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- Atlanta, GA
new job!

Our client, a global leader in the manufacture of coatings and raw materials for coatings, requires an experienced Quality Control Manager for their Atlanta, GA area production facility. ResponsibilitiesSupervise an industrial laboratory staff of 12 technicians and be responsible for hiring, performance reviews, disciplinary actions as required. Coordinate laboratory testing activities with raw material suppliers, customers and other internal technical teams. Employ industrial chemical testing

- Los Angeles, CA
new job!

Data Scientist JOS000000567 Full-Time/Regular EmploymentDegree in Statistics or related field.Prior experience as Data ScientistCompany is experiencing rapid growth.Experience with financial transaction data.Payment industry experience is a plus.R, PythonSAS, SPSSDevelop rules and models to detect risk in portfolios.Multivariate Regression, Logistic Regression, clustering algorithms, Support Vector Machines, Decision TreesPredictive ModelingRelocation assistance may be available.Targeting....

- San Jose, CA
new job!

This role initiates, directs, and executes scientific research and/or development strategies to create profitable produce/ vegetable products. Responsibilities: --- Research and/or develop genetic testing, analysis, and evaluation. --- Develop program strategy and participate in achieving strategies. --- Develop and coordinate the inbred line development. --- Coordinate screening and development of lines and end products. --- Develop, conduct and evaluate tolerance for species at seedling....


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 Manager 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....


Position Summary: The Manager Strategic Analytics will work closely with members of the Marketing, Finance and IT departments. The analyst will be responsible for creating measurable campaign test designs, building statistical models (Regression, tree-based, time series and more), model implementation, and model monitoring, writing and maintaining SAS code. The ideal candidate will have a balanced background in both Statistics and Business Analytics. The ideal candidate will possess the....


Regulatory Affairs Team Lead New Jersey Massachusetts Our client, a global pharma company has a new opportunity for a Team Lead level professional with Regulatory Affairs/Oncology expertise to drive US and Global Oncology projects. This is a full-time Team leader level role driving regulatory strategy of oncology drugs. Independently manages all regulatory business strategies for oncology products throughout lifecycle. Responsible for the regulatory strategy of submissions for all products as....


Regulatory Affairs Project Manager Job – Medical DeviceOur client needs a Regulatory Affairs Project Manager to support Asia Pacific (Japan, China, South Korea and Taiwan) regulatory approvals for implantables. Comfort and experience working hands on with design and validation reports and other technical files is needed.RequirementsPrevious experience authoring or approving design and validation reports a plus (strong technical writing skills).Experience in Regulatory Affairs with US Class III


Our pharma client needs two Sr.Clinical Operations Associates for a one-year contract. They will work with the Clinical Trial Manager and Operations Study Lead in the operational execution of assigned clinical studies. RequirementsScience degree preferably in science or health-related field Previous experience of working on a clinical study Good Clinical Practices, ICH guidelines, PhRMA code, CFR Guidelines, clinical research ethics, HIPAA and patient privacy laws (plus applicable local....

- San Diego, CA

Our client - a major Pharmaceutical company in SoCal - is looking for Analytical Chemists. These Chemists will work within the company's Analytical R&D department. Responsibilities will include:Method Development / Method ValidationDevelopment of stability studies Performing literature searches Documenting/Recording all experimental activities in laboratory notebooksThe Qualified Candidate will have analytical methods development experience in a pharmaceutical environment. (4-10+....


The company is a leading, privately held national food service company serving business and industry, education, healthcare and the entertainment sectors with on-site dining, catering, vending and beverage services. RESPONSIBILITIES: Primary point of contact for all quality assurance and food safety related topics and company liaison to clients and regulatory agencies for safety inquiries, issues and concerns. Process and standards expert responsible for initiatives, development, improvement,....


Manufacturer of artisan proof and bake and ready to bake croissants, Danish, puff pastry, strudels, muffin batters and breads supplying the Food Service, Retail and In-Store Bakery, C-Stores and Travel and Leisure channels. Responsibilities: Responsible to ensure compliance to company quality and food safety policies and federal, state, and local regulatory requirements to include the Food Safety Modernization Act (FSMA). Ensures compliance to company quality procedures, ingredient....


A Project Planner is needed by our pharmaceutical client in Irvine, CA. This is a one-year on-site position.Requirements:Life science and/or business degree with at least 5 years of experience in the industry, preferably with a sponsor or CRO.MS degree and PMP certification desirable.Strong knowledge of and experience with clinical study/trial operations processes.At least three years of Project Management experience required.OverviewThe Contract R&D Project Planner is responsible for....


R&D APPLICATION ENGINEER - INDUSTRIAL GAS - HEALTHCARE - MEDICAL EQUIPMENT - MEDICAL DEVICE Our client, a Fortune 300 company and leading global supplier of atmospheric gases and equipment is seeking a Healthcare Applications Engineer based out of their state-of-the-art Technology Center for global plant engineering and research and development. SCOPE: As a member of the Healthcare Applications team, the successful candidate will work with the regional healthcare business leaders to....


***RETAINED SEARCH**** My best client, a $850MM Global Manufacturer, has recently created a brand new position of VP of R&D to head up worldwide R&D efforts within their Advanced Materials Division. The Advanced Materials Division's primary focus is supplying the semiconductor industry with the tools it needs to produce semiconductor based products like microchips, solar cells, LEDs, etc..... The primary mission of the VP of R&D is: Allow the company to continually adapt its....


Senior Clinical Trials Project Manager Elmsford, NY or Glasgow, DE (Relocation Provided) Competitive Pay, Bonus, 4 weeks PTO, 6% 401K, Great benefits We have a new opening for a Senior Clinical Project Manager with a longstanding client; a multi-billion ($8B+) global medical diagnostics/instrumentation company. They have strong revenue growth, a stable environment, very low turnover, and offer the opportunity to work on customized, complex medical products that impact people's lives. A lot


This position will have oversight of Quality Systems implementation and management; audit support; Quality Assurance and Quality Control operations; and compliance for the Fiber Business Group in accordance with established practices, processes, regulations, guidelines and standards in a safe and efficient manner. Essential Duties and Responsibilities: Take leadership and ownership of Quality, ensuring product design Quality relative to manufacturing and product safety, and regulatory....


Responsibilities:Manage cleaning and sanitation employees in a food manufacturing facility;Train new sanitation employees in proper cleaning SSOPs, chemical use and safety procedures;Ensure uniform pre-operational standards through inspection and training;Solve concerns in regards to GMP, SSOP, SQF, SDS, and Process Control programs;Inspect plant, stored equipment, and environment for cleanliness;Establish and maintain a Master Sanitation Schedule for the entire facility and....

- East Hanover, NJ

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....

- Hopkinsville, KY

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 five years’ experience in Food Safety....


Director of Quality Assurance My client is focused on cell therapy products, and they actively seek a QA Director. The ideal candidate will take on the following tasks:Establish, develop and manage the quality management system for the firm.Build the quality department infrastructure to assure compliance to company, industry standards and the applicable regulatory requirements.Interface with external personnel (vendors, partners and regulatory bodies) and internal personnel (management and....

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