QC Analyst

To support our continued growth, the Quality Control department at our Weert site is expanding and currently looking for an experienced and motivated:

QC Analyst (Full-time)

The Quality Control (QC) department plays a key role in ensuring product quality and regulatory compliance. Responsibilities include analytical method validation, testing of raw materials, in-process controls, intermediates, active pharmaceutical ingredients (APIs), and stability studies.

Our QC lab is equipped with a broad range of state-of-the-art analytical technologies, including GC (MS), (U)HPLC (MS-MS), ICP (MS), NMR, IC, FT-IR, wet chemistry techniques, and more.

In this role, you will:

• Carry out analytical testing intended for release of (critical and project) raw materials, intermediates and final products, based on approved methods of analysis.
• Compare the results against established specifications.
• Report and examines aberrant and OOS- and OOT-results. Where possible, suggests solutions and/or improvements.
• Carry out analytical protocols for stability studies, retests of reference standards and validation of analytical methods.
• Write analytical reports for stability studies and validation of methods.
• Calculate, interpret and report the obtained test results.
• Write/review procedures and work instructions.
• Work in close collaboration with project teams and manufacturing to discuss timelines, flag and discuss deviations from procedure and share results.

You'll bring

• an MBO degree with three years experience / HBO-level.
• Knowledge of analytical chemistry acquired through education and/or working experience in a pharmaceutical environment.
• Broad (practical) analytical knowledge of analytical techniques, for example (U)HPLC (MS), GC (MS), Titration, FT-IR, NMR, IPC-MS
• Knowledge of Good Manufacturing Practices (GMP).
• Strong communication skills, both verbally and in writing. Fluent in English and Dutch.
• A good working and quality attitude, accurate, with an eye for detail.

Job offer

At Symeres, you'll be part of a dynamic and rapidly expanding Solid State team. You'll have access to state-of-the art analytical instrumentation and the opportunity to develop and implement innovative ideas and techniques in a collaborative and supportive environment.

An exciting position in a dynamic fast-growing organization with an attractive remuneration package and opportunities for learning and development.

Application

Please send an email with your CV to:

Further information on the specifics of this position can be obtained from the Team Leader QC, Michiel van Geijn, by email:

More information about the Symeres organization can be found on our website:

More about Symeres

Symeres is the leading mid-sized transatlantic contract research organization for drug discovery and development needs. With over 600 highly educated scientists and professionals in six locations in Europe and two in the USA, we offer best-in-class solutions for drug discovery and drug development, from small- to medium-sized molecule hits. We are large enough to matter, and small enough to care. Our services span across early stage hit finding all the way to the delivery of early clinical drug substance API. Making molecules matter. Together.

Soort dienstverband: Fulltime, Uitzicht op vast, Bepaalde tijd

Contractduur 12 maanden

Salaris: €2.900,00 - €3.900,00 per maand

Ervaring:

• werken op QC afdeling: 2 jaar (Vereist)

Toestemming om in Nederland te werken:

• Netherlands (Vereist)

Werklocatie: Fysiek