Production Supervisor
hace 1 día
Ready to turn chemistry into impact? Join Curaleaf International as a **Production Supervisor**, where your technical expertise and leadership will power the production of next-generation medicinal products.
This is a full time role, based on site in Alicante, Spain.
**About the Role**:
As **Production Supervisor**, you'll play a key role in leading chemical synthesis and manufacturing operations for Active Pharmaceutical Ingredients and investigational medicinal products. Leading from the front, you will promote a culture of safety, accountability, and operational excellence throughout every stage of production, ensuring full compliance with GMP standards.
**Duties include but won't be limited to**:
- Ensuring equipment, materials, and production areas are prepared and ready for batch execution
- Reviewing and verifying batch records, logbooks, and documentation for accuracy and completeness
- Supervising, mentoring, and training production operators, ensuring KPIs and adherence to all policies and procedures are met
- Leading shift meetings and communicating production goals, issues, and updates effectively
- Supporting technology transfer and process scale-up from R&D to production scale
- Identifying, escalating, and documenting process deviations or non-conformities
- Verifying material and product movements, labeling, CoAs, and traceability documentation
- Assisting the Production Manager and QA in investigations, CAPAs, and continuous improvement activities
- Participating in audits and inspections as required
**About You**:
This hands-on role is ideal for a technically strong professional in organic chemistry who thrives in a fast-paced, quality-driven environment and takes pride in maintaining the highest standards of safety, documentation, and production excellence.
Essential criteria:
PhD in Organic Chemistry (or equivalent)
Experience in chemical process development or GMP manufacturing of APIs
Strong understanding of reaction mechanisms, scale-up challenges, and process safety
Excellent organizational and problem-solving skills
Good communication and leadership abilities
Computer literacy (MS Office, ERP, batch management software)
It would also be beneficial to have:
Experience in technology transfer from R&D to manufacturing
Proven experience in writing, reviewing, and approving batch documentation under GMP
Familiarity with ICH Q7, EU GMP Part II
Knowledge of analytical techniques (HPLC, GC, NMR) and process analytical tools (PAT)
Fluency in English (technical reading/writing)
**About Us**:
- At Curaleaf International, we're not just participating in the cannabis industry-we're leading it._
Curaleaf International is shaping the future of cannabis through its commitment to research and product excellence. Powered by a strong presence at all stages of the supply chain, its unique distribution network throughout Europe, Canada and Australasia brings together pioneering research with cutting-edge cultivation, extraction, and production. Amidst a rapid growth trajectory, the emphasis on quality and expertise aims to ensure the delivery of safe and legal cannabis.
Curaleaf International's network includes a clinic, pharmacy, and laboratory in the UK; cultivation and EU-GMP processing facilities in Portugal; an EU-GMP processing, quality assurance and research site in Spain; Four20 Pharma wholesaler and distributor in Germany; a Polish wholesaler and clinic; and the EU-GMP producer Northern Green Canada.
Curaleaf International is part of Curaleaf Holdings, Inc., a leading international producer and distributor of consumer cannabis products.
**Our Vision**: To shape the future of cannabis through our commitment to research and product excellence
**Our Mission**: To be the world's leading cannabis company consistently delivering superior products and services and driving the global acceptance of cannabis.
**Our Values**:Lead & Inspire Commit to Win Driven to Deliver Excellence Customer Obsession One Curaleaf
We value progression and development, offering competitive wages and benefits as well as lots of opportunity in a rapidly growing organisation.
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