Urwah Admin

Sun Pharma Laboratories Ltd

<div><div><div><div><div><h1 class="jobSectionHeader"><b>Title: </b><b>Senior Manager - EHS
</b></h1></div></div></div></div><div><div><div><div>Date: Sep 24, 2025
</div></div></div></div><div><div><div><div>Location: Guwahati - Plant
</div></div></div></div><div><div><div><div>Company: Sun Pharma Laboratories Ltd<br>
</div></div></div></div><p></p><div><div><div><div><div><div><div><div><div><div><b>Job Title:</b></div></div><div><br>
<div>
Sr.Manager EHS</div></div><div><br>
<div><b>
Business Unit:</b></div></div><div><br>
<div>
Sun Global Operations</div></div></div><div><br>
<div>
<div><b>Job Grade</b></div></div><div><br>
<div>
G9B</div></div><div><br>
<div><b>
Location :</b></div></div><div><br>
<div>
Guwahati</div></div></div><div></div><div><br>
<div>
<div>At Sun Pharma, we commit to helping you &ldquo;Create your own sunshine&rdquo;&mdash; by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.</div>
<div>
Are You Ready to Create Your Own Sunshine?</div><br>
<div></div>
<div>
As you enter the Sun Pharma world, you&rsquo;ll find yourself becoming &lsquo;Better every day&rsquo; through continuous progress. Exhibit self-drive as you &lsquo;Take charge&rsquo; and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we &lsquo;Thrive together&rsquo; and support each other&rsquo;s journeys.&rdquo;</div><br>
<div></div>
<div><b>
Key responsibilities: as Site EHS Lead</b></div><br>
<div></div>
<ul>
<li>EHS compliance at plant.</li>
<li>Maintain safe &amp; pollution free environment within the plant.</li>
<li>To build up the EHS Culture inside the plant by organizing EHS awareness programs.</li>
<li>Implement EHS promotional activities at plant</li>
<li>To make the workplace free from hazard and maintain the plant with acceptable risk.</li>
<li>To establish EHS Global culture at site.</li>
<li>Educate, train &amp; motivate the employees and contractors to conduct their activities in a safe and environmentally responsible manner.</li>
<li>To establish &amp; sustain EHS Management system at plant.</li>
<li>To comply EHS legal and other requirements applicable the site.</li>
<li>To create and maintain green belt inside plant premises.</li>
<li>To supervise all EHS related activities in plant.</li>
<li>Ensuring safe working environment at the site.</li>
<li>Implementation and sustaining of EHS Management System (ISO45001:2018 &amp; ISO14001:2015) at site.</li>
<li>Adherence to maintenance of loss prevention equipment as per site specific (Fire Hydrant system, Fire Alarm system, &amp; PA system, Fire extinguishers, safety shower and eye wash, emergency lights)</li>
<li>Preparation and implementation of emergency response procedure for the emergency prone scenarios applicable to site.</li>
<li>Closure of action items under EHS responsibility.</li>
<li>Conduct monthly EHS review meeting is conducted with Site Leadership team, Contractor Safety, emergency response team and Plant EHS committee meeting (as per regulatory requirement)</li>
<li>Promoting Safe Behavioral Change by improving the awareness and capability of people</li>
<li>To develop EHS CAPEX budget for the site and track them for complete.</li></ul></div><br>
</div><br>
<div><div><div><b>Travel Estimate</b></div></div></div><div></div><div><br>
<div>
<div><b>Job Requirements</b></div></div></div><div><br>
<div>
<div><b>Educational Qualification</b></div></div><div><br>
<div>
M.Sc./B.Tech/Post Diploma in Industrial Safety</div></div></div><div><br>
<div>
<div><b>Experience</b></div></div><div><br>
<div><i>
Tenure</i>: 15+ years</div></div></div><div><br>
<div>
<div><b>Your Success Matters to Us</b></div><br>
<div><b>
</b></div><div>At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. <i>Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let&rsquo;s create a brighter future together!</i></div></div></div><div></div><div><br>
<div>
<div><b><i>Disclaimer: </i></b><i>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).</i></div></div></div></div></div></div></div></div></div></div></div><p></p>

