Product Certification and Laboratory Manager (Riga, Latvia) MF.

Kronospan
Chirk
1 year ago
Applications closed

Related Jobs

View all jobs

Director, Clinical Operations Lead

Senior Director, Project Operating Model and Leadership Excellence

Radiopharmaceutical QP

Data Privacy Manager

Senior Project Manager, R&D: Drug Development

Technical Assessor

- Oversee laboratory operations in compliance with product certifications and EN standards, ensuring the highest level of accuracy and reliability in testing procedures.
- Maintain existing product certifications (document management, regular audits) and obtain new certifications, demonstrating a commitment to continuous improvement and regulatory excellence.
- Work with EN standards and CE marking, playing a crucial role in maintaining the company's competitive edge in the European market.
- Analyze product quality with a keen eye for detail, driving the development of superior products.
- Collaborate with production managers to resolve defects efficiently, fostering a culture of quality and innovation.

Requirements

- Higher technical education.
- Fluent Latvian and English.
- Higher education in chemistry or materials science, showcasing a strong foundation in scientific principles.
- Precision and high sense of responsibility, essential traits for maintaining rigorous standards.
- Computer skills: MS Office, databases, enabling efficient and accurate data management.
- Experience with physical and mechanical property testing methods is preferred, underscoring expertise in quality assessment and control.

What we offer

•Monthly base salary for this position is 2500-2700 EUR gross. The final offer will depend on your qualifications, competencies, and professional experience.
•Challenging position within a multinational organization.
•Broad experience and professional development.

Please, pay attention to the fact, that we are located in Bolderaja region.
If you are interested in this opportunity, please send us your resume to are thrilled to meet you!
We will contact the candidates who will be invited for a job interview.

Darba apraksts
Laboratorijas uzraudzība saskaņā ar produktu sertifikātiem un EN normām.
Esošo produkcijas sertifikātu uzturēšana (dokumentācijas vadība, regulārie auditi), jaunu sertifikātu iegūšana.
Darbs ar EN standartiem un CE marķējumu.
Produkcijas kvalitātes analīze.
Defektu novēršana sadarbībā ar ražošanas vadītājiem.

Prasības kandidātiem
Augstākā izglītība ķīmijas vai materiālzinātnes jomās.
Precizitāte un augsta atbildības sajūta.
Iemaņas darbā ar datoru: MS Office, datubāzes.
Vēlama pieredze darbā ar fizikāli mehānisko īpašību testēšanas metodēm.

Uzņēmums piedāvā
Starptautisku un sakārtotu darba vidi.
Mācības kvalifikācijas paaugstināšanai.
Stabilu atalgojumu un sociālās

Subscribe to Future Tech Insights for the latest jobs & insights, direct to your inbox.

By subscribing, you agree to our privacy policy and terms of service.

Industry Insights

Discover insightful articles, industry insights, expert tips, and curated resources.

Jobs

CSL Behring Jobs UK: Careers, Salaries, Locations & How to Get Hired

CSL Behring is one of the world’s leading biopharmaceutical companies specialising in plasma-derived therapies, recombinant proteins, gene therapy, vaccines, and rare disease treatments. If you’re a UK job seeker looking for a career with real purpose, strong scientific standards, and long-term progression, CSL Behring roles can be an excellent fit, especially if you have experience in biotech, pharma manufacturing, quality, engineering, supply chain, clinical operations, regulatory, pharmacovigilance, or commercial. This guide is written for UK candidates who want to understand what CSL Behring jobs typically involve, which roles to target, where opportunities may be based, what skills recruiters look for, and how to tailor your application to stand out.

Careers

How Many Biotechnology Tools Do You Need to Know to Get a Biotech Job?

If you are trying to break into biotechnology or progress your career, it can feel like the list of tools you are expected to know is endless. One job advert asks for PCR, another mentions cell culture, another lists bioinformatics pipelines, automation platforms or GMP systems. LinkedIn makes it worse, with people sharing long skills lists that make you wonder if you are already behind. Here is the reality most biotech employers will not say out loud: they are not hiring you because you know every tool. They are hiring you because you understand biological systems, can work accurately and safely, follow protocols, interpret results and contribute reliably to a team. Tools matter, but only when they support those outcomes. So how many biotechnology tools do you actually need to know to get a job? The answer depends on the role you are targeting, but for most job seekers it is far fewer than you think. This article breaks down what employers really expect, which tools are essential, which are role-specific, and how to focus your learning so you look employable rather than overwhelmed.

Jobs

What Hiring Managers Look for First in Biotechnology Job Applications (UK Guide)

Hiring managers in biotechnology do not start by reading your CV word for word. They scan for credibility, relevance and risk. In a regulated, evidence-driven sector like biotech, the first question is simple: is this person safe, competent and genuinely capable of contributing in this environment? Whether you are applying for roles in research, manufacturing, quality, regulatory, clinical, bioinformatics or commercial biotech, the strongest applications make the right signals obvious in the first 10–20 seconds. This in-depth guide explains exactly what hiring managers in UK biotechnology look for first, how they assess CVs, cover letters and portfolios, and why capable candidates are often rejected. Use it as a practical checklist before you apply.

🍪 We use cookies to enhance your browsing experience on our website. By continuing to use this site, you consent to the use of cookies as described in our Cookie Policy. You can review our Cookie Policy for more information.