Eugia Pharma Hiring Formulation R&D
- Company Overview
- Job Role & Responsibilities
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Why Join Eugia Pharma?
- Frequently Asked Questions (FAQs)
- Summary Table
Meta Title: Ph.D/M.Pharm Formulation R&D Complex Injectables | Eugia Pharma
Meta Description: Eugia Pharma hiring Formulation R&D (Complex Injectables) — Ph.D/M.Pharm/B.Pharm/M.Sc | 4–8 yrs | Patancheru, Telangana.
Advance your career in formulation science with Eugia Pharma Research Centre — a research-led organization focused on developing complex injectable therapies that address unmet clinical needs. Eugia is inviting experienced formulation scientists for its Formulation R&D — Complex Injectables group at its development site near Patancheru, Sangareddy, Telangana.
If you have solid experience in sterile injectable product development, hands-on exposure to Quality by Design (QbD) and Quality by Research (QbR) approaches, and a passion for translating lab innovation into regulatory-ready CMC packages, this role offers a high-impact platform to grow and contribute to advanced therapeutics.
Company Overview
Eugia Pharma Research Centre is part of a progressive pharmaceutical organization committed to scientific excellence and regulatory compliance. The company invests in cutting-edge R&D for complex dosage forms, particularly sterile injectables such as emulsions, suspensions, peptide formulations, and microsphere depot systems. Eugia’s research footprint emphasizes robust process development, scalable manufacturing, and timely regulatory submissions to global markets.
Working at Eugia places you within a multidisciplinary environment where formulation scientists, analytical experts, process engineers, and regulatory professionals collaborate to bring novel and high-value injectable therapies from concept to clinic.
Job Role & Responsibilities
Position: Formulation R&D – Complex Injectables
Qualification: Ph.D / M.Pharm / B.Pharm / M.Sc
Experience: 4 to 8 years
Location: Eugia Pharma Research Centre, Phase III, TSIIC, Epip, Pashamylaram Village, Patancheru Mandal, Sangareddy, Telangana 502307
As a Formulation R&D scientist specializing in complex injectables, you will lead formulation design, process optimization, and CMC-ready documentation for sterile parenteral products. Your work will directly support product development for regulated markets and include cross-functional coordination with analytical, QA/RA, and pilot manufacturing teams.
Key Responsibilities:
- Lead formulation development projects for complex injectables: emulsions, suspensions, peptide formulations, microsphere depot systems, and other advanced sterile dosage forms.
- Design experiments using QbD and QbR principles to define critical material attributes (CMAs) and critical process parameters (CPPs).
- Develop robust, scalable processes amenable to GMP pilot and commercial manufacturing; demonstrate understanding of SS/SUB equipment impacts on sterile processes.
- Plan and execute pre-formulation, formulation screening, excipient compatibility and stability studies aligned with ICH guidelines.
- Prepare and contribute to CMC sections for regulatory submissions for regulated markets; interact with RA to ensure dossier readiness.
- Perform technology transfer to pilot/manufacturing, support equipment qualification and process validation activities.
- Conduct risk assessments, failure mode analysis and implement mitigation strategies for sterile product development.
- Author technical reports, SOPs, protocols, method validation documents, and summary reports ensuring data integrity and traceability.
- Mentor junior scientists and provide hands-on training for aseptic technique, sterile handling, and formulation characterization.
- Collaborate with analytical development for assay, impurity, particle size, sterility, endotoxin and other critical quality attributes testing.
Impact: Your contributions will ensure Eugia’s injectable candidates meet regulatory expectations for quality, safety, and efficacy — accelerating patient access to advanced therapeutics.
Eligibility / Qualifications
Minimum Qualifications:
- Ph.D. in Pharmaceutics, Pharmaceutical Technology, or related discipline — preferred; OR
- M.Pharm / B.Pharm / M.Sc in Pharmaceutics, Pharmaceutical Chemistry, Biotechnology or related fields with strong formulation experience.
Experience: 4–8 years in formulation R&D with demonstrable expertise in sterile/aseptic injectable development.
Core Competencies & Skills:
- Hands-on experience in formulation of emulsions, suspensions, peptides, microspheres / depot systems.
