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Formulation/Process Development Technical Services

Quality Assurance &
Quality Control


Regulatory Affairs

Analytical, Bioanalytical, Microbiology & Toxicology

Manufacturing & Operations

Validation

Business Development

Medical Writing

Clinical Operations, Clinical Research, MD's

Clinical Research Associates

Pharmacology/
Pharmacokinetics


Project Management

Other

Listings posted January 10, 2012



Some of the listings are posted below. We suggest candidates interested in advanciing their career contact us via phone or email with their resume attached. We will contact you as soon as possible to have a confidential conversation. Please know that these listings can change immediately and not all inclusive. The areas we specialize in our listed.

Formulation, Research & Development

Formulation Scientist

Job Number 996

An expanding CRO has an opportunity for an experienced formulation scientist with a broad background that would include solid dosage experience. A BS degree is required and a minimum of 5 to 7 years hands on experience. Client will consider PhD candidate with less experience but must have ability to work in a fast paced environment and enjoy multiple projects. Company is located in the southeast with excellent compensation and benefits.

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Operations

Vice President, Operations (Filled)

Job Number 986

A multi-national company has an opportunity for a strong leader in operations. Will build their own team and have responsibilities for establishing complete operations as new site head. Experience required from scale up to commercial manufacturing. Person needs to have demonstated success in managing all facets of operations including production, engineering, human resources, validation, QA/QC, and interfaced with R & D from scale up to techncial transfer, both in and out. Must have experience in preparing budgets and working knowledge of P & L. Southeast location. Competitive compensation and benefits.

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Director/ Senior Director, Supply Chain(Filled)

Job Number 989

Our client, a growing biotech company has a new opportunity for a seasoned supply chain specialist. Individual will be the initial person in production, production planning, and supply chain operations. You will be dealing with CMO, CRO companies in selection, negotiating contracts, and maintenance of relationships. Will be dealing with KPI's, and responsible for preparing company for commercial operations.

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Regulatory Affairs


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Director, CMC Regulatory Affairs

Job Number 984

Our client in New Jersey has an immediate need for an experienced leader in Regulatory Affairs with strong CMC strategic, as well as hands on experience in branded products. Individual must have a strong scientific background to provide guidance to the global project teams dealing with regulatory issues. Person should have a PhD in sciences and a minimum of twelve years experience and six years in recent CMC regulatory dealings working with multi-national regulatory agencies. Person will interact with R&D, manufacturing, and QA on CMC issues. Responsibilities will include leadership and coordination of US and EU organizations.

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Analytical Chemist

Analytical Chemist

Job Number 997

Our client located in the southwest has openings for two analytical chemists. Individuals must have a minimum of a BS degree and experience with HPLC(prefer Waters), Empower data system, dissolution testing, method development, and method validation in an R & D environment. Individuals must be able to write protocols and reports suitable for FDA submission.Company is growing and needs to complement their staff with qualified individuals who like working in a fast paced environment. Competitive salary and benefits. Immediate openings.


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Manufacturing & Operations



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Validation

Business Development

Medical Writing

Clinical Operations, Clinical Research, MD's

 

Director, External Data Operations, Clinical Operations

Job Number 988

Our client, a global pharmaceutical company in New Jersey, has an opportunity for an experienced individual to lead a global organization responsible for the data management of all electronically sourced clinical trial data which includes successful sourcing, loading and cleaning externally sourced clinical data into the clinical data management system as well as cleaning lab data collected directly from clinical sites on CRF's. Responsibilitiesof the group include vendor data specifications, data query management, laboratory test dictionary maintenance and the development and maintenance of loading standards. EDO has global responsibility for the support of Phase I through Phase IV studies and is part of the Global Data Operations organization. The successful candidate will have excellent leadership and communication skills. A qualified candidate must have a minimum of a BS/BA in a science discipline with at least 10-15 years experience in data management, clinical, bioanalytical, or computer science experience.

Competitive compensation and benefits.

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Clinical Research Associates



Pharmacology/Pharmacokinetics


Project Management









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