À propos du poste
The primary purpose of the Post-Production Label Printing Specialist role is to process label printing requirements for commercial batches, BUD batches, label testing and other printing needs with precision and accuracy associated with our post-production manufacturing.
Responsibilities:
In addition to performing the responsibilities associated with processing label printing for production batches, this individual will also be responsible for the following:
· Communicating and relaying inventory needs and shortages to procurement or warehouse teams.
· Support marketing and sales requests for sample sales kit label needs.
· Coordinate with SME’s regarding label modifications, regulatory updates and harmonization programs.
· Support post-production continuous improvement initiatives.
· Continuous monitoring of batch records for errors, completions of review and verification signatures.
· Clerical tasks including data entry, batch tracking, inventory control.
· Establish key performance indicators in alignment with department goals, maintain and report applicable area or organizational metrics.
· Collaborate with pharmacists, supervisors, supply chain and other manufacturing teams to author, review or revise applicable SOPs, batch records, and other operational related documents.
· Conduct technical training for post-production manufacturing operations.
· Conduct review of post-production operations to ensure compliance to procedures.
· Other tasks and duties as assigned by Area Management.
· Investigate, document findings and influence assessment for deviations.
· Actively participate in teams conversations with SMEs within post-production.
· Commitment to maintaining consistency and compliance with established procedures.
· Assist assigned functional area leads in driving problems to resolution.
Distinguez-vous !
Profile/Experiences
· Skilled, flexible worker with strong people skills and an extensive background in cGMP manufacturing.
· Excellent time management skills and ability to self-direct in managing concurrent requirements.
· commitment to maintaining consistency and compliance with established procedures.
· Knowledge and experience in Current Good Manufacturing Practices (cGMP) regulations, documentation, and compliance.
· Experience in batch paperwork and processes.
· Minimum of 6 months cGMP post-production experience.
· Direct experience in processes acclimated to post-production.
· Excellent communication and organizational skills with an ability to prioritize effectively and work cross-functionally to deliver results within established timelines.
· Must be detail oriented, able to work in a fast-paced environment.
· High school diploma or equivalent required
Notre proposition
Fagron offers exciting opportunities for personal and professional growth. We provide an open and truly dynamic environment which supports and encourages you to develop your skills and talents.