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Hyderabad, Telangana, India • On-site
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Lead late-stage CMC deliverables, including technical scale-up, registration batches, and the development of robust manufacturing processes. Manage relationships with CMOs/CDMOs and collaborate with cross-functional teams to ensure continuous product supply and regulatory compliance.
Requires an M. Pharm in Pharmaceutics or related pharmaceutical sciences with at least 10 years of industrial experience in technical scale-up and technology transfer. Must have hands-on experience with oral and sterile formulations and a proven track record of working with external manufacturing sites.
Job Title: Scientist - I (Process Expert) – Late-Stage CMC
Reporting to: Associate Director - Late-Stage CMC
Location: Hyderabad
Qualification: M. Pharm (Pharmaceutics / Pharmaceutical Technology / Pharmaceutical Sciences)
At least 10 years of industrial experience technical scale up & technology transfer.
Hands-on experience with oral and sterile formulations
Experienced in working with external manufacturing sites (CMOs)
Carry out: QbD process risk assessment & mitigation plan with First Time Right (FTR) approach from technical scale up through commercial supply to achieve Derive a robust & reproducible manufacturing process while interfacing with CMC team, QA, RA
Carry out: Execution of technical scale up and registration batches, define design space and control strategy to achieve new product submission and commercial launch with adherence to timelines while interfacing with multidiscipline team including CMC, quality and regulatory team.
Support: New product launch activities and commercial manufacturing as per business requirement to achieve Continues product supply while interfacing with multidiscipline team including CMC, quality and regulatory team.
Support & Ensure: Identification of CDMO & CMOs meeting global regulatory standards and develop request for proposals to achieve reliable partners to support drug product registration and commercial supply while interfacing with multidiscipline team including CMC, quality and regulatory team.
Support & Ensure: Driving late-stage CMC deliverables in collaboration with internal and external stake holders to achieve Timely completion of projects in line with the requirements while interfacing with CRO/CMO and Project Management
Carry out: Troubleshooting and root cause analysis using best in class scientific approaches to address challenges faced during product life cycle to achieve Continues product supply while interfacing with CMC, QA, RA, CMO/CDMO
Carry out: Prepare and review protocols, reports, validation plans and other technical documents like batch record, stability protocol & report to achieve Compliance to quality systems while interfacing with CMC team, QA, and RA
Carry out /Support: Represent and collaborate with relevant global forums/stake holders to inculcate best practices in industry related to pharmaceutical technology to create a competitive advantage to achieve Capability building while interfacing with Internal a& external stake holders.
Projects milestones – timely completion
Technology – Contribute to technology development, through external partners.
Unlocking opportunities to deliver life-changing solutions to patients. Guidelines: re.ferring.com/social-guidelines
Ferring Pharmaceuticals is a privately owned specialty biopharmaceutical group committed to building families and helping people live better lives. We are leaders in reproductive medicine with a strong heritage in gastroenterology and urology and are at the forefront of innovation in uro-oncology gene therapy. Ferring was founded in 1950 and employs more than 7,500 people worldwide. The company is headquartered in Saint-Prex, Switzerland, and has operating subsidiaries in more than 50 countries which market its medicines in over 100 countries. Community guidelines available here: https://re.ferring.com/Ferring-LinkedIn-Community-Guidelines Social Media Privacy Notice available here: https://www.ferring.com/social-media-privacy-notice/
Offices: -, St-Prex, 1162, CH
There are currently 433 open science & research positions in Hyderabad, India listed on Clera. New openings are added daily as companies post roles.
Companies currently hiring include Amgen, Novartis, Sanofi, Thermo Fisher Scientific, Bristol Myers Squibb, among others. Browse the listings above to see every active employer.
Yes — 124 of the 433 open science & research positions offer remote or hybrid work (21 remote, 103 hybrid).
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.
