Senior Associate

Avani Consulting; Mysuru; In loco; INR 500.000 - 800.000; Tempo pieno

Descrizione del lavoro

Avani Consulting in Mysuru (Nanjangud) is seeking an Associate / Sr. Associate Quality Assurance with 7-9 years of pharmaceutical QA experience to join our team.

Key responsibilities include IPQA activities on the shop floor, reviewing GMP documentation and batch records, approving BCR/ECR, ensuring line clearance for manufacturing and packing, and supporting QA release of finished products. The role requires strong QA and regulatory discipline.

Competenze

• 7-9 years of experience in pharmaceutical QA.
• Experience with IPQA, GMP documentation, and batch records.
• Knowledge of deviations, CAPA, change controls, and regulatory data integrity.

Mansioni

• Handle IPQA activities and shop-floor QA monitoring.
• Review GMP documentation and batch-related records.
• Review/approve BCR/ECR and cleaning validation documents.
• Perform Line Clearance for manufacturing and packing operations.
• Review BMR/BPR and support QA release of finished products.
• Review/approve IQ, OQ and PQ documentation.
• Prepare, revise and manage SOPs and QMS documents.
• Participate in internal audits, self-inspections and compliance activities.
• Handle Deviations, Change Controls and CAPA.

Conoscenze

IPQA

GMP docs

BMR/BPR

Line clearance

IQ/OQ/PQ

SOPs & QMS

Internal audits

Deviations & CAPA

Data integrity

cGMP compliance

LMS administration

Formazione

MSc Chemistry

Life Sciences

B.Pharm

M.Pharm

D.Pharm

Strumenti

LMS administration

Descrizione del lavoro

Hiring: Associate / Sr. Associate Quality Assurance (QA) - Only Male Candidates

Experience: 7 - 9 years of relevant experience in Pharmaceutical Quality Assurance.

Location: Mysuru (Nanjangud)

Educational Qualification:

M.Sc. Chemistry / Life Sciences

B.Pharm / M.Pharm / D.Pharm

CTC: 5 - 8 LPA

Key Responsibilities:

• Handle In-Process Quality Assurance (IPQA) activities and shop-floor QA monitoring.
• Review GMP documentation and batch-related records.
• Review and approve BCR/ECR and cleaning validation documents.
• Perform Line Clearance for manufacturing and packing operations.
• Review BMR/BPR.
• Support QA release of finished products.
• Review/approve IQ, OQ and PQ documentation.
• Prepare, revise and manage SOPs and QMS documents.
• Participate in internal audits, self-inspections and compliance activities.
• Handle/support Deviations, Change Controls and CAPA.
• Knowledge of LMS administration, regulatory requirements, data integrity and cGMP compliance will be an added advantage.