Quality Assurance Job at SAVA Healthcare | Pharma Job Opportunity | Apply Now
Looking for a Quality Assurance Job or a Pharma Job in a rapidly growing pharmaceutical company? SAVA Healthcare is offering an excellent opportunity for the role of Executive – Corporate Quality Assurance in Pune. This Quality Assurance Job is ideal for candidates seeking a Pharma Job with hands-on experience in artwork approval, regulatory compliance, and quality systems.
- Job Title: Executive – Corporate Quality Assurance
- Job Location: Corporate Office, Viman Nagar, Pune
- CTC to be offered: 4 LPA to 6 LPA
About the Company
SAVA Healthcare is amongst the fastest emerging pharmaceutical companies in India with global reach to customers in Canada, Ukraine, the CIS, Asia, Latin America, Africa & FWA. With manufacturing units in Surendranagar, Malur, and in the near future in Indore, it holds various accreditations and produces a wide variety of dosage forms across therapeutic categories.
Their GMP-compliant, state-of-the-art manufacturing facility for Tablet, Oral Dry Powder, Capsule, Nasal sprays, DPIs, Cream, Gel, and Ointment formulations with dedicated manufacturing sections supported by an In-House R&D Center, focuses on Formulation and Analytical Development with an annual turnover of more than 200 crores and a manpower of 500+ employees engaged across locations.
Job Description
- Oversee preparation, approval, and quality control of in-house and third-party artworks
- Ensure compliance with regulatory standards
- Coordinate with cross-functional departments
- Maintain accurate documentation throughout the process
Key Responsibilities
- Prepare and compile AWIF for in-house and third-party artworks
- Coordinate with Medical, Marketing, DRA, Plant, PMT, and TPM teams
- Review artworks and obtain necessary approvals
- Manage customer approvals for foreign language artworks
- Finalize and approve artworks for CDR file release
- Handle printer PDF approvals and shade card approvals
- Conduct pre-dispatch and visual inspections for third-party products
- Review certificates of analysis and coordinate discrepancies
- Support batch release documentation and logistics coordination
- Maintain data, reports, and compliance documents
- Record and manage market complaints
- Coordinate investigation reports with manufacturing plants
- Review and compile reports for resolution
Qualifications and Skills
- Bachelor’s degree in Pharmacy, Chemistry, or related field.
- Proven experience in artwork approval and quality assurance processes.
- Strong knowledge of regulatory requirements for pharmaceutical products.
- Excellent communication and coordination skills.
- Ability to work effectively in a cross-functional team environment.
- Detail-oriented with strong organizational and documentation skills.
