Specialist, QC Bioanalytical

Specialist, QC Bioanalytical We use first and third-party cookies, which are necessary for the website's correct functioning, and which allow us to analyse your browsing and offer you several functionalities within the website.  For further information, please check our Cookies Policy. In order to accept all the cookies, click ACCEPT; in order to refuse them, click DECLINE.# People come first at Ferring## Specialist, QC Bioanalytical Apply:
Parsippany, New Jersey, United States:
Full time:
Posted Yesterday:
End Date:
November 6, 2026 (12 days left to apply):
R0038553##
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* Job Description:

** As a privately-owned, biopharmaceutical company, Ferring pioneers and delivers life-changing therapies that help people build families and live better lives. Our independence helps us cultivate an entrepreneurial spirit and long-term perspective that enables us to achieve growth and scale, while remaining agile and true to our ‘people first’ philosophy. Built on a 70-year plus commitment to science and research, Ferring is relentless in its pursuit of science that drives powerful discoveries and therapies to help people build families, stay healthy, and stand up to the world’s oldest enemy: disease.  

As
** Specialist, QC Bionalytical**, you will be responsible for performing bioanalytical testing and analysis of raw materials, in-process samples, and finished products to ensure compliance with regulatory requirements and internal quality standards.  With Ferring, you will be joining a recognized leader, identified as one of “The World’s Most Innovative Companies” by Fast Company, and honored by Fortune with inclusion on its “Change the World List,” for addressing society’s unmet needs.

Ferring US is also Great Places to Work Certified, distinguishing it as one of the best companies to work for in the country.
** Responsibilities:
*** Conduct bioanalytical testing and analysis using a variety of techniques such as Cell-Based Assay, ELISA, PCR and HPLC.
* Perform assays for the quantification of biomarkers, proteins, nucleic acids, and other analytes.
* Execute routine QC testing, method validation, verification, and transfer activities in accordance with regulatory guidelines.
* Maintain and troubleshoot analytical instrumentation to ensure optimal performance and data integrity.
* Document test results, observations, and deviations accurately in laboratory notebooks and electronic systems.
* Collaborate with cross-functional teams including Research & Development, Manufacturing, and Quality Assurance to support product development and process improvement initiatives.
* Participate in investigations of out-of-specification (OOS) results and non-conformances, and implement corrective and preventive actions (CAPAs) as needed.
* Adhere to Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP) and Good Documentation Practices (GDP) in all laboratory activities.
* Contribute to the continuous improvement of laboratory procedures, protocols, and documentation.  
** Requirements:
*** Bachelor’s or Master’s degree in biology, Cell and Molecular Biology, Biochemistry, Biological Chemistry, Pharmaceutical Sciences, or related field.
* A minimum of 2 years of experience in bioanalytical testing within a GMP, QC Analytical or in the biotechnology or pharmaceutical industry.
* Working knowledge following Standard Operating Procedure (SOP)
* Proficiency in analytical techniques such as ELISA, PCR, Flow Cytometry, Spectroscopy and HPLC (preferred).
* Understanding of regulatory requirements (FDA, EMA, ICH) for bioanalytical method validation and sample analysis.
* Strong problem-solving skills and attention to detail.
* Effective communication and interpersonal skills, with the ability to work collaboratively in a…