Senior Manager - Block Head Production (OSD)
Sun Pharmaceuticals, Inc
**Job Title:**
Block Head (Production)
**Business Unit:**
SGO
**Location :**
Sikkim-2
**Sub-Function:**
Formulation Production
**Job Classification Code:**
JC2141
**Job Classification Label:**
Block Head
**Job Family:**
Manufacturing
**Sub-Job Family:**
Production
**Key Responsibilities**
**Position Summary**
This role is responsible for overseeing the operations of a specific block within the manufacturing facility, ensuring efficient production processes, compliance with quality and safety standards, and meeting production targets.
+ To meet the production targets
+ To ensure the implementation of current Good Manufacturing Practices and SOPs at work place
+ To maintain and improve the product quality as per standard
+ To ensure Accuracy, Reliability, validity, integrity and completeness of the cGxP data/records
+ To plan the department activities as per weekly delivery schedule for OSD and Liquid orals
+ To ensure the effective control on man, machine and material in the department
+ To participate and coordinate various on-going qualification and validation activities
+ Collaborate with the site quality head, QA & QC head in ensuring that the production is aligned to the quality standards and regulatory requirements
+ To ensure the completeness of all the trainings (Sops, Technical, Developmental and Regulatory etc.) assigned to block personnels
+ To organize and implement the on-job training activities in the department
+ To ensure the implementation of EHS practices during work
+ To ensure the maintenance of equipment and upkeep of department constantly
+ To control the rejection during manufacturing and packing operations
+ To do counseling and grievance handling of the subordinates
+ To prepare, review and approve the Standard Operating Procedures
+ To evaluate deviations, change controls and other quality documents for appropriate conclusion
+ To ensure the market compliant investigations as per the track wise module and its timely closure and awareness training to all the concerned persons
+ Handling of QMS related activities of Block
+ To carry out the batch failure investigation for root cause identification and accordingly appropriate corrective action and preventive action taken
+ To review and approve the equipment qualification protocols, process validation protocols, reports, specifications and master formulae
**Job Requirements**
**Educational Qualification**
M.Sc. /B Pharma / M.Pharm
**Experience**
_Tenure_ : 18-20 years
**_Disclaimer:_** _The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s)._
We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.
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