Quality Specialist

At Adalvo, we're not just a company - we're a team of passionate individuals driven by our mission to consistently deliver high-quality products and services to our partners. We are positive, we are fast, we are always on target , we are Adalvo ! 🎯 🚀

We are looking for an enthusiastic Quality Assurance Specialist to join our dynamic Quality s team. If you're someone who thrives in a fast-paced environment and loves tackling new challenges, then this is the perfect opportunity for you.

SUMMARY OF POSITION

The Quality Assurance Specialist will provide support to QA team by contributing to all activities involving quality assurance and compliance with applicable regulatory requirements and assuring that Company standards are maintained, and product integrity is preserved.

RESPONSIBILITIES

Primary responsibilities of this role include the following:

• Supporting in the maintenance of internal quality systems and GxP activities.
• Supporting in the drafting, reviewing, issuing and archiving of GxP documents.
• Ensuring that documents issued are incompliance with good documentation practices.
• Preparing and reviewing SOPs related to Adalvo operations
• Providing support to Quality team in the handling of deviations, change controls, CAPAs, complaints and risk assessments.
• Assisting in internal and external audits and in the preparation of corrective and preventive actions (CAPA) and their respective follow up.
• Supporting and assisting in training activities and monitoring SOP training gaps.
• Supporting and assisting the QP/RP in qualification of vendors and customers.
• Supporting and assisting the QP/RP in review of distribution and release documentation.
• Providing support in investigations related to deviations, complaints and recalls.
• Supporting continuous improvement activities related to Adalvo.
• Participating in quality management review meetings and assist in any follow upsrequired.
• Keep abreast with latest requirements related to GMP and GDP.
• Approve materials, vendors and customers in SAP after quality review.
• Support in the transfer of samples required for submission purposes.

QUALIFICATIONS & REQUIREMENTS

• Education - University degree in pharmacy, chemistry or another science-based discipline (minimum Bachelor’s degree). The person must not have been deprived of legal capacity to hold a position in the pharmaceutical industry.
• Professional experience – preferably not less than 5 years of work experience in the production and/or control of pharmaceuticals.
• To be well acquainted with the European standards on Good Manufacturing Practice (EU-GMP) and Good Distribution Practice (GDP), as well as other international GMP standards.
• Good command of English
• Good computer skills

CORE COMPETENCIES

Business Focus

Drive for Results

Building Team Spirit

Customer Service

Embracing Change

Quality

Why join us?

🎯 Exciting Challenges: Every day brings new opportunities to learn and grow.

🎯 Supportive Environment: We foster a culture of collaboration, where your ideas are valued, and your voice is heard.

🎯 Career Development: We're committed to helping you reach your full potential through ongoing training and development opportunities.

🎯 Recognizing Excellence: We recognize and appreciate hard work and dedication by offering competitive compensation packages and employee rewards programs that acknowledge contributions and achievements.

🎯 Fun and Inclusive Culture: We believe in celebrating our successes and building strong connections within our team.

Ready to Ignite Your Passion?

If you're ready to take the next step in your career and join a business committed to consistently deliver high-quality products and services, then we want to hear from you! Send us your resume today!

Kindly be informed that only selected candidates will be contacted.