India's DMPLOI - Jobs & Networking AppSymbio Generics has announced exciting career opportunities at VPL Chemicals, Dabaspet for experienced pharmaceutical professionals in Quality Control (QC), Quality Assurance (QA), and Production departments. Candidates with relevant experience in API Pharma manufacturing and quality functions are invited to apply for multiple positions ranging from Executive to Assistant Manager levels.
This recruitment drive is an excellent opportunity for professionals seeking career growth in the pharmaceutical API industry.
Company Overview
Company Name: Symbio Generics
Work Location: VPL Chemicals, Dabaspet
Industry: Pharmaceutical API Manufacturing
Symbio Generics is known for its commitment to quality, compliance, and innovation in pharmaceutical manufacturing. The company offers a professional work environment with opportunities for learning and career advancement.
Job Details
Particulars Details
Company Name
Symbio Generics
Location
VPL Chemicals, Dabaspet
Departments
QC, QA, Production
Positions
Executive, Senior Executive, Assistant Manager, Deputy Manager, Junior Executive
Experience
2–10 Years
Qualification
Diploma, B.Pharm, M.Sc, M.Pharm or relevant qualification
Industry
API Pharma
Department-wise Open Positions
Quality Control (QC)
1. Executive – API Pharma
Experience: Relevant API QC experience
2. Senior Executive – API Pharma
Experience: API Quality Control operations and laboratory activities
3. Assistant Manager – API Pharma
Preferred Exposure: Formulations, especially Pellets & Granules
Quality Assurance (QA)
Assistant Manager – API Pharma
Preferred Exposure: Formulations with experience in Pellets & Granules manufacturing and quality systems.
Production Department
1. Assistant Manager / Deputy Manager – API Production
Requirements:
Currently handling Assistant Manager level responsibilities
Minimum 8–10 years of experience
Strong knowledge of QMS (Quality Management System)
Shop-floor production experience in API manufacturing
2. Junior Executive / Executive – API Production Operators
Requirements:
Experience in API production operations
Knowledge of manufacturing processes and GMP practices
Eligibility Criteria
Educational Qualification
Candidates should possess any of the following:
Diploma
B.Pharm
M.Sc
M.Pharm
Any other relevant qualification suitable for the job role
Experience Required
Minimum: 2 Years
Maximum: 10 Years
Required Technical Skills
For QC Professionals
HPLC Analysis
GC Analysis
Instrument Calibration
Stability Studies
Raw Material & Finished Product Testing
Laboratory Documentation
For QA Professionals
GMP Compliance
QMS Documentation
Change Control
Deviation Management
CAPA Implementation
Audit Handling
For Production Professionals
API Manufacturing Processes
Batch Manufacturing Records (BMR)
Process Monitoring
Equipment Operations
Safety Compliance
Shop-floor Management
How to Apply?
Interested candidates can share their updated CV and referral form through the official recruitment email:
Email ID: careers@symbiogenerics.com
Candidates are advised to mention the department and position applied for in the email subject line.
Example Subject: Application for QC Senior Executive – API Pharma
Why Join Symbio Generics?
Growing pharmaceutical organization
Exposure to API manufacturing operations
Opportunities for leadership roles
Professional and compliance-driven work culture
Career advancement opportunities
Technical FAQs
1. What analytical instruments are commonly used in API Quality Control?
API QC laboratories primarily use HPLC, GC, UV-Visible Spectrophotometers, Dissolution Testers, Karl Fischer Titrators, and analytical balances for testing raw materials, intermediates, and finished products.
2. What is the role of QMS in pharmaceutical manufacturing?
QMS (Quality Management System) ensures that pharmaceutical products consistently meet quality standards through documentation, deviation management, CAPA, change control, and compliance monitoring.
3. What are CAPA and Deviation in QA?
Deviation refers to any departure from approved procedures, while CAPA (Corrective and Preventive Action) is implemented to identify root causes and prevent recurrence of quality issues.
4. Why is GMP important in API production?
Good Manufacturing Practices (GMP) ensure product quality, patient safety, regulatory compliance, proper documentation, and controlled manufacturing processes.
5. What is the significance of HPLC in pharmaceutical QC?
High-Performance Liquid Chromatography (HPLC) is used for assay determination, impurity profiling, content uniformity testing, and stability analysis of pharmaceutical products.
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