KLM Laboratories Pvt. Ltd., a leading global pharmaceutical company specializing in dermatology, pediatrics, and cosmeceuticals, is hosting a Walk-in Drive on June 22, 2025, at our manufacturing unit in Vadodara, Gujarat.
With a mission to improve lives through innovative healthcare solutions, our USFDA and PIC/s-approved facility at Horizon Industrial Park, Vadodara, invites enthusiastic professionals to join our team in Quality Control, Quality Assurance, Production, Engineering, Environmental Health & Safety, Regulatory Affairs, Research & Development, and Analytical Development.
About KLM Laboratories
Established in 2010, KLM Laboratories is headquartered in Mumbai with a state-of-the-art manufacturing unit in Vadodara (100,000 sq. ft.) and a head office in Surat. Known for being India’s top prescriber of Itraconazole (2013) and launching a Pediatric Dermatology division (2017), we manufacture tablets, capsules, ointments, lotions, and creams for 35+ countries.
Our Vadodara plant complies with USFDA, PIC/s, WHO-GMP, and Schedule M standards, supported by 500+ employees and a 4.0/5 job security rating on AmbitionBox.
Walk-in Drive Details
We’re hiring for multiple roles at our Vadodara manufacturing unit. Below are the event details:
| Event Details | Information |
|---|---|
| Date | June 22, 2025 (Sunday) |
| Time | 10:00 AM to 3:00 PM IST |
| Venue | 261, GIDC Makarpura, Bharti House, Bank of Baroda Lane, Vadodara, Gujarat-390010 |
| Job Location | Horizon Industrial Park, Near Bamangam, Ta. Karjan, Vadodara-391243, Gujarat |
| Application Email | career@klmlab.com |
| Contact Number | +91 9227897864 |
| Note | Only candidates with relevant experience are eligible |
Job Opportunities
Below are the open positions, qualifications, experience, and roles at our Vadodara facility, focusing on semi-solid and oral dosage forms.
1. Quality Control (QC)
- Designation: Officer / Sr. Officer / Executive
- Qualification: B.Sc. / M.Sc. / B.Pharm / M.Pharm
- Experience: 2–8 years
- Role: Instrument Analysis, Reviewer
- Responsibilities:
- Perform HPLC, GC, UV, and dissolution testing for semi-solids and oral dosage forms.
- Conduct stability studies and raw material analysis.
- Ensure cGMP and GLP compliance for USFDA audits.
- Skills: Proficiency in analytical instruments, method validation, and documentation.
2. Quality Assurance (QA)
- Designation: Officer / Sr. Officer / Executive
- Qualification: B.Sc. / M.Sc. / B.Pharm / M.Pharm
- Experience: 2–8 years
- Role: QMS, Documentation, IPQA, Validation
- Responsibilities:
- Manage QMS (e.g., CAPA, deviations, change controls).
- Conduct IPQA for semi-solid manufacturing and filling.
- Prepare validation protocols and support USFDA inspections.
- Skills: Knowledge of cGMP, SOPs, and audit preparedness.
3. Production
- Designation: Officer / Sr. Officer / Assistant Manager
- Qualification: M.Sc. / B.Pharm / M.Pharm
- Experience: 2–12 years
- Role: Manufacturing & Filling of Semi-Solid & Liquid Products
- Responsibilities:
- Oversee manufacturing and filling of ointments, creams, and liquids.
- Ensure batch record compliance and process optimization.
- Manage cleanroom operations per USFDA standards.
- Skills: Expertise in semi-solid production, cGMP, and team management.
- Designation: Operator
- Qualification: ITI / Diploma
- Experience: 2–5 years
- Responsibilities:
- Operate manufacturing and filling equipment for semi-solids.
- Maintain BMR and SOP adherence.
- Skills: Familiarity with cleanroom equipment and aseptic processes.
4. Packing – Production
- Designation: Operator
- Qualification: ITI / Diploma
- Experience: 2–5 years
- Role: Secondary Packing, Auto Cartonator, Serialization
- Responsibilities:
- Execute secondary packing and serialization for semi-solids and liquids.
- Operate auto-cartonators and ensure packing compliance.
- Skills: Knowledge of packing line automation and cGMP.
5. Engineering
- Designation: Executive / Sr. Executive
- Qualification: B.E. / B.Tech (Mechanical / Electrical)
- Experience: 6–8 years in API manufacturing.
- Role: Maintenance & Project Engineer
- Responsibilities:
- Perform preventive maintenance on manufacturing and cleanroom equipment.
- Support project execution for facility upgrades.
- Skills: Expertise in mechanical/electrical systems, GMP, and project management.
6. Environmental Health & Safety (EHS)
- Designation: Officer / Sr. Officer
- Qualification: Diploma (Health & Safety) / Master of Industrial Hygiene & Safety
- Experience: 3–8 years
- Role: EHS Statutory Compliance
- Responsibilities:
- Ensure compliance with EHS regulations (e.g., OSHA, GPCB).
- Conduct safety audits and training for chemical handling.
- Skills: Knowledge of EHS standards, hazard analysis, and compliance reporting.
7. Packaging & Development
- Designation: Packaging Development Engineer
- Qualification: Any Graduate
- Experience: 10–10 years
- Role: Primary & Secondary Packaging Development
- Responsibilities:
- Design and develop primary (e.g., tubes, pumps) and secondary packaging for semi-solids.
