Job Overview
| Particulars | Details |
|---|---|
| Position | Multiple Pharma Vacancies |
| Company | Farmson Basic Drugs Pvt. Ltd. |
| Location | Vadodara |
| Job Type | Full-Time |
| Category / Department | Pharma |
| Application Mode |
🏢 About Farmson Basic Drugs Pvt. Ltd.
Farmson Basic Drugs Private Limited operates in the pharmaceutical industry with a focus on the manufacturing of Active Pharmaceutical Ingredients (APIs) and intermediate products. The company serves pharmaceutical markets and emphasizes manufacturing quality, regulatory compliance, and operational excellence.
Company Mission
The organization focuses on delivering pharmaceutical products through reliable manufacturing practices, quality-driven processes, and compliance with applicable industry standards.
Company Vision
Farmson Basic Drugs aims to strengthen its position in the pharmaceutical manufacturing sector by combining technical expertise, quality systems, innovation, and continuous improvement.
Core Values
🔹 Quality and consistency
🔹 GMP and regulatory compliance
🔹 Technical excellence
🔹 Safety and responsibility
🔹 Continuous improvement
🔹 Professional integrity
🔹 Teamwork and collaboration
What Makes Them Different
Farmson Basic Drugs provides professionals with opportunities to work across a diverse pharmaceutical manufacturing ecosystem. Employees can gain exposure to areas ranging from API production and analytical testing to regulatory affairs, quality systems, R&D, engineering, instrumentation, and EHS.
Leadership / Company Philosophy
The company's work culture emphasizes technical capability, quality compliance, operational discipline, and continuous improvement. Its focus on regulated pharmaceutical manufacturing provides employees with an environment where expertise, accuracy, safety, and professional development are important parts of day-to-day operations
📍 Farmson CII Model Career Centre
2nd Floor, Cooperative House
Besides McDonald’s
Near Manisha Chowkdi
Old Padra Road
Vadodara-20, Gujarat, India
💡 Editor's Note / Preparation Tip
📄 Resume Preparation Tips
1️⃣ Clearly mention your current department, designation, total experience, and relevant pharmaceutical experience.
2️⃣ Highlight specific expertise such as API manufacturing, GMP, HPLC, GC, QA, QC, ADL, regulatory affairs, or engineering systems.
3️⃣ Include experience with relevant equipment, processes, instruments, and software where applicable.
4️⃣ Mention your educational qualification prominently and ensure your experience aligns with the position you're targeting.
5️⃣ Keep an updated copy of your resume ready for the walk-in and highlight your most relevant achievements.
🎯 Interview Preparation
1️⃣ Revise key concepts related to GMP, GDP, QMS, and pharmaceutical compliance.
2️⃣ Prepare department-specific technical questions based on the role you're applying for.
3️⃣ QC/ADL candidates should revise HPLC, GC, UV, IR, method validation, and analytical testing.
4️⃣ Production candidates should prepare topics related to API manufacturing, batch operations, dispensing, granulation, and GMP.
5️⃣ Engineering and EHS candidates should revise maintenance, utilities, PLC/DCS/SCADA, safety, risk assessment, and incident investigation.
💡 Professional Tips
1️⃣ Research the specific department you want to join before attending the walk-in interview.
2️⃣ Carry multiple copies of your updated resume and organize all supporting documents in advance.
3️⃣ Be prepared to explain your current responsibilities and the technical challenges you have handled.
4️⃣ Quantify your achievements wherever possible, such as production scale, audit performance, process improvements, or quality metrics.
5️⃣ Demonstrate a strong understanding of quality, safety, compliance, and continuous improvement—key priorities in pharmaceutical manufacturing.
📝 Job Description
Below is a fully rewritten, original LinkedIn-style post that preserves the job information while avoiding direct copying or close paraphrasing of the source.
🚨 Walk-In Interview | Multiple Pharma Vacancies | Farmson Basic Drugs Pvt. Ltd.
💊 Build Your Career in API Manufacturing, Quality, R&D & Technical Operations!
Farmson Basic Drugs Private Limited is conducting a Walk-In Interview on 26 July 2026 for experienced professionals across multiple departments in its pharmaceutical and API manufacturing operations.
