Group Leader - CDMO

Jubilant Pharma, LLC; Hinoba-an; On-site; PHP 5,629,000 - 9,381,000; Full time

Job summary

Jubilant Ingrevia Limited is seeking a Group Leader - Pharma CDMO to head a team of scientists focusing on route scouting, process development, scale-up, technology transfer, and commercialization for global CDMO customers.

You will drive innovation, ensure timely project execution, support customer interactions, and maintain regulatory and safety compliance to deliver commercially viable manufacturing processes.

Qualifications

• 12+ years of relevant experience in Pharma CDMO, API or Fine Chemical process development.
• Strong expertise in synthetic organic chemistry, scale-up, and process optimization.
• Experience in pilot plant operations, scale-up processes and commercial manufacturing support.
• Proven experience in leading scientific teams and managing multiple projects.
• Excellent communication, documentation and project coordination skills.

Responsibilities

• Lead process research and development activities for pharmaceutical APIs and intermediates.
• Drive route scouting, non-infringing route development, process optimization, and cost reduction initiatives.
• Identify critical process parameters and establish robust, scalable manufacturing processes.
• Troubleshoot complex synthetic challenges and process-related issues.
• Prepare technology transfer packages, batch manufacturing records, and process reports.

Skills

12+ years experience

Synthetic organic chemistry

Scale-up & process optimization

Leadership & project management

Communication & documentation

Education

M.Sc./Ph.D. in Organic Chemistry or related

Tools

ELN systems

Automation & AI-enabled tools

Job description

Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S Bhartia and Mr. Hari S Bhartia with strong presence in diverse sectors like Pharmaceuticals, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Jubilant Bhartia Group has four flagships’ Companies- Jubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited. Currently the group has a global workforce of around 43,000 employees.

JubilantIngreviaisnowamemberoftheeliteGlobalLighthouseNetwork(GLN) oftheWorldEconomicForum(WEF)

Celebrating our Culture and People.

We are proud to be aGreat Place to Work certified!

Jubilant Ingrevia history goes back to 1978 with the incorporation of VAM Organics Limited, which later became Jubilant Organosys and then Jubilant Life Sciences and now demerged to an independent entity as Jubilant Ingrevia Limited, which is listed in both the stock exchanges of India. Over the years, company has developed global capacities and leadership in chosen business segments.

Ingrevia is born out of a union of ‘Ingredients’ and ‘Life’ (‘Vie’ in French). Jubilant Ingrevia Limited is committed to offering high-quality and innovative life science ingredients to enrich all forms of life.

Jubilant Ingrevia, a global integrated Life Science products and Innovative Solutions provider serving, Pharmaceutical, Nutrition, Agrochemical, Consumer and Industrial customers with our customised products and solutions that are innovative, cost-effective and conforming to excellent quality standards.

Jubilant Ingrevia Limited offers a broad portfolio of high-quality ingredients that find application in a wide range of industries. Jubilant Ingrevia’s portfolio also extends to custom development and manufacturing for pharmaceutical and agrochemical customers on an exclusive basis.

Ourbusinessissplitacross3businessverticals,withgloballeadership acrossourkeyproductlines.

Speciality Chemicals: The Specialty Chemical business of Jubilant Ingrevia manufactures Pyridine, Picolines and its forward integration derivatives, which finds application in agrochemicals, pharmaceuticals, dyes, solvents, metal finishes, fine chemicals, semiconductors etc.

We have also launched new platform of Diketene & its value-added derivatives for multiple industry use. We are an established ‘partner of choice’ in CDMO, with more investment plans in GMP & Non-GMP multi-product facilities for Pharma, Agro and Semi-conductor customers.

Chemical Intermediates: The Chemical Intermediates business has acetic anhydride and value added anhydrides and aldehydes catering to various industries.

Nutrition & Health Solutions: The Nutrition & Heath Solutions business unit offers B3 & Picolinates (Chromium & Zinc) which are fully backward integrated. Our ingredients find application in animal nutrition, human nutrition, personal care, etc. We provide high-quality feed & food additives having application in poultry, dairy, aqua & pet food industry. In Human Nutrition & Health Solutions, we offer food ingredients & premix solutions to nutrition.

