Navin Fluorine Quality Control Vacancies Walk In Interview Dewas
Navin Fluorine International Ltd., part of the prestigious Padmanabh Mafatlal Group, is hiring for its Quality Control department at the Dewas facility in Madhya Pradesh. As a premier technology-driven CDMO organization serving top global pharmaceutical clients, Navin Molecular offers exceptional career opportunities in life sciences manufacturing. Read on for complete walk-in interview details and qualifications required.
Navin Fluorine Hiring for below positions
1. Department: Quality Control
Designation: Sr Executive – Quality Control
Experience: 8 – 10 years
Qualification: M. Sc (Chemistry)/ B. Pharma/ M. Pharma
Key skill or job description: The role requires hands-on experience in Quality Control activities, including operation of analytical instruments such as HPLC, GC, UV, KF, and related laboratory equipment. The incumbent should possess sound knowledge of GMP, data integrity, laboratory investigations (OOS/OOT), analytical method validation, documentation practices, and regulatory compliance. Candidates with a strong safety mindset and adherence to safe laboratory practices will be preferred.
2. Department: Quality Control
Designation: Executive – Quality Control
Experience: 6 – 8 years
Qualification: M. Sc (Chemistry)/ B. Pharma/ M. Pharma
Key skill or job description: The role requires hands-on experience in Quality Control activities, including operation of analytical instruments such as HPLC, GC, UV, KF, and related laboratory equipment. The incumbent should possess sound knowledge of GMP, data integrity, laboratory investigations (OOS/OOT), analytical method validation, documentation practices, and regulatory compliance. Candidates with a strong safety mindset and adherence to safe laboratory practices will be preferred.
3. Department: Quality Control
Designation: Sr Officer – Quality Control
Experience: 4 – 6 years
Qualification: M. Sc (Chemistry)/ B. Pharma/ M. Pharma
Key skill or job description: The role requires hands-on experience in Quality Control activities, including operation of analytical instruments such as HPLC, GC, UV, KF, and related laboratory equipment. The incumbent should possess sound knowledge of GMP, data integrity, laboratory investigations (OOS/OOT), analytical method validation, documentation practices, and regulatory compliance. Candidates with a strong safety mindset and adherence to safe laboratory practices will be preferred.
4. Department: Quality Control
Designation: Associate – Quality Control (Off-roll)
Experience: 1 – 2 years
Qualification: B. Sc/ M. Sc (Chemistry)/ B. Pharma
Key skill or job description: Candidates who have successfully completed Apprenticeship training in the Quality Control (QC) function will be preferred for Associate position.
Who Can Apply
Candidates with a background in chemistry or pharmacy holding B.Sc, M.Sc, B.Pharma, or M.Pharma degrees with relevant practical experience in pharmaceutical analytical laboratories and cGMP environments can apply.
Career Growth at Navin Fluorine
Joining Navin Fluorine International Ltd. provides professionals with strong long-term stability and career acceleration. Being part of the legacy Padmanabh Mafatlal Group established in 1967, employees gain extensive hands-on experience with modern CDMO practices, high-end analytical technologies, global regulatory compliance, and a safety-first workplace culture.
Walk In Interview Details
Date: Saturday, September 12, 2026
Time: 10:00 AM to 02:00 PM
Venue: New Industrial Area No. 2, A.B. Road, Dewas, Madhya Pradesh, 455001
If you are unable to attend in person, share your CV directly to the official email address: careers.dewas@navinmolecular.com
Important Notes / Remarks
The role requires hands-on experience in Quality Control activities, including operation of analytical instruments such as HPLC, GC, UV, KF, and related laboratory equipment.
The incumbent should possess sound knowledge of GMP, data integrity, laboratory investigations (OOS/OOT), analytical method validation, documentation practices, and regulatory compliance.
Candidates with a strong safety mindset and adherence to safe laboratory practices will be preferred.
Candidates who have successfully completed Apprenticeship training in the Quality Control (QC) function will be preferred for Associate position.
Frequently Asked Questions
1. What standard original documents should candidates carry during a pharma walk-in interview?
Candidates are generally advised to carry updated hard-copy resumes, recent passport-size photographs, last 3 months’ pay slips, appointment letters, and photo ID proofs.
2. What is the distinction between contract manufacturing CDMO services and standard API manufacturing?
CDMO (Contract Development and Manufacturing Organization) partners focus on specialized custom synthesis and complex molecule development for global innovator clients, unlike generic bulk drug manufacturing.
3. Why are GMP and data integrity guidelines critical in analytical chemistry laboratories?
Good Manufacturing Practices and strict data integrity ensure product safety, complete traceability, accurate laboratory testing records, and international regulatory compliance for clinical-grade pharmaceuticals.
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| Navin Fluorine Quality Control Walk In Interview at Dewas |