Senior Manager - EHS

<div><div><div><div><div><h1 class="jobSectionHeader"><b>Title: </b><b>QC &amp; Training Manager
</b></h1></div></div></div></div><div><div><div><div>Date: Sep 24, 2025
</div></div></div></div><div><div><div><div>Location: Vile Parle - Office
</div></div></div></div><div><div><div><div>Company: Sun Pharma Laboratories Ltd
</div></div></div></div><div><div><div><div><div><div><div><div><div><div><b>Job Title:</b></div></div><div><br>
<div>
Quality Compliant and Training Manager (Clinical Trials)</div></div><div><br>
<div><b>
Business Unit:</b></div></div><div><br>
<div>
Clinical Research</div></div></div><div><br>
<div>
<div><b>Location:</b></div></div><div><br>
<div>
Mumbai</div></div></div><div></div><div><br>
<div>
<div>At Sun Pharma, we commit to helping you <b>&ldquo;Create your own sunshine&rdquo;</b>&mdash; by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.</div>
<div>
Are You Ready to Create Your Own Sunshine?</div><br>
<div></div>
<div>
As you enter the Sun Pharma world, you&rsquo;ll find yourself becoming &lsquo;Better every day&rsquo; through continuous progress. Exhibit self-drive as you &lsquo;Take charge&rsquo; and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we &lsquo;Thrive together&rsquo; and support each other&rsquo;s journeys.&rdquo;</div><br>
<div></div>
<div><b>
Key responsibilities:</b></div><br>
<div></div>
<div>
This role will be responsible for oversight on end-to-end clinical trial activities from quality perspective. This role will be accountable for Quality Compliance (QC) activities of Clinical Trial Medical Science team and Operations team, Clinical Trial Supply Management (CTSM) team, and Clinical Data Management team by way of Review of all study related activities, processes, procedures and adherence to applicable regulations and guidelines to ensure 24x7 Inspection/audit readiness.</div>
<div>
This role will be responsible for establishing the procedures and trainings of teams which ensure protection of human subjects from research risk, reliability/Integrity of the data, and thereby assures internal consistency and Quality Compliance measures.</div><br>
<div></div>
<div><b>
Systems and Processes:</b></div>
<ul>
<li>Develop, implement and maintain a Quality Management System (QMS) for clinical trial team in consultation with Head Quality Compliance &amp; Training and ensure oversight on team on quality aspect as per defined SOPs and applicable regulations.</li>
<li>Implement and oversee the Quality Compliance procedures/processes/systems for clinical trials managed by the Medical science and Clinical Operations department.</li>
<li>To assist in designing a process to write, review and approve the risk assessments for new trials and for ongoing projects and working closely with Project Managers and Operation Head as needed.</li>
<li>To ensure a process in place to provide assurance on review of all study documentation for accuracy, consistency and completeness.</li>
<li>Ensure effective systems and processes in place to maintain consistency and quality compliance parameters in medical science, operations, data management and drug depot for end-to-end activities of each function as per applicable regulatory requirements.</li>
<li>Work with Clinical Research QC team, Medical Science team, Clinical Operations team, Clinical Data Management team and Study Management team to create and implement study specific QC plans that outline the scope of Quality Compliance procedures to be followed during clinical trials, ensuring QC processes are in alignment with SOPs and study protocols.</li>
<li>Ensure completeness of training of study team on SOPs and job specific training as per role and responsibilities. Ensure periodic review of training files for all study team.</li>
<li>Assess and identify the training requirement of study team and ensure completion of training.</li>
<li>Well versed with electronic systems used in Clinical Trial operations, Data Management and Project Management which includes project specific deliverables tracking and important milestone related alarms, protocol compliance tracking, deviations tracking and electronic systems used for managing Trial Master File (TMF) and Drug accountability.</li>
<li>Assist in developing system/process to work with the clinical trial team to schedule pre-execution and post-execution QC activities to ensure that all requirements of the QC plans are planned as required and executed.</li>
<li>Plan, design, and update process and systems for clinical trial activities like development and utilization of QC assessment parameters and other QC tools designed to document/track the QC review process for clinical research activities in line with recent regulatory requirement.</li>
<li>Ensure Quality Management System at Medical Science, Data Management team, Operation team to ensure the department is ready for audit/inspection 24x7.</li>
<li>Ensure periodic review of Vendors and renewals as per applicable policies &amp; procedures.</li>
<li>Identify and recommend process improvement initiatives where required.</li>
<li>Create and evaluate metrics to assess performance and implement plans for course correction.</li></ul><br>
<div></div>
<div><b>
Activities:</b></div>
<ul>
