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Associate Director, Compliance Jobs

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Associate Director, Consultative Solutions

Medivo

Location: New York, NYType: Full TimeMin. Experience: Experienced Summary: Medivo?s Lab Exchange (LVX) is a network of 140 labs across the U.S. The LVX gathers lab datasets from multiple labs then harmonizes the data so it is able to be tracked at patient, physician, practice,

9/7/2014  New York, NY  Save This Job

Senior Manager/Associate Director, Clinical Quality Assurance (14-131)

FibroGen

Description: FibroGen seeks a Clinical Quality Assurance (CQA) Associate Director / Senior Manager to support the company?s Clinical Quality Assurance program. The incumbent will conduct and manage Good Clinical Practice (GCP) related quality audits (e.g., investigator site and

9/7/2014  San Francisco, CA  Save This Job

Associate Director/Director Regulatory Affairs

Cytokinetics

Description: Cytokinetics, Inc. is a clinical-stage biopharmaceutical company dedicated to the discovery and development of novel small molecule therapeutics that modulate muscle function for the potential treatment of serious diseases and medical conditions. Working

9/9/2014  South San Francisco, CA  Save This Job

Associate Director/Director, Quality Assurance (14-137)

FibroGen

Description: FibroGen seeks a Quality Assurance Associate Director / Director to support the manufacture of Drug Substance and Drug Product at Contract Manufacturing Organizations (CMO) and Contract Research Organizations (CRO) to ensure FibroGen products are in compliance with

9/7/2014  San Francisco, CA  Save This Job

Director / Associate Director Regulatory Affairs

Catabasis

Catabasis Pharmaceuticals, Inc. is dedicated to the discovery and development of innovative, effective and safe medicines to treat inflammatory and metabolic diseases. We are assembling a team of highly motivated and experienced professionals who are committed to improving the

9/1/2014  Cambridge, MA  Save This Job

Senior Manager/Associate Director, Commercial IT (079)

Relypsa

SUMMARY: The Senior Manager / Associate Director of Commercial IT role will provide strategic and operational leadership for applications including CRM, customer master, aggregate spend, case management, data warehouse and analytics. This role will be responsible for business

10/17/2014  Redwood City, CA  Save This Job

Senior Manager/Associate Director, Quality Assurance (14-119)

FibroGen

Description: FibroGen seeks a Quality Assurance Senior Manager/Associate Director to support the manufacture of Drug Substance and Drug Product at Contract Manufacturing Organizations (CMO) and Contract Research Organizations (CRO) to ensure FibroGen products are in compliance

9/7/2014  San Francisco, CA  Save This Job

Associate Director, Chemical Development (14-139)

FibroGen

Description: Reporting to the Department Senior Director, the successful incumbent will work on all process chemistry aspects of new small molecule pharmaceuticals Responsibilities will include: Coordinate process development and optimization at a CMO Verify process

10/7/2014  San Francisco, CA  Save This Job

Associate Director, Procurement (074)

Relypsa

SUMMARY: We are looking for candidates who have a strong Procurement background including pharmaceutical experience and a track record in driving supply chain and cost of goods improvements with particular emphasis on in API sourcing. This position will be responsible for

10/17/2014  Redwood City, CA  Save This Job

Associate Director, Procurement (074)

Relypsa

SUMMARY: We are looking for candidates who have a strong Procurement background including pharmaceutical experience and a track record in driving supply chain and cost of goods improvements with particular emphasis on in API sourcing. This position will be responsible for

10/17/2014  Redwood City, CA  Save This Job

Drug Safety Associate (14-157)

FibroGen

Description: The Drug Safety Associate will be responsible for the review, evaluation and management of adverse event reports from FG-4592, FG-3019, and other clinical trials in accordance with FDA, EMEA, CFDA, other applicable health authorities and ICH guidelines and

9/7/2014  San Francisco, CA  Save This Job

Clinical Trial Associate

VaxInnate

Temp to Perm Opportunity VaxInnate is a small biotech company discovering, developing and preparing to commercialize innovative vaccines based on its Toll-like receptor technology platform. VaxInnate has seasonal and pandemic influenza vaccines currently in clinical development

10/20/2014  Cranbury, NJ  Save This Job

Research Associate III/ Senior Research Associate, Analytical Development (057)

Relypsa

SUMMARY: Work with minor instructions in analytical method development, qualification and improvement for methods to analyze small molecule compound(s). Perform routine testing to support in-process control and development for drug substances and drug products analyzes. This

10/17/2014  Redwood City, CA  Save This Job

Regulatory Affairs Associate/Specialist

FibroGen

Description: FibroGen seeks a goal driven, dynamic individual in the Regulatory Affairs department. This position provides proactive support and technical assistance to more experienced regulatory personnel and reports directly to either an Associate Director or Director of

9/7/2014  San Francisco, CA  Save This Job

Senior Clinical Research Associate

Catabasis

We are seeking a Senior Clinical Research Associate to join the Clinical Operations team at Catabasis. The role will be a key contributor to the company?s clinical development and primarily responsible for the hands-on management and monitoring of clinical studies in

9/1/2014  Cambridge, MA  Save This Job

Staff Scientist I, Quality Control (025)

Relypsa

SUMMARY: Work as part of a team in the identification and resolution of CMC method related issues. Evaluate, and implement novel and viable analytical technologies for characterization of polymers. Conduct method transfer between contract service providers. Assist in protocol

9/17/2014  Santa Clara, CA  Save This Job

Scientist/Staff Scientist I, Analytical Development (058)

Relypsa

SUMMARY: Work independently in analytical method development, qualification and improvement for small molecule compound(s). Coordinate routine testing to support in-process control and development for drug substances and drug products. This position reports to an Associate

10/17/2014  Santa Clara, CA  Save This Job

Sr. Quality Engineer

Astute Medical, Inc.

Job ID#: 55131 Background: This position will be responsible for ensuring Astute Medical establishes and maintains compliance to ISO13485 & 21CFR Part820. Astute Medical is a developer of in vitro diagnostics. Position title will be based on experience. Emphasis placed

8/31/2014  San Diego, CA  Save This Job

Companies: Associate Director, Compliance Jobs