- Evaluate packaging compatibility and stability.
- Skills: Expertise in packaging design, material selection, and regulatory requirements.
8. Regulatory Affairs
- Designation: Executive / Sr. Executive
- Qualification: B.Pharm / M.Pharm
- Experience: 6–10 years
- Role: Dossier Preparation for ROW Market
- Responsibilities:
- Prepare CMC dossiers for Rest of World (ROW) markets.
- Ensure compliance with regulatory guidelines (e.g., WHO, PIC/s).
- Skills: Proficiency in dossier compilation, CMC documentation, and regulatory submissions.
9. Research & Development (R&D)
- Designation: Scientist (Various Levels)
- Qualification: M.Pharm / Ph.D.
- Experience: 2–5 years
- Role: Semi-Solid & Oral Dosage Form Development
- Responsibilities:
- Develop semi-solid (e.g., ointments, creams) and oral dosage forms (tablets, capsules).
- Conduct formulation trials and scale-up studies.
- Skills: Knowledge of QbD, formulation development, and stability studies.
10. Analytical Development Laboratory (ADL)
- Designation: Scientist (Various Levels)
- Qualification: M.Sc. / M.Pharm
- Experience: 2–5 years
- Role: Analytical Method Development & Validation
- Responsibilities:
- Develop and validate analytical methods for semi-solids using HPLC, GC, and UV.
- Support stability testing and regulatory submissions.
- Skills: Expertise in method development, validation, and instrument handling.
Why Join KLM Laboratories?
KLM offers a rewarding career in a globally recognized pharmaceutical company. Benefits include:
- Competitive Salary: Officers earn ₹3–8 LPA; Executives ₹6–12 LPA in Vadodara.
- Global Exposure: Work in a USFDA/PIC/s-approved facility serving 35+ countries.
- Career Growth: Training in HPLC, QMS, formulation development, and regulatory affairs.
- Supportive Environment: Rated 4.0/5 for job security and 3.8/5 for work culture (AmbitionBox).
- Challenges: Employees note below-market salaries and Monday–Saturday work (70% report 6-day weeks).
Why These Roles Matter
These roles drive KLM’s production of semi-solid and oral dosage forms, ensuring quality for dermatology and pediatric markets. Your work in QC, R&D, or Regulatory Affairs supports KLM’s global expansion, leveraging Vadodara’s 1,800+ pharma job ecosystem.
Growth Opportunities
KLM invests in training for QbD, analytical validation, and USFDA compliance, with exposure to global audits. Employees value learning opportunities (3.8/5) but note limited salary growth (3.2/5).
Work Environment
The Vadodara facility features cleanrooms, HPLC labs, and semi-solid filling lines, fostering a quality-driven culture (3.8/5). Expect shift-based roles for production and a desk-based environment for R&D/QC, with 64% office-based work and flexible timings (60%).
How to Attend
Join us on June 22, 2025, from 10:00 AM to 3:00 PM at GIDC Makarpura, Vadodara. Bring:
- Updated resume.
- CTC breakup (current salary details).
- Passport-size photograph.
- Educational certificates.
- Experience letters/payslips.
If unable to attend, email your resume to career@klmlab.com with the subject line “[Department] – [Designation]” (e.g., “QC – Officer”). Contact +91 9227897864 for queries. Note: Only candidates with relevant experience are eligible.
Verified by Trusted HRs
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Preparation Tips
- QC/QA: Highlight HPLC, IPQA, or QMS experience.
- Production: Detail semi-solid manufacturing or filling expertise.
- R&D/ADL: Emphasize formulation or method development projects.
- Regulatory: Showcase dossier preparation for ROW markets.
- Prepare for questions like “How do you validate an HPLC method?” or “What ensures cGMP in semi-solid production?”
Important Disclaimer
KLM Laboratories maintains a transparent recruitment process. We do not charge fees or use free email services (e.g., Gmail, Yahoo) for job offers. Verify opportunities through career@klmlab.com or KLM Careers. Report suspicious activities to feedback@klmlab.com or +91-22-61279855.
Stay Safe from Fraud
- Confirm offers through official KLM channels.
- Avoid sharing personal or financial information with unverified sources.
- Contact HR for clarifications.
Why Vadodara?
Vadodara, Gujarat, is a pharma manufacturing hub with 1,800+ jobs, hosting KLM’s USFDA-approved facility in Horizon Industrial Park. Its connectivity and proximity to Surat (130 km) make it ideal for industrial careers.
Join KLM’s Mission
KLM Laboratories is dedicated to improving lives through innovative healthcare solutions. By joining our Vadodara team, you’ll contribute to USFDA-compliant semi-solid and oral dosage forms for global markets. Attend our walk-in drive on June 22, 2025, or apply online to join our 500+ strong team!
Next Steps
Arrive early for registration on June 22, 2025. The selection process may include technical interviews (e.g., HPLC validation, QMS processes) and document verification. Selected candidates will receive spot offers or follow-up communication.
Contact Us
For queries, email career@klmlab.com, call +91 9227897864, or visit KLM Contact. Stay updated via KLM Careers.
Innovate with KLM
Join KLM Laboratories to advance pharmaceutical innovation in Vadodara. Attend our Walk-in Drive on June 22, 2025, and contribute to global healthcare!
