• Pharmaceutical Industry with production plant in the area of Barcelona
• Shift Supervisor to lead a team of 6-7 people

A pharmaceutical industry located in the area of Barcelona (Vallés Occidental) is looking to hire a Shift Supervisor to lead a team of approximately 6 people, rotating between morning and afternoon shifts, with an initial training period on a split shift.

As a Shift Supervisor, you'll lead a team of manufacturing operators to ensure production runs efficiently, safely, and in compliance with procedures and GMP standards. You'll play a key role in people development, quality, process improvement, and daily operations.

????? Your Main Responsibilities?? Team & People Management

• Ensure a safe, clean, and organized work environment.


• Assign daily tasks to team members and ensure proper execution.


• Set performance goals, provide feedback, and coach your team.


• Support and escalate any issues related to safety, process, materials, or equipment.


• Provide technical guidance in aseptic production, formulation, and packaging areas.

?? Training & Compliance

• Coordinate and deliver training to ensure team members are skilled and compliant.


• Support inspection readiness in collaboration with Quality teams.


• Promote a Right First Time approach across operations.

?? Production Oversight

• Operate and supervise complex manufacturing systems.


• Review batch records and ensure alignment with production schedules.


• Troubleshoot basic equipment or process issues when needed.

?? Deviation & Quality Management

• Ensure deviations are properly identified, documented, and investigated.


• Partner with QA to support investigations and CAPA implementation.


• Help maintain high-quality standards in every step of production.

?? Continuous Improvement

• Suggest and implement improvements in SOPs, manufacturing records, and training materials.


• Represent Manufacturing in cross-functional initiatives and projects.


• Drive efficiency and quality through continuous improvement.

• A meaningful role in a company committed to quality and continuous improvement.


• The chance to lead, grow, and make a real impact.


• A dynamic and collaborative environment.


• Career development and training opportunities.


• Permanent contract.


• Rotate between morning and afternoon shifts, with an initial training period on a split shift.


• Salary according to experience and market salary.

Required Qualifications

• Bachelor's degree with 4.-5 years of experience in manufacturing filling area GMP manufacturing and 2+ years of experience leading manufacturing teams in aseptic area.


• Minimum 2 years of experience in a lead or supervisor position.


• Solid understanding of pharmaceutical manufacturing and cGMP principles.

Preferred Qualifications

• Bachelor's degree in a relevant field.


• Experience supervising teams in aseptic manufacturing.


• Skilled in coaching, training, and team development.


• Strong problem-solving and root cause analysis skills.


• Experienced in reviewing SOPs, training materials, and batch documentation.