BDR Hiring Tech Transfer & Pellets
- Company Overview
- Job Role & Responsibilities
- Executive / Officer – F&D OSD (Technology Transfer)
- Executive / Officer – F&D OSD (Pellets)
- Eligibility / Qualifications
- Location & Work Environment
- Application Process
- Why F&D OSD Careers Offer Strong Growth
- Frequently Asked Questions (FAQs)
- 1. Is regulated market experience mandatory?
- 2. Are freshers eligible?
- 3. What equipment experience is preferred?
- 4. What is the job location?
- 5. How do I apply?
- Job Summary
BPharm MPharm F&D OSD Jobs Halol Vadodara
BPharm/MPharm F&D OSD Tech Transfer & Pellets vacancies (3–8 yrs) at BDR Pharma, Halol Vadodara. Apply now.
BDR Pharmaceuticals, a Great Place to Work certified organization, is hiring experienced professionals for its Formulation & Development (F&D) – OSD division at Baska, Halol (Vadodara). The company is inviting applications for Executive/Officer roles in Technology Transfer (OSD) and Pellet Formulation Development. Candidates with 3–8 years of hands-on formulation development experience in regulated markets are encouraged to apply.
If you are searching for formulation development jobs in Gujarat, technology transfer OSD careers, pellet dosage formulation roles, or FDA-compliant pharma R&D opportunities, this opening offers strong exposure to regulatory submissions, QbD-based optimization, and commercial-scale manufacturing.
Company Overview
BDR Pharmaceuticals is an established pharmaceutical organization known for its focus on complex generics and regulated market products. The company operates advanced formulation development laboratories and manufacturing facilities aligned with USFDA and international regulatory requirements.
The F&D OSD division plays a critical role in:
- Developing non-infringing formulations
- Managing patent landscape analysis (Para I, II, III, IV filings, NCE-1 projects)
- Supporting technology transfer and site transfer activities
- Executing exhibit batches and regulatory submission batches
- Ensuring Quality by Design (QbD) compliance
Formulation Development professionals working in regulated OSD environments gain exposure to CTD Module 3 documentation, bioequivalence study support, stability studies, and FDA deficiency responses.
Job Role & Responsibilities
BDR is hiring for the following positions:
Executive / Officer – F&D OSD (Technology Transfer)
Qualification: B.Pharm, M.Pharm
Experience: 3–8 Years
Key Responsibilities:
- Conducting literature and patent searches (Para I–IV, NCE-1 projects)
- Developing non-infringing formulations and manufacturing processes
- Designing formulation strategies aligned with regulatory guidelines
- Performing pre-formulation studies and prototype batch development
- Applying optimization techniques such as DOE and OFAT under FDA QbD guidelines
- Preparing laboratory and pivotal stability batches for bioequivalence studies
- Reviewing analytical data and proposing specifications for RM, in-process, and finished products
- Planning exhibit batches and preparing documentation as per CTD Module 3.2.P.2
- Responding to FDA deficiencies with technical justifications
- Handling site transfer activities from dossier review to commercial batch execution
- Preparing technical documents including MFR, MPR, BMR, protocols (hold time, stability, in-use)
- Troubleshooting OOS and OOT investigations during exhibit batches
- Providing technical training through tech transfer presentations
Hands-on equipment experience required:
- Rapid Mixer Granulator (RMG)
- Fluid Bed Processor
- Coating machine
- Roller compactor
- Softgel equipment
- Hot Melt Extrusion (HME)
Strong knowledge of Quality Management Systems (QMS) and regulatory documentation is mandatory.
Executive / Officer – F&D OSD (Pellets)
Qualification: B.Pharm, M.Pharm
Experience: 3–8 Years
Key Responsibilities:
Formulation Development Support:
- Assisting in pellet dosage formulation development
- Conducting lab-scale trials and optimization studies
- Performing dissolution testing, particle size analysis, and stability studies
- Maintaining accurate laboratory documentation
Process Optimization & Tech Transfer:
- Supporting scale-up and technology transfer for pellet formulations
- Developing cost-effective and scalable processes
- Troubleshooting manufacturing issues in collaboration with production teams
Regulatory Compliance:
- Preparing development reports and regulatory dossiers
- Ensuring adherence to global regulatory guidelines
- Supporting documentation for submission batches
Project Coordination:
- Collaborating with cross-functional R&D, QA, and manufacturing teams
- Participating in project planning and milestone tracking
- Identifying risks and proposing mitigation strategies
Candidates must have strong understanding of solid oral dosage forms and pellet formulation principles.
Eligibility / Qualifications
Educational Qualifications (comma-separated):
B.Pharm, M.Pharm (Pharmaceutics, Industrial Pharmacy, Pharmaceutical Technology)
Experience Requirements:
- 3–8 years in OSD formulation development
- Exposure to technology transfer and exhibit batches
- Knowledge of CTD documentation and FDA regulatory requirements
Core Competencies:
- Quality by Design (QbD) principles
- DOE and OFAT optimization techniques
- Stability study execution
- OOS/OOT investigation handling
- Regulatory dossier preparation
Candidates without regulated market formulation exposure may not meet role expectations.
Location & Work Environment
Location: Baska, Halol (Vadodara), Gujarat
Halol is a key pharmaceutical manufacturing hub with several USFDA-approved facilities. Working in this region offers strong exposure to export-focused pharmaceutical development and commercial-scale manufacturing.
Compensation will be based on experience, regulatory exposure, and technical expertise in formulation development and technology transfer.
Application Process
Interested candidates may send their updated CV to:
recruit.baska@bdrpharma.com
vishal.sharma@bdrpharma.com
Application Steps:
- Update resume highlighting technology transfer or pellet formulation experience.
- Mention QbD, DOE, and regulatory submission exposure clearly.
- Include equipment handling experience.
- Email CV with relevant subject line.
Shortlisted candidates will be contacted for further evaluation.
Why F&D OSD Careers Offer Strong Growth
Formulation & Development roles in regulated OSD environments are among the most technically demanding positions in pharmaceutical R&D. Professionals in this domain directly influence product approval timelines, patent strategy execution, and commercial success.
Key growth advantages:
- Exposure to USFDA regulatory submissions
- Patent and Para IV project experience
- Technology transfer leadership
- Process optimization expertise
- High-value regulatory documentation exposure
These competencies significantly enhance long-term earning potential and leadership prospects.
Frequently Asked Questions (FAQs)
1. Is regulated market experience mandatory?
Yes, especially for Technology Transfer roles.
2. Are freshers eligible?
No. Minimum 3 years of experience is required.
3. What equipment experience is preferred?
RMG, FBP, coating machine, roller compactor, HME, softgel equipment.
4. What is the job location?
Baska, Halol (Vadodara), Gujarat.
5. How do I apply?
Send your CV to recruit.baska@bdrpharma.com or vishal.sharma@bdrpharma.com.
Job Summary
| Company | BDR Pharmaceuticals |
|---|---|
| Vacancies | Executive/Officer – F&D OSD (Technology Transfer); Executive/Officer – F&D OSD (Pellets) |
| Required Education | B.Pharm, M.Pharm |
| Experience | 3–8 Years |
To apply for this job email your details to vishal.sharma@bdrpharma.com
