Key Responsibilities

a. Responsible for issuance of BPCRs/ECRs, Protocols, Seal, Formats, Registers/Logbooks/ Bound books, Controlled / Uncontrolled copy, Controlled /Display copy of SOP, Numbering of Qualification.(IQ/OQ/PQ/RQ/DQ/URS/SAT).

b. Responsible for tracking, updating and handling of all master documents like BPCRs, ECRs, SOPs, reviewing & checking of filled BPCR/ECR, Specification, Document Archival activity.

c. Responsible for review of Raw material, Packing material, in-process, intermediate, finish, cleaning specification & test method for master after approval.

d. Responsible for master, issuance, tracking and retrieval of SOPs to all departments.

Qualification and Experiences

a. Masters in Science (Chemistry)

b. Minimum 0-1 year of work experience from pharma, preferably in quality assurance workplace

c.



Knowledge and Experience in US FDA approval, GMP compliance.

Competencies / Skills

a. Ability to work under pressure to meet specific timelines & targets

b. Strong analytical skills

c. Strong communication and collaboration skill

Job Type: Permanent

Pay: ₹10,051.47 - ₹13,535.13 per month

Benefits:
- Versatile schedule
- Food provided
- Paid sick time
- Paid time off
- Provident Fund

Application Question(s):
- Are you fresher ?
- Where is your current location ?
- Are you ready to work in QA ?
- If selected, How soon you can join ?

Location:
- Vapi, Gujarat (Vapi, Valsad District) (required)

Work Location: In person

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