<li>Should be effective team player who can work closely with different study teams and collaborate well with team members to achieve defined QC targets.</li>
<li>Develop and implement a risk-based and flexible approach to Quality Compliance (QC) within the function, which will ensure that trial participants and data are safeguarded in compliance with applicable regulatory requirements and best practices.</li>
<li>Identify and decide team members job specific SOP training requirements in view of their role and maintain oversight of training to ensure all team members are trained on each SOP as required.</li>
<li>Preparation of SOPs related to QC function and support in review of SOPs specific to Medical science, Clinical team and Data Management team.</li>
<li>Quality review of the clinical trial medical science related activities like Synopsis, Protocol, Clinical Study Report (CSR) and appendices, and SOPs in line with ICH GCP requirement, Indian and global regulatory requirement.</li>
<li>Quality review of the clinical trial operation related activities, related tools, plans and documentation like site feasibility, site selection visit, site initiation, Ethic committee documentation, monitoring site specific reports, Site Documents, logs and close out activities in line with ICH GCP requirement, Indian and global regulatory requirement.</li>
<li>Ensure Quality review of SOPs and oversight on quality parameters specific to Clinical Trial Supply Management (CTSM) and other activities like receipt, handling of study sample, labelling, storage, temperature monitoring systems and distribution to trial sites.</li>
<li>Final QC review of study close out activities including returned goods reconciliation, inventory destruction processing and archiving of documents.</li>
<li>Review and communication of QC findings to respective department in stipulated timelines.</li>
<li>Arrange monthly meeting or meetings as and when required depending on criticality of the issues with concerned team to discuss and communicate the findings from QC reviews to the internal stakeholders via QC summaries, reports as required.</li>
<li>Maintain the repository of QC findings as per the department and specific function and present the trend analysis, training requirement and action plan with timelines to Head Medical Affairs and clinical for course correction on quarterly basis.</li>
<li>Ensure training of SOPs, on job training and reviewing training files on regular basis.</li>
<li>QC review and Support in preparation of clinical study manuals/documents/Plan such as the IMP handling manual, Study plans.</li>
<li>Ensure record maintenance for all activities for traceability in line with regulatory requirement.</li></ul></div><br>
</div><br>
<div><div><div><b>Job Requirements</b></div></div></div><div><br>
<div>
<div><b>Educational Qualification</b></div></div><div><br>
<div>
B Pharma</div>
<div>
M Pharma/PG Diploma in Clinical Research</div></div></div><div><br>
<div>
<div><b>Experience</b></div></div><div><br>
<div>
&gt;5 years experience in a CRO/Pharma/Biotech organization in Quality department with experience of Quality activities in Clinical Research department.</div></div></div><br>
<div>
<div><ul><li>Strong eye for detail and ability to spot inconsistencies a must and good conflict management skills.</li>
<li>Must have experience in handling audits &amp; inspections of DCGI, US FDA.</li>
<li>Thorough knowledge of recent GCP guidelines, ICMR guidelines, Drugs and Cosmetic Act regulations and other applicable regulations pertaining to clinical trials.</li>
<li>Experience of working in matrix business environments preferred.</li>
<li>Strong track record of success as demonstrated through annual performance ratings and/or professional accomplishments and awards.</li>
<li>Quality oriented mindset and skill set.</li>
<li>Experience in auditing processes and procedures, including the development of plans for corrective and preventive action (CAPA).</li>
<li>In-depth working knowledge of clinical trial regulations, good clinical practice (GCP) guidelines and other frameworks, and their implications for clinical research.</li>
<li>Proactive approach to reviewing, updating and improving processes based on current knowledge of the regulatory requirements.</li>
<li>Have strong analytical and problem-solving skills and the ability to present solutions.</li>
<li>Able to work under pressure and prioritize workload effectively, able to ensure timely completion of tasks to high quality in a matrix organization.</li>
<li>Eye for details, Sense of urgency &amp; desire to excel.</li>
<li>Proficiency with Excel or other quality management systems/ tools.</li>
<li>Result oriented and performance driven.</li>
<li>Excellent interpersonal &amp; communication skills to effectively interact with a broad range of audience.</li></ul></div></div><div></div><div><br>
<div>
<div><b>Your Success Matters to Us</b></div><br>
<div><b>
</b></div><div>At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. <i>Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let&rsquo;s create a brighter future together!</i></div></div></div><div></div><div><br>
<div>
<div><b><i>Disclaimer: </i></b><i>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).</i></div></div></div></div></div></div></div></div></div></div></div><p></p>

