Job Description

To be responsible for the overall activities of plant. To be responsible for the production and manpower planning of plant. To ensure that products are produced and stored according to appropriate procedures & documentation in order to obtain/maintain the required quality. To review and ensure the batch production records (BMR & BPR etc.) are executed as per standards. To ensure that the qualification of Equipment's and Instruments are done. To ensure that the appropriate validations are done for products. To check and ensure minimum stock of consumables, Log books and Status Labels. Ensuring preventive maintenance of all equipment's and instrument calibrations as per schedule. Co-ordinate with service departments (QA, QC, IT, stores, E&M, EHS, projects, SCM & Finance) for various production related activities. To ensure and verify the SAP stocks for RM, intermediates and FG materials To attend GMP and safety trainings & implement the trainings outcome at workplace. To ensure that the required initial and continual training of department personnel are carried out and adapted according to the need To check and ensure production related inputs in SAP system and FG transfer. To be responsible for investigations for market complaints, deviations, quality incidents and take appropriate CAPA against the non-conformity / Root cause. Participation in management reviews on process performance, quality and advocating continual improvement. To be responsible for timely, effective communication and escalation process exists to raise quality issue to the appropriate levels of management. To be responsible for production activities are being followed as per the pre-defined procedure and cGMP. To be responsible for audit readiness and compliance within the stipulated timelines. To be responsible for compliance of legal and other requirements related to ISO and OHSAS standards To be responsible for identification of risk, hazards, environmental aspects and evaluation and review the same. To be responsible to develop the objective and targets under the ISO and OHSAS standards Identify the EHS training needs for awareness and competence of department personnel. To be responsible for the work of his senior in the absence of senior or authorization from senior. Responsible to handle all the QMS documentation works such as Change controls, Deviation investigations, Market complaint investigations, Corrective and Preventive actions, Preparation / review of protocols, Qualification & validation activities, SOP preparation or revision, Batch record preparation / review / approval. Complete the assigned training activities in LMS within timeline and should provide trainings to associates as per requirement in LMS Handling of Internal and External audits, Visits, Safety audits etc. and their compliance. To involve in the CSV (Computer System Validation) related activities. To perform review activities in ENSUR, Docusign & Trackwise system To perform approval of training contents / questionnaires in LMS

In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth.
Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices.

Equal employment opportunity

Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics.



We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice.

Piramal Critical Care (PCC), under Piramal Pharma Limited (PPL), a subsidiary of Piramal Enterprises Limited, is the third largest producer of Inhaled Anaesthetics and a global player in hospital generics. Motivated by its vision to deliver critical care solutions for patients and healthcare providers across the globe, PCC is committed to enabling sustainable and profitable growth for all its stakeholders.


PCC maintains a wide presence across the USA, Europe and more than 100 countries across the globe. Its rich product portfolio includes Inhalation Anaesthetics such as Sevoflurane, Isoflurane and Halothane as well as Intrathecal Baclofen therapy, for spasticity management. PCC has wholly-owned, state-of-the-art manufacturing facilities in the US and India that have successfully cleared periodical inspections by the US FDA, UK MHRA and other regulators.


Its core strength lies in a highly qualified global workforce of more than 400 employees across 16 countries. PCC is focused on further expanding its global footprint through new product additions in the critical care space.


Committed to corporate social responsibility alongside Piramal Group, PCC collaborates with various partner organizations and proudly takes an active role in providing hope and resources to those in need, as well as caring for the environment.