Bachwell Hiring Trainee / Research Associate
- Company Overview
- Job Role & Responsibilities
- Trainee / Research Associate – ADME & DMPK (02 Vacancies)
- 1. ADME & DMPK Responsibilities
- 2. Pharmacology (In Vivo & In Vitro)
- 3. Global Regulatory Responsibilities (Trainee Level)
- Eligibility / Qualifications
- Required Educational Qualifications (comma-separated)
- Experience
- Desired Skills
- Location & Salary
- Application Process
- Why Choose a Career in ADME & DMPK Research
- Frequently Asked Questions (FAQs)
- Who can apply for this position?
- Is prior ADME experience mandatory?
- Is this role compliant with global regulatory standards?
- Where is the job located?
- How do I apply?
- Summary Table
MPharm Pharmacology Fresher Vacancy | Hyderabad
Trainee Research Associate ADME DMPK vacancy in Hyderabad. M.Pharm Pharmacology freshers eligible. 2 openings.
Bachwell Pharma is inviting applications from M.Pharm (Pharmacology) freshers for the position of Trainee / Research Associate in ADME & DMPK and Pharmacology (In Vivo & In Vitro) at its Genome Valley, Hyderabad facility. This opportunity is designed for candidates who want to build a scientific career in preclinical research, drug metabolism studies, and global regulatory-compliant drug development programs.
The role directly supports global markets regulated by agencies such as the US FDA, EMA, and PMDA, where high-quality pharmacokinetic and safety data are mandatory before a drug progresses to clinical trials. If you are searching for pharmacology jobs for freshers, ADME DMPK trainee roles, drug metabolism research careers, or preclinical research jobs in Hyderabad, this position offers structured exposure to international regulatory standards and GLP-compliant research systems.
Company Overview
Bachwell Pharma operates in the preclinical research and drug development domain, supporting pharmaceutical and biotech clients targeting global regulatory approvals. The organization focuses on ADME (Absorption, Distribution, Metabolism, and Excretion), DMPK (Drug Metabolism and Pharmacokinetics), and pharmacology studies that generate critical data for IND and NDA submissions.
The Hyderabad facility, located in Genome Valley, provides access to advanced laboratory infrastructure, LC-MS/MS systems, cell culture platforms, and in vivo research models. The company aligns its research operations with GLP (Good Laboratory Practice) standards and ICH regulatory guidelines to ensure global compliance.
Working at Bachwell Pharma offers early-career scientists hands-on training in regulated laboratory practices, bioanalytical methods, pharmacokinetic modeling, and safety pharmacology assessments.
Job Role & Responsibilities
Trainee / Research Associate – ADME & DMPK (02 Vacancies)
Department: ADME & DMPK and Pharmacology (In Vivo & In Vitro)
Location: Genome Valley, Hyderabad, India
Experience: Fresher
Qualification: M.Pharm (Pharmacology)
This position plays a technical role in generating scientific data required for global regulatory submissions. As a trainee, you will work under senior scientists and contribute to experimental design, execution, and documentation aligned with international compliance standards.
1. ADME & DMPK Responsibilities
ADME & DMPK studies determine how a drug behaves inside the body and whether it is suitable for further development.
In Vitro Assays:
- Conduct microsomal stability studies to evaluate metabolic stability
- Perform plasma protein binding experiments
- Assess intrinsic clearance and enzyme interactions
Metabolite Identification (MetID):
- Use LC-MS/MS (Liquid Chromatography–Mass Spectrometry) for metabolite profiling
- Analyze metabolic pathways and identify potential toxic metabolites
- Generate analytical reports compliant with regulatory expectations
Permeability Studies:
- Conduct Caco-2 permeability assays
- Evaluate absorption potential for oral drug candidates
- Support bioavailability assessment for global market submissions
2. Pharmacology (In Vivo & In Vitro)
Pharmacology studies focus on evaluating drug efficacy, mechanism of action, and safety profile.
In Vivo Studies:
- Assist in animal dosing and sample collection
- Monitor pharmacokinetic parameters at defined time intervals
- Maintain ethical and regulatory compliance in animal research
PK/PD Modeling:
- Support correlation of plasma drug concentration (PK) with biological effect (PD)
- Assist in data compilation and statistical interpretation
Safety Pharmacology:
- Screen for off-target effects
- Monitor potential cardiac or CNS impact of drug candidates
- Assist in safety data generation for regulatory dossiers
3. Global Regulatory Responsibilities (Trainee Level)
Since this role supports global markets, documentation and data integrity are critical.
- Maintain laboratory notebooks and electronic records as per GLP
- Follow ICH guidelines and international compliance frameworks
- Ensure raw data traceability and audit readiness
- Support preparation of study reports for regulatory submissions
- Maintain adherence to SOPs and quality systems
As a trainee, your role is technical and data-driven. Accuracy, discipline, and scientific curiosity are essential.
Eligibility / Qualifications
Required Educational Qualifications (comma-separated)
M.Pharm Pharmacology
Experience
- Freshers are eligible
- Strong academic foundation in pharmacokinetics, drug metabolism, and preclinical pharmacology preferred
Desired Skills
- Basic understanding of ADME and DMPK principles
- Knowledge of LC-MS/MS and bioanalytical techniques (academic exposure acceptable)
- Familiarity with GLP and regulatory documentation concepts
- Strong analytical and scientific writing skills
- Good communication and teamwork abilities
Location & Salary
Location: Genome Valley, Hyderabad, India
Genome Valley is one of India’s leading biotech and pharmaceutical research hubs, offering exposure to CROs, R&D centers, and global life sciences operations.
Salary: As per company standards and industry norms for trainee-level preclinical research roles.
Application Process
Interested candidates can share their updated resume at:
WhatsApp Contact: +91 9014502249
Candidates are advised to mention “Trainee – ADME & DMPK” in the subject line.
Why Choose a Career in ADME & DMPK Research
ADME & DMPK research is one of the most critical phases in drug development. Regulatory authorities demand detailed pharmacokinetic, metabolic, and safety data before approving clinical trials.
Starting your career in ADME & DMPK provides:
- Strong foundation in preclinical drug development
- Exposure to global regulatory standards (FDA, EMA, PMDA)
- Career growth in bioanalysis, PK/PD modeling, or regulatory toxicology
- Opportunities in CROs, pharma R&D centers, and biotech companies
- High-value technical skill development in LC-MS/MS and drug metabolism research
This role is ideal for candidates targeting pharmacology research jobs, drug metabolism careers, preclinical research associate roles, and ADME DMPK fresher vacancies in Hyderabad.
Frequently Asked Questions (FAQs)
Who can apply for this position?
Candidates with M.Pharm in Pharmacology are eligible. Freshers are welcome.
Is prior ADME experience mandatory?
No. This is a trainee-level opportunity designed for freshers.
Is this role compliant with global regulatory standards?
Yes. Work aligns with GLP and ICH guidelines supporting global markets.
Where is the job located?
Genome Valley, Hyderabad, India.
How do I apply?
Email your updated CV to the provided email IDs and mention the position clearly.
Summary Table
| Company | Bachwell Pharma |
|---|---|
| Vacancies | Trainee / Research Associate – ADME & DMPK (02) |
| Required Education | M.Pharm (Pharmacology) |
| Experience | Fresher |
To apply for this job email your details to sreddy@bachwellpharma.com
