Director of Quality Control
Job Description

A leading company in the medical device industry is currently seeking a Director of Quality Control to join their team. For the right candidate, this is a fantastic opportunity with great growth prospects. Details:

1) Define and set Quality Standards for each R&D function and across multiple therapeutic areas and ensure that quality checks are performed across the business
2) Build quality control team and methodology, including collaboration with other functional managers and groups to deliver a comprehensive quality control effort
3) Identify risk, support in the development and track effective use of CAPAs across departments
4) Perform in-process checks and define and utilize metrics to monitor and report on compliance
5) Drive accountability and continuous improvement through training, SOPs and workflows as needed to proactively improve quality, efficiency, and standardization
6) Direct the implementation and maintenance of the company's quality system, reporting on the performance of the quality system for review and improvements as required
7) Direct and track social compliance audits required by customers
8) Review, test and approve all licensed products prior to production or 3rd party testing
9) Enforce Standard Operating Procedures with the goal of maintaining quality and safety in accordance with the company's standards, based on current regulations and up to date product development procedures
10) Perform comparison testing of competitive product for sales
More questions? Want to know the Salary range? Keep reading.

The best way to get more details is to click ‘Apply’, upload your resume, and ENTER YOUR QUESTIONS in the ‘Cover Letter’ field. A recruiter will call you and answer all of your questions (if they feel you are a fit for the role). Your resume will be kept CONFIDENTIAL – we respect your privacy. Our Recruiters are more likely to respond to your questions if they know you are *seriously* interested, and prefer to know a little bit about your background before calling.

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TAGS: Biotechnology Jobs, Pharmaceutical Jobs, Medical Device Jobs, Small Molecule, Biologic, Oncology, Hematology, Dermatology, Neurology, Cardiology, Urology, Nephrology, Vaccine, Disease, Drug Development, Surgery, Physician, EMR, Healthcare, Life Sciences, Scientist, R&D, Clinical Research, Clinical Trial, Regulatory Affairs, Nutraceutical, Surgeon, MD, Hospital, Immunology, Quality, QC, Validation, Engineer, QA, Manufacturing, Engineering, Aseptic, Sterility, Hospital, Research and Development, Medical Affairs, Drug Safety



Job Requirements

1) University degree is required (preference will be given to those with degree in relevant field, though all candidates are welcome and encouraged to apply)
2) Appropriate full-time work experience is mandatory (no students or fresh graduates please)
3) Recent experience in the medical device industry is strongly preferred
4) Preference will be given to people have recent experience in quality

Our client is seeking an enthusiastic individual who can bring added value and a new approach to their business. If you believe this is a challenge you can be successful at, please apply ASAP.

Company Overview

Sterling-Hoffman Life Sciences is the premier recruitment firm in North America for companies involved in the research, clinical development, manufacturing and distribution of drugs and devices that allow patients to live healthier and more fulfilling lives. Leveraging a network of relationships in every major city – including New York, San Francisco, Raleigh-Durham, Chicago, Dallas, Denver and Los Angeles – Sterling-Hoffman Life Sciences is ideally positioned to assist fast growing CROs, pharmaceutical companies, biotech firms and medical device players in their quest to recruit the best people.


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  • Director of Quality Control @ Sterling Life Sciences

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