Job Description

Position Overview:

We are looking for a dedicated and detail-oriented

QC Officer

to join our

office-based Quality Control team

. This role is focused on

documentation, review, and coordination activities

, without involvement in laboratory testing. The QC Officer will play a key role in maintaining the integrity of quality systems and supporting regulatory and quality assurance functions.

Key Responsibilities:

Document Review & Preparation:

Prepare and review key quality documents such as: ST/MoA (Specifications and Methods of Analysis) AMV (Analytical Method Validation documents) Finished Product Specifications Certificate of Analysis (CoA) Stability protocols and reports Other documents

Validation Support:

Draft and review validation protocols and reports in alignment with applicable guidelines and internal SOPs.

Quality Standards Oversight:

Establish and review specifications for finished products and APIs in accordance with regulatory and internal quality standards.

Regulatory Support:

Assist the Regulatory Affairs team with documentation for submissions, audits, and query responses.

Quality System Awareness:

Apply knowledge of QA principles, including: CAPA (Corrective and Preventive Actions) Change Control Deviation handling and documentation

Audit Participation:

Support internal and external audits (regulatory or customer) through documentation readiness and audit coordination.

Cross-functional Support:

Provide assistance on any quality-related assignments or projects as directed by QC leadership.

Qualifications & Skills:

Education:

Bachelor's or Master's degree in Pharmacy, Chemistry, or related field.

Experience:

2-5 years in a QC documentation or compliance role within the pharmaceutical or healthcare industry.

Skills Required:

Strong understanding of GMP, ICH, and regulatory requirements Proficient in preparing and reviewing quality documents Knowledge of QA concepts such as CAPA and audit management Excellent organizational and communication skills Attention to detail and commitment to compliance

Work Environment:

This is a

non-laboratory, office-based position

. Collaboration with QA, Regulatory Affairs, and other departments is essential. Some participation in plant visits or audits may be required, but routine lab work is

not part of this role

.
Job Types: Full-time, Permanent

Pay: ?20,000.00 - ?35,000.00 per month

Schedule:

Day shift
Ability to commute/relocate:

Ahmedabad, Gujarat: Reliably commute or planning to relocate before starting work (Required)
Education:

Bachelor's (Required)
Experience:

Quality control: 2 years (Required) Pharmaceutical manufacturing : 1 year (Preferred)
Willingness to travel:

25% (Preferred)
Work Location: In person

Application Deadline: 18/07/2025