- Strong grasp of QbD/QbR methodology, DoE (Design of Experiments), statistical analysis and process optimization.
- Familiarity with CMC documentation and global regulatory expectations (ICH, USFDA, EMA) for sterile injectables.
- Practical exposure to sterile processing, aseptic fills, lyophilization, sterilization techniques (filtration, terminal sterilization) and stability programs.
- Proficiency in analytical characterization techniques relevant to injectables: particle sizing (DLS, laser diffraction), rheology, HPLC, LC-MS, endotoxin testing, sterility testing.
- Excellent technical writing skills for SOPs, protocols, validation reports and regulatory dossiers.
- Strong teamwork, project management, and cross-functional communication skills.
Desirable:
- Prior experience with peptide therapeutics or biologics formulations.
- Experience in technology transfer to pilot or GMP manufacturing and support during validation runs.
- Knowledge of single-use technologies and their impact on sterile process development.
Relevant courses (comma-separated): Pharmaceutics, Pharmaceutical Technology, Pharmaceutical Chemistry, Biopharmaceutics, Biotechnology, Analytical Chemistry, Process Engineering, Quality Assurance, Regulatory Affairs.
Location & Salary
Location: Eugia Pharma Research Centre — Phase III, TSIIC, EPIP, Pashamylaram Village, Patancheru Mandal, Sangareddy, Telangana 502307.
Work Type: On-site R&D role at Patancheru facility.
Compensation: Competitive and commensurate with experience, academic background (Ph.D preferred), and core competency. Specific package will be discussed during the interview and will align with industry standards for formulation R&D roles in biotech/pharma.
Application Process
Please send your updated CV / resume along with a cover note highlighting relevant formulation projects, publications (if any), and your availability to the contact below. Shortlisted candidates will be contacted for technical interviews and may be requested to present a brief project/technical summary.
Email: Reshma.Thota@eugiapharma.com
Application tip: In your email subject line, mention: “Application – Formulation R&D (Complex Injectables) — [Your Name]” and include a one-page summary of a recent injectable formulation project you led or contributed to.
Apply early — positions are limited and selection will be on a rolling basis.
Why Join Eugia Pharma?
- Work at a focused R&D center dedicated to complex sterile injectables — ideal for scientists who want to make meaningful contributions to advanced drug delivery.
- Exposure to end-to-end formulation development — from pre-formulation to technology transfer and regulatory submissions.
- Collaborative multi-disciplinary teams with experienced R&D, analytical, and regulatory professionals.
- Opportunities for patentable innovations, publications, and professional growth in formulation science.
- A culture that values scientific rigor, data integrity, and employee development.
Frequently Asked Questions (FAQs)
1. What qualifications are mandatory for this role?
A Ph.D is preferred; however, candidates with M.Pharm/B.Pharm/M.Sc and 4–8 years of relevant injectable formulation experience will also be considered.
2. What types of injectables will I work on?
You will work on complex sterile forms such as emulsions, suspensions, peptide formulations, and microsphere depot systems.
3. Is this an on-site role?
Yes. The role is based at Eugia’s R&D centre in Patancheru (Sangareddy), Telangana.
4. How do I apply?
Send your CV and a one-page project summary to Reshma.Thota@eugiapharma.com with the subject line noted above.
5. What is the expected salary range?
Compensation is competitive and will be aligned to your experience, academic qualifications, and market benchmarks. Exact figures will be shared during the recruitment process.
6. Will I be involved in regulatory submissions?
Yes. The role requires CMC documentation experience and collaboration with regulatory affairs for dossier preparation for regulated markets.
Summary Table
| Category | Details |
|---|---|
| Company | Eugia Pharma Research Centre |
| Vacancies | Formulation R&D – Complex Injectables |
| Required Education | Ph.D, M.Pharm, B.Pharm, M.Sc (Pharmaceutics, Pharmaceutical Technology, Biotechnology) |
| Experience | 4 to 8 Years |
| Location | Patancheru, Sangareddy, Telangana (EPIP) |
| Reshma.Thota@eugiapharma.com |
To apply for this job email your details to Reshma.Thota@eugiapharma.com