The recruitment drive includes opportunities in Production, Packing, Regulatory Affairs, Quality Control, Microbiology, Analytical Development, Quality Assurance, R&D, Engineering, Utilities, Instrumentation, EHS, and ETP. Candidates with relevant pharmaceutical, chemical, engineering, and technical experience are encouraged to attend and explore career opportunities with an organization focused on quality, GMP compliance, and manufacturing excellence. 🧪🏭
Position Details
Company: Farmson Basic Drugs Private Limited
Industry: Pharmaceuticals / API Manufacturing / Chemicals
Experience: 1–15 Years, depending on the position
Work Type: Full-Time, On-Site
Location: Vadodara, Gujarat
Qualifications: M.Pharm / B.Pharm / M.Sc. / B.Sc. / Diploma / B.E. / PDIS, depending on the role
Walk-In Date: 26 July 2026 (Sunday)
Time: 9:30 AM – 5:00 PM
Venue: Farmson CII Model Career Centre, 2nd Floor, Cooperative House, Besides McDonald’s, Near Manisha Chowkdi, Old Padra Road, Vadodara-20
Preferred Skills
⭐ Prior experience in API manufacturing environments
⭐ Familiarity with Glatt equipment and processes
⭐ Knowledge of dispensing and granulation operations
⭐ Experience with GMP-compliant production systems
⭐ Exposure to analytical method validation
⭐ Experience in pharmaceutical QMS and compliance activities
⭐ Knowledge of plant utilities and instrumentation
⭐ Experience with PLC, DCS, and SCADA systems
⭐ EHS and ETP experience
⭐ Strong understanding of pharmaceutical regulatory expectations
Detailed Job Description / Responsibilities
Candidate Requirements
🎓 Production: M.Pharm / B.Pharm / M.Sc. / B.Sc. Chemistry – 2–6 Years
🎓 Packing: Any Graduate – 3–6 Years
🎓 Regulatory Affairs: M.Pharm / M.Sc. Chemistry – 4–15 Years
🎓 QC & Microbiology: M.Sc. / B.Sc. Chemistry or Microbiology – 1–10 Years
🎓 ADL: M.Pharm / M.Sc. / B.Sc. Organic or Analytical Chemistry – 5–10 Years
🎓 QA: M.Sc. / B.Sc. Chemistry – 3–10 Years
🎓 R&D: M.Sc. Organic Chemistry – 1–3 Years
🎓 Engineering / Utility / Instrument / EHS / ETP: Diploma / B.E. Mechanical or Instrumentation / B.Sc. / M.Sc. / PDIS – 2–15 Years
📌 Note: Experience requirements and qualifications vary by department and position.
Why Join Farmson Basic Drugs?
💊 Build your career within an established API manufacturing environment
📈 Explore multiple career paths across technical and pharmaceutical functions
🧪 Gain exposure to GMP, quality systems, and advanced pharmaceutical practices
🏭 Work across critical areas of manufacturing and plant operations
📚 Develop expertise in quality, regulatory, analytical, and technical functions
🤝 Work in a professional and compliance-focused environment
🚀 Access opportunities for professional growth and continuous learning
💼 Receive compensation aligned with experience and role requirements
How to Apply
🚨 Walk-In Interview
📅 Date: 26 July 2026 (Sunday)
⏰ Time: 9:30 AM – 5:00 PM
📍 Venue: Farmson CII Model Career Centre, 2nd Floor, Cooperative House, Besides McDonald’s, Near Manisha Chowkdi, Old Padra Road, Vadodara-20
📌 Candidates should carry:
✔️ Updated Resume / CV
✔️ Passport-size Photograph
✔️ Educational Certificates
✔️ Experience Certificates
✔️ Recent Payslips
✔️ Other Relevant Supporting Documents
📩 Unable to attend the walk-in?
Send your updated CV to: recruitment@farmson.com
📞 Contact: 7227060620
Know someone who would be a great fit? Tag them or share this opportunity with your network! 🚀
🎯 Key Responsibilities
- ✓ Production – Direct Compression & Plant Operations
- ✓ Manage production batches and plant activities according to approved plans and procedures.
- ✓ Follow GMP requirements throughout manufacturing operations.
- ✓ Maintain accurate batch and production documentation.
- ✓ Support activities involving dispensing, granulation, and relevant manufacturing processes.
- ✓ Packing
- ✓ Execute packing activities according to approved procedures and production requirements.
- ✓ Maintain appropriate GMP and packaging-related records.
- ✓ Ensure compliance with quality and documentation requirements.
- ✓ Regulatory Affairs
- ✓ Prepare, review, and maintain regulatory documentation.
- ✓ Support regulatory compliance activities and documentation requirements.
- ✓ Coordinate relevant information across internal teams.
- ✓ Contribute to maintaining pharmaceutical regulatory and quality standards.
- ✓ Quality Control & Microbiology
- ✓ Perform testing of raw materials, in-process materials, finished products, and stability samples.
- ✓ Conduct chemical and microbiological analysis as applicable.
- ✓ Operate laboratory instruments and maintain accurate analytical records.
- ✓ Follow laboratory procedures, GMP requirements, and quality standards.
- ✓ Analytical Development Laboratory (ADL)
- ✓ Support analytical method development and validation activities.
- ✓ Perform analytical testing using relevant laboratory techniques and instruments.
- ✓ Prepare appropriate analytical documentation and reports.
- ✓ Support qualification and validation activities as required.
