India's DMPLOI - Jobs & Networking AppSynthimed Labs Private Limited has announced a Walk-in Interview Drive for Freshers and Experienced professionals in multiple departments, including Production, Quality Control (QC), DRA, and Engineering. Candidates with qualifications such as M.Pharm, M.Sc, B.Sc, Diploma in Chemical Engineering, and ITI are invited to attend the interview.
This recruitment drive offers excellent career opportunities in the pharmaceutical API manufacturing industry.
Overview
Particulars Details
Company Name
Synthimed Labs Private Limited
Job Type
Walk-in Interview
Industry
Pharmaceutical (API Manufacturing)
Interview Date
24 July 2026 (Friday)
Interview Time
09:00 AM to 03:00 PM
Job Location
Derabassi, Punjab
Selection Mode
Walk-in Interview
Walk-in Interview Details
Venue:
Synthimed Labs Private Limited
Vill Bhagwanpur, Barwala Road,
Derabassi, Punjab
Date: 24 July 2026 (Friday)
Time: 09:00 AM to 03:00 PM
Documents Required
Candidates should carry:
Updated Resume/CV
Passport-size Photograph
Original Educational Certificates
Experience Certificates (if applicable)
Government Photo ID Proof
Job Openings
1. Executive – DRA
Department: DRA
Qualification:
M.Pharm
M.Sc
Experience:
3–5 Years
Required Skills:
Hands-on experience in API regulatory submissions
Documentation
Regulatory compliance
2. Trainee Associate – Production
Department: Production
Qualification:
B.Sc
Experience:
Freshers
Required Skills:
API Manufacturing
Production operations
GMP awareness
3. Assistant Officer / Officer – Production
Department: Production
Qualification:
B.Sc
Diploma in Chemical Engineering
Experience:
1–4 Years
Required Skills:
API Manufacturing
Chemical Manufacturing
Process handling
4. Assistant Officer / Officer – Quality Control
Department: Quality Control
Qualification:
B.Sc
M.Sc
Experience:
1–4 Years
Required Skills:
HPLC
Gas Chromatography (GC)
Wet Laboratory Testing
Raw Material Analysis
5. NAPS Trainee – Engineering
Department: Engineering
Qualification:
ITI
Experience:
Freshers
Required Skills:
Electrical Maintenance
Mechanical Maintenance
RAC (Refrigeration & Air Conditioning)
Candidate Preference
Candidates having API manufacturing background will be given preference.
Synthimed Labs is an Equal Opportunity Employer and actively encourages female candidates to apply.
Why Join Synthimed Labs?
Professional career growth
Collaborative work environment
Comprehensive employee benefits
Learning and development opportunities
Exposure to API pharmaceutical manufacturing
Stable career with a growing pharmaceutical company
Selection Process
Walk-in Registration
Document Verification
Technical Interview
HR Interview
Final Selection
Technical Skills Expected
Depending on the role, candidates should have knowledge of:
API Manufacturing
Good Manufacturing Practices (GMP)
Regulatory Affairs (DRA)
HPLC Operation
Gas Chromatography (GC)
Wet Laboratory Testing
Chemical Process Manufacturing
Engineering Maintenance
Documentation Practices
Quality Management Systems (QMS)
Tips for Candidates
Reach the venue before reporting time.
Carry all original documents and photocopies.
Wear formal attire.
Revise technical concepts related to your department.
Be prepared to explain your academic projects or previous work experience.
Conclusion
The Synthimed Labs Walk-in Interview 2026 is a valuable opportunity for both freshers and experienced candidates seeking careers in the pharmaceutical sector. With openings across Production, Quality Control, DRA, and Engineering, eligible candidates are encouraged to attend the interview with all required documents.
Technical FAQs
1. What is API manufacturing in the pharmaceutical industry?
API (Active Pharmaceutical Ingredient) manufacturing involves producing the active chemical substance responsible for the therapeutic effect of a medicine under strict GMP and quality standards.
2. What is HPLC and why is it important in Quality Control?
High-Performance Liquid Chromatography (HPLC) is an analytical technique used to identify, quantify, and verify the purity of pharmaceutical products and raw materials.
3. What does a DRA Executive do?
A Drug Regulatory Affairs (DRA) Executive prepares and submits regulatory documents, ensures compliance with national and international guidelines, and supports product registrations.
4. What is GMP in pharmaceutical manufacturing?
Good Manufacturing Practices (GMP) are quality guidelines that ensure medicines are consistently manufactured, tested, and controlled according to regulatory standards.
5. What technical knowledge should a Production candidate possess?
Production candidates should understand API manufacturing processes, SOPs, GMP, batch manufacturing records (BMR), equipment operation, safety procedures, and process documentation.
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