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Our client, a growing Pharmaceutical company located in the Philly area is looking for a Sr. Regulatory Affairs Associate. This Associate will be involved in the preparation and submission of regulatory filings and will interact with regulatory agencies. Specific duties are as follows:Compiling and reviewing ANDAs, Amendments, Supplements, Annual Reports, etc. for FDA submissions. Working with functional business units in order to obtain documentation required for submissions Evaluating....

- Brewster, NY

Our client - a growing Pharmaceutical company is looking for a Site Quality Head for their facility in the Brewster NY area. This is a newly created position at a newly acquired site. This position reports to the VP of Quality. The Site Quality Head will provide leadership for the Quality unit and as well as departmental personnel. (The Quality unit will consist of Quality Assurance and Quality Control.) This position is responsible ensuring cGMP compliance by establishing and overseeing....


Our client, a growing Pharmaceutical Company on Long Island is looking for a Director QA/QC. The Director will have oversight of all QA functions covering manufacturing, packaging and distribution. This position will ensure compliance with cGMP's for manufacture and packaging of all products. These responsibilities will include developing, approving and maintaining in-house QA SOP's for operating areas as well as hosting FDA inspections, customer audits, and outside third party audits.....


The primary focus of the Vice President, US Regulatory Affairs is to lead & develop the direct reports within the Therapeutic Area Additionally the Vice President, US Regulatory Affairs will serve as the RA Business partner to the Global Vice President and the US Leadership team offering regulatory opportunities and business evaluations aimed at expanding the The Company's US business. Will report to Global Head of Regulatory Affairs and have a dotted line report to the....

- Edison, NJ

Our client - a growing Pharmaceutical Company in Central NJ is looking for a Project Engineer The Project Engineer will manage various capital projects from concept through completion. The Project Engineer will also: Implement capital projects and actively participate in cost reduction efforts. Improve manufacturing and utility operations through process improvement techniques. Support manufacturing, facility and utility operations by troubleshooting practices, change requests, conceptual....


Our Client - a major Pharmaceutical Company in NJ - is looking for a Lab Manager to oversee between 8-12 Chemists in their Analytical R&D labs. This position will oversee Scientists in the development and transfer of Analytical Methods for IND/NDA candidates. Additionally - this position will oversee other forms of Routine Testing to include Dissolution, Stability etc. The Lab Manager will also be responsible for leading and overseeing lab investigations in order to determine root cause.....


Our client - a major Pharmaceutical Company in the Philadelphia area - is looking for a Regulatory Affairs Associate - Labeling.The Labeling Associate will be responsible for the development, revision, review, and approval of labeling content for submission to FDA, as well as any post marketing labeling changes.They will also be responsible for the creation of labeling in both SPL and PLR format as well as monitoring changes to Reference Listed Drug (RLD) products.This company has an extensive


Our client - a major Pharmaceutical Company in Central NJ - is looking for a Sr. Regulatory Affairs Associate. The Sr. Regulatory Affairs Associate with be responsible for preparing, reviewing, performing Gap Analysis, and submitting Drug Master Files (Type II, IV and V) according to US FDA requirements. This person will also serve as a regulatory representative on cross-functional teams. These teams are responsible for supporting products throughout the various stages of development and....


Our client - a fast growing generic pharmaceutical company located in central NJ is looking for a Sr. Scientist with hands-on expertise in Solid Dose Formulation. This candidate will be responsible for projects from Formulation through manufacture of the Submission Batch.The qualified Chemist will have significant knowledge and experience in the areas of formulation and process development, scale up and optimization of solid-dosage forms.They will also provide technical leadership in the areas


Our client - a growing Pharmaceutical company in the Bensalem, PA area is looking for a Project /Validation Engineer. The Project / Validation Engineer will be responsible for projects in the following areas: Manufacturing / Processing / Packaging / Plant Qualified Candidates will have Bachelor Degree in Engineering (Chemical, Mechanical or Pharmaceutical) with a strong preference for experience in the Pharmaceutical Industry. Responsibilities will include: Overseeing projects for new....


