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- Raritan, NJ
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We are looking for a Formulation Scientist with experience formulating Parenteral Dosage Forms. The Formulation Scientist will work at our client - a Pharmaceutical Company located in Raritan NJ. The qualified candidate will have experience with Pre-Formulation, Formulation, Scale-up of Parenteral Dosage Forms. Experience with Lyophilized products will be a plus. The Formulation Scientist will be involved in Literature Searches, writing Experimental protocols, identifying CPP's & QTPP's....

- Plainsboro Center, NJ

Sr. Quality Engineer Industry: Medical Equipment / Devices Assures Regulatory and Quality compliance in the area of verification and validation, design controls, and design transfer engineering for Integra’s biomaterial products.Contributes to and executes engineering schedules and plans.Supports new product launches in compliance with EMA, FDA, and Notified Body requirementsReviews and approves written reports and engineering documentation as necessary.Executes tactical implementation of....


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....


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+....


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....

- Pittsburgh, PA

My client’s team is growing and they look to add a new Scientist to their team. The ideal candidate will solve technically challenging problems, develop new and improved products and services, and liaise with a team of technical professionals focused on patient health. The ideal candidate will take on the following tasks:Create algorithms to advance the company strategy of improving outcomes for at-risk patients.Collaborate with physicians, software engineers, and data scientists to identify....


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....


Minimum Requirements: B.S. Chemical Engineer, Mechanical Engineer, Chemistry with a minimum 8+ years of experience out of chemicals, pharmaceuticals, biotech, foods, or something very closely related. Candidates must have two years’ previous supervision experience, but they do not need to have prior plant management experience. They should have supervised at least 15 operators. Pluses would be: previous budget responsibility, previous maintenance experience or experience overseeing....


WIll be responsible for managing product lifecycle Iinvestigations, analysis, recommendations, and implementation of product involvements. Will be involved with statistical data analysisof the manufacturing process and QC data.A Bachelor's degree is required along with 2 - 3 years related experience and/or trainingin a biotech company. Any experience as a Medical Technologist would be a plus. Essential duties include: - Perform product improvement and development activities to include pilot....

- Lexington, KY

Company Information: The company is a $2B, privately-held manufacturer of all-natural animal feed additives, agricultural additives, food/beverage additives and various other related products. Four of this company’s manufacturing facilities are located within driving distance of Lexington, KY and overall, this company has over 4,500 employees in 120+ countries throughout the World. Job Description: This person will work at the World HQ for a rapidly growing additives manufacturer and will....


The positions serves as the site’s Oral Solid Dosage (OSD) platform leader and reports directly to the Sr. Director of Process Development. Responsibilities include management and oversight of multiple early and late stage development projects and support personnel. Job Functions: Demonstrates technical expertise in OSD technology and methodologies. Lead site related process development, scale-up, commercialization and tech transfer responsibilities Collaboratively develop project strategies....

- Cincinnati, OH

Job Description: Responsibilities include supporting daily compliance and systems activities. Performs audits (internal and vendor audits), supports change control program, complaints and any customer services related to Documentation Center. Also works with manufacturing to identify resolution to events while working with Quality Management. The candidate will perform general QA work, using their ability as a skilled contributor in completing tasks where judgment is required in resolving....

- Cambridge, MA

CLINICAL PROGRAM MANAGER MUST BE STRONG CLINICAL OPERATIONS BACKGROUND Clinical OPERATIONS Program Manager position assigned one or multiple compounds and they would be responsible for the clinical operations (planning, execution and oversight of activities) Working with our PRA Embedded team study execution team to ensure studies and executed and plans are in place to make sure things are on track for timelines and budgets Cross functional team work within Company and outside of Company....


We are working with a client in the Madison area in need of a Senior Quality Control Analyst. This client is a manufacturer of pharmaceutical ingredients. This position is for an experienced analyst with experience in qPCR and molecular technologies. This opportunity requires this person to be independent and a creative thinker. Responsibilities:Responsible for performing complex and routine laboratory analysis and testing of raw material, finished product and special products.All work is....

- Durham, NC

ICITIZENSHIP: US Citizen or Permanent Resident [Green Card Holder] . - NO H1B Ideal candidates should have extensive knowledge of Linux and excellent communication skills. Relevant areas of expertise might include large-installation systems administration experience and strong programming and scripting ability, but specific knowledge of and level of experience in any of these areas is less critical than exceptional intellectual ability. We will consider candidates at all levels of experience,....

- Indianola, PA

NO H1B, CONTRACT or HIRE. FULL TIME w2 ONLY!! CITIZENSHIP: US Citizen or Permanent Resident [Green Card Holder] JOB DESCRIPTION *Design and develop medical device software. *Lead the design and development of medical device software - Defines requirements for design elements at the module level. - Responsible for design and integration of high complexity design elements and modules. - Applies understanding of product line and clinical applications to develop product or process functionality. -


Our client - a Pharma company in Central NJ - is looking for someone with strong experience with scale-up/tech transfer of sterile dosage forms (ideally Parenterals). In addition to having strong technical skills - the Qualified Candidate will have good “soft skills” since they will also be interfacing with CMOs. The Company said that they can fill this position at either a Manager or Sr. Manager level. This position requires BS in Chemical Engineering, Physical or Analytical Science or....


Senior Electrical Engineer We are currently seeking an experienced Electrical Engineer to join our clients technical team. In addition to acting as the lead electrical engineer on projects, you will provide technical guidance to their junior design staff and have the opportunity to work on a range of projects.Position Responsibilities:Lead Electrical Engineer on projects.Responsible for production and review of narratives, drawings, and specifications for all assigned projects.Construction....


Our client - a growing Pharmaceutical company in Raritan, NJ is looking for a Sr. Scientist. The ideal candidate will have experience developing novel LC-MS Methods. They will also have experience developing quantitative analysis methods using mass spectrometric techniques. The qualified candidate will have strong knowledge of high resolution LC-MS (especially structural characterization/elucidation work of small molecules) as well as experience in troubleshooting MS methods. Any experience....

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