Abryl Laboratories Pvt. Ltd., a rapidly growing pharmaceutical company specializing in injectable formulations, has announced exciting career opportunities for experienced professionals in its Quality Assurance (QA) and Quality Control (QC) departments. The positions are based at the company’s state-of-the-art Injectable Plant located in Dera Bassi, Punjab.

This recruitment drive is an excellent opportunity for candidates with experience in regulated injectable manufacturing facilities operating under USFDA and EU-GMP standards.

Open Positions

1. Quality Assurance (QA) – Validation & Qualifications

Department: Quality Assurance

Section: Validation & Qualifications

Experience: 2–10 Years

Qualification: B.Pharm

The selected candidates will be responsible for validation activities, equipment qualification, process qualification, and ensuring compliance with regulatory guidelines in injectable manufacturing operations.

2. Quality Control (QC)

Department: Quality Control

Section: GLP / RM / FG / PM

Experience: 2–5 Years

Qualification: M.Sc. (Chemistry)

Technical Skills: HPLC, GC

Candidates should possess strong analytical expertise and hands-on experience in handling chromatographic instruments while ensuring compliance with Good Laboratory Practices (GLP).

Preferred Candidate Profile

Abryl Laboratories is seeking professionals who possess:

Experience in injectable regulatory manufacturing facilities

Exposure to USFDA and EU-GMP regulatory requirements

Strong documentation and compliance knowledge

Good analytical and problem-solving skills

Ability to work effectively in a quality-driven environment

Job Location

Dera Bassi, Punjab

How to Apply

Interested candidates can share their updated resumes through the following contact details:

Email: hr.2@abryl.in

WhatsApp: 9882859675

Candidates meeting the eligibility criteria are encouraged to apply at the earliest and become part of a growing pharmaceutical organization committed to quality and innovation.

Technical FAQs

1. What is the importance of Validation and Qualification in pharmaceutical manufacturing?

Validation and Qualification ensure that equipment, systems, utilities, and manufacturing processes consistently produce products meeting predefined quality standards and regulatory requirements.

2. What is the role of HPLC in Quality Control laboratories?

High Performance Liquid Chromatography (HPLC) is used to identify, quantify, and analyze active pharmaceutical ingredients, impurities, and finished products with high accuracy and precision.

3. What is the difference between IQ, OQ, and PQ?

IQ (Installation Qualification): Verifies proper installation of equipment.

OQ (Operational Qualification): Confirms equipment operates according to specifications.

PQ (Performance Qualification): Demonstrates consistent performance under actual operating conditions.

4. Why is experience in USFDA and EU-GMP regulated plants important?

Regulated plants follow stringent quality systems, documentation practices, and compliance standards, preparing professionals to meet international pharmaceutical manufacturing requirements.

5. What is the purpose of GC (Gas Chromatography) in pharmaceutical testing?

Gas Chromatography is primarily used for residual solvent analysis, volatile compound testing, impurity profiling, and ensuring compliance with pharmacopeial standards.