QC & Training Manager

<div><div><div><div><div><h1 class="jobSectionHeader"><b>Title: </b><b>Product Manager (Cardio Diabetes)
</b></h1></div></div></div></div><div><div><div><div>Date: Sep 24, 2025
</div></div></div></div><div><div><div><div>Location: Sun House - Corporate Office
</div></div></div></div><div><div><div><div>Company: Sun Pharma Laboratories Ltd
</div></div></div></div><div><div><div><div><div><div><div><div><div><div><b>Job Title:</b></div></div><div><br>
<div>
Product Manager (Cardio-Diabetes)</div></div><div><br>
<div><b>
Business Unit:</b></div></div><div><br>
<div>
India Business</div></div></div><div><br>
<div>
<div><b>Location :</b></div></div><div><br>
<div>
Mumbai</div></div></div><div></div><div><br>
<div>
<div>At Sun Pharma, we commit to helping you <b>&ldquo;Create your own sunshine&rdquo;</b>&mdash; by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.</div>
<div>
Are You Ready to Create Your Own Sunshine?</div><br>
<div></div>
<div>
As you enter the Sun Pharma world, you&rsquo;ll find yourself becoming &lsquo;Better every day&rsquo; through continuous progress. Exhibit self-drive as you &lsquo;Take charge&rsquo; and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we &lsquo;Thrive together&rsquo; and support each other&rsquo;s journeys.&rdquo;</div><br>
<div></div>
<div><b>
Key responsibilities:</b></div>
<ul>
<li>Development of marketing and promotional plans for products to support the end consumer&rsquo;s need</li>
<li>Monitor business performance and support the portfolio with the help of regular tracking</li>
<li>Market intelligence through primary research and customer connect</li>
<li>Writing and executing strategic business and marketing plans in collaboration with important prescribers, opinion leaders, round tables, and other advisory groups</li>
<li>Joint financial responsibility for budgets (advertising and promotion, conferences and symposia, sales brochures and other product documentation, website content, literature), as well as analysis of budget income and costs;</li>
<li>initiating and coordinating marketing activities and projects</li>
<li>Presentation to staff and training field staff for the same</li>
<li>Visiting national and international congresses, hospitals, and key opinion leaders (KOLs);</li>
<li>Translating the corporate brand strategy in close collaboration with headquarters, together with logos and visuals, working with corporate product budgets (approval for expenditure on projects, local communication strategies), and providing input into corporate product strategy;</li>
<li>Discussion partner for first, second, and third-line professionals such as general practitioners, medical specialists, pharmacists, and other medical professionals, and for other DMU members (decision-making units) such as local and national formulary committees and insurance companies;</li>
<li>Organizing advisory councils, acting as a discussion leader or chairman, or giving product presentations.</li>
<li>Collaboration with internal &amp; external media to ensure the proper execution of strategies</li></ul></div></div><div></div><div><br>
<div>
<div><b>Travel Estimate</b></div></div><div><br>
<div>
Max. 1 week in a month</div></div></div><div><br>
<div>
<div><b>Job Requirements</b></div></div></div><div><br>
<div>
<div><b>Educational Qualification</b></div></div><div><br>
<div>
B. Pharma + MBA - Marketing OR Pharma Management</div></div></div><div><br>
<div>
<div><b>Experience</b></div></div><div><br>
<div>
3 to 4 years of experience in Pharma Marketing</div></div></div><div><br>
<div>
<div><b>Therapy Exposure</b></div></div><div><br>
<div>
Cardio-Diabetes therapy exposure is preferred</div></div></div><br>
<div>
<div><ul><li>Able to foster collaborative relationships</li>
<li>Proven track record of launching and managing successful products</li>
<li>Strong analytical and problem-solving skills</li>
<li>Proficiency in product management tools</li>
<li>Good in communication and presentation</li>
<li>Science driven marketing strategies</li></ul></div><br>
</div><br>
<div><div><div><b>Your Success Matters to Us</b></div><br>
<div><b>
</b></div><div>At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. <i>Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let&rsquo;s create a brighter future together!</i></div></div></div><div></div><div><br>
<div>
<div><b><i>Disclaimer: </i></b><i>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).</i></div></div></div></div></div></div></div></div></div></div></div><p></p>

Product Manager (Cardio Diabetes)