Jubilant Ingrevia Limited is supported by five state-of-the-art manufacturing facilities in India. We practice world-class manufacturing processes in our day-to-day operations, assuring our customers with unmatched quality and timely delivery of products through innovations and cutting-edge technology. Transforming Manufacturing for Operational Excellence & Sustainability with “zero tolerance to any non-compliance” is the core focus of Jubilant Ingrevia Manufacturing.

We have 5 world-class manufacturing facilities i.e. One in UP at Gajraula, Two in Gujarat at Bharuch and Savli, Two in Maharashtra at Nira and Ambernath.

Environment Sustainability

The company is committed to environmental sustainability and supports green chemistry by prioritising the use of bio inputs in manufacturing. Jubilant is one of the world’s largest producers of Acetaldehyde from the bio route.

Organization : - Jubilant Ingrevia Limited

Location : - Corporate Office

Job Summary

The Group Leader - Pharma CDMO will lead a team of scientists involved in route scouting, process development, scale-up, technology transfer, and commercialization of pharmaceutical APIs & intermediates and specialty ingredients for global CDMO customers. The role involves driving innovation, ensuring timely project execution, supporting customer interactions, maintaining regulatory and safety compliance, and delivering commercially viable manufacturing processes.

Key Responsibilities

• Lead process research and development activities for pharmaceutical APIs and intermediates.
• Drive route scouting, non-infringing route development, process optimization, and cost reduction initiatives.
• Identify critical process parameters and establish robust, scalable manufacturing processes.
• Troubleshoot complex synthetic challenges and process-related issues.
• Support impurity profiling, control strategy development, and specification setting.
• Manage multiple CDMO projects from feasibility assessment to commercialization.
• Ensure RfP, feasibility study, sample delivery, and project milestones are achieved within agreed timelines.
• Monitor project progress and provide regular technical updates to management and customers.
• Coordinate cross-functional activities with Analytical, IP, QA, EHS, Procurement, Business Development, and Manufacturing teams.
• Manage multiple CDMO projects from feasibility assessment to commercialization.
• Ensure feasibility study, sample delivery, and project milestones are achieved within agreed timelines.
• Monitor project progress and provide regular technical updates to management and customers.
• Coordinate cross-functional activities with Analytical, IP, QA, EHS, Procurement, Business Development, TAC and Manufacturing teams.
• Support process validation, engineering batches, and plant troubleshooting.
• Prepare technology transfer packages, batch manufacturing records, and process reports.
• Participate in plant campaigns and commissioning activities when required.
• Lead, mentor, and develop a team of Research Associates, Senior Research Associates, Research Scientists, and Senior Research Scientists.
• Ensure effective project allocation and resource utilization.
• Drive a culture of innovation, accountability, collaboration, and continuous learning.
• Support talent development, succession planning, and capability building within the team.
• MaintainGLP-compliant documentation¿and ensure lab safety and organization.
• Promote safe handling of hazardous chemicals and high-risk reactions.
• Ensure proper documentation in ELN and other digital systems.
• Promote ELN utilization, data integrity, automation, and AI-enabled tools.
• Drive productivity improvement and First-Time-Right execution.

The Person

Qualifications:

• M.Sc./Ph.D. in Organic Chemistry, Process Chemistry or related discipline or related discipline
• 12+ years of relevant experience in Pharma CDMO, API or Fine Chemical process development
• Strong expertise in synthetic organic chemistry, scale-up, and process optimization.
• Experience in pilot plant operations, scale-up processes and commercial manufacturing support.
• Proven experience in leading scientific teams and managing multiple projects.
• Excellent communication, documentation and project coordination skills.

What’s on Offer:

• Opportunity to work with the only Indian company in Global Lighthouse Network under World Economic Forum in the chemical sector.
• Competitive salary and benefits package.
• Career growth opportunities in a rapidly evolving industry

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Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances.

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