regulatory Affairs & Technical ServicesRoles and Responsibilities:Maintains all (electronic/hard) files

- Charlotte, NC
new job!

Job DescriptionThe IT Service Desk is the central point of contact for all IT related incidents and service requests. The role of the Desktop Support Technician is to provide 1st level support for all company 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 phone, e-mail....

- Rockford, IL
new job!

The Compliance Manager will provide a broad range of compliance services in support of Quality Department. Essential Duties and Responsibilities include the following. · Performing periodic GMP/food safety related audits in internal manufacturing and distribution facilities, supplier audits in a variety of food processing/packaging environments, label compliance audits, and maintenance- food safety related performance audits. · Responsible for Managing the Company’s Tracegains System and....

- Cincinnati, OH
new job!

Job Description: Responsibilities include supporting daily compliance and systems activities. Performs audits (internal and vendor audits), supports change control program, complaints and any customer services related to Documentation Center. Also works with manufacturing to identify resolution to events while working with Quality Management. The candidate will perform general QA work, using their ability as a skilled contributor in completing tasks where judgment is required in resolving....


Company is seeking a Principal Engineer to lead projects in the Biologics process development and clinical manufacturing projects. The individual will design, develop, scale-up and optimize drug substance and drug product unit operations for protein therapeutics. Experience managing projects from Discovery integration through GMP manufacturing, with both internal and external partners are required. The candidate should have strong technical, communication and interpersonal skills, be able to....


Seeking an experienced Quality Assurance professional with proven leadership skills, a collaborative work style, a passion for learning, and one who is decisive and takes initiative. As QA Supervisor you will lead all facets of the Quality Assurance Department including Quality Programs, Food Safety, Sanitation Programs, Customer Programs, Data Management, Process Improvement and Laboratory Analyses. You will be a key member of the management team driving a culture that values progress but....

- Any US State
new job!

Title: Formulation Chemist Develop new pharmaceutical products. Pilot scale batches, test a variety of product dosage forms including tablets, liquids, powders, soft chews, sustained release products and ointments. Document laboratory and pilot scale batches to meet GMP requirements. Performs routine and non routine testing on new product formulations using established analytical procedures. B.S. Chemistry Degree 5 yrs experience in a chemistry or pharmaceutical related field Previous....

- Parsippany, NJ
new job!

Our client - a growing Pharmaceutical company in Northern NJ - is looking for a Sr. Regulatory Affairs Associate. The Sr. Regulatory Affairs Associate will helps to put together and submit regulatory submissions to the FDA. These submissions will include: ANDAs, Amendments, Supplements, Annual Reports etc. (There may be additional work involving 505 (b)(2) submissions as well.) This position will also involve effective interaction with other departments with regards to the information required

- East Hanover, NJ
new job!

To be considered for this position you must have at least 7 or more years of regulatory affairs experience in the area of In Vitro Diagnostics (IVD) along with hands-on preparation of 510K submissions for IVD products. Strongly prefer someone form the medical device industry (not pharmaceutical mfg). Any experience dealing with face-2-face meetings with regulators (like Pre-Submission meetings) will be considered a valuable asset. Provide regulatory strategies for products, including....


Excellent oppt'y for a Medical Technologist to work for a medical lab manufacturer and utilize their lab knowledge as a Technical Support Specialist. Will be instrumental during the installation process as a trainer, and documenting the lab procedures. Area to be covered is approx 150 mile radius of San Jose (Sacramento - Stockton - San Jose), and maybe a bit south of San Jose. Can reside almost anywhere is this area. Will also be involved with direct problem solving covering reagents, kits,....

- Newark/Princeton Area, NJ
new job!

Our client, a Fortune 150 Medical Diagnostics Equipment Manufacturer, is looking for a Senior QA Auditor to join Division Team in Central New Jersey area and independently conduct assigned audits to assess compliance to applicable business/division requirements, external standards/regulations and Corporate Quality System requirements across multiple Plants within Division. Participate in audits of manufacturing and commercial affiliate sites.in US and CanadaManage and/or participate in....


The R&D Formulation Scientist will be responsible for all aspects of product development for topical cosmetic and OTC products, such as formulation development, sourcing raw materials, and oversee the process from scale-up through launch. Working on multiple projects simultaneously, this individual is responsible for designing experiments to support product development in a team based environment, and will conduct hands-on laboratory and bench work, while participating in multi-functional....


We are seeking a Engineering and Manufacturing Systems Analyst to be located at the Chattanooga, TN manufacturing facility. This is a rare ground floor opportunity with a leading global manufacturer. This position is due to growth and is just one of the first of many to follow at this location and within the organization. The company is growing rapidly and the opportunities are developing daily for this and other positions here. Start now! The sky is the limit. This is an exciting opportunity....


Title: Director Regulatory Affairs Oversee Regulatory Affairs (Animal Health) – USA & Canada (SME) FDA audits – Point Player with FDA Regulatory strategy, labeling, and promotional material Facilitate product transfers Degree – Scientific 10+ yrs Reg Affairs Experience


Title: Pharmaceutical CMC Manager Oversees research efforts of the CMC team within the Pharmaceutical Development Group. Evaluates needed resources to meet the project expectations for CMC support and anticipates gaps to avoid project delays. Formulates a plan for building the CMC section of each project. Coordinates with key players inside and outside Research & Development to ensure CMC needs are met BS in Chemistry, Engineering, or related science10 years experience in chemistry-related

- Any US State

Title: Sr Reg Affairs Mgr Regulatory compliance with relevant regulations managing submissions with regulatory authorities. Ensures compliance with relevant regulations. Manage regulatory documents, pre and post approval.. Education: BS Science Minimum 7+ yrs animal health regulatory experience, Previous relationship with FDA

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