QA Job at SAVA Healthcare | Apply now for the Chemistry Job
Are you looking for a rewarding QA job or a Chemistry job in Pune with strong career growth in the pharmaceutical industry? SAVA Healthcare is hiring an Executive for its Corporate Quality Assurance (CQA) department at the Viman Nagar corporate office. This full-time Quality Assurance job offers the opportunity to work with global markets, manage artwork approvals, ensure regulatory compliance, and contribute to high-quality pharmaceutical manufacturing. If you’re passionate about quality systems, documentation, and cross-functional coordination, this role is an excellent step forward in your QA career.
About the Company
SAVA Healthcare is a rapidly growing Indian pharmaceutical company with an international footprint across Canada, Europe, Asia, Africa, and Latin America. Known for its strong commitment to quality, ethics, and innovation, SAVA operates GMP-compliant, state-of-the-art manufacturing facilities and robust in-house R&D centers specializing in formulation and analytical development. With an annual turnover exceeding 200 crores and a workforce of 500+ employees, SAVA Healthcare continues to expand globally. For individuals seeking meaningful growth in a QA job, Quality Assurance job, or Chemistry job in Pune, SAVA offers a dynamic, collaborative, and future-ready workplace.
Job Details
- Job Title: Executive – Corporate Quality Assurance
- Location: Corporate Office, Viman Nagar, Pune
- CTC to be offered: 4 LPA to 6 LPA
- Experience: 2 to 4 Years
Job Overview:
We are looking for a detail-oriented and organized Executive – Corporate Quality Assurance to manage artwork preparation, approval processes, batch release activities, and documentation for both in-house and third-party manufacturing. This role is perfect for professionals building a long-term career in QA jobs and pharmaceutical quality systems.
Key Responsibilities:
Preparation & Approval of In-house Artworks:
- Review and compile Artwork Information Form (AWIF) for artwork development (Domestic/Export commercial/Registration dossier/Domestic tender).
- Coordinate with the Medical department for leaflet requirements and updates.
- Conduct initial review of developed artwork.
- Obtain necessary approvals from Marketing, Medical, DRA, Plant, PMT, and other relevant departments.
- Follow up with Marketing for customer approval on foreign language artworks.
- Final review and approval of artwork for CDR file release.
- Coordinate with the purchase department for the printer’s PDF approval.
Preparation & Approval of Third-Party Manufacturing Artworks:
- Review and compile AWIF for third-party manufacturing artworks.
- Liaise with the Contract Manufacturing Division (CMD) for mock-up size requirements.
- Coordinate with Medical for leaflet needs.
- Conduct initial artwork review.
- Obtain necessary approvals from Marketing, Medical, DRA, Plant, PMT, TPM, and other relevant departments.
- Coordinate the customer approval process for foreign language artworks.
- Final review and approval of artwork for CDR file release.
- Manage shade card approvals and maintain artwork status.
Batch Releases for Third-Party Manufacturing Products:
- Conduct pre-dispatch inspections for third-party manufacturing products.
- Perform visual inspections of received samples.
- Review certificates of analysis and FP reports.
- Coordinate with TPM for sample or report discrepancies.
- Prepare and review certificates of analysis when applicable.
- Coordinate with logistics for the certificate of analysis for batch release.
- Maintain data for third-party release and manufacturing products.
- Manage TPM-related reports and compliance documents.
Handling of Market Complaints for Third-Party Manufacturing Unit:
- Record and document complaints received from marketing.
- Coordinate with manufacturing plants for investigation reports.
- Review and compile investigation 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.
