Position Summary

We have an exciting opportunity for a Quality Control Chemist to join our team in Berlin. The main responsibilities of a QC Chemist are to carry out analytical testing, documentation and reporting. The QC chemist may also be required to perform method development, method performance characterisation including validation or participate in research projects. All QC Chemists are expected to actively be involved in housekeeping of the labs including supporting maintenance of testing infrastructure

Role and Responsibilities

Carry out GMP-compliant analytical testing of samples
Sampling and testing of chemicals (esp. process raw materials and polymers) and proteins, using the necessary associated ‘wet’ chemistry and instrumental techniques
Ensuring samples and products are handled appropriately according to standard operating procedures and work instructions
Preparing test records, participation in drafting analysis reports, stability reports and Certificates of Analysis
Participation in development of analytical procedures for the analysis of raw materials, in-process samples and pharmaceutical products
Performing instrumental analysis to assist in method development
Researching literature and pharmacopeia for methods when necessary
Assist the other members of the QC team with method development tasks
Ensuring GMP-compliant maintenance and qualification of QC equipment
Organizing and carrying out equipment qualification as requested by the QC Manager, ensuring all qualification documents are complete for equipment release
Ensuring all qualifications are done as described in the SOPs
Manage the necessary documentation as required by standard operating procedures

Requirements

BSc or higher degree in Pharmacy, analytical Chemistry, Chemistry, Biochemistry or related. Or appropriate vocational training plus 5 year experience in an analytical lab doing analysis
Experience with method development and execution of detector-coupled (e.g. UV/VIS, RI, ELS) analytical separation (HPLC, U(H)PLC, GPC) technics of primarily proteins and peptides including sample preparation
Use of chromatography data systems (CDS) in instrument control and data processing
Use of office software such as spreadsheets in data evaluation and text processing programs
Experience with analytical techniques: HPLC-(UV/RI/ELS/CAD), spectrophotometric analysis (UV/VIS, IR) especially on peptides, proteins and/or synthetic polymers
Strong analytical interpretation skills
General technical user knowledge in analytical instrumentation
Intermediate to good English and German language competency (level B2/C1) in speech and writing
Self-motivated, well organized, and pro-active learner
Ability to work independently in a structured manner
Ability and willingness to train and instruct coworkers in newly developed testing methods
Team player especially concerning work and lab organisation

About us

Biosynth® is an innovative life sciences reagents, custom synthesis and manufacturing services company headquartered in Staad, Switzerland. We are by scientists, for scientists, securing supply chains with consistent quality, across the globe. As a trusted supplier, manufacturer and partner to the pharmaceutical, life science and diagnostic industries, as well as food, agrochemical and cosmetic customers, we have facilities on three continents and a rapid global distribution network. Our main production laboratories are located in Switzerland, the UK, Slovakia and China, with peptide and antibody production in the US, the Netherlands. Enzyme projects are based in Austria, bioconjugation projects are based in Germany and biological IVD reagents in Ireland.

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Carbosynth LLC

Jobs:

Quality Control Chemist (m/w/d)

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