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Analyst, Quality Control M/F/D

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Vacancy details

General information

Legal structure (logo)

Company / Establishment

SEQENS is an integrated global leader in pharmaceutical solutions and specialty ingredients, delivering outstanding performance, unrivalled market responsiveness and tailor-made solutions to our customers.
Our mission is to bring R&D and industrial performance to our clients' projects with our unique skill set and a broad range of technologies.

SEQENS operates 24 manufacturing plants and 10 R&D centers in Europe, North America and Asia with 3,200 employees. More than 300 scientists, engineers and experts develop tailor-made solutions for our customers and ensure that products are successfully transferred into production.  

Reference

2022-763  

Position description

Job Family / Sub-family

Quality & Regulatory - Quality Control

Contract type

Permanent

Job title

Analyst, Quality Control M/F/D

Position Context:

Ø Purpose of the position:
The analyst is responsible for providing accurate and timely results for the samples submitted for analysis to support the manufacturing and research and development departments.

Main tasks :

 

Ø Main missions:
·         Use liquid chromatography, gas chromatography, ultraviolet spectroscopy, infrared spectroscopy, titrimetry, and other techniques to assess the quality of samples.  The resulting data is interpreted by the analyst and submitted for review.  The analyst is also responsible for ensuring that the instruments used for analysis are calibrated to industry standards.    

·         Write laboratory operating procedures.       

·         Maintain chemical inventory.

·         Maintain reference standard program.

·         Perform secondary data review for analyses completed by other analysts.

·         Ensure appropriate levels of laboratory supplies.        

Required skills :

BA/BS in Chemistry or related discipline, or comparable educational and professional experience
 
Excellent verbal and written communication skills are essential; a thorough understanding of the techniques described above is essential to accurately assess the validity if the data generated
Previous experience in a current Good Manufacturing Practices (cGMP) laboratory or manufacturing environment preferred.

Position location

Job location

USA, Massachusetts, Newburyport


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