<div><div><div><div><div><h1 class="jobSectionHeader"><b>Title: </b><b>Operational Excellence Manager
</b></h1></div></div></div></div><div><div><div><div>Date: Sep 24, 2025
</div></div></div></div><div><div><div><div>Location: Sikkim I - Plant
</div></div></div></div><div><div><div><div>Company: Sun Pharma Laboratories Ltd
</div></div></div></div><div><div><div><div><div><div><div><div><p><b>Job Title:</b></p></div><div><br>
<p>
Manager, Operational Excellence</p></div><div><br>
<p><b>
Business Unit:</b></p></div><div><br>
<p>
Operation Excellence</p></div></div><div><br>
<div>
<p><b>Job Grade</b></p></div><div><br>
<p>
G11A</p></div><div><br>
<p><b>
Location :</b></p></div><div><br>
<p>
Gangtok</p></div></div><p></p><div><div><br>
<ul>
<li>Drive OE framework at site.</li>
</ul><ul><li>Work on capacity debottlenecking.</li>
</ul><ul><li><b>OEE Tracking and improvement</b> of all areas including bottlenecks</li>
</ul><ul><li>Change over time tracking and reduction for all areas including bottlenecks using SMED.</li>
</ul><ul><li><b>Batch cycle time improvement</b> for concerned products.</li>
</ul><ul><li><b>Yield improvement</b> on the basis of high value and high-volume products.</li>
</ul><ul><li>Idea generation, Implementation, Saving tracking every month.</li>
</ul><ul><li>Facilitation of performance dialogues in all area.</li>
</ul><ul><li>Site performance dashboards updation on monthly basis.</li>
</ul><ul><li>Successfully delivered all operation excellence training.</li>
</ul><ul><li>Facilitation and conducting all Quality Circle activities.</li>
</ul><ul><li>All activity under the programme to achieve continues excellence (PACE) to be completed successfully.</li>
</ul><ul><li>Driving the Kaizen initiative at whole site and monthly R&amp;R conducted for the same.</li>
</ul><ul><li>Transfer the understanding of all lean tools like 5s, Poka Yoke, PDCA etc to shop floor.</li></ul></div></div><p></p><div><br>
<div>
<p><b>Travel Estimate</b></p></div></div><p></p><div><br>
<div>
<p><b>Job Requirements</b></p></div></div><div><br>
<div>
<p><b>Educational Qualification</b></p></div><div><br>
<p>
MBA preferred / B.E. or B. Tech</p></div></div><div><br>
<div>
<p><b>Experience</b></p></div><div><br>
<p><i>
 </i>10-12+ years, TPM, Value Stream Mapping (VSM), Bottleneck improvement</p></div></div><div><br>
<div>
<p><b>Your Success Matters to Us
</b></p><p>At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. <i>Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let&rsquo;s create a brighter future together!</i></p></div></div><div><br>
<div>
<p><b><i>Disclaimer: </i></b><i>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).</i></p></div></div></div></div></div></div></div></div></div><p></p>

