Senior Dispensary Technician - Late shift

Dechra; Skipton; Sur place; GBP 17 000 - 25 000; Plein temps

Avantages offerts par ce poste

Free onsite parking

Average 36 hour working week

22 days annual holiday + Bank Holidays

Option to buy a week's holiday each年

8% Employer Pension Contribution

Résumé du poste

Dechra is seeking a Senior Dispensary Technician at its Skipton site in North Yorkshire. You will act as the SME for dispensing operations, ensuring GMP/SOP compliance while guiding a team and maintaining data integrity in batch records.

The role includes coaching staff, managing safety, and coordinating with the Manufacturing Supervisor. The position features a late shift (2pm-10:30pm, Mon-Thurs, plus every other Friday) with a strong emphasis on quality, risk assessment, and continuous

Qualifications

• Experience in GMP production facilities.
• Strong Health & Safety knowledge and compliance.
• Experience with Oracle systems.
• Ability to manage time and workload effectively.
• Excellent communication within production teams.

Responsabilités

• Act as SME for day-to-day dispensing operations.
• Ensure SOP/GMP adherence across paperwork, picking, dispensing, and Oracle.
• Train technicians and deliver shift briefings.
• Promote safety culture and participate in risk assessments.
• Review batch documentation and maintain data integrity.
• Escalate non-conformances and support problem resolution.
• Lead on shopfloor engagement and team coaching.

Connaissances

Communication skills

GMP knowledge

Safety awareness

People coaching

Outils

Oracle

Description du poste

Senior Dispensary Technician - £Competitive

Shift details: Late shift, 9DF, 2pm-10.30pm (Mon-Thurs), every other Friday 12pm-8.30pm

Based at our Skipton, North Yorkshire manufacturing site.

We are Dechra a growing, global specialist within the world of veterinary pharmaceuticals. Our expertise is in the development, manufacture, marketing and sales of high-quality products exclusively for veterinarians worldwide.

The role

• Act as the subject matter expert (SME) for day-to-day dispensing operations within the department.
• Support dispensing process across paperwork, picking, dispensing, and Oracle, ensuring adherence to Standard Operating Procedures (SOPs) and Good Manufacturing Practice (GMP) standards.
• Support and guide the team. Make routine decisions regarding safety and GMP, notifying the Manufacturing Supervisor or Manager, as a matter of urgency, if there has been any serious failure of safety or GMP which could affect staff safety or product quality.
• Train technicians on procedures, best practices, and GMP expectations.
• Deliver shift briefings and ensure effective communication both ways with the shopfloor.
• Advocate on shopfloor for employee engagement and people plan initiatives to create a positive working culture.
• Support onboarding of new team members.
• Promote and uphold site safety culture - actively participate in safety walks, risk assessments, and incident reviews.
• Ensure all dispensing activities are performed in accordance with EHS policies and permit conditions.
• Drive strong housekeeping standards to maintain a safe working environment.
• Ensure team's adherence to risk assessments and input to updates where required.
• Promote active participation in hazard identification and resolution of open hazards.
• Prepare and review batch documentation, logbooks, and electronic records to ensure data integrity.
• Assisting in updating and completion of GMP documentation such as SOP's and BMR'S.
• Escalate any non-conformances whilst ensuring they are documented appropriately and contributing to the investigation where required.
• Drive right first time (RFT) execution through technician coaching and real-time support on the shop floor.
• Review dispensary telemetry alarms and upscale issues to supervisor.
• Troubleshoot equipment issues to minimize downtime and maintain schedule adherence.
• Support plan delivery through effective resource and process management,

KPIs

• RFT and deviation closure rates.
• Compliance with GMP and EHS standards.
• Plan schedule adherence.
• Training completion and competency verification.

You

Essential

• Experience of low to medium volume production, manual/semi-automated processes.
• Good knowledge and understanding of Health & Safety compliance.
• Proven industry experience from a highly regulated GMP production facility,
• A working knowledge and practical experience of pharmaceutical manufacture and ability to manage time and workload effectively.
• Ability to communicate effectively, both within the production team and cross functionally.

Desirable

• Knowledge of computerised systems such as Oracle.
• Proven ability to lead projects and teams.

Reward

• Competitive basic salary depending on the shift
• Free onsite parking
• Average 36 hour working week
• 22 days annual holiday + Bank Holidays
• Option to buy a week's holiday each year
• 8% Employer Pension Contribution