ANALISTA CONTROL DE CALIDAD ANILLO (VACACIONES DE VERANO)
Chemo Villaquilambre, Castilla and Leon, Spain
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Overview
Sample and analyze, using different analytical techniques (GC, HPLC, TLC, KF), API, intermediate samples or final samples, completing the work bulletins for each product, and perform verifications of HPLC, GC, KF, Analytical Balances. Follow GMP guidelines and Standard Operating Procedures (SOPs) concerning weekly cleaning of the work area to ensure the quality of different products, proper functioning of equipment, and facilitate decision-making. All activities should adhere to safety regulations and the use of personal protective equipment as per operational risks.
Responsibilities
- Analyze samples using techniques such as GC, HPLC, TLC, KF to ensure product quality.
- Complete analytical documentation for GMP compliance.
- Perform analytical transfers and train QC analysts in new methods.
- Verify the performance of laboratory equipment including HPLC, GC, KF, and balances.
- Manage and control chemical reagent stocks following established protocols.
- Maintain and clean laboratory equipment.
- Adhere to approved analytical methods and SOPs.
- Train new team members in specific activities and functions.
Qualifications
- Education : Bachelor's degree in Sciences.
- Languages : Fluent Spanish; intermediate English is a plus.
- Experience : Minimum 1 year in relevant functions, with experience in HPLC, GC, Physico-chemical analysis.
- Knowledge : GMP environment experience; FDA knowledge is advantageous.
- Travel : Willing to travel occasionally.
- Personal Skills : Ability to work independently, prioritize tasks, meet deadlines, motivate teams, and handle a fast-paced environment with multiple demands.
- Seniority level : Not Applicable
- Employment type : Full-time
- Job function : Quality Assurance
- Industry : Pharmaceutical Manufacturing
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