Operational Excellence Manager

<div><div><div><div><div><h1 class="jobSectionHeader"><b>Title: </b><b>Medical Advisor
</b></h1></div></div></div></div><div><div><div><div>Date: Sep 18, 2025
</div></div></div></div><div><div><div><div>Location: Sun House - Corporate Office
</div></div></div></div><div><div><div><div>Company: Sun Pharma Laboratories Ltd
</div></div></div></div><div><div><div><div><div><div><div><div><div><div><b>Job Title:</b></div></div><div><br>
<div>
Medical Advisor</div></div><div><br>
<div><b>
Business Unit:</b></div></div><div><br>
<div>
Medical Services</div></div></div><div><br>
<div>
<div><b>Location :</b></div></div><div><br>
<div>
Mumbai</div></div></div><div></div><div><br>
<div>
<div>At Sun Pharma, we commit to helping you <b>&ldquo;Create your own sunshine&rdquo;</b>&mdash; by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.</div>
<div>
Are You Ready to Create Your Own Sunshine?</div><br>
<div></div>
<div>
As you enter the Sun Pharma world, you&rsquo;ll find yourself becoming &lsquo;Better every day&rsquo; through continuous progress. Exhibit self-drive as you &lsquo;Take charge&rsquo; and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we &lsquo;Thrive together&rsquo; and support each other&rsquo;s journeys.&rdquo;</div><br>
<div></div>
<div><b>
Key responsibilities:</b></div><br>
<div></div>
<ul>
<li>Core scientific member of cross-functional franchise team and a disease area expert, responsible for scientific enablement of respective business cluster</li>
<li>Conceptualization and project management of wide range of medical activities that are aligned to the respective franchise strategy like:
<ul><li>New Product Ideation</li>
<li>New Product Evaluation</li>
<li>Therapeutic rationale &amp; relevant Medical support for regulatory submissions</li>
<li>Preparation of SEC presentations &amp; defense in SEC meeting</li>
<li>Pre-launch &amp; launch preparations including product monograph, training manuals, training &amp; CME slides</li>
<li>Franchise Medical Education programs</li>
<li>Promotional and non-promotional material review &amp; approval</li>
<li>Answering queries</li>
<li>Marketing and Sales training</li>
<li>Real World Clinical Research and Publications &ndash; Planning and Execution</li>
<li>Advisory board meetings</li>
<li>Developing Insight driven Medical Plans</li>
</ul></li><li>Interaction &amp; Engagement of identified Key Opinion leaders in a peer-to-peer capacity through medical affairs activities, in alignment with the overall strategic plan to shape disease areas of interest</li>
<li>A therapeutic area scientific expert, responsible for discussing the scientific data pertaining to products on proactive and reactive basis, obtain insights into patients&rsquo; treatment trends and insights in the disease areas of interest and to be considered a trusted scientific counterpart</li>
<li>Responsible for identifying knowledge gaps, practice gaps and data gaps and provide recommendations for devising medical &amp; product education programs, evidence generation and special projects</li>
<li>Ability to convert insights on disease trends and treatment patterns from KOLs into viable and formidable solutions to shape the therapeutic areas of interest</li>
<li>Devise optimal training plan to ensure flow of latest medical developments in the given to sales &amp; marketing team</li>
<li>Jointly responsible with marketing teams to support optimal patient outcomes through communication of data, information, and insights to shape disease areas of interest</li>
<li>Represent the organization in various internal &amp; external scientific platforms</li>
<li>Collaborate with thought leaders to conduct therapy specific reviews, meta-analysis, case studies, case series, patient reported outcomes and publish them in journals of repute</li>
<li>Receiving and processing scientific information requests received from physicians &amp; internal stakeholders</li>
<li>Ability to handle complex questions from health care professionals related to company products or disease area to satisfaction</li>
<li>Responsible for ensuring that all promotional materials are approved within stipulated timelines and in alignment with company approval process</li>
<li>Conduct of robust medical evaluation of new products through thorough desk research and interactions with KOLs</li></ul></div></div><div></div><div><br>
<div>
<div><b>Travel Estimate</b></div></div><div><br>
<div>
Less than 1 week in a month</div></div></div><div><br>
<div>
<div><b>Job Requirements</b></div></div></div><div><br>
<div>
<div><b>Educational Qualification</b></div></div><div><br>
<div>
MD Pharmacology</div></div></div><div><br>
<div>
<div><b>Experience</b></div></div><div><br>
<div>
1-3 years working experience in the pharmaceutical industry or research company in a capacity of HO Medical Advisor or Sr. Medical Advisor</div></div></div><br>
<div>
<div><ul><li>Training in medical writing, clinical trial methodologies, research design and ICH &ndash; GCP will be added advantage</li>
<li>Must have working knowledge of Indian regulations pertaining to Health care professionals&rsquo; interactions (MCI code of ethics for doctors &amp; UCPMP Code for Pharma) and Drugs and Cosmetic Act regulations pertaining to clinical trials and new drug approvals</li>
<li>Strong academic record with deep knowledge of the therapeutic area, strength in research with knowledge of research methodologies and interpretation of medical data</li>
<li>Strategic mindset with scientific acumen and communication skills in order to be accepted by leading specialists in peer-to-peer capacity</li>
<li>Experience with complex business environments preferred</li>
<li>Strong track record of success as demonstrated through annual performance ratings and/or professional accomplishments and award</li></ul></div><br>
</div><br>
<div><div><div><b>Your Success Matters to Us</b></div><br>
<div><b>
</b></div><div>At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. <i>Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let&rsquo;s create a brighter future together!</i></div></div></div><div></div><div><br>
<div>
<div><b><i>Disclaimer: </i></b><i>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).</i></div></div></div></div></div></div></div></div></div></div></div><p></p>

