Lead a team focused on the development of personalized medicine utilizing your expertise in translational medicine, biomarker discover, companion diagnostics, and patient population identification.
Develop Preclinical Strategies to optimize patient selection;
*** Analyze and interpret genomic, transcriptomic, proteomic, metabolomic, and pharmacogenomic data sets derived from patient samples, databases and medical monitors
*** Discover molecular markers, such as combinations of somatic mutations ...
We are looking for a Laboratory Medical Technologist to join our clinical team at one of the area's leading medical facilities. We combine the extensive testing capabilities of a large laboratory with ground breaking research.
Ideally, this position is for an individual who is a dedicated Laboratory Technologist with experience in Toxicology.
To qualify, you must have:
· Clinical Diagnostics experience. Preferably, Toxicology experience.(Performing a variety of automated and manual test. ...
our client in Malvern, PA is looking for a planning analyst with SAP experience. This is a long term consulting position. If interested, please apply to this ad
The primary scope of this position will require creation/maintenance of master data, bills of material, master recipes, data tables, and management of interfaces between manufacturing execution systems (MES) and SAP. Additionally, the position is required to schedule and maintain ongoing production planning activities in the co-ordination ...
Contract: 6 Months - extension
Pay Range: $24 - $27/hr
*Previous pharmaceutical expereince required
The purpose of the QA Coordinator is to provide support to the site when implementing new products, review of records to ensure compliance with local and regulatory guidelines, and to execute Quality Systems actions. This is done through direct intervention between this role and other staff in the facility. This role may develop, implement and administer input and in-process ...
Are you a Regulatory Affairs professional looking for a new and exciting opportunity near Philadelphia? Our client is a global biotechnology company in the enviable position of having a strong and growing balance sheet; a promising pipeline with novel drugs targeting great unmet medical needs and serious diseases; two FDA approved products that are today saving and improving lives. Relocation available! Please apply today if you possess the required experience!
The top competencies that ...
Order: PS # 90911
Title: In-house Clinical Research Associate
Location: Wilmington, DE
Openings: 2 OPENINGs
Contract Length: 12 Month Contracts
5 years of Pharmaceutical experience
JOB DESCRIPTION / DETAILS:
(9081) Clinical Research Associate (2 Openings, 12 Month Contracts)
Degree / College Major: Biological science or health care
Number of Years Work Experience Required: 5
Primary Job Responsibilities and Qualifications:
5+ years pharmaceutical, ...
Summary Description: Ph.D. level scientist to oversee and advise the Company regarding its laboratory operations, review and write SOPs, and initiate research in related areas. The Company provides services for referring physicians and patients involving the cryopreservation of adipose tissue as well as the processing of adipose tissue for the isolation, expansion, and cryopreservation of adipose stromal cells (ASC; adult stem cells) and related media for clinical uses. The individual will oversee ...
*Please note that this is a contract assignment. Candidates cannot start an assignment until background check and drug test is completed*
0 or more years prior experience in biological/pharmaceutical/chemical manufacturing environment. Working knowledge of Microsoft Outlook, Internet Explorer, Excel, Word, Powerpoint, MS Project. Strong written and oral communication skills as necessary for documentation authoring, conducting meetings and creating / ...
::Contact Steve for more details at 815-756-1221. Attach resume when responding to this posting::
The Manager will be responsible for all ISO and Quality Systems. Will have 3 direct reports.
- BS/MS Chemistry, Biology or related degree
- 5-10 years in a chemical manufacturing environment
- Experience working with polymer technologies
- 5+ years of management of ISO or Plant quality systems
- Greenbelt or Blackbelt certification
- Working knowledge of regulatory guidelines
Contract Length: 8 months, possible to renew
The candidate will be responsible for preparing global CMC regulatory submissions for company’s marketed drug products. The position will have responsibility for executing global regulatory strategy for anticipated analytical, manufacturing and packaging changes, compilation of post approval regulatory submissions including annual reports, renewals, supplemental applications, variations and other maintenance dossiers and coordination of ...
!!! PERM!!!! - PROCESS ENGINEER
This is an active process engineering role in the design of biological industrial wastewater treatmentfacilities. Major work tasks to include process design & engineering, overseeing pilots, and commissioning of full scale facilities. Dynamic work environment in a team atmosphere.
Duties may include, but not be limited to:
Process design of biological industrial wastewater treatment plants
Mass balances & design calculations
Develop PFD’s & P&ID’s
Working knowledge ...
Full time opportunity for a Chemical Buyer for a manufacturing company located north of Charleston,SC (Georgetown). Must be willing to relocate to the Georgetown,SC area. Coastal SC. Low cost of living.
Products are found in many of the products used around the world every day. Our customers manufacture a wide assortment of products in the textiles, cosmetics, detergents, paper products, plastics and other industries.
Effectively negotiates pricing and contracts with ...
Senior Food Scientist - Beverage Focus
Reporting to the Director of Research & Product Development, the Senior Food Scientist develops new juices, organic products, nutrient beverages, drinks, cocktails, teas, and sauces as well as line extensions. Responsible for the development, formulation and duplication of new products from conception to shelf and for management of development from bench top to manufacturing start-up.
Performs lab analysis and conducts market product ...
JOB ID: PA21179
Job Title: Forensic Scientist
Company: Job Chit Chat
Industry/Environment: Biology (a growing company with a family atmosphere)
• Obtain DNA profiles from evidence
• Write reports of results
• Maintain national DNA database
• Concentration and attention to detail
• Microsoft Office, Excel, PowerPoint, Outlook
• Maintain relationships with detectives and officers
Salary: $19/Hour DOE
Hours: Full Time
This is a great opportunity for someone who desires to learn, grow and be a part of the organ donation, recovery and allocation team. This position offers tremendous growth and rapid advancement potential.
The Referral Intake Specialist triages all calls related to deaths and organ/ tissue referred to GLDP; Initially screens all tissue referrals to determine suitability, notifies in-house coordinator of all referrals that are suitable; Documents all referrals received and enters them into GLDP ...
Director Regulatory Affairs - CMC
The Director, Regulatory Affairs-CMC is responsible for CMC-related regulatory activities. This person develops and implements regulatory strategies related to CMC throughout drug development from Phase 1 through Phase 4. The Director is also responsible for assessing the regulatory requirements of CMC changes, coordinating and contributing to regulatory ...
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