Sr. Regulatory Affairs Associate Our Client - a growing Pharmaceutical Company in NJ is looking for a Sr. Regulatory Affairs Associate. This position will be involved in preparing and submitting various regulatory filings. The Sr. Regulatory Associate will have frequent interaction with regulatory agencies. Primary Responsibilities will include: - Compiling and reviewing ANDAs, Amendments, Supplements, Annual Reports, etc. for FDA submissions. - Interacting with the Company's various business....

- Piscataway, NJ

The HR Director will be responsible for implementing and overseeing the Company’s HR and business strategy. This position will work closely with the Company’s CSO and the CFO. The Director will sit on the Human Resources Leadership Team and is responsible for the successful HR oversight of assigned client groups.The HR Director will support the company’s R&D and Finance Departments - and will provide a wide range of HR Generalist support to include:Organization DesignTalent....

- Edison, NJ

Our client - a fast growing Manufacturing company located in central NJ is looking for a Manager - Logistics. The Manager - Logistics will be responsible for the following:Domestic/International freightNegotiating Supplier ContractsDeveloping /Implementing Process/Cost ImprovementsPerforming both Service & Expense AnalysisDevelop, Implement & Oversee Global Freight StrategyWorks w/ Supply Chain to perform Comparison AnalysesWorks w/ Supply Chain to prepare inventory projections. Will....

- Chesterfield, MO

Our client, a growing Pharmaceutical company in Missouri, is looking for a Validation Manager. The client is looking for someone who wants to join an organization where they can truly make a difference. The Manager will oversee all Validation operations (i.e. Process, Cleaning, and Packaging)as well Equipment Qualification (IQ/OQ/PQ). The Manager will be responsible for writing and implementing Process, Cleaning, Packaging Validation as well as Equipment Qualification policies, SOPs, Master....


Our client, a major Laboratory Equipment Manager, is looking for a Marketing Communications Specialist. This position is with an established company that has not only been around for over 100 years but also has a phenomenal company culture. The Specialist will create communications programs that will successfully promote the company and its products utilizing various multimedia packages (Brochures, Fact Sheets, Video, POP Displays etc.) The Specialist will also develop email marketing....

- Chesterfield, MO

COMPUTER VALIDATION SPECIALIST Our Client, a growing Pharmaceutical Company located in Missouri, is looking for a Computer Validation Specialist. They are looking for someone who truly wants to have the opportunity to make an impact. The Computer Validation Specialist will be responsible for validation for all computer related qualification / validation protocols. They will be responsible for writing and implementing protocols for Database Application, Automated Manufacturing and Packaging....

- Morristown, NJ

Our client, a growing Pharmaceutical company in NJ is looking for a Sr. Scientist to perform Method Development & Method Validation in support of both Drug Substance & Drug Product. The Sr. Scientist will also be involved with chemical characterization and stability evaluation studies. The qualified candidate will have a Ph.D. with 5-12+ years of experience and must be experienced with HPLC, GC, LC/MS UV, IR, NMR etc. Additionally the Sr. Scientist needs to be able to work....

- Chesterfield, MO

Our Client, a growing Pharma Company in Missouri is looking for a Validation Specialist.This is a great company with a great culture!The Validation Specialist will be involved in all aspects of Validation (Process, Cleaning, Equipment Qualification (IQ/OQ/PQ) etc.).They will coordinate all validation related activities with regards to equipment and processes as well as write Summary Reports (closeout reports when applicable) for validation/qualification protocols.The Validation Specialist....


Our Client, a growing Pharmaceutical Company in Missouri, is looking for Manufacturing / Production Operators (2). The Manufacturing / Production Operators should be open to working a 1st or 2nd Shift. They will be involved in the operation of various Pharmaceutical Production Machinery & Procedures to include: Coating/Encapsulating/Granulating/Milling/Drying/Dispensing/Mixing etc. The Manufacturing / Production Operators will be responsible for accurate Batch Record & Logbook....


Our client, a growing Cosmetics company, is looking for a Process Engineer who will be involved the scale-up of both new & existing products in all areas (Color Cosmetics, Skin Care etc.) This position will interface with personnel in both R&D as well as Manufacturing. The Process Engineer will be involved with Process Improvement, Root Cause Analysis, First Production Batches, Optimizing Manufacturing and Filling Processes etc. The Process Engineer will work with both in-house as well

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