Leben Life Sciences Hiring 2026 – Sr. Officer / Executive R&D Formulation Development Jobs in Akola
Leben Life Sciences Pvt. Ltd. (LLS) is hiring experienced pharmaceutical professionals for its R&D – Formulation Development team in Akola, Maharashtra.
The opening is for the position of Sr. Officer / Executive – R&D (Formulation Development). Candidates with an M.Pharm qualification and 3 to 8 years of relevant formulation development experience can consider this opportunity.
The role involves working on Oral Solid Dosage (OSD) and Semisolid formulations, including formulation optimization, pre-formulation studies, scale-up, technology transfer, stability studies and related documentation.
Leben Life Sciences Recruitment 2026 – Job Highlights
| Particular | Details |
|---|---|
| Company | Leben Life Sciences Pvt. Ltd. |
| Position | Sr. Officer / Executive – R&D |
| Function | Formulation Development |
| Experience | 3–8 Years |
| Qualification | M.Pharm |
| Dosage Forms | OSD & Semisolid |
| Location | Akola, Maharashtra |
| Work Type | Full Time / On-site |
| Markets | EU, ROW & Domestic |
About Leben Life Sciences
Leben Life Sciences Pvt. Ltd. (LLS) is a pharmaceutical organization involved in formulation development and manufacturing.
The company works on pharmaceutical products intended for EU, Rest of World (ROW) and Domestic markets. The supplied recruitment information highlights its work across Oral Solid Dosage and Semisolid formulations, along with formulation development, scale-up and commercialization activities.
For experienced formulation professionals, the advertised role focuses on hands-on R&D activities combined with documentation, quality requirements and cross-functional coordination.
Sr. Officer / Executive – R&D Formulation Development
The selected professional will be part of the R&D – Formulation Development function at Akola.
Position Details
Job Title: Sr. Officer / Executive – R&D (Formulation Development)
Department: R&D – Formulation Development
Experience: 3–8 years
Qualification: M.Pharm
Location: Akola, Maharashtra
Employment: Full Time / On-site
The position is particularly relevant to professionals who have practical experience in solid and semisolid dosage-form development.
Eligibility Criteria
Candidates should have:
- M.Pharm qualification
- 3–8 years of experience in pharmaceutical formulation development
- Practical experience with OSD and/or Semisolid dosage forms
- Understanding of pre-formulation activities
- Knowledge of drug–excipient compatibility studies
- Experience with formulation optimization
- Understanding of QbD principles
- Exposure to scale-up and technology transfer
- Experience with stability studies
- Knowledge of formulation development documentation
- Understanding of cGMP requirements
Experience coordinating with QA, QC and Production teams will also be relevant to the position.
Key Technical Skills
The role requires practical formulation development knowledge rather than only academic understanding.
Important areas include:
Oral Solid Dosage Development
Candidates should have experience with OSD products such as tablets and/or capsules, including formulation trials and optimization activities.
Semisolid Formulations
Experience working with semisolid dosage forms is relevant to the advertised position.
QbD-Based Development
Knowledge of Quality by Design (QbD) principles is expected for formulation optimization and development activities.
Pre-Formulation
The role includes pre-formulation work and drug–excipient compatibility studies to support formulation development.
Scale-Up and Technology Transfer
Candidates should understand activities involved in moving formulations from laboratory development toward larger-scale manufacturing and technology transfer.
Key Responsibilities
The advertised responsibilities include:
- Developing and optimizing OSD and Semisolid formulations
- Applying QbD principles during formulation development
- Conducting pre-formulation studies
- Performing drug–excipient compatibility studies
- Executing laboratory formulation trials
- Supporting scale-up activities
- Participating in technology transfer
- Preparing and maintaining formulation development documents
- Preparing MFR and PDR-related documentation
- Preparing stability protocols and maintaining related records
- Managing stability studies according to requirements
- Coordinating with QA, QC and Production
- Supporting product development and commercialization
- Following cGMP and applicable regulatory requirements
- Supporting products intended for EU, ROW and Domestic markets
Documentation Responsibilities
Documentation is an important part of formulation R&D.
