Job Title : Quality Control Analyst
Location : BilthovenNetherlands
Industry : Pharmaceutical
We are seeking a Quality Control Analyst to join our dynamic team in the pharmaceutical industry. The ideal candidate will have experience in laboratory testing and analysis with strong knowledge of Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). This position will offer opportunities for growth and development in a fastpaced environment.
Key Responsibilities :
Analysis & Testing : Perform chromatographic tests and analyses (e.g. HPLC GC FTIR UV) on samples ensuring compliance with specifications and standards. Handle independent instrumental analysis and release of Finished Product (FP) analysis as per commitment dates.
Documentation & Compliance : Document all activities using valid procedures and standard formats to maintain accuracy and integrity. Ensure timely updates to documentation and handle deviations in compliance with GMP standards.
Equipment & Facility Maintenance : Maintain laboratory working areas equipment and facilities in compliance with SOPs. Perform validation qualification and calibration of equipment as per schedule.
Collaboration & Communication : Foster good relations with internal teams including Lab Planning QA and Lab Assistants. Provide timely responses to both internal and external customer queries.
Process Improvement : Participate in audits (GMP / customer) suggest costsaving measures and contribute to process automation initiatives for continuous improvement.
Safety & Compliance : Ensure all activities comply with safety norms and GLP. Handle samples and chemicals according to safety standards and disposal procedures.
Key Requirements : Education :
Bachelor s degree in Chemistry Pharmacy or related field. Alternatively secondary vocational education (MBO) with 5 years of relevant experience or higher professional education (HBO) with 13 years of experience.
Experience :
13 years of experience in a pharmaceutical quality control function.
Skills :
Proficiency in using chromatographic instruments adherence to GLP and GMP strong attention to detail and good communication skills.
Key Interactions :
Internal : Collaborate daily with Lab Planning Lab Assistant and QA teams.
External : Work with service engineers for instrumentrelated issues and external audits.
Key Challenges :
Managing delays due to changes in planning or instrument breakdowns.
Addressing challenges around procurement of necessary materials and instruments.
Requirements
Min 1 to 3 yrs experience.
Educational qualifications : B. Sc Chemistry OR Bachelor of pharmacy. In Dutch terms Secondary vocational education
Experience and working knowledge of CGMP regulations is required.
1. Should be Experienced in :
Maintenance of the Laboratory in the Pharma industry
Reporting of abnormal observations of OOS OOT analytical incidences
Performing analysis
2. Key Skills English language is required.
3. Please source candidates who are already based in the Netherlands
Benefits
Competitive Salary
Career Growth & Development
WorkLife Balance
Health & Wellness Benefits
Min 1 to 3 yrs experience. Educational qualifications : B. Sc Chemistry OR Bachelor of pharmacy. In Dutch terms, Secondary vocational education Experience and working knowledge of CGMP regulations is required. 1. Should be Experienced in : Maintenance of the Laboratory in the Pharma industry Reporting of abnormal observations of OOS, OOT, analytical incidences Performing analysis 2. Key Skills - English language is required. 3. Please source candidates who are already based in the Netherlands
Key Skills
Computer,IT Audit,CAD CAM,ABAP,Exterior Designing,HR Operations
Employment Type : Full Time
Experience : years
Vacancy : 1
Quality Control • Nederhemert, Gelderland, Netherlands