Executive-Sr. Executive-MSTG

Sun Pharma

Bhopal, Indore District, Dewas

On-site

INR 500,000 - 900,000

Full time

8 days ago

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Job summary

Sun Pharma, Dewas, is seeking an Executive/Sr. Officer to support execution and monitoring of trials, scale-up and exhibit batches, coordinating with manufacturing and development teams.

The role requires preparing new product documents (MR sheet, batch manufacturing record, BOM, risk reports, sampling protocol), regulatory responses, site transfer support, and participation in regulatory audits to ensure compliance and product robustness.

Qualifications

Educational qualification: M.Pharma
Experience: Tenure: 2-5 Years

Responsibilities

To provide support for execution and monitoring of trial, scale up and exhibit batches.
To prepare new product documents like material requirement sheet, batch manufacturing record, bill of material, risk assessment reports, contamination reports, sampling protocol, reports, exhibit batch manufacturing record and exhibit protocols and reports etc.
To prepare new product documents like sampling protocol and trial batch reports investigation report/Justification report, additional activity protocol, regulatory evaluation etc.
To provide the regulatory response.
To send samples of trial / exhibit batches to formulation and development department.
To conduct training of protocols for batch execution.
To prepare site transfer documents and provide support during site transfer activities of the products.
To monitor the scale up batch/characterization batch and process qualification batches if required.
To share process knowledge to cross functional departments through presentation for smooth technology transfer whenever required.
To prepare investigation report/Justification report, additional activity protocol, regulatory evaluation etc.
To prepare site transfer documents and provide support during site transfer activities of the products.
To prepare and evaluate product history and process parameters for technical remediation and improvement of product robustness.
To prepare investigation report/Justification report, additional activity protocol, regulatory evaluation etc.
To monitor the scale up batch/characterization batch and process qualification batches.
To prepare site transfer documents and provide support during site transfer activities of the products.
To prepare and submit the investigation reports for OOS, OOT and any failure for exhibit/validation/commercial batch manufacturing and during stability testing.
To prepare product containment approach and risk assessment for new product.
To prepare and arrange placebo for quality control testing if required.
To participate in various regulatory audits to support the plant.

Education

M.Pharma

Job description

Job Title

Executive/Sr. Officer

Business Unit

MSTG

Job Grade

G12A/12B

Location

Dewas

At Sun Pharma, we commit to helping you Create your own sunshine” – by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.

Are You Ready to Create Your Own Sunshine?

As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.

Job Responsibilities

To provide support for execution and monitoring of trial, scale up and exhibit batches.
To prepare new product documents like material requirement sheet, batch manufacturing record, bill of material, risk assessment reports, contamination reports, sampling protocol, reports, exhibit batch manufacturing record and exhibit protocols and reports etc.
To prepare new product documents like sampling protocol and trial batch reports investigation report/Justification report, additional activity protocol, regulatory evaluation etc.
To provide the regulatory response.
To send samples of trial / exhibit batches to formulation and development department.
To conduct training of protocols for batch execution.
To prepare site transfer documents and provide support during site transfer activities of the products.
To monitor the scale up batch/characterization batch and process qualification batches if required.
To share process knowledge to cross functional departments through presentation for smooth technology transfer whenever required.
To prepare investigation report/Justification report, additional activity protocol, regulatory evaluation etc.
To prepare site transfer documents and provide support during site transfer activities of the products.
To prepare and evaluate product history and process parameters for technical remediation and improvement of product robustness.
To prepare investigation report/Justification report, additional activity protocol, regulatory evaluation etc.
To monitor the scale up batch/characterization batch and process qualification batches.
To prepare site transfer documents and provide support during site transfer activities of the products.
To prepare and submit the investigation reports for OOS, OOT and any failure for exhibit/validation/commercial batch manufacturing and during stability testing.
To prepare product containment approach and risk assessment for new product.
To prepare and arrange placebo for quality control testing if required.
To participate in various regulatory audits to support the plant.

Job Requirements

Educational Qualification: M.Pharma

Experience: Tenure: 2-5 Years

Your Success Matters to Us

At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together!

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).

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