Aculife healthcare hiring for we are hiring AGM / DGM - Production

Pharma Vacancy
Aculife Healthcare Pvt. Ltd company is a part of $3 billion Nirma Group & it is one of world's largest Infusion & Injectable Company, having a State-of-the art manufacturing facility spread over 550 acres of land located near Ahmedabad, Gujarat. Aculife healthcare has global operation in more than 100 countries and it has subsidiaries in Brazil, Mexico & Vietnam. The manufacturing facility has 2 plants with FFS technology, 1 Glass injectable plant and a one dedicated R&D center equipped with advance technology and unmatched research team. Aculife has best in class quality infrastructure with the aim to assure high level of quality assurance through QBD & QAR, Aculife has developed strong footprint globally and have 1000 registrations to cater the demand of regulated and semi regulated market. Company's domestic business is driven by 3 divisions in therapeutic area of Critical care, Parentral Infusion & Parentral Nutritions, at the same time we are the most preferred contract manufacturers for top Indian pharmaceutical companies.

We at Aculife nurture the talent and have more than 3000+ satisfied employees, out of which around 300+ field force spread across the country. In pursuit of our expansion plan, we are hiring AGM / DGM - Production
Job Responsibilities

• Ensure all activity related to administrative and technical function of department are

as per schedule & approved procedure.

• To control & improve the aseptic practices & behavior in routine activity.

• To plan and execute the monthly production and raw materials & packing materials

Requirement schedule.

⚫ To follow the safety norms and c-GMP procedures.

⚫To Handle & support the action required for internal and external audits including regulatory audits.

• To response the observations observed by auditors during inspections • Review and handling of Change Controls, Deviations, Incidents, Customer complaint, OOS, CAPA etc

• Review of Qualification (Equipment, Area, Utility), Cleaning and Process Validation documents and ensure completion of activities as per schedule/Planner.

• Review of documents related to GMP, SOPs, Operating manual and Batch records.

⚫ Technology transfer support to F&D and Regulatory support for submission related tasks. Water system, Environment monitoring report review and take necessary action for any failure.

• To ensure implementation of c-GMP, GEP and Quality Systems.

To ensure cost control in the area of manufacturing expenses, waste and down time reduction.

Interested candidates may apply or WhatsApp on - 9727523477/


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