Career
WORK WITH US
Would you like to join our team?
Are you interested in our work and would you like to grow with us?
Send us your CV and a cover letter to the following email address recruitment@moonpharm.ch
No. 1 Engineer
Requirements:
Bachelor of Engineering, with experience in the pharmaceutical sector or equivalent with a minimum of 3 years of experience in Quality Assurance
Experience in project management, including the development and execution of validation protocols for equipments, tools and premises
Interpersonal skills
Excellent organizational and problem solving skills
Knowledge of safety regulations in the workplace
Knowledge of English level B2
Your Responsibilities:
Responsible for engineering projects developed in line with quality and safety requirements
Responsible for the maintenance of areas and equipments
Support the QA for the identification of critical quality parameters for new equipments, structures, premises
Support the QA in the development and review of validations and qualifications (DQ, OQ, IQ, FAT, SAT etc.)
Ensure validation protocols are performed and documented in compliance with GMPs
Supervise the work carried out by external personnel
Contribute to the continuous improvement of processes, premises and equipments by participating in meetings, seminars and projects on site
No. 1 Production Manager
Degree in science, chemistry, CTF or similar
Similar experience of at least 3-5 years in pharmaceutical manufacturing and research with excellent knowledge of GMP standards
Personnel management skills
Attitude to leadership and interpersonal and communication skills
Excellent organizational skills and propensity for problem solving
Orientation towards achieving objectives
Knowledge of English at B2 / C1 level
Activities:
Manage projects for the development of new pharmaceutical products
Process and formulation optimization in relation to existing pharmaceutical products
Ensure that the production and storage of medicines is done in accordance with existing rules
Issue and approve instructions related to production, warehouse and ensure their correct execution
Issues, approves, ensures the review and approval of production and warehouse documentation (Batch Record, Master Record, logbook etc.)
Ensures and controls the state of efficiency of the premises and equipment of its department and takes care of their maintenance
Ensures the execution of validations
Ensures the necessary training of its staff
Ensures hygiene in the facilities
Verify and participate in the selection of material suppliers, subcontractors and service providers
Verify the choice and control of the storage conditions of raw materials, materials and products
Ensures proper management of production and warehouse documentation, monitoring of compliance with cGMP
Participate in self-inspection, investigation and sampling activities aimed at keeping under control the factors that can affect the quality of the products