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- Hazelwood, MO

Our client, a major Pharmaceutical Company in the Hazelwood, MO area is looking for a Director - Engineering The Director - Engineering will:Oversee the development of Engineering (Project & Facility) & Maintenance programsProvide Leadership on all Capital Projects to include both planning & implementationCreate Facility Use Master PlansProvide Engineering & Maintenance experience in the start-up/validation of SystemsHire and maintain a staff of technically strong....

- Hazelwood, MO

Our client, a major Pharmaceutical Company in Hazelwood, MO area is looking for a VP Operations. The position will: Oversee all the Manufacturing/Engineering/Supply Chain activities in the company Be responsible for the safe and efficient operation of all manufacturing sites within the company and to ensure GMP standards are maintained Develop and execute policies / goals /objectives / financial plans approved by the VP & the GM The qualified candidate with have a minimum of 12 years of....


Our client - a growing Pharmaceutical company in the St Louis, MO area - is looking for a Principal Scientist in Analytical R&D. This company is going through a major expansion. The Principal Scientist will be responsible for Method Development & Method Validation in support of both Drug Substances & Drug Products. Experience in HPLC, GC, AA, FTIR, and ICP-MS is a must. BS/MS/PH.D. in Chemistry or related. Additional responsibilities will include: Identifying and assimilating....

- St. Louis, MO

Our client - a growing Pharmaceutical company in the St Louis, MO area - is looking for a Manager - Analytical R&D. This company is going through a major expansion. The Manager will be responsible for leading a team of Chemists who will be responsible for Method Development & Method Validation in support of both Drug Substance & Drug Product. Responsibilities will include: Leading the Team in a manner that ensures both a good work environment as well as ensuring that all....

- East Hanover, NJ

Our client - a growing Generic Pharmaceutical company in Northern NJ is looking for 2 Formulation Scientists. The Scientists will responsible for Formulation Projects from “Cradle to Grave”. The ideal candidate will have experience in pre-formulation as well as formulation development/optimization. They will also have experience in tech transfer & scale-up. The Scientists will also be responsible for writing Development Reports, CMC sections etc. The positions require a BS/MS in Chemistry....


Our client - a growing Specialty Pharmaceutical Company located in Central NJ is looking for an Formulation Scientist. The Formulation Scientist will be responsible for formulation and scale-up activities associated with Generic & Rx sterile injectable drug products. The Formulation Scientist will be work on the development of both small molecule & peptide compounds. This is a newly created position. The Qualified Candidate will have an MS/Ph.D in Pharmaceutical Sciences or related....


Our Client, a growing Pharmaceutical company located in Costa Mesa, CA is looking for a Principal Scientist - Analytical R&D. This is a newly created position open as a result of an ongoing expansion. The Principal Scientist - Analytical R&D will:Develop novel methods to solve challenging analytical problemsValidate and transfer analytical methods.Manage multiple projects and ensure timely delivery of all deliverables and will also establish, direct, coordinate and monitor activities....

- East Hanover, NJ

Our client - a growing Generic Pharmaceutical company in Northern NJ is looking for 2 Analytical Chemists. The ideal candidates will have experience performing Method Development / Method Validation / Method Transfer. Pharmaceutical Industry experience with HPLC / GC/ UV/Vis / FTIR / Particle Size Analyzer etc., as well as having experience writing Reports & SOPs is a must. The positions require a BS/MS in Chemistry or related with industrial experience (2-7 Years) in Analytical R&D....

- Piscataway, NJ

Our client - a growing Pharmaceutical Company based in NJ is looking for a Chemist to work in Analytical R&D. This is a newly created addition to staff. And if you are strong performer in the lab, and want to be rewarded for your efforts, you will want to work at this Company. The Chemist will perform analytical method development, method validation and method transfers in support of Formulation Development of new products. The Chemist should be strong in HPLC, GC etc. and ideally have....

- Fort Washington, PA

Our Client, a growing Pharmaceutical company in the Fort Washington, PA area is looking for a Sr. Process Engineer. This company has experienced tremendous growth over the past two years and will continue to grow at a fast pace in 2016. The Sr. Process Engineer will be responsible for projects involving:Tech TransferScale-UpSubmission BatchesProcess ValidationThe qualified candidate will have extensive experience working with Solid Dosage Forms and should have strong knowledge in Granulation,....