Medical Advisor

<div><div><div><div><div><h1 class="jobSectionHeader"><b>Title: </b><b>Mechanical- Projects Manager
</b></h1></div></div></div></div><div><div><div><div>Date: Sep 24, 2025
</div></div></div></div><div><div><div><div>Location: Sun House - Corporate Office
</div></div></div></div><div><div><div><div>Company: Sun Pharma Laboratories Ltd<br>
</div></div></div></div><p></p><div><div><div><div><div><div><div><div><p><b>Job Title:</b></p></div><div><br>
<p>
Engineering &amp; Projects - Mechanical Engineers</p></div><div><br>
<p><b>
Business Unit:</b></p></div><div><br>
<p>
Sun Global Operations</p></div></div><div><br>
<div>
<p><b>Job Grade</b></p></div><div><br>
<p><b>
G10 - Manager 1</b></p></div><div><br>
<p><b>
Location :</b></p></div><div><br>
<p>
New green field site (Pithampur - Indore)</p></div></div><p></p><div><br>
<div>
<p>At Sun Pharma, we commit to helping you <b>&ldquo;Create your own sunshine&rdquo;</b>&mdash; by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.</p>
<h3 class="jobSectionHeader"><b>
Are You Ready to Create Your Own Sunshine?</b></h3><br>
<p></p>
<p>
As you enter the Sun Pharma world, you&rsquo;ll find yourself becoming &lsquo;Better every day&rsquo; through continuous progress. Exhibit self-drive as you &lsquo;Take charge&rsquo; and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we &lsquo;Thrive together&rsquo; and support each other&rsquo;s journeys.&rdquo;</p><br>
<p></p>
<p><b>
Key responsibilities:</b></p>
<ul>
<li>Based on received drawings &amp; documents, assign work and timelines and ensures the implementation of the same.</li>
<li>Ensure collection of data; do analysis to achieve relevant construction quality and safety.</li>
<li>Help overcome constraints, work out alternatives to the design in case of difficulties</li>
<li>Retention of records in respective area. Preparation &amp; completeness of documentation for Qualifications.</li>
<li>Give final acceptance of construction quality for piping and utilities.</li>
<li>Review measurements sheets.</li>
<li>Ensure schedule updates in primavera and send progress reports in terms of schedule work quantity, progress, constraints, snaps and etc.</li>
<li>Coordination with Boiler Inspector and other statutory agencies.</li>
<li>Execute construction quality audits for piping and utilities.</li>
<li>Help overcome constraints, work out alternatives to the design in case of difficulties.</li>
<li>Responsible for construction quality; finishes, Operations, Performance and safety at site.</li>
<li>He will report quantity variation and scope change.</li>
<li>Ensure collection of data; do analysis to achieve relevant construction quality and safety.</li></ul><br>
<p></p>
<ul>
<li>Develop, evaluate and optimize HVAC system designs for pharmaceutical projects.</li>
<li>Lead HVAC projects from concept to completion, ensuring timely delivery within budget.</li>
<li>Review and develop HVAC systems that maximize energy efficiency and comply with sustainability standards.</li>
<li>Ensure designs meet local, national and international HVAC codes and regulations.</li>
<li>Review in detail the engineering drawings, technical specifications and generate reports.</li>
<li>Engage with user to understand requirements and provide tailored HVAC solutions.</li>
<li>Work closely with consultants, contractors and other engineers to integrate HVAC systems seamlessly into overall design.</li>
<li>Evaluate and select HVAC equipment vendors and suppliers.</li>
<li>Stay updated on the latest HVAC technologies and integrate them into design processes.</li>
<li>Develop cost-effective solutions while maintaining design integrity and system performance.</li>
<li>Working with the customer to define scope of project, creating functional specifications.</li>
<li>Reviewing of the technical submittals as per specification, Drawings &amp; Design from the consultants.</li>
<li>Preparation of product technical specification and approval of the supplier technical data sheet.</li>
<li>Analyze HVAC systems and equipment whenever necessary to find inefficiencies or malfunctions and create solutions to optimize performance and increase the efficiency of operation.</li>
<li>Create and submit detailed bids that outline costs and timelines for construction projects in accordance with deadlines.</li>
<li>Conceptual, Basic and Detailed Design of HVAC system starting from Area Classification Zoning, Pressure Zoning, AHU Zoning as per discussion with Process Departments.</li>
<li>Design of P&amp;ID, ducting layout and Piping Layout etc.</li>
<li>System selection such as AHU, Dehumidifiers, Humidifiers, Exhaust Blowers and VRF system. Reviewing of the Vendors technical Data Sheet.</li>
<li>Preparation of Validation Documents, Commissioning &amp; Validation execution of Clean Room &amp; HVAC Systems (Such as DQ, IQ &amp; OQ) in Pharmaceutical Industries as per the required standards.</li></ul></div></div><p></p><div><br>
<div>
<p><b>Travel Estimate</b></p></div></div><p></p><div><br>
<div>
<p><b>Job Requirements</b></p></div></div><div><br>
<div>
<p><b>Educational Qualification</b></p></div><div><br>
<p>
B.E. in Mechanical Engineering.</p></div></div><div><br>
<div>
<p><b>Experience</b></p></div><div><br>
<p><i>
Tenure</i>: 5 to 10 Years of experience in relevant field in Pharmaceutical Industry.)</p>
<ul>
<li>Design and engineering of the centralized air conditioning and ventilation system in pharmaceutical industry.</li>
<li>Installation, commissioning and qualification of HVAC system.</li>
<li>Hands on experience for the review and approval of HVAC system.</li>
<li>Sound knowledge in all aspects (cost, schedule, quality) of project controlling and reporting.</li>
<li>Leadership skills for the management of the project</li>
<li>Solid analytical and data interpersonal skills.</li>
<li>Sound computer skills (MS office, MS Project)</li></ul></div></div><p></p><div><br>
<div>
<p><b>Your Success Matters to Us</b></p><br>
<p></p>
<p>
At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. <i>Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let&rsquo;s create a brighter future together!</i></p></div></div><p></p><div><br>
<div>
<p><b><i>Disclaimer: </i></b><i>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).</i></p></div></div></div></div></div></div></div></div></div><p></p>

