Post : Production Manager



Post : Production Manager

Job Description
• To manufacture a product that is compliant to SISPQ.
• To ensure GMP and GDP is followed at all levels of manufacturing and relevant activities.
• To coordinate with Projects and Engineering department during commissioning, qualification and maintenance activities.
• Responsible for organizing production schedule to meet the commitment to the supply chain department.
• To evaluate the Risk Analysis for equipment and processes.
• Supporting in managing the resources, planning and ensuring the coordination and control of formulation and filling department.
• To support Validation team to execute the validation and qualification activities as per the pre-approved protocols.
• To ensure the work place and equipment are maintained clean and hygienic all the time.
• To escalate the potential quality events to superiors and take part in investigations and root cause analysis.
• To initiate Change controls related to processes or process equipment pertaining to compounding area.
• To supervise Production operations and ensure the production plan is achieved with respect to quality, quantity, timelines, performance KPIs and HSE standards.
• To supervise, motivate and allow team personnel to develop his/ her competencies and potential in order to perform his/ her job better.
• To support and implement continuous improvements within his/her perimeter.

Duties & Responsibilities


• Responsible for Effective Operations of Equipment for compounding and filling area in Insulin facility.
• Ensure operations to be carried with budget planning and its effective utilization.
• To contribute in the definition and execution of the site strategy and is in-charge of implementing Operational Excellence standards (e.g: lean program).
• Supporting in fostering motivation and excellence in his perimeter.
• Responsible for timely support in execution and documentation of validations and other relevant activities.
• Responsible for preparation & Review of SOPs, batch production records and relevant documents pertaining to compounding & filling area.
• Act as a key point of contact for internal and external audit preparations.
• Act as an interface between manufacturing team and cross functional teams during investigations, change approvals, lean management and several miscellaneous activities.
• Improve the existing facility in terms of equipment and practices in compliance with site quality procedures.
• Define ways of working based on the goals and priorities.
• Ensure continuous improvement of Industrial performance in compounding and filling area.
• Simplify ways of working and establish low hierarchy.
• In-line with APU concept, take decisions in given boundaries to meet business requirements.


• Train the staff on compounding operations as per Sanofi group strategy.
• Acquire relevant equipment and process training with respect to compounding and filling relevant operations.
• Prepare the team for various regulatory inspections/ audits and GMP compliance

Cross functional

• Responsible for co-ordinating with QA, QC, Validations, Engineering, HSE and Projects to support in respective relevant activities.
• Support activities conducted by cross functional departments such as HSE, Lean management and facilitate exchange of information.


• To identify, correct and promptly report unsafe conditions, behaviours, or potentially hazardous situations.
• To animate a strong, proactive culture oriented towards promoting positive behaviours at all times.
• To demonstrate visible commitment to HSE and have the special responsibility to lead by example

Candidate Profile

• Minimum of Bachelor’s/Masters degree in Pharmacy/M.Sc
• Minimum of 7 years’ experience.
• Pharmaceutical industry experience is a must.
• Act for change: Adapt to changing circumstances in positive and enthusiastic manner.
• Cooperate Transversally: Develop and maintain effective cross functional working relationships and partnerships.
• Develop people: Share best practices and expertise to improve team member’s competencies.
• Excellent communication skills.
• Capacity to imbibe new technologies.
• High levels of confidence and problem solving capabilities.
• Knowledge on GMP/ GXP and technicalities involved in manufacturing relevant activities.
• Language requirements: Fluency in English (reading, writing and listening).

Additional Information
Experience : 5+ years
Qualification : M.Sc, B.Pharm, M.Pharm
Location : Toopran Mandal, Telangana
Industry Type : Pharma
Functional Area : Production
End Date : 25th December, 2018

Interested candidates can apply online through

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