Global Calcium Pvt. Ltd. is inviting applications for the position of IPQA (In-Process Quality Assurance) at its Unit-III pharmaceutical manufacturing facility. This opportunity is ideal for professionals with 1–4 years of experience in pharmaceutical quality assurance, particularly those with hands-on exposure to in-process quality monitoring, GMP compliance, and batch documentation.
The company is looking for detail-oriented candidates who can ensure strict adherence to GMP guidelines, documentation standards, and manufacturing quality controls within pharmaceutical production lines.
Working in IPQA provides an excellent opportunity to contribute directly to product quality, regulatory compliance, and manufacturing efficiency within a growing pharmaceutical organization.
Job Overview
Company: Global Calcium Pvt. Ltd.
Department: Quality Assurance – IPQA
Industry: Pharmaceutical Manufacturing
Experience Required: 1–4 Years
Location: India
Application Mode: Email / WhatsApp
Key Responsibilities
As an IPQA professional, the selected candidate will be responsible for ensuring quality compliance during manufacturing operations.
Key responsibilities include:
Performing in-process line clearance before starting manufacturing and packaging operations
Monitoring manufacturing processes to ensure GMP compliance
Issuing and controlling Batch Manufacturing Records (BMR) and Batch Packing Records (BPR)
Reviewing BMR and BPR documentation for accuracy and compliance
Conducting in-process quality checks during production stages
Handling deviations, documentation corrections, and quality observations
Supporting quality teams in maintaining regulatory and internal quality standards
Required Qualifications
Candidates applying for the IPQA role should meet the following requirements:
1–4 years of experience in pharmaceutical manufacturing quality assurance
Hands-on experience in IPQA activities within pharma plants
Knowledge of BMR/BPR documentation systems
Understanding of GMP guidelines and regulatory requirements
Strong documentation and communication skills
Ability to monitor manufacturing lines and maintain quality compliance
Educational qualification typically preferred:
B.Pharm / M.Pharm / BSc / MSc (Chemistry or related field)
Salary and Benefits
The salary for this role depends on experience, technical expertise, and company policies.
Typical expected compensation includes:
Estimated Salary Range: ₹2.8 LPA – ₹5 LPA
Opportunity to work in a regulated pharmaceutical manufacturing environment
Exposure to quality assurance systems and GMP practices
Career growth opportunities within the QA and compliance domain
How to Apply
Interested and eligible candidates can apply by sharing their updated resume using the contact details below.
Email: suganya@globalcalciumpharma.in
WhatsApp: 9843444102
Applicants are encouraged to apply early and share this opportunity with other professionals who may be interested in pharmaceutical quality assurance roles.