نیچرز اُنلی

منتشر شده 5 سال پیش

Job Description

Over all job review: Production supervisor is responsible for reporting of technical documents associated with GMP testing, investigations, change controls, raw material methods, and technical reports in support of new and existing raw materials, methods verification/validation and regulatory submissions. And work directly under Regulatory manager. - Ensure all compliance of production and GMP processes are met - Ensure compliance of GMP and SOP - Coordinate with QA, QC, and Purchase departments for planning and availability of materials - Ensures all necessary components / resources are available and capable to meet production schedule and established quality standards and goals. - Perform all assigned duties according to departmental SOP’s and cGMP’s. - Remain current on proper procedures by reviewing current, revised, and new SOP’s relating to the job and to the department. - Perform tasks as required to support the production / packaging of product to provide on-time - Assist daily production in operating and monitoring technical, computerized, production machinery, ensuring quality standards are maintained. - Perform other duties as assigned. - Accurately matching material and inventory to ensure that appropriate supplies are on hand. - Managing input and output rate of APIs and finished products .Matching staticties of APIs and paking materials to avoid any gap. - Gathering data like batch records and stability tests - Coordinating with RO about whatever is happening in factories in a daily basis as daily reports ,regarding commercial team ,Production team ,Warehouse team ,lab and finance team's issues.

Requirements

- Master degree in related majors such as Pharma chemistry, pure chemistry, Food industry, - Two (2) years of experience in Supervision and production in a pharmaceutical factory - Ability to go on mission for around maximum 20 days a month inside and outside of the country in case of need - Advance knowledge of IPQC - Proficient in Microsoft Word, Excel, and SAP. - Experience working in a GMP regulated environment preferred. - Experience working in an Aseptic production environment preferred. - Knowledge and application of fundamental concepts of manufacturing, including CGMP/QSR. - Ability to communicate effectively (verbal, written and presentation skills). - Ability to work effectively with peers and supervisors. - Analytical and problem-solving skills. - Demonstrated managerial ability. - Detail oriented and the ability to manage multiple task. - Ability to work and communicate with others in a professional and effective manner, within a team-oriented environment. - Ability to work any shift (up to 12-hours) as required dependent on business needs.

برای مشاهده‌ی شغل‌هایی که ارتباط بیشتری با حرفه‌ی شما دارد،