Team Member-visual Inspection

**Company Description**
Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because **Good Health Can’t Wait**.

We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries.

For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity - to strengthen our core further (the next steps) and to build the future (the new bets).

‘The Next and the New’ is how we aim to continue to be the partner of choice - purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose - helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency

Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.
**Job Description** Job summary**
We are seeking a diligent individual with on Hands experience in Automatic visual inspection machine qualification and operations.

**Roles & Responsibilities**
- You will be responsible for qualification and operations of visual inspection machines.
- You will ensure proper documentation, and preparation of component specifications, Standard Operating Procedures (SOPs) and other related documents.
- You will be responsible for preparation of KNAPP samples and approach on visual inspection qualification process.

**Qualifications**
**Educational qualification**:A Bachelor’s in Pharmacy, Diploma in Pharmacy, BSc, MSc.

**Minimum work experience**: 3 years of experience in automatic visual inspection machine qualification and operations.

**Skills & attributes**:
**Technical Skills**
- Should have skills and experience on GDP SAP, operational and QMS documentation.
- Should have experience to operate Automatic visual inspection machine, high voltage leak test equipment’s.
- Should have experience on KNAPP samples and approach on visual inspection qualification.
- Should have experience on equipment qualifications, validations, Protocol etc.
- Should have exposure on automation and equipment life cycle management.
- Should have skills for MS office, excel and data management.
- Should have experience in execution of batches in MES without exceptions.

**Behavioural skills**
- Strong team skills, actively contributing to collaborative efforts and fostering a positive team environment.
- Diligence and sincerity in tasks and responsibilities, ensuring a thorough and earnest approach to work.

**Additional Information** About the Department**
**Biologics**
Currently operates in the Global Biosimilars business - a segment that is poised for attractive and sustained growth over the next 10-15-year time horizon.
With a robust portfolio of biosimilar products across key therapeutic areas, covering ~US$80+ Bn in innovator sales - future business pipeline covers a variety of product classes and therapy areas, and new modalities. Fully integrated organization with over two decades of experience in developing, manufacturing and commercializing multiple biosimilar products.
With a Product Development engine that has end-to-end capabilities - in-house clone development, upstream and downstream process development, bioanalytical development and proprietary formulation.
Supported by a Clinical and Regulatory team with experience in executing complex biosimilar programs with innovative global trial designs.
We have a proven experience in commercial-scale manufacturing across a variety of technology platforms with global quality standards and a highly competitive cost structure
Rich experience of commercializing high-quality biosimilars in multiple markets with over 900,000 patients having benefited from our products till date.

**Benefits Offered**
At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalis