339589BR
Feb 22, 2022
India

Job Description

With 64 manufacturing sites in 26 countries, our aspiration is to become the top manufacturer of innovative and generic medicines in the industry.

Your key responsibilities:
Your responsibilities include, but are not limited to:

• GMP & abiding and ensuring compliance to the Health, Safety & Environment policy. Ensure compliance with Pharmacopoeia/Group. Requirements /local and International authorities. Completion of all trainings assigned to individuals role. To ensure the integrity of data at workplace. To follow current Good Manufacturing Practices and Good Documentation Practice.
• Follow Standard Operating Procedures of Manufacturing and their documents. Maintain cleanliness in the work area, equipment and Machine. To allot & follow up of work as per plan. Co-ordination with cross-functional department. Provide training to new joining associate.
• Follow the procedure of miscellaneous material at the time receiving and handling the material. To supervise the work as per allocated job in respective department as per Production norms and Quality norms adhering to Good Manufacturing Practices. Plan & procure the material as per daily production requirement. Filling Batch Manufacturing records.
• Maintain the shop floor records; carry out in process checks and record. Co-ordination with engineering department for various maintenance activities. To maintain & ensure compliance at shop floor. To handle associates in the shift, their work allocation & target allocation for the shift. To prepare protocol reports for deviations, quality events & for track wise actions. To conduct trainings of associates at shop floor.
• Change control, Quality Event and deviation handling as per SOP. To raise CR and Deviation in track wise and support in investigation and implementation of CAPA. To handle MES.

Diversity & Inclusion / EEO

Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Minimum Requirements

What you’ll bring to the role:
• D. Pharm / B. Pharm
• Minimum 5 to 6 years of experience in OSD facility in reputed Pharmaceutical Company handling various equipment and production process.
• Operations Management and Execution
• Collaborating across boundaries, Functional Breadth
• Excellent oral and written English communication skills.

Commitment to Diversity & Inclusion:

Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve.
Join our Novartis Group Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network

Why Sandoz?
500 million patients were touched by Sandoz generic and biosimilar medicines in 2020 and while we’re proud of this, we know there is more we could do to continue to help pioneer access to medicines for people around the world.
How will we do this? We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working.
We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying!
Imagine what you could do here at Sandoz!
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Novartis Technical Operations
NTO SANDOZ TECHOPS
India
Mumbai
Technical Operations
Full Time
Regular
Yes
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339589BR

Executive Production (Granulation)

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