Introduction to Ardena

As a leading Contract Development and Manufacturing Organization (CDMO), Ardena partners with pharmaceutical companies of all sizes—from emerging biotech to global industry leaders—united by the mission to help biopharma innovators navigate drug development with precision, quality, and speed, bringing their molecules from discovery to the clinic and market. Our fully integrated services span drug substance and drug product development, manufacturing, nanomedicine, clinical logistics, bioanalytical services, state research, fill & finish, and CMC regulatory support.

With a rapidly growing international footprint, Ardena is home to over 750 professionals across six strategic locations—Belgium (Ghent), the Netherlands (Oss and Assen), Sweden (Södertälje), Spain (Pamplona), and Somerset, New Jersey (the US). Our open and transparent culture is built on collaboration, ownership, and innovation, guided by our We CARE values. We foster a communicative environment where mutual respect, accountability, and excellence empower our team.

We are looking for skilled and motivated professionals eager to grow their careers in an exciting and fast-paced environment. Whether you’re an experienced expert or just starting out, Ardena provides a dynamic workplace where you can contribute to meaningful drug development projects, expand your knowledge, and be part of a global team committed to making a difference. As an international organization, we help you navigate a career path that expands your possibilities beyond borders, opening doors to personal and professional growth without limits. Your potential to grow is limitless with us.

If you are ready to take on new opportunities, work alongside industry experts, and contribute to the future of medicine, Ardena is the place for you.
  

WHAT YOU WILL WORK ON

YOUR ROLE

The Shift Supervisor (second shift) will lead the training, monitoring and supervising of the production staff. Responsible for employee assignments, safety, quality, production rates, material reconciliation, production reports, timelines and aligning on strategic goals to improve line efficiencies and output. This position requires a working knowledge of commercial and clinical manufacturing applications regarding study phases I through IV within a 24/7 operation. Experience with advanced unit dose filling and solid dosage processing equipment. Responsible for maintaining Class 100,000 clean rooms along with manufacturing and packaging of controlled substances II through V.

YOUR KEY RESPONSIBILITIES

• Monitors, organizes and performs all functions associated with commercial and clinical manufacturing and packaging and assures compliance to GMPs, SOPs, FDA, DEA and OSHA rules and regulations.
• Work seamlessly with partnering Team leaders and direct report technicians in ensuring productive and compliant operations within and between shifts
• Develops and Implements relevant Standard Operating Procedures, Site Quality procedures in ensuring 100% compliance, increases productivity and creates/maintains a culture of Continuous Improvement.
• Oversees unit operations consisting of and not limited to Hot Melt Extrusion, Fluid Bed, high speed Encapsulation, Compression, Coating, Milling, Blending, Sifting and other processes where assigned.
• Maintain compliance for PPE at the equipment and its vicinity through personal compliance and supervision for compliance by other personnel near the manufacturing and packaging equipment.

YOUR PROFILE 

• A Bachelor’s degree within an area of Science & Technology (i.e. Engineering, Mathematics, Chemistry, Physics) with at least 1+ years of experience working in the pharmaceutical industry, food manufacturing environment, or relevant industries (regulated by GMP standards and requirements).
• Prior experience leading projects or groups is required.
• 1+ years of supervisory experience is preferred, or 4+ years of experience working in relevant industries (regulated by GMP standards and requirements).
• Minimum 2+ years of experience in a leadership role within the pharmaceutical industry. 
• Knowledge of cGMP and ability to complete compliance/regulatory records and documents, processes, procedures, and practices for conformance to these requirements. 
• Knowledge of regulatory, compliance & quality requirements for packaging and labeling operations Ability to implement procedures to increase productivity and decrease downtime is required. 
• Experience overseeing both primary and secondary manufacturing and packaging operations including entering data accurately in batch records and logbooks is preferred. 
• Experience entering data necessary for production rates, labor hours and downtime is required.                                                                                                                                                      

WHAT WE OFFER

At Ardena, we recognize that our people drive our success. We offer:

✔ A competitive salary with a tailor-made benefits package, including: medical, dental and vision benefits effective day one of employment
✔ Paid Time Off
✔ A dynamic, global work environment with career growth opportunities
✔ Access to Ardena Academy, our internal learning platform for professional development
✔ A chance to contribute to groundbreaking drug development projects that make a real impact

HOW TO APPLY

Want to know more? Contact [Hiring Manager Name] at [Email] or call [Phone Number].

Ready to start your career path with Ardena? Click the application button and join us in shaping the future of drug development!