- Performing daily laboratory activities related to applying analytical methods and conducting stability studies analyses, which includes: conducting analyses, processing data, drafting reports and relevant documentation, presenting/discussing results when necessary, and validating raw data
- Validating analytical methods based on established protocols and under the supervision of the technical leader
- Relevant work experience with Liquid Chromatography (U)HPLC
- Prior experience in a similar laboratory role involving the application of existing methods
- Familiarity with Empower
- Strong team player
- Proficiency in French
- Basic level of English (A2)
- Experience in developing and/or validating analytical methods
- Aptitude for working in a regulated environment, with initial exposure to the pharmaceutical industry within a GMP setting
- We establish analytical protocols
- We devise and validate novel analytical methods
- We conduct studies including characterization, stability, pharmacokinetics, biomarker assessments, immunogenicity testing, and batch release evaluations.
- The consolidation of its laboratories in a single site (Donstiennes, Belgium)
- A workforce of 250 highly skilled professionals
- An array of analytical methodologies and cutting-edge equipment
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LAB ANALYST - Thuin, België - QUALITY ASSISTANCE S.A.
Beschrijving
Scope
To accommodate our continuous expansion, we are actively in search of a Laboratory Analyst specialized in Physico-Chemistry.
Join us in working on cutting-edge biopharmaceutical products currently in various development stages (non-clinical and clinical).
You will be an essential part of a team dedicated to managing projects outsourced by our clients.
These projects involve tasks related to developing, validating, and applying analytical methods as per specific protocols for characterizing and ensuring the quality of biomolecules.
Your mission
You will directly report to the Chromatography Technical Leader.
You will collaborate with a team of 5/6 members.
As part of this role, you will be responsible for:
Your profile
Scientific background required
Mandatory
Added advantages
Reasons to join Quality Assistance
Are you seeking a professional environment that combines expertise with a personal touch? Do you envision a workplace built on mutual respect, communication, and support, where you can thrive?
This is your chance to become part of our analytical CRO! Our shared objective is accelerating the accessibility of novel medications.
You will enjoy a competitive compensation package aligned with industry standards, inclusive of numerous perks such as meal vouchers, health insurance coverage, group insurance, bonuses, and in some roles, a company vehicle with fuel card.
Upon commencing your role, you will engage in a comprehensive training program tailored to your profile and responsibilities.
Were you aware that in 2023, we welcomed and trained 23 new team members? Additionally, we promoted 25 staff members (vertical mobility), with 2 internal candidates securing new positions.
We present various opportunities for you to integrate into your new workplace environment, fostering relationships with your colleagues through after-work activities, sports, team-building events, departmental gatherings, year-end celebrations, BBQs, family-oriented functions, and more. We prioritize the well-being of our team members: offering complimentary fitness classes, fresh fruit and sugar-free beverages, daily lunch and bread delivery, free car wash, ironing services through vouchers, access to books and board games, and additional amenities.
You are becoming a part of an organization that values your input and considers your needs
About Quality Assistance
Quality Assistance stands out as a prominent European Contract Research Organization (CRO) delivering the full spectrum of analytical services mandated by EMA and FDA regulations for the innovation and commercialization of new human medicinal products.
From candidate selection to clinical trials and market approval, Quality Assistance serves its clients with tailored solutions:
These assessments are conducted to evaluate the Quality, Safety, and Effectiveness of provided pharmaceuticals.
With a legacy of over 40 years of expertise in the analytical sciences domain, Quality Assistance distinguishes itself in the market with:
The Quality Assistance framework adheres to GMP, GLP, and GCLP/GCP standards.
