Packaging Supervisor - 2nd Shift

Are you ready to join a growing, global drug development and manufacturing organization that puts people first? Come to Adare! We work closely with our pharmaceutical industry partners during all phases of drug development and commercial manufacturing with a mission of improving the lives of patients and medicines essential to people all over the world. Every role within Adare offers you a unique, customized experience with a chance to make a real impact that is critical to our success. With the help of people like you dedicated to our mission, Adare is transforming lives by transforming drug delivery!

Join our mission at Adare!

What can Adare offer you?

• Medical/dental/vision/life – low employee premiums
• 401k with a highly competitive match
• Generous PTO, including floating holidays
• Career growth and internal opportunities
• Tuition reimbursement
• Relocation assistance
• Performance-based bonus
• Employee Recognition Programs

We are seeking to hire a 2nd ShiftPackaging Supervisorto join our Manufacturing Operations team…

If any of the below describes you, we would love to meet you!

Job Summary

The Packaging Supervisor is a crucial role as a shift leader in Adare’s packaging operations. This Supervisor will be responsible for ensuring the packaging of client products in compliance with regulatory requirements, operational plans, and company policies. This position will support Adare through a high growth time, and will be expected to play an important role in the interviewing, onboarding, and training of employees.

Responsibilities and Learning Opportunities

• Lead and guide packaging floor personnel to ensure efficient use of equipment and materials for high-quality product outcomes in accordance with cGMP and production plan.
• Provide coaching, counselling, and development to direct staff, provide input on performance reviews.
• Maintain alignment with department goals and objectives.
• Promote safe work practices and compliance with policies and environmental, health, and safety standards.
• Train personnel on equipment, processes, and SOPs.
• Develop and manage packaging schedules within budget.
• Ensure timely project completion and participate in qualification and validation activities.
• Perform investigations for OOS, partner with Quality to create and implement CAPA’s
• Investigate and resolve problems, propose process improvements and foster collaboration.
• Monitor processes, generate reports, and provide operational direction.
• Review documentation for compliance standards and establish timelines.
• Participate in multi-functional project teams and perform additional tasks as required.

Requirements

• Bachelor’s degree in engineering, pharmaceuticals, related life sciences, or equivalent with 4+ years of experience; Associates’ degree with 6+ years’ of experience, or 8+ years’ experience with a certification.
• Experience in tablet or capsule packaging, manual visual inspection, and finished product packaging with serialization.
• Strong communication, leadership, and problem-solving skills.
• Proficient in investigations, technical writing, MS Office applications, and leading operational teams.
• Familiarity with FDA cGMPs and regulations.
• Ability to work in office and biotechnology manufacturing environments.
• Flexibility for different shifts and overtime

Benefits

• Medical/dental/vision/life – low employee premiums
• 401k with a highly competitive match
• Generous PTO, including floating holidays
• Career growth and internal opportunities
• Tuition reimbursement
• Relocation assistance
• Performance-based bonus
• Employee Recognition Programs