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Manager, Quality Control Analytical in Burlington, MA at AMRI

Date Posted: 5/9/2019

Job Snapshot

Job Description

AMRI provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries.

The Manager, Quality Control Analytical is an integral part of the AMRI team, contributing to our success by managing the routine and non-routine analytical chemistry assays of raw materials, in-process samples, finished formulations, and special projects. This role will oversee the day-to-day functions of the QC Analytical department, and manage a team of chemists.

Join our talented workforce, where a commitment to excellence and a customer focused attitude is everything. We pursue excellence because our work has the power to improve patients’ lives with the pharmaceuticals we develop and manufacture.

In this role, you will:

  • Manage the Quality Control Team Performance of analytical testing fo incoming, in­ process and final products, and stability samples
  • Ensure that the analytical chemistry functions are completed in accordance with the Company and governmental standards of safety and quality, and that all experimental documentation is complete and timely
  • Supervise a team of scientists including, but not limited to, the motivation, education, efficiency, performance management and productivity of these individuals
  • Build a sense of customer confidence in departmental results. Will be responsible for providing liaison communication with key members of client organizations

Job Requirements

Required

  • Bachelor’s degree in Chemistry or a scientific discipline with relevant coursework or work experience in analytical chemistry
  • Experience in pharmaceutical/biotechnology or medical device industry

 

Preferred

  • 7 years’ experience in a GMP or FLP environment, working with HPLC
  • Advanced scientific degree preferred
  • Proficient use of computer software, including Microsoft Office Suite (excel, word)
  • Strong organizational skills with the ability to multi-task
  • Proficient in HPLC method development and method validation with extensive experience with multiple other analytical techniques and analytical equipment.
  • Prior experience and knowledge in FDA GMPs (21 CFR, 211, 820, and/or 600); ISO 9001 and 13485.


Shift:  Standard 8

Albany Molecular Research, Inc. is committed to providing equal opportunity to all job seekers including qualified individuals with disabilities. If you have any difficulty using our online application system due to a disability or believe you need a reasonable accommodation to search for a job opening or submit an application, you may use the alternative email address "jobs@amriglobal.com" to contact us about your interest in employment or you may call us at 518.512.2000.

Please note: The above-referred email address and telephone number are dedicated communication lines designed exclusively to assist job seekers whose disability prevents them from being able to apply online. Messages left for other purposes will not receive a response.

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AMRI is committed to providing equal opportunity to all job seekers including qualified individuals with disabilities. If you have any difficulty using our online application system due to a disability or believe you need a reasonable accommodation to search for a job opening or submit an application, you may use the alternative email address jobs@amriglobal.com to contact us about your interest in employment or you may call us at 518.512.2000.

Please note: The above referenced email address and telephone number are dedicated communication lines designed exclusively to assist job seekers whose disability prevents them from being able to apply online. Messages left for other purposes will not receive a response.