Head Production department pharma вакансия 111966718

Вакансия:	Head Production department pharma
Работодатель:	OOO Novugen Pharma
Обновлено:	27.11.2024 12:40:08
Регион:	Ташкент
Опыт работы:	Более 6 лет
Оплата:	ЗП не указана
Тип занятости:	Полная занятость
Описание:	Job Purpose: The Production Manager oversees the manufacturing process to ensure efficient and effective production operations. This includes managing production schedules, coordinating resources, and ensuring quality standards are met in accordance with regulatory requirements of Uzbekistan and EAEU compliance level. The role is critical in optimizing production performance and achieving company objectives. This position expectation is to have deep knowledge in production procedures, operation of production equipment and hands on experience on solid dosage manufacturing operations. Must have experience and understanding to face international inspection. This role is critical for the smooth running of all production lines and quality output with continuous improvement in the system, processes and cost optimization. Strategic & Key Result Areas: Production Efficiency: Implement strategies to enhance production efficiency and reduce downtime. Quality Management System: Ensure all products meet established quality standards and specifications, also ensure the compliance level as defines in the GMP guidelines to follow good practices in production and maintain data integrity in each processes and equipment. Resource Management: Optimize the use of labor, equipment, and materials to achieve production goals. Cost Management: Develop and manage budgets to control production costs and improve profitability. Safety Compliance: Ensure a safe working environment by adhering to health and safety regulations. Team Leadership: Lead, develop, and motivate the production team to achieve high performance. Productivity Enhancement: Identify and implement continuous improvement initiatives to streamline production processes, improve OEE in each functions such as granulation, compression, blistering and encapsulation Reporting & Analysis: Monitor production metrics, analyze data, and prepare reports to track performance and identify areas for improvement. Job Description: Key Responsibilities: Plan, coordinate, and manage the production schedule to meet production targets. Monitor production processes to ensure they are running efficiently and effectively. Responsible for manufacturing of products as per written instruction in the BMR, ensuring 100% compliance during production and control all CPPs and CQAs. Responsible for writing URS of production equipment and other accessories as per current GMP standards. Responsible for the successful FAT, SAT, DQ, IQ,OQ and PQ of production equipment in coordination with validation. Manage and allocate resources, including labor, equipment, and materials. Responsible for the improve OEE of production equipment and set targets to achieve on continuous basis. Estimate Costs and prepare CAPEX and OPEX budgets Reviewing of written SOP and other documents pertaining to the manufacturing and engineering operation Ensuring and monitoring compliance of production activities with GMP, facilitating and ensuring self-inspection, internal audit according to schedule and strong follow up of observation for CAPA. Facility, system and procedure should be aligned as per local and EAEU standards and must pass all inspections. Lead, motivate and develop the team in line with company policies, setting KPIs and monitoring and reporting performance to the immediate supervisor. Participation in Product/ process validation of Area and equipment qualification in coordination with validation team. Responsible for the investigation and RCA against deviation and inspection findings related to production activities. Ensure compliance with health and safety regulations and promote a safe working environment. Lead, train, and develop the production team to enhance their skills and performance. Implement and oversee continuous improvement initiatives to optimize production processes. Prepare and present production reports and performance metrics to senior management. Collaborate with other departments to ensure seamless production operations. Position Profile: Qualifications: Bachelor’s or Master degree in pharmaceutical technology, Chemistry, or a related field. Proven experience as a Production Manager or in a similar role for a minimum of 5 years in CIS countries. Proficient knowledge of Russian and English is a must Strong understanding of production management, quality control, and budgeting. Excellent leadership and team management skills. Proficiency in production management software and tools. Strong problem-solving and decision-making abilities. Good communication and interpersonal skills. Knowledge of health and safety regulations. Personal Attributes: Analytical and detail oriented. Proactive and results-driven. Ability to work under pressure and meet deadlines. Strong organizational and multitasking skills. Commitment to continuous improvement. Remunerations Depending on experience. Transportation from Tashkent to Syrdyra. Annual bonus if results are met. Special/extra bonus on passing/clearing of EuroAsia (Russia, Kazakhstan or Belarus) GMP audit.

Контактная информация доступна авторизованным пользователям

Авторизоваться

Создать резюме

• В начало