- ✓ Quality Assurance
- ✓ Support quality systems and GMP compliance activities.
- ✓ Review and maintain quality-related documentation.
- ✓ Participate in validation, qualification, and QMS activities.
- ✓ Ensure processes and documentation meet applicable quality requirements.
- ✓ Research & Development
- ✓ Support chemical synthesis and laboratory-scale research activities.
- ✓ Design and perform synthesis reactions under appropriate procedures.
- ✓ Maintain accurate research documentation and experimental records.
- ✓ Contribute to process development and optimization activities.
- ✓ ️ Engineering, Utility & Instrumentation
- ✓ Support plant maintenance and engineering operations.
- ✓ Maintain utilities and manufacturing infrastructure.
- ✓ Work with instrumentation and relevant control systems.
- ✓ Support PLC, DCS, and SCADA-related activities where applicable.
- ✓ Ensure equipment reliability and operational continuity.
- ✓ EHS & ETP
- ✓ Promote compliance with environmental, health, and safety requirements.
- ✓ Support workplace risk assessments and safety initiatives.
- ✓ Assist in incident investigation and corrective actions.
- ✓ Contribute to maintaining a strong safety culture and environmental compliance.
💡 Required Qualifications & Skills
🚀 Career Guidance & Interview Insights
To help you succeed, we've compiled original preparation guides, resume keywords, and growth analytics for this category of role.
This Multiple Pharma Vacancies role is a chance to contribute directly to life sciences, patient care, or pharmaceutical advancements. You will work within strict compliance frameworks, ensure rigorous quality standards, and collaborate with technical or medical experts. It is a career path that blends scientific excellence with a deep sense of social purpose.
Healthcare and pharmaceutical professionals grow through specialized scientific experience. Entry-level starts as Lab Technician, Chemist, or Quality Associate, progressing to Senior QA/QC Analyst. Advancement leads to Lab Supervisor, Clinical Project Manager, and senior management roles like Quality Director, VP of Regulatory Affairs, or Chief Scientific Officer.
Expected Technical & Behavioral Questions:
- Q1: How do you ensure compliance with WHO/GMP guidelines during laboratory operations?
Answer Tip: Mention strict adherence to Standard Operating Procedures (SOPs), detailed batch records, regular equipment calibration, and sanitization cycles. - Q2: What steps do you take when a quality deviation is detected in a product batch?
Answer Tip: Outline immediate isolation of the batch, raising a deviation report, root cause analysis (RCA), and initiating CAPA (Corrective and Preventive Action). - Q3: How do you manage safety protocols while handling toxic chemicals?
Answer Tip: Discuss using Material Safety Data Sheets (MSDS), wearing appropriate Personal Protective Equipment (PPE), proper ventilation, and chemical spill kits.
To pass automated ATS (Applicant Tracking System) screening and catch the recruiter's eye, tailor your resume with the following tips:
- Keywords to include: Quality Control (QC), GMP Compliance, FDA Regulations, SOP Documentation, HPLC/GC analysis, Batch Validation, Clinical Trials, Pharmacovigilance.
- Format: List laboratory skills and instruments handled (e.g. HPLC, spectrophotometer) in a dedicated technical matrix.
- Quantify Results: E.g., 'Validated 15 batch formulations under GMP guidelines with zero quality defects.'
Estimated compensation for this role type in India is ₹2,40,000 - ₹3,80,000 per annum (Fresher analyst). The actual salary package offered depends on factors such as company size, work mode (remote or on-site), individual technical proficiency, and negotiations during final HR rounds.
Key credentials: GMP Certified Professional (ASQ), Certified Clinical Research Coordinator (CCRC), or specialized laboratory training certificates in high-performance liquid chromatography (HPLC) and safety standards.
Frequently Asked Questions
1️⃣ When is the Farmson Basic Drugs Walk-In Interview?
The walk-in interview is scheduled for 26 July 2026 (Sunday) from 9:30 AM to 5:00 PM.
2️⃣ Which departments are hiring?
Openings are available across Production, Packing, Regulatory Affairs, QC, Microbiology, ADL, QA, R&D, Engineering, Utility, Instrumentation, EHS, and ETP.
3️⃣ What experience range is required?
The experience requirement varies by role, ranging from approximately 1 to 15 years.
4️⃣ Which educational backgrounds are eligible?
Depending on the position, qualifications include M.Pharm, B.Pharm, M.Sc., B.Sc., Diploma, B.E. in Mechanical/Instrumentation, and PDIS.
5️⃣ Is API experience mandatory?
Relevant API manufacturing experience is preferred for many technical positions. Candidates should review the requirements of their target department before attending.
6️⃣ What documents should candidates bring?
Candidates should carry their updated CV, passport-size photograph, educational and experience certificates, payslips, and other relevant supporting documents.
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