At SINCERITAS, we cultivate and process pharmaceutical-grade cannabis into medicinal products to improve patient health and provide relief. Offering cutting-edge solutions for numerous medical needs, we strive to meet every client’s unique requests by tailor-making each product.
 

We are a team of experienced science professionals that use industry-standard practices in agricultural and pharmaceutical techniques to manufacture high-quality medicinal cannabis products consistently and reliably. Our products are developed to retain all of the plant’s essential components and ensure a maximum medicinal effect, particularly in patients with rare and difficult-to-treat conditions.
 

Through ongoing scientific research and development, we aim to unlock the full therapeutic potential of cannabis, opening the doors to new and revolutionary medical treatments.
 

Sinceritas is made up of talented diverse team of over 100 employees who deliver innovative solutions that add value across a variety of Business Service functions. Our company culture is build on three pillars: Science.Progress.Trust
 

SINCERITAS offers premium workspace at our facility in Rosoman and administrative office in Skopje.

 

Job Title: Head of Quality Assurance - Pharmaceutical Industry

Job Summary:

The Head of Quality Assurance in the pharmaceutical industry is a leadership role responsible for ensuring that all products meet regulatory requirements, industry standards, and internal quality standards. This position plays a crucial role in maintaining and improving the quality management system within the organization. The individual in this role will lead a team of quality professionals, develop and implement quality assurance strategies, and collaborate with cross-functional teams to drive continuous improvement in product quality and compliance.

Key Responsibilities:

1. Leadership and Team Management:
   • Provide strategic leadership to the Quality Assurance (QA) team, ensuring a high level of engagement, motivation, and professional development.
   • Build and maintain a high-performance culture within the QA department.
   • Foster collaboration and effective communication within the QA team and with other departments.
2. Quality Management System (QMS) Development:
   • Establish, implement, and maintain the QMS in accordance with regulatory requirements and industry best practices.
   • Ensure that the QMS is continuously improved and aligned with organizational goals.
3. Regulatory Compliance:
   • Stay current with applicable regulatory requirements and industry standards, and ensure the organization's compliance.
   • Interact with regulatory authorities and participate in regulatory inspections.
4. Quality Audits and Inspections:
   • Plan and execute internal and external quality audits to assess compliance with regulatory requirements and company standards.
   • Prepare and lead the organization through regulatory inspections.
5. Risk Management:
   • Implement and oversee a risk management program to identify and mitigate quality risks across the organization.
6. Document Control and Training:
   • Establish and maintain document control processes to ensure the accuracy and accessibility of quality documentation.
   • Develop and oversee training programs to ensure that personnel are adequately trained on quality processes and procedures.
7. Supplier and Vendor Management:
   • Establish and maintain processes for evaluating and monitoring suppliers and vendors to ensure the quality of incoming materials and services.
8. Continuous Improvement:
   • Drive a culture of continuous improvement, utilizing quality metrics and key performance indicators to identify and implement opportunities for enhancing product quality and operational efficiency.

Qualifications and Experience:

• Bachelor's or advanced degree in a relevant scientific or engineering discipline.
• Extensive experience in quality assurance within the pharmaceutical industry, including leadership roles.
• In-depth knowledge of regulatory requirements, such as FDA, EMA, and other relevant authorities.
• Strong understanding of GMP (Good Manufacturing Practice) principles.
• Excellent leadership, communication, and interpersonal skills.
• Experience in managing and leading teams.
• Familiarity with quality management tools and methodologies.

What we offer:

By investing in new development capabilities, state-of-the-art manufacturing facility, and partnerships we have the opportunity to shape the future of SINCERITAS and give more patients access to affordable, high-quality medicines - sustainably. Our dynamism and entrepreneurial spirit are driven by an open, collaborative culture, supported by our talented and ambitious colleagues who, in return for the use of their skills, experience an agile and collegial environment with impactful, flexible careers in which diversity is welcome and personal development is encouraged!

In addition to a basic salary in line with market, we offer:

1. Organized transport from Skopje to Rosoman

2. Provided meal for all the employees

3. Collective insurance for all the employees

 

EMPLOYEE LOYALTY & LONG-TERM BENEFITS

Seniority Salary Increase Tiers

Private Health Care Loyalty Incentive

Vacation Voucher Benefit

Additional information: Candidates who meet the above conditions can send their CVs in English via Fast Apply.