The supplied job information specifically mentions exposure to documents and activities such as:
- MFR
- PDR
- Stability protocols
- Formulation development documentation
- Technical documents
- Technology transfer documentation
Candidates should therefore be comfortable maintaining accurate and controlled R&D records.
Markets Covered
The formulation development activities associated with this role support products intended for:
- European Union (EU) markets
- Rest of World (ROW) markets
- Domestic market
This means candidates should be familiar with working in a regulated pharmaceutical development environment and following applicable quality and documentation practices.
Cross-Functional Collaboration
Formulation development generally involves coordination with several pharmaceutical functions.
For this position, the supplied requirements specifically mention coordination with:
- Quality Assurance (QA)
- Quality Control (QC)
- Production
The selected candidate may need to work with these teams during development, scale-up, technology transfer and commercialization activities.
Career Opportunity for Formulation R&D Professionals
This position is aimed at experienced professionals rather than freshers. Candidates with 3–8 years of formulation development experience can review the opening if their background matches the OSD and/or Semisolid requirements.
The role brings together laboratory formulation development, QbD, stability, scale-up, technology transfer and pharmaceutical documentation.
How to Apply for Leben Life Sciences Jobs
Eligible candidates can share their updated CV with the recruitment team.
Email: career@lebenlifesciences.com
For additional information, the supplied recruitment details provide the following contact number:
Contact: 7498035480
Candidates should mention their relevant formulation development experience clearly in their CV, particularly experience involving OSD, Semisolid formulations, QbD, scale-up and technology transfer.
What to Highlight in Your Resume
Candidates applying for this position can make their relevant experience easier to identify by mentioning:
- M.Pharm specialization
- Total formulation R&D experience
- OSD formulation experience
- Semisolid formulation experience
- Product development projects
- QbD experience
- Pre-formulation studies
- Drug–excipient compatibility studies
- Scale-up experience
- Technology transfer experience
- Stability studies
- MFR/PDR documentation
- cGMP knowledge
- QA/QC/Production coordination
Quick Job Summary
| Job Information | Details |
|---|---|
| Company | Leben Life Sciences Pvt. Ltd. |
| Job Role | Sr. Officer / Executive – R&D |
| Function | Formulation Development |
| Qualification | M.Pharm |
| Experience | 3–8 Years |
| Dosage Forms | OSD & Semisolid |
| Location | Akola, Maharashtra |
| Work Mode | On-site |
| Markets | EU, ROW & Domestic |
| Application Email | career@lebenlifesciences.com |
| Contact | 7498035480 |
Frequently Asked Questions
Q1. What position is available at Leben Life Sciences?
Leben Life Sciences is hiring for a Sr. Officer / Executive – R&D (Formulation Development) position in Akola, Maharashtra.
Q2. What qualification is required?
The advertised educational requirement is M.Pharm.
Q3. How much experience is required?
Candidates should have 3 to 8 years of experience in pharmaceutical formulation development.
Q4. Is this a fresher job?
No. The advertised position requires 3–8 years of relevant formulation development experience.
Q5. What dosage forms are involved?
The role focuses on Oral Solid Dosage (OSD) and Semisolid formulations.
Q6. Is QbD experience required?
Knowledge and experience with QbD-based formulation optimization are mentioned among the requirements.
Q7. Does the role involve scale-up and technology transfer?
Yes. Scale-up and technology transfer are specifically mentioned as part of the role.
Q8. Which markets does the formulation team support?
The supplied recruitment information mentions EU, ROW and Domestic markets.
Q9. How can I apply for this Leben Life Sciences vacancy?
Eligible candidates can send their updated CV to career@lebenlifesciences.com. The supplied contact number is 7498035480.
Q10. Where is the job located?
The position is based in Akola, Maharashtra, and the supplied details identify it as a full-time, on-site role.
