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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....

- Cranford, NJ
new job!

Global Pharmaceutical company is hiring a \ for their growing company. Our Clinical Trainer is responsible for identifying and implementing Clinical Development staff training needs. They may benchmark Clinical SOPs and insure SOP training is completed and up to date. The Clinical Operations Trainer may also periodically co-monitor and evaluate staff performance and provide guidance for performance, improvement and adherence to FDA and SOP requirements. They may liaise with US and Taiwan....


Global Pharmaceutical Leader is looking for consultant (all levels) Clinical Managers for their growing Clinical Development team Accountable for leading the operational study team, which is responsible for the execution and delivery of quality studies, including in-process quality control activities (e.g. quality checks and balances to ensure inspection readiness, enrollment, metrics, milestones, timelines and budget). This position requires advanced knowledge of the functional disciplines....

- work from home, FL
new job!

Global Pharmaceutical company (headquarted in West Palm BEach, Florida) is growing and needs a Strong Clinical Lead (someone who mas managed the CRAs and the clinical study trials but can also monitor when needed as Snr CRA). Snr Clinical Research Associate for oncology trials. Must have five to eight years of experience with at least two years of oncology experience. Must come from a Sponsor company (Pharma or Biotech) and be bi-lingual (spanish speaking - many sites are in Latin America).....


Our client is a world leader in laboratory equipment and services, and has an opportunity for a Technical Sales Representative (TSR) for its industry leading analytical instrumentation used in R&D laboratories. The TSR will be selling products for Atomic Force Microscope and Nanomaterials Testing include indentation testers, scratch testers, tribometers (high temperature and linear reciprocating), and calotest instruments (coating thickness characterization).This position will be covering....

- Kansas City, MO
new job!

Our client is a world leader in the manufacturing and distribution of analytical instrumentation used in R&D Laboratories. Due to continuing growth they have opening for a Field Service Engineer to be based in the Kansas City, St. Louis or Springfield. This position may also conduct supplemental travel into other territories on a regular basis.Requirements:The preferred candidate will have an A.S. or B.S. in electronics engineering or Chemistry or engineering or other technical degrees as....


The Manager Regulatory Affairs will be responsible for the following: Leading the preparation and filing of regulatory applications (IND, NDA, BLA).Coordinating/meeting with various functional areas in order to identify and obtain information required for regulatory submissions.Developing and/or reviewing regulatory documents (IND, NDA, BLA) in order to ensure that all submissions are of high quality.Leading the preparation of responses to questions from Regulatory Authorities.Developing and....

- Boston, MA

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....


Great opportunity to join an expanding global leader as the site Manager, Analytical QC laboratory with responsibility to provide internal and external customers with accurate, reliable and timely test results for raw materials, in-process and finished goods for this cGMP compliant environment. Strong leadership skills are required to develop, train and manage a team of chemists and technicians supporting this 4 shift operation. Responsibilities: --- Manage and direct the Quality Control/....


Join a Global Company as the strategic North American (NA) Team Leader supporting Analytical/ Synthesis (Methods Development); Product Metabolism, Product Safety (registration); and Regulatory Compliance (EPA). Participate on the Global Leadership Team while developing a challenged, problem-solving analytical team responsible for performing/ delivering scientific studies to ensure a sustainable product safety and registration success. The successful candidate will have a strong background in....

- Pittsburgh, PA

Director of Regulatory and Clinical Operations The ideal candidate will take on the following tasks: · Contribute to the strategic planning of the company’s regulatory affairs · Lead the implementation of the company’s regulatory strategy and provide evidence-based opinions and advice · Manage all relations with FDA and 510k submission · Provide management with continuous input on regulatory matters and their interactions with business development, clinical development, commercialization,....


Top Tier Global Pharmaceutical company is expanding and looking for two Medical Director (for Clinical) must be Medical Doctor with MD degree Can have experience in oncology or even internal medicine and have experience with clinical development. Competitive salary and benefits and bonus, 401k, long term incentives and short term incentives and more Provide medical support for the study team:Global primary contact person during the course of the study for medical;Responsible for content of....


QUALIFICATIONS: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions ESSENTIAL KNOWLEDGE, SKILLS AND ABILITIES: Good understating of cross-contamination, personal hygiene and GMP's Good written/verbal skills Follow all applicable safety....


Director of Regulatory The ideal candidate will take on the following tasks: · Contribute to the strategic planning of the company’s regulatory affairs · Lead the implementation of the company’s regulatory strategy and provide evidence-based opinions and advice · Manage all relations with FDA and 510k submission · Provide management with continuous input on regulatory matters and their interactions with business development, clinical development, commercialization, financial planning,....


The Head of Device SRM (Supplier Relationship Management) manages device supplier relationships. This is a strategic role that will develop and implement internal policies and be influential in decision making across major functional areas: - Develop and manage Suppliers for clinical and commercial devices - Development and implementation for legal and financial aspects of the alliance - Contribute to negotiation of contract terms and conditions, including the management of amendment....


Director Analytical Method Development & Validation (GMP BiopharmaceuticalPhD preferred or MS with LOTS (5+ mgt, 10+ GMP)Analytical Method Devt, qualification and validation experience requiredComplex and New Method workLarge Cell experience is a mustWould love to have protein Characterization and analyticsGMP and STRONG leadership (team up to 60-100), Financial Management


Specialty Pharmaceutical company is expanding the Somerset, NJ location- Looking for a Supervisor, QA Documentation This position serves as a dedicated resource for the administration of controlled documentation and documentation systems at the companys Somerset site. Associated documentation, systems and activities provide support for all facets of material, process and product development, validation, manufacture, testing, storage, service and distribution. It also applies to controlled....


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....


JOB PROFILE: Responsible for the laboratory testing, formulation modifications, quality assurance functions of a growing Sanitation Chemicals operation. This is very much a hands-on role requiring a chemistry background. ISO compliance REQUIREMENTS: BS Chemistry or similar degree Laboratory testing, formulation experience ISO experience No state income taxes, reasonable cost of living in Central Florida


Top Tier Global Pharmaceutical company is expanding their Austin, Texas location $25-30/hour on w-2 with full benefits For the perfect fit for the level III position, it would be someone who also possesses the below mentioned level II experience, with possible experience as a supervisor. (This role is an introductory lead/supervisor position who will oversee the work that the two level II specialists will be producing). Furthermore, previous experience interacting with sites of manufacture.....

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