Mechanical- Projects Manager

<div><div><div><div><div><h1 class="jobSectionHeader"><b>Title: </b><b>Manager-II
</b></h1></div></div></div></div><div><div><div><div>Date: Sep 24, 2025
</div></div></div></div><div><div><div><div>Location: Guwahati - Validation/Quality Engineering
</div></div></div></div><div><div><div><div>Company: Sun Pharma Laboratories Ltd
</div></div></div></div><div><div><div><div><div><div><div><div><div><p><b>Job Title:</b></p></div><div><br>
<p>
Executive/Sr Executive &ndash; Process Engineering OSD</p></div><div><br>
<p><b>
Business Unit:</b></p></div><div><br>
<p>
Sun Global Operations</p></div></div><div><br>
<div>
<p><b>Job Grade</b></p></div><div><br>
<p>
G12A/G11B</p></div><div><br>
<p><b>
Location :</b></p></div><div><br>
<p>
Guwahati</p></div></div><p></p><div><br>
<div>
<p>At Sun Pharma, we commit to helping you <b>&ldquo;Create your own sunshine&rdquo;</b>&mdash; by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.</p>
<p>
Are You Ready to Create Your Own Sunshine?</p><br>
<p></p>
<p>
As you enter the Sun Pharma world, you&rsquo;ll find yourself becoming &lsquo;Better every day&rsquo; through continuous progress. Exhibit self-drive as you &lsquo;Take charge&rsquo; and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we &lsquo;Thrive together&rsquo; and support each other&rsquo;s journeys.&rdquo;</p><br>
<p></p>
<p><b>
Key responsibilities:</b></p>
<p>
Diagnose malfunctioning of systems, apparatus and components to locate the root cause of a breakdown and correct the problem.</p>
<p>
Carry out scheduled maintenance activity and inspect systems, equipment, and components to identify hazards, defects and the need for adjustment or repair to improve overall efficiency of the system and equipment</p>
<p>
Schedule and undertake periodic maintenance of all equipment.</p>
<p>
Preparation, maintain and update the SOPs, maintenance schedules, planners etc. periodically</p>
<p>
Responsible for overall calibration activity in OSD, SH and Warehouse</p>
<p>
Provide prompt response to user whenever there is a breakdown and resolve the issue as quickly as possible</p>
<p>
Assist in forecasting requirements and scheduling expenses for the consumable items, spare parts in the department</p>
<p>
Keep record of all stock and supplies of all equipment spares, items, instruments and assist the management in forecasting requirements and scheduling expenses to maintain the consumables</p>
<p>
Working in collaboration with the production team to formulate the best cost-effective manufacturing process</p>
<p>
Perform energy audit internally and recommend alternative sources of energy for effective cost and energy savings</p>
<p>
Ensure that all utility supply, gadgets and instruments are switched off after close of work daily.</p>
<p>
Learn new skills and attend training programs in other to increase knowledge of trends and best practices in the industry</p>
<p>
Provide safe working environment for members of staff and ensure accidents and mishaps are prevented.</p>
<p>
Provide 24 hours a day maintenance services or assign technical staff to do so</p>
<p>
Supervise electrical works when new projects are undertaken</p>
<p>
Support the company in increasing profitability by managing resources efficiently and making necessary recommendations</p>
<p>
Follow GEP in daily work culture to build enhance performance and efficiency of equipment, system and organization</p>
<p>
Follow GMP practices, guidelines, schedules and SOPs.</p>
<p>
Preparation, recording, update, maintain the schedules, planner, SOPs, records as per standards.</p>
<p>
Prepare QRB Data for Preventive Maintenance and Calibration at the end of every month</p></div></div><p></p><div><br>
<div>
<p><b>Travel Estimate</b></p></div></div><p></p><div><br>
<div>
<p><b>Job Requirements</b></p></div></div><div><br>
<div>
<p><b>Educational Qualification</b></p></div><div><br>
<p>
B. Tech /Instrumentation</p></div></div><p></p><div><br>
<div>
<p><b>Experience</b></p></div><div><br>
<p><i>
Tenure</i>: 05 to 10 years</p></div></div><div><br>
<div>
<p><b>Your Success Matters to Us
</b></p><p>At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. <i>Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let&rsquo;s create a brighter future together!</i></p></div></div><p></p><div><br>
<div>
<p><b><i>Disclaimer: </i></b><i>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).</i></p></div></div></div></div></div></div></div></div></div></div><p></p>

Manager-II

Join Sun Pharma Laboratories Ltd and explore 8   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.