Associate QC Chemist

Proclinical Group; Cambridge (MA); On-site; USD 60,000 - 80,000; Full time

Job summary

Join a leading pharmaceutical company as an Associate QC Chemist in Cambridge, MA. You will be essential in performing analytical testing of siRNA drug products and contribute towards regulatory submissions. Ideal candidates will have a BS in a relevant field and 1+ years of laboratory experience.

Qualifications

• 1+ years of relevant experience in an analytical laboratory setting.
• Preferred experience in Quality Control / GMP.
• Experience with oligonucleotides or oligosaccharides is a plus.

Responsibilities

• Perform analytical testing of drug substances and products.
• Analyze and trend stability data for regulatory submissions.
• Contribute to stability and compatibility studies.

Skills

Analytical Testing

Chemical Instruments

Data Analysis

Education

BS in Biology, Chemistry, Biochemistry, Pharmacology

Job description

Associate QC Chemist - Contract - Cambridge, MA

Be the backbone of innovation and join a leading pharmaceutical company to help keep life-changing science moving forward!

Proclinical is seeking an Associate QC Chemist to join our client's team in Cambridge, MA.

Primary Responsibilities:

The successful candidate will be responsible for performing analytical testing of siRNA drug substances, drug products, intermediates, and critical raw materials using UV spectrophotometry, osmometry, water content titration, and other chemistry instruments.

Qualifications:

• BS in Biology, Chemistry, Biochemistry, Pharmacology or related discipline.
• 1+ years of relevant experience in an analytical laboratory setting. Previous Quality Control / GMP experience is preferred.
• Preferred - experience with physico-chemical test methods of oligonucleotides. Alternatively - experience with physico-chemical test methods of oligosaccharides or proteins.
• Experience working at a multi-site company and/or with CMOs is helpful

The Associate QC Chemist's responsibilities will be:

• Perform testing of stability, stress, forced degradation, photostability, excursion management, compatibility, and ASAP studies.
• Prepare and perform set downs of study plan with stakeholders.
• Analyze and trend stability data, archive data.
• Contribute analytical data to stability sections of regulatory submissions

Compensation:

• $30.00 - $33.00 Per Hour

If you are having difficulty in applying or if you have any questions, please contact Shannon Briggs at [e-mail]

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

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