Seeking a skilled Formulation Supervisor for Ordan, a leading Swedish medical company. Join us now!
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– BSc in Industrial or Chemical Engineering.
– Minimum of one year of experience working in the quality field preferably within a pharmaceutical company.
– Knowledge and practical experience of Good Manufacturing Practices.
– Auditing and inspection skills.
– Statistical and analytical skills.
– Knowledge of quality tools and process improvement tools.
– Knowledge of relevant regulatory requirements.
– Preferable knowledge and courses in ISO 9001.
– Good command of English language.
– Strong computer skills including Microsoft Office and databases.
– The ability to work collaboratively and as part of a team.
– Strong verbal and written communication and problem-solving skills.
The candidate will be responsible for:
– Conducting onsite and desktop compliance audits to ensure the effectiveness of the systems and procedures in place.
– Assisting in conducting departmental internal audits.
– Participating in the required investigations and actions resulting from external audits and inspections, customer complaints, or any suggested projects.
– Performance monitoring of manufacturing processes and quality systems through key performance indicators and process improvement tools.
– Performing the studies required for risk evaluation and assessment of operations and systems.
– Participating in suppliers and service providers assessment and evaluation and auditing.
– Assisting in quality related training needed for company employees.
Candidates should send their resumes to the following email address and add the position in the title:
[email protected]
ordan Sweden Medical is looking to hire a Formulation_Supervisor with the following requirements:
Formulation Supervisor Duties and Responsibilities:
1. Ensure that the Standard Operating Procedures (SOPs) and GMP requirements that relate to the preparation and development of medicinal formulas are implemented.
2.Follow up with the rules and regulations of GLP and their implementation.
3. Execute the stages of the formula preparation in coordination with the R&D Manager.
4. Document the processes related to the materials mixing and preparation of products on the designated records.
5. Participate effectively in stabilizing the methods of products preparation and review the documents related to increasing the size of the trial batches to the production batch sizes.
6. Participate in coordinating with the Stability Studies Specialist to review the results of the accelerated stability studies that provide initial indication on the studied formulas.
7.Ensure that the mixing processes comply with the universal regulations related to the medicinal manufacturing.
8.Participate in training R&D department employees.
Formulation Supervisor Requirements and Qualifications:
إقرأ أيضا:وظائف عمل في شركة ENI في ابوظبي· Bachelor’s degree in Pharmacy .
· At least 5 years in Pharmaceutical industries.
Skills Required:
1. Courses in GMP and registration required inside and outside Jordan.
2. Clinical studies and their requirements.
3. Scientific research methods and scientific reports writing technics.
4. Good knowledge at GMP & GLP
Primary location:
Amman 851831 Jordan
Organization:
Joswe Medical
Job Function:
Formulation Supervisor
Please send your updated resume to the following email address: [email protected]