Consumer food processor and distributor to national retailers, independent grocers and online retailers. Responsibilities: Manage a portfolio of new product development projects of all commercialization tasks in the new product development process from prototype to launch to product / packaging changes, optimization projects and product deletions. Optimize and communicate project timelines, process for new products, line extensions, product changes, product deletions, speed to market....

POSITION SUMMARY: Independently responsible for the efficient and thorough investigation of process deviations and customer complaints, determination of root cause, and initiation of corrective/preventative actions designed to adequately address and correct the Quality related deficiencies identified during the investigation process. Responsible to provide proactive corrections based on noted trends to minimize the potential for repeat incidents that may lead to, or result in, the issuance of....

Global Pharmaceutical and Vaccine company is expanding the Marketing division: Objective: To maximize company dose and dollar sales volume in a manner consistent with profit goals. Expectations: ·Achieve forecast as planned. ·Develop realistic and achievable forecast in concert with Marketing and Sales Management. ·Use information systems and reports to monitor and direct the progress of sales and profits toward monthly, trimester and annual sales objectives. PRODUCT LINE MANAGEMENT Objective:

Our client is an industry leader and global manufacturer of paints and coatings for a variety of applications and is in need of an experienced industrial coatings chemist with specific experience in the development of powder coatings. They offer a state of the art laboratory facilities and exciting growth potential. ResponsibilitiesDevelop and update formulas for powder coatings by performing analyses and performance tests. Develop test batches and production scale formulas for powder....

General Job Description: This position would support drug product packaging and combination product development on cross functional teams through all phases of development. Engineer would evaluate materials and designs, execute design verification, prepare design control documents and support usability/human factors assessments. Key Area of Responsibilities: Key areas of responsibility for Human Factors and Design Control Engineer include:Evaluate materials, design, and configuration of....

We are looking for a Project Manager with cGMP/Pharma experience who will be responsible for delivering projects on time within budget and scope. The Project Manager should have a background in business skills, management, budgeting and analysis.Roles and Responsibilities:Coordinate internal resources or third parties/vendors for the flawless execution of projectsEnsure that all projects are delivered on-time, within scope and within budgetDeveloping project scopes and objectives, involving....

Our client is a world leader in laboratory equipment and services and has an opportunity for a Sales Director Americas for their Materials Characterization product lines. This new position is based in the Mid-Atlantic region and will be responsible for all sales and marketing activities of the materials characterization products with company operations and distributors throughout North, Central and South America. The successful candidate will have sales and marketing responsibility for the....

NO VISA's Our client is a rapidly growing company that is on a mission to reinvent the way scientific research is done. They are a SaaS company that bridges software, hardware, and innovation. You will be responsible for architecting, managing and scaling the entire IOT platform that is built on Rancher/Docker and AWS. The RoleTake ownership for health, scalability and availability of our cloud services and IOT platform.Automate the deployment pipeline between our pre-production to production....

Summary of Key ResponsibilitiesProduce high quality and on-time writing deliverables.Plan, write, edit, and format key documents with minimal supervision, including clinical protocols, investigator brochures, clinical study reports, integrated safety and efficacy summaries and related documents. Other documents may include informed consent forms, health authority briefing books, and scientific publications.Facilitate efficient review and finalization process for documents produced internally....

Reporting directly to the Quality Systems and Compliance manager, the Quality Auditor will have responsibility to audit scheduling, planning, execution and documentation of quality system audits of internal processes for the Greenville location. This position will also be responsible for maintaining a library of standards and for reviewing all applicable regulations, standards and communicating requirements to site leadership. This position will provide cGMP / GXP, technical and auditing....