9 дней назад
Process Technician Senior Coordinator (12 Month Fixed Term Contract) (Biopharma)
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Process Technician Senior Coordinator (Biopharma): Managing manufacturing and packaging processes for Botanical Drug Product batches in a regulated production environment with an accent on cGMP compliance, batch documentation, and product quality. Focus on coordinating production schedules, performing routine microbiological testing, training technicians, and implementing process improvements.
Location: Sittingbourne, UK; onsite production role with flexible working hours when production processes overrun.
Company
is a global biopharmaceutical company developing and manufacturing medicines for serious diseases, with a focus on oncology, neuroscience, sleep disorders, and epilepsy.
What you will do
- Manage manufacturing and packaging processes for Botanical Drug Product batches in accordance with cGMP and EH&S requirements.
- Deliver production schedules, process batch documentation, equipment records, cleaning activities, and quality documentation.
- Perform routine microbiological testing in the Commercial Manufacturing Suite.
- Coordinate production activities with supply chain, warehouse, engineering, QC, and QA teams.
- Train and coach technicians on manufacturing processes, new procedures, and process changes.
- Identify and implement improvements that increase efficiency and reduce costs.
Requirements
- At least 3 years of experience in a regulated production environment, ideally pharmaceutical, chemical, or food manufacturing.
- Experience supervising or leading teams in the pharmaceutical or a related industry.
- Knowledge of cGMP, cGxP, EH&S requirements, standard operating procedures, and quality documentation.
- Strong attention to detail, numeracy, written and verbal communication skills, and teamwork.
- Working knowledge of Microsoft Excel and Word.
- Pharmaceutical industry qualifications such as NVQs or equivalent are preferred.
Culture & Benefits
- Work in a patient-focused, science-driven biopharmaceutical environment.
- Collaborate with internal departments and key stakeholder groups across manufacturing operations.
- Take part in continuous improvement initiatives across production and packaging processes.
- Fixed-term contract for 12 months with responsibilities supporting production, quality, safety, and environmental standards.
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