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- South Bend, IN
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Company Background For over 30 years, this research laboratory has been manufacturing and distributing a variety of enzymes and cofactors used in basic coagulation research. They are known and trusted by coagulation communities worldwide for their purified coagulation factors and research reagents. This research laboratory seeks an energetic Technical Specialist to join their team. Position Overview Technical Specialist reports to the Laboratory Manager. Responsibilities/DutiesPurify proteins....

- Any US State

Open CMC (Pharma) position ... Direct technical CMC for drug development projectsHands on Formulation / Process DevelopmentPost approval maintenance of productsTroubleshoot manufacturing with CDMO's Assess manufacturing changes Maintain CMC, DMF, GMP-QA electronic filesStrong chemistry backgroundHow studies need to be runResponsible for preparation of post approval supplements and other regulatory documents PhD, MS or BS Exp: 5+ yrs

- Milwaukee, WI

Excellent oppt'y for a Medical Technologist to work for a medical lab instrument 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. This position can be based almost anywhere in Wisconsin as long as you are within a 45 minute to 1 hour drive from a major airport.Will also be involved with direct problem solving covering reagents, kits, procedures, adaptations, and

- Los Angeles area, CA

Excellent oppt'y for a Medical Technologist to work for a medical lab instrument 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. This position can be based almost anywhere in the greater Los Angeles CA area:Will also be involved with direct problem solving covering reagents, kits, procedures, adaptations, and software upgrades.Your lab knowledge will also be....

- San Jose, CA

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,....


Our client is a producer of Bio-pharmaceuticals. They have developed core competencies in the development of processes and products derived from natural sources both animal-based and plant-based. They have an immediate opening for a Regulatory Affairs Specialist. RESPONSIBILITIES:This position will provide regulatory support for development and commercial programs.In this role, you will plan, coordinate and oversee regulatory activities.These activities include the preparation of document....

- San Francisco Bay Area, CA

Director, Research - Immuno-OncologyOur pre-clinical stage client is working on exciting technology in the field of Immuno-Oncology.This newly created critical leadership has 4 direct reports currently. Ideal candidate will be a Ph.D with strong industry experience in a pre-clinical setting in Immuno-Oncology. This person will outline, implement, and lead the company research strategy and growth towards commercialization. Every day, they will make decisions that matter. Qualifications:Define....


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....


Job Description: We are seeking an experienced and determined professional with a passion for Project Management. As a consultant you will primarily work with clients in the pharmaceutical industry. You will engage directly with key decision makers and have the potential to create true impact. Tasks will mainly relate to Project Management of or within large investment projects. We are looking for a candidate with strong leadership and communication skills who is driven by a desire for....

- Sacramento, CA

Well-established Medical Device Manufacturer seeks a Field Clinical Specialist based in the Sacranebto area for their line of Interventional Cardiology products, marketed to Interventional Radiologists, Interventional Neuroradiologists, Interventional Cardiologists and Vascular Surgeons. The Field Clinical Specialist will provide clinical insight and educational support/training on the technical applications of company products (physicians, nurses and other medical personnel). The Field....


Global Pharmaceutical company in Northern NJ is expanding and is looking for Packaging Mechanic Serialization Our company is a niche pharmaceutical company that develops, manufactures and markets generic and branded prescription pharmaceuticals as well as animal and consumer health products. We specialize in difficult-to-manufacture sterile and non-sterile dosage forms including: ophthalmic, injectables, oral liquids, OTCs, topicals, inhalants, and nasal sprays. We market our products to....


Global Pharmaceutical company is expanding: OBJECTIVES: - The Project Manager is required to identify and resolve project risks with proposed resolution plan (ad hoc and planned), with escalation to senior stakeholders where appropriate. - They will execute their day-to-day activities in line with company Category Management Framework, with a strong focus on strategic sourcing initiatives which aim to qualify and select suppliers that meet the needs of the business at maximum financial....


DIRECTOR / SENIOR DIRECTOR, REGULATORY AFFAIRS – CMC Our client, a progressive biopharmaceutical company, has a new opportunity for a Senior Director level Regulatory Affairs professional with CMC expertise in the San Francisco Bay area, to drive US and Global Regulatory projects. This is a full-time Senior Director level role with a primary focus on the discovery and development of oncology drugs. Independently manages all regulatory CMC business for oncology products throughout lifecycle.....


The Senior Director, Product Quality and Occupational Toxicology is responsible for providing robust, scientifically-sound hazard and risk assessments to support product quality activities, primarily associated with manufacturing, and health and safety of the workplace for employees handling proprietary and non-proprietary chemicals used in the production of our products.The Senior Director is primarily accountable for product quality/occupational toxicology, working in collaboration with....


My client seeks a Manager of Safety Assessments to oversee a team of toxicologists, chemists, and other technical experts. The ideal candidate will take on the following tasks: Deliver high quality safety assessments of chemicals and products covering toxicological endpoints for a wide-range of ingredientsOversee 8+ PhD scientists and provide coaching, problem-solving, and supportDirect the overall production of safety assessments, including responsibility for meeting the metric goals and....


My client seeks a Senior Scientist to elevate R&D efforts – the ideal candidate will assist with nanotechnology product development and help manage a small group. The ideal candidate will possess the following qualities:MS/PhD in Organic Chemistry or Materials ScienceDemonstrated experience in micro- and nanofabrication and clean room experienceHands-on experience with organic and polymer synthesisProduct commercialization experienceStrong track record of research productivity demonstrated


Major Pharmaceutical and Manufacturing company is looking to hire 6 Production Line Operators - Sterile Fillers for a contract w-2, full benefits start in December and goes to April or May (and can then be renewed) $16-18/hour Must be able to work overtime and third shift All Production Line Operators (Sterile Fillers) are responsible for all activities associated with the manufacturing and filling operations, required to produce sterile drug products under aseptic conditions. Must have....

- Charlotte, NC

A leading provider of innovative solutions in the field of polyolefin compounded resins used in the manufacture of automotive plastic parts and components is searching for a Product Developer. The Product Developer will be a resin compounding professional with command of diverse practices in applications and complex concepts and principles in Automotive product design and end use performance. This knowledge is acquired through deep and/or broad experience typically combined with an academic/....


My client is focused in the oncology space, and they seek a Project Manager to take on the following tasks:Support project development activities and the overall coordination of proof-of-concept, proof-of-efficacy preclinical research projects, non-clinical toxicology and pre-IND activities for internal projects.Collaborate with a cross functional team including internal scientists and CROs to prepare study designs, manage budgets to perform the studies, and oversee the study from initiation....

- Kalamazoo, MI

SUMMARY: Management Business Solutions is actively seeking a 2nd Shift Certifying Scientist for our client in Kalamazoo, MI. The Toxicology Scientist will be responsible for reviewing, certifying and reporting results of biological specimens. The ideal candidate will have experience working in a laboratory environment and be familiar with fundamental and advanced techniques of separation science. RESPONSIBILITIES: Follow standard operating procedures in confirming samples for drugs in a high....

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