Avencia Molecules has announced an excellent hiring opportunity for candidates seeking Pharmaceutical Quality Control Jobs, Production Chemist roles, and Quality Assurance careers in Gujarat. The company is recruiting for 13 vacancies across Quality Control, Production, and Quality Assurance departments at its Panoli, Ankleshwar facility. Both freshers and experienced professionals are invited to apply.
This recruitment drive offers a promising opportunity for B.Sc, M.Sc, B.Pharm, M.Pharm, and Life Sciences graduates who want to build a career in pharmaceutical manufacturing, quality systems, GMP compliance, and production operations.
Company Overview
Avencia Molecules is a pharmaceutical manufacturing company located in GIDC Estate, Panoli, Ankleshwar, Gujarat. The company focuses on quality-driven manufacturing practices and provides career opportunities for professionals interested in pharmaceutical production, quality assurance, and quality control functions.
Ankleshwar is one of India’s leading pharmaceutical and chemical manufacturing hubs, making it an attractive destination for professionals seeking long-term growth in the pharma sector.
Job Highlights
Company Name: Avencia Molecules
Location: Panoli, Ankleshwar, Gujarat
Industry: Pharmaceutical Manufacturing
Experience: Freshers and Experienced Candidates
Total Openings: 13
Employment Type: Full-Time
Available Positions
QC Chemist – 4 Vacancies (Male)
Production Chemist – 5 Vacancies
QA Officer – 4 Vacancies (2 Male, 2 Female)
Total Vacancies: 13
Eligibility Criteria
Candidates with the following qualifications are encouraged to apply:
• B.Sc Chemistry
• M.Sc Chemistry
• B.Pharm
• M.Pharm
• Life Sciences Graduates
• Pharmaceutical Chemistry Graduates
• Analytical Chemistry Graduates
• Industrial Chemistry Graduates
Experience Requirement
• Freshers Eligible
• Experienced Candidates Eligible
Quality Control Chemist – Roles & Responsibilities
Quality Control professionals are responsible for ensuring pharmaceutical products meet quality standards before release.
Key Responsibilities
• Conduct routine laboratory testing and analysis
• Perform testing of raw materials and finished products
• Maintain analytical records and laboratory documentation
• Follow GLP and GMP guidelines
• Support investigations related to deviations and quality issues
• Ensure accurate recording of test results
• Participate in continuous quality improvement initiatives
Required Skills
• Laboratory Testing
• Chemical Analysis
• GMP Compliance
• Documentation Practices
• Quality Systems Knowledge
Production Chemist – Roles & Responsibilities
Production Chemists play a critical role in pharmaceutical manufacturing and batch execution.
Key Responsibilities
• Monitor manufacturing and production activities
• Ensure compliance with standard operating procedures
• Maintain production records and batch documentation
• Support process optimization initiatives
• Coordinate with QA and QC teams
• Follow GMP and safety requirements
• Assist in resolving production-related issues
Required Skills
• Pharmaceutical Manufacturing
• Batch Processing
• Production Documentation
• Process Monitoring
• GMP Compliance
Quality Assurance Officer – Roles & Responsibilities
Quality Assurance professionals ensure compliance with pharmaceutical quality systems and regulatory standards.
Key Responsibilities
• Review manufacturing and quality documents
• Monitor adherence to GMP requirements
• Conduct in-process quality checks
• Support audit and compliance activities
• Participate in deviation investigations and CAPA implementation
• Maintain quality documentation and records
• Ensure compliance with quality management systems
Required Skills
• Quality Assurance Systems
• GMP Documentation
• Compliance Management
• Audit Support
• CAPA Activities
• Quality Monitoring
Salary and Benefits
Expected Salary Range
• Freshers: ₹2.2 LPA – ₹3.5 LPA
• Experienced Candidates: ₹3.5 LPA – ₹6.5 LPA
Additional Benefits
• Opportunity to work in a GMP-regulated environment
• Exposure to pharmaceutical manufacturing operations
• Career growth opportunities
• Learning and development in quality systems
• Hands-on experience with industry-standard practices
Why Candidates Should Apply
This hiring drive is particularly attractive because it welcomes freshers along with experienced professionals. Candidates will gain valuable exposure to:
• Pharmaceutical manufacturing operations
• Quality control laboratory practices
• GMP documentation and compliance
• Quality assurance systems
• Regulatory requirements
• Production management processes
How to Apply
Interested candidates can send their updated resume directly to the company.
Email ID: hr@avenciamolecules.com
Contact Number: +91 6359440444
Application Location
Plot No. 3505, GIDC Estate, Panoli, Ankleshwar, Gujarat – 394116
