Unit Head Production

Job Summary

We are seeking an individual to oversee batch manufacturing ensuring adherence to cGMP (Current Good Manufacturing Practices) providing training and coordinating day-to-day activities. Responsibilities include minimizing machine downtime managing subordinate staff assuring compliance with standards and SOPs (Standard Operating Procedure) leading regulatory audits compiling reports ensuring safety norms and budget management.

Roles & Responsibilities

You will be responsible for enforcing cGMP for batch manufacturing in order to obtain high-quality products and achieve targeted production within a span of control.

You will be responsible for imparting general and cGMP training to the subordinates based on the need to nurture talent and motivation in them.

You will be responsible for coordinating with interdepartmental functions to carry out day-to-day activities in a smooth manner minimizing loss of utilization.

You will be responsible for ensuring adherence to the maintenance plan for machines to reduce downtime leading to increased product yield and productivity.

You will manage and evaluate the work performed by subordinate staff to ensure the implementation of GMP standards and SOP.

Your role includes assuring the adherence to in-house specifications SOPs Master formulas and approvals as well as ensuring compliance with the companys Quality policies.

You will lead the Regulatory audit team and handle Regulatory Audits internationally ensuring plant readiness for Regulated Markets.

Compiling daily weekly and monthly reports and submitting them to the leadership team is part of your responsibilities.

You will ensure safety norms as per the EHS (Environment Health and Safety) policy of the site meeting 100% guidelines.

Your role involves preparing the departments budget and executing it effectively to achieve organizational objectives.

You will build a development plan and align yourself with the goals of the organization.

Qualifications :

Educational qualification : .

Minimum work experience : 15 to 20 years of experience preferably in a manufacturing environment with a focus on cGMP compliance and regulatory audits

Skills & attributes :

Technical Skills

Experience in handling and overseeing Injectables Process Equipment

Knowledge of maintenance planning for machines and the proficiency in compiling and analysing daily weekly and monthly reports for leadership review.

Regulatory audit leadership and experience in handling international Regulatory Audits.

Familiarity with safety norms and the implementation of EHS policies.

Budgeting skills for preparing and effectively executing departmental budgets.

Behavioural Skills

Leadership and managerial skills to manage and evaluate subordinate staff.

Strong communication and coordination skills for interdepartmental collaboration and smooth day-to-day activities.

Commitment to nurturing talent and motivation through training programs.

Detail-oriented mind set for ensuring adherence to specifications SOPs and quality policies.

Strategic thinking and goal alignment for effective organizational development.

Additional Information :

About the Department

Global Manufacturing Organisation (GMO)

At Dr. Reddys Laboratories we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence we are a leading force in the pharmaceutical industry.

We operate 19 state-of-the-art manufacturing plants across Hyderabad Vizag Baddi Mexico Shreveport and Mirfield comprising 8 OSD facilities 3 Injectables facilities and 8 API facilities.

Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1150 drug master files across key therapy areas such as Oncology Cardio-vascular Central Nervous System and Anti-Diabetes. he World Economic Forum has recognised our largest manufacturing facility in Bachupally Hyderabad as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive meeting business imperatives and meeting our ambitious ESG goals. Building such factories of the future is integral to innovation and to build healthcare of the future.

Benefits Offered

At Dr. Reddys we actively help to catalyse your career growth and professional development through personalised learning programs.

The benefits you will enjoy at Dr. Reddys are on par with the best industry standards. They include among other things and other essential equipment joining & relocation support family support (Maternity & Paternity benefits) learning and development opportunities medical coverage for yourself and your family life coverage for yourself.

Our Work Culture

Ask any employee at Dr. Reddys why they come to work every day and theyll say because Good Health Cant Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations but as a means to help patients lead healthier lives and were always attuned to the new and the next to empower people to stay fit. And to do this we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system they can make magic.

For more details please visit our career website at Work :

No

Employment Type : Full-time

Key Skills

Hr Internship,B2C,Analysis,Drafting,Automobile Service,Arabic

Experience : years

Vacancy : 1