Our Client, a growing mid-sized Pharma company located in Upstate NY, is looking for a Sr. Manager/Associate Director - Regulatory CMC. The responsibilities are listed below: Works with Project Management, Operations, Subject Matter Experts (SMEs) etc. to manage Project Timelines.Assists with the planning, writing and reviewing of regulatory / technical documents and CMC regulatory modules with multi-disciplined project teams and SMEs.Will correspond and interact with regulatory agencies,....


Our client - a growing Pharmaceutical Company based in Central NJ - is looking for a Scientist - Preformulation. This is a newly created position. The Scientist will have the following responsibilities.Will develop strategies (both Preformulation & Formulation) in order to identify any liabilities/problems that could impact both drug substance and drug product development.Will develop and preform various studies (e.g. Solubility, Formulation Screening, Degradation) etc.Will develop....


Our client - a major Pharmaceutical company is looking for a Director - Regulatory Affairs. The Director will serve as the Regulatory Strategist for development projects throughout drug development life-cycle and will have responsibility for providing US regulatory input to Global development plans. Responsibilities are as follows:Develop and implement Regulatory Strategies for both development projects as well as mature products and ensures input to the global development plans.Provide US....


Our client - a growing Pharmaceutical Company in Central NJ - is looking for an Analytical Chemist. This Chemist will be responsible for:Performing method development/method validation for complex Injectable formulations (small molecule and/or peptide formulations).Working with External Labs for Method Validation/Method TransferThis is a newly created role. The Qualified candidate will have an MS/Ph.D. with between 2-8 years of Industry experience in Analytical R&D with small molecule....

- Buffalo, NY

Our client, a global Pharmaceutical company located in Upstate NY, is continuing to expand.The Company is looking for Production Supervisors on all shifts with experience in any dosage forms (solids, liquids, sterile etc.)The Production Supervisors will be responsible for:Supervising personnel as well as coordinating Production Processes.Ensuring compliance with cGMPs as well as Company SOPsConducting Deviation InvestigationsPerforming root cause analysis and implementing CAPA.Experience in an


Clinical Project Manager (CPM) The CPM will be responsible for: Managing early phase clinical trials as well as managing & scheduling the CRAs assigned to the project. Preparing the project/monitoring plan for the studies. Monitoring budgets and fund expenditures for the assigned trials Preparing the Study Budgets. Performing Site Qualification Visits Implementing Contingency Plans in order to meet timelines Experience: 6+ years of Clinical trial management experience Doctorate,....


Clinical Project Manager (CPM)The CPM will be responsible for:Managing early phase clinical trials as well as managing & scheduling the CRAs assigned to the project.Preparing the project/monitoring plan for the studies. Monitoring budgets and fund expenditures for the assigned trialsPreparing the Study Budgets.Performing Site Qualification VisitsImplementing Contingency Plans in order to meet timelinesExperience:6+ years of Clinical trial management experienceDoctorate, Masters or....

- Morristown, NJ

Our client - a major Pharma company located in the Morristown area is looking for a CRA Manager (U.S.) The CRA Manager will be responsible for:Managing & training of the Sr. CRAs, CRAs, and contract CRAs in U.S.Assigning workloads to the CRAs and ensuring that the proper resources are in place at the various sites for both current and future clinical studies.Ensuring that all studies being monitored are GCP compliant and adhere to the Company’s SOPs.

- St. Louis, MO

Our Client, a Pharma Company located in St. Louis, MO is looking for a VP-Quality. The VP-Quality will have overall responsibility for QA/QC/Validation/Regulatory Compliance, Investigations etc. The VP will oversee that all aspects of operations in the company in order to confirm that they are GMP compliant. Additionally - this position will ensure that products manufactured by the Company meet all appropriate quality standards, both internal & external. The VP will be responsible for....

- New Brunswick, NJ

Our client, a major Pharmaceutical Company, is looking for a Principal Scientist to work in their Analytical R&D department. The Principal Scientist will be responsible for managing 2-4 Scientists as well as managing their own Projects. The Principal Scientist should have solid experience in Method Development / Method Validation in the Pharma/Biotech industry. Ideally they should have Analytical experience with Products in any of the following areas: Injectables, Peptides, Emulsions,....

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