Quality Assurance Specialist role at Micro Crispr Pvt. Ltd. | Apply Now
Are you ready to redefine compliance in the life sciences sector? Micro Crispr Pvt. Ltd. is currently offering one of the most dynamic Quality Assurance Jobs in the industry. We are seeking a dedicated Specialist to join our next-generation manufacturing ecosystem. This role stands out among Pharma Jobs by placing you at the exciting intersection of science, strict GMP compliance, and innovation. If you are passionate about ensuring the safety of life-changing therapies through precision, this is the perfect opportunity to advance your career.
- Job Title: Quality Assurance Specialist
- Location: Vapi, Gujarat.
About the Company
Micro Crispr Pvt. Ltd. is building a next-generation manufacturing ecosystem focused on advanced biologics and viral vector platforms. We foster a culture that values scientific rigor and bold thinking, offering employees the opportunity to work on cutting-edge therapeutic platforms. Join us to gain exposure to global quality standards in a high-visibility role that sets the standard for Pharma Jobs in the region.
Key Responsibilities
- Support the implementation and maintenance of the Quality Management System (QMS) in compliance with GMP and regulatory standards.
- Manage the lifecycle of controlled documents, including SOPs, specifications, protocols, and batch records.
- Perform document review to ensure accuracy, completeness, and data integrity.
- Participate in handling deviations, CAPA, change controls, and investigations.
- Assist in preparation for internal and external audits.
- Ensure effective archival and retrieval of quality documents.
- Collaborate with manufacturing, QC, and validation teams to support operational excellence.
- Promote a strong culture of compliance and continuous improvement
Qualifications for Pharma Jobs in QA
Education:
-
M.Pharm / B.Pharm or related discipline.
Experience & Skills:
- 1–5 years of experience in Quality Assurance within biologics, sterile manufacturing, vaccines, or regulated pharmaceutical environments.
- Exposure to GMP documentation practices and regulatory expectations.
- Working knowledge of QMS processes such as deviations, CAPA, and change control is preferred.
- Strong attention to detail with excellent organizational skills.
- Ability to work in a fast-paced, highly regulated environment.
Preferred (but not mandatory):
- Exposure to viral vectors/cell & gene therapy.
- Audit participation.
- Experience in electronic QMS systems.
