QC Team Lead

4 weeks ago

Malmo, Skåne, Sweden Institut Straumann AG Full time

About Straumann Group:

The Straumann Group is a global leader in tooth replacement and orthodontic solutions that restore smiles and confidence. It unites global and international brands that stand for excellence, innovation and quality in replacement, corrective and digital dentistry, including Anthogyr, ClearCorrect, Medentika, Neodent, NUVO, Straumann and other fully/partly owned companies and partners. In collaboration with leading clinics, institutes and universities, the Group researches, develops, manufactures and supplies dental implants, instruments, CADCAM prosthetics, orthodontic aligners, biomaterials and digital solutions for use in tooth correction, replacement and restoration or to prevent tooth loss.
Headquartered in Basel, Switzerland, the Group currently employs more than 11,000 people worldwide. Its products, solutions and services are available in more than 100 countries.
People and culture are the Straumann Group's greatest assets; they are the keys to high performance and sustainable success. We strive for a culture that builds trust and collaboration, fosters diversity, embraces change, promotes agility, learning and innovation, creates opportunities, allows people to make mistakes and encourages them to take both responsibility and ownership. The fundamental driver of our culture is the player-learner mindset, which we seek to inspire and nurture in every employee.

Biora AB produces regenerative products for dentists and is a production unit in Malmö, Sweden, with approx 35 employees. Biora is a part of the international dental company Straumann AG with HQ in Basel, Switzerland. Straumann is the leading producer of implant and products for dental tissue regeneration. Straumann engages about 13,000 employees and is active in more than 70 countries.

Job Description:

We are seeking a driven operational QC Team Leader who will lead the quality assurance of our products. In the role of QC Team Leader, you will report to the Quality Manager. This is a full-time position that involves approximately 50% operational work. The position is permanent and will commence as soon as possible.

Main Responsibilities:

  1. Lead and develop QC operations and QC staff.
  2. Act as the contact person between QC, Logistics, and Production.
  3. Be responsible for QC planning and prioritization.
  4. Participate in the daily work in QC.
  5. Ensure that QC operations effectively deliver safe and reliable analysis results.
  6. Be responsible for quality control of raw materials, processes, intermediates, and finished products.
  7. Approve or reject raw materials, packaging materials, media, and finished products. Document results in reports as required.
  8. Issue, review, and approve documents such as product specifications, QC methods, instructions, specifications, sampling instructions, QC analyses, stability reports, test protocols, validation protocols, and reports.
  9. Lead/participate in the validation of test methods and processes, QC equipment, and QC premises.
  10. Initiate, evaluate, review, and approve change requests, deviations, and lab investigations.
  11. Participate in and conduct risk assessments.
  12. Drive and/or participate in various types of development projects related to QC.
  13. Participate in inspections of contract laboratories and suppliers, as well as inspections from external bodies, customers, etc.
  14. Communicate with external suppliers and laboratories regarding analyses and validations.
  15. Ensure that QC staff are trained, educated, and certified according to operational needs.
  16. Contribute to identifying and implementing improvements in the work environment.
  17. Drive continuous improvement of the quality system.

Qualifications:

We are looking for someone with a degree in natural sciences/chemistry or equivalent. We prefer candidates with at least 5 years of experience in laboratory work in a regulated environment and/or quality assurance work or quality responsibility within manufacturing, quality control, or production. You should have a good knowledge of relevant standards and regulations, as well as experience in product release according to requirements. Experience in a leadership role is advantageous. Good communication skills in Swedish and English, both spoken and written, are essential. Additionally, you should have good computer skills (Office). Knowledge of regulatory documentation and medical technology products and regulations, such as clean rooms, sterilization, packaging, risk analyses, etc., is a plus.

As a person, you are passionate about leadership, analytical, meticulous, and structured. You achieve results by developing employees and fostering good collaboration across functional boundaries. You have a holistic perspective and are driven to continuously develop and improve the organization, employees, and yourself. You address problems as they arise and come up with your own initiatives and suggestions.

For more information about the position, please contact Eva Sigfridsson at +47 730 497713. Applications are processed on an ongoing basis.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or disability.

Employment Type: Full Time

Location: Sweden: Malmö

Travel Percentage: 0 - 10%

Requisition ID: 17186

#J-18808-Ljbffr

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