Quality Control Specialist

Workplace: Władysławowo

Your responsibilities

• Independent performance of qualitative tests of materials and finished products, carrying out in-process control (IPC) and monitoring the quality of the production environment and process media, supporting quality control at subsequent stages of medical device and pharmaceutical product manufacturing.
• Preparation and collection of samples, reagents, and materials necessary for tests, with attention to the correctness and timeliness of conducted analyses.
• Monitoring the quality of processes and products, analyzing test results, and identifying and reporting non-conformities to support the maintenance of required quality standards.
• Cooperation with the production department and other individuals involved in the quality control process, combined with maintaining documentation of tests and quality records.
• Ensuring proper conditions for conducting tests by monitoring the condition of laboratory equipment and maintaining cleanliness standards in the laboratory and production areas.[DM1.1]
• Participation in the development, updating, and improvement of quality documentation, particularly research methods, instructions, and procedures.[

Our requirements

• Relevant education: chemistry, biology, biotechnology, or related fields[DM3.1]
• Minimum one year of practical laboratory experience, enabling independent performance of tests.
• Knowledge of analytical techniques used in a quality control laboratory, including practical knowledge of pipetting techniques.
• Ability to work with quality documentation and knowledge of quality standards, e.g., ISO 13485
• Ability to organize own work, analytical thinking, and accuracy in conducting tests.
• Proactiveness, openness to cooperation, and readiness for stationary work in the laboratory.

Nice to have

• Experience in performing microbiological tests.

What we offer

In 2026, in the engagement survey, our employees rated their satisfaction with the company as a workplace at 79%!

How do we work?

MAKE IT REAL. We work close to the product and the results of our work. We create solutions for the health tech industry – from idea and research, through processes and production, to the market and patient health.

SEE MORE. DO MORE. We work cross-departmentally, allowing you to gain experience beyond your own part of the process, draw on the knowledge of various specialists, and actively influence your role and the company's way of operating.

BETTER THAN YESTERDAY. We create an environment of an ambitious, developing organization where we build new standards, improve our work methods, and seek more effective solutions. We value curiosity, initiative, and readiness to learn from experience.

Additionally, we offer our Employees:

• Stable employment conditions – employment contract for 12 months, followed by an indefinite period, and flexible start times between 7:00 AM and 9:00 AM.

• Additional benefits – group insurance (Generali/UNIQA), FitProfit sports card, quarterly bonus.

• Development opportunities – training and conferences, TalkPal for language learning, clear career paths, quarterly feedback process, and annual competency assessment.

• Employee and integration initiatives – running team, book discussion club, integration meetings, and joint birthday celebrations.

• Comfortable working conditions – coffee, tea, parking, Hutników – our outdoor zone for work and integration, well-equipped workstations and quality tools, and no dress code.

Benefits

• life insurance
• flexible working hours
• integration meetings
• no dress code
• coffee / tea
• employee parking
• birthday celebrations
• opportunity to acquire a sports card

Recruitment process

1. Application – we verify formal requirements and review your experience.

2. HR Interview – we describe the position, get to know your competencies, motivation, and check your fit with the organization.

3. Office Meeting – you will meet with HR and the Department Manager to discuss the role details; sometimes we also invite candidates to complete a practical task.

4. Offer – we submit a written proposal and jointly set the start date.

We provide feedback at every stage because we believe it is part of a partnership relationship.

Biovico Sp. z o.o.

Biovico is a manufacturing company operating in the HealthTech industry, with an extensive R&D department and international sales. It specializes in the creation of high-quality medical devices and pharmaceutical products. Operating within the Wilandt Brothers (HLDG) holding, together with its sister company Implai, we co-create a cohesive ecosystem connecting biotechnology, pharmaceuticals, medical devices, and equipment, delivering effective and innovative solutions for professionals and patients worldwide.

Currently, due to the need to strengthen the Quality Control team with a person having practical laboratory experience, we are looking for a candidate for the position of: Quality Control Specialist

Please add the following clause to your CV: I hereby consent to the processing of personal data contained in this document for the purpose of the recruitment process in accordance with the Act of May 10, 2018, on the protection of personal data (Journal of Laws of 2018, item 1000) and in accordance with Regulation (EU) 2016/679 of the European Parliament and of the Council of April 27, 2016, on the protection of natural persons with regard to the processing of personal data and on the free movement of such data, and repealing Directive 95/46/EC (GDPR).