KLM Laboratories Hiring Production Officers
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities:
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Why Join KLM Laboratories?
- FAQs
- Job Summary Table
Production Officer (B.Pharm/M.Pharm) | KLM Laboratories | Vadodara
KLM Laboratories hiring Production Officers (B.Pharm/M.Pharm/M.Sc) with 2–5 yrs experience at Vadodara, Gujarat.
KLM Laboratories Pvt. Ltd., a reputed pharmaceutical manufacturing company in Vadodara, invites qualified professionals to join its Production Department as Production Officers. The role offers an opportunity to work in a state-of-the-art pharmaceutical setup that adheres to stringent regulatory standards while ensuring consistent product quality and operational excellence.
Company Overview
KLM Laboratories Pvt. Ltd. is a trusted pharmaceutical organization dedicated to manufacturing high-quality formulations compliant with global standards such as WHO-GMP, USFDA, and MHRA. With a strong focus on innovation, safety, and quality, KLM Laboratories continues to expand its product portfolio across therapeutic segments while ensuring compliance with international regulatory requirements.
Our Vadodara facility is equipped with modern production infrastructure designed for efficiency, safety, and sustainability. Employees at KLM enjoy a professional environment that encourages continuous learning, teamwork, and growth.
Job Role & Responsibilities
Designation: Officer
Department: Production
Experience: 2 to 5 Years
Qualification: B.Pharm / M.Pharm / M.Sc
Location: Vadodara, Gujarat
Key Responsibilities:
- Perform on-line documentation of all production activities in Batch Manufacturing Records (BMR) and logbooks.
- Conduct calibration and daily verification of weighing balances as per the standard schedule.
- Ensure that equipment and production areas are cleaned and operated in accordance with approved Standard Operating Procedures (SOPs).
- Obtain line clearance from Quality Assurance (QA) prior to initiating operations.
- Allocate work to operators and workmen as per the daily or batch production plan.
- Monitor and ensure temperature and humidity controls within specified limits during production processes.
- Conduct in-process checks at various intermediate stages of batch manufacturing and filling.
- Initiate and document online rejections, deviations, incidents, and change controls as per quality standards.
- Oversee validation batches, ensuring compliance with established protocols.
- Maintain production areas in compliance with regulatory audit requirements (e.g., USFDA, WHO-GMP, MHRA).
- Follow all labeling procedures for areas, equipment, and products.
- Manage receipt and verification of dispensed raw materials from the warehouse.
- Coordinate with Quality Control (QC) for timely product release.
- Verify and ensure product yield after each manufacturing stage as per batch records.
Note: The above duties are indicative and not exhaustive. The company reserves the right to modify responsibilities based on operational needs.
Eligibility / Qualifications
Educational Requirements:
- B.Pharm, M.Pharm, or M.Sc in Pharmaceutical Sciences, Chemistry, or related disciplines.
Experience:
- 2 to 5 years of relevant experience in pharmaceutical production operations (OSD, liquids, injectables, or other dosage forms).
Relevant Courses (comma-separated): B.Pharmacy, M.Pharmacy, Industrial Pharmacy, Pharmaceutical Technology, Process Validation, Quality Management Systems, GMP Documentation.
Skill Requirements:
- Strong understanding of cGMP and documentation practices.
- Knowledge of manufacturing equipment and process validation requirements.
- Ability to work efficiently in a regulated production environment.
- Good communication and teamwork skills for coordination with QA, QC, and other departments.
Location & Salary
Job Location: Vadodara, Gujarat
Employment Type: Full-time, Permanent
Salary: Commensurate with experience and industry standards
Working Environment: WHO-GMP and USFDA-compliant facility with strong safety and compliance culture.
Application Process
Interested candidates meeting the above criteria can apply by sharing their resume to:
Email: career@klmlab.com
Please include “Application – Production Officer (Vadodara)” in the subject line and attach your latest CV with details of education, work experience, and current CTC.
Why Join KLM Laboratories?
- Opportunity to work in a globally compliant manufacturing facility with exposure to multiple dosage forms.
- Learn and grow under the guidance of experienced pharmaceutical professionals.
- Collaborative work environment fostering quality, safety, and innovation.
- Regular training and skill development programs aligned with Good Manufacturing Practices (GMP).
- Competitive compensation and growth-oriented career path.
FAQs
1. What qualifications are required for this role?
Candidates with B.Pharm, M.Pharm, or M.Sc degrees in pharmaceutical or chemical sciences are eligible.
2. What experience is preferred?
Applicants should have 2 to 5 years of hands-on experience in pharmaceutical production, preferably in a regulated facility.
3. Is experience with GMP documentation mandatory?
Yes, knowledge of Good Manufacturing Practices (GMP) and documentation standards is essential.
4. Where is the job located?
The role is based at Vadodara, Gujarat in KLM Laboratories’ manufacturing facility.
5. How do I apply?
Send your updated resume to career@klmlab.com with the subject line “Production Officer Application – Vadodara.”
Job Summary Table
| Category | Details |
|---|---|
| Company | KLM Laboratories Pvt. Ltd. |
| Vacancies | Production Officer |
| Required Education | B.Pharm / M.Pharm / M.Sc |
| Experience | 2–5 Years |
| Location | Vadodara, Gujarat |
| career@klmlab.com | |
| Department | Production |
To apply for this job please visit Vadodara,%20Gujarat.
