Abryl Laboratories Hiring QA, QC, and Production

B.Pharm, M.Sc Openings – Abryl Laboratories Injectable Plant, Dera Bassi

Apply for QA, QC, and Production roles at Abryl Laboratories USFDA-approved injectable plant in Dera Bassi. 2–6 years experience required.

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Abryl Laboratories Pvt. Ltd., a USFDA-approved injectable manufacturing company, is inviting experienced professionals to join its Dera Bassi facility. The company seeks skilled individuals in Quality Assurance, Quality Control, and Production departments who have a solid background in sterile injectable manufacturing operations. This is an excellent opportunity for pharma professionals aiming to grow their careers with a reputed, globally compliant organization.

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Company Overview

Abryl Laboratories Pvt. Ltd. is a trusted name in sterile pharmaceutical manufacturing, specializing in injectables for regulated and emerging markets. With its state-of-the-art facility located in Dera Bassi, Abryl operates under strict USFDA, EU-GMP, and WHO regulatory guidelines. The company focuses on quality, innovation, and patient safety—ensuring that every product meets international standards.

Abryl’s manufacturing plant is equipped with advanced production lines, automated filling systems, modern autoclaves, and a strong Quality Management System (QMS). The organization provides a collaborative work environment that encourages technical excellence, continuous learning, and compliance-driven growth.

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Job Role & Responsibilities

Abryl Laboratories is hiring for the following positions:

1. Quality Assurance (QMS)

Department: Quality Assurance
Experience: 4–6 Years
Qualification: B.Pharm

Key Responsibilities:

• Manage and monitor Quality Management System (QMS) processes including deviations, CAPA, and change controls.
• Ensure compliance with cGMP, USFDA, and WHO guidelines.
• Conduct internal audits and support external regulatory inspections.
• Maintain documentation control systems and ensure data integrity.
• Collaborate with production and QC teams to address quality issues promptly.

Preferred Skills:

• Strong knowledge of QMS documentation and investigation management.
• Experience with sterile injectable facilities.

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2. Quality Control (Method Validation)

Department: Quality Control
Section: Analytical / Method Validation
Qualification: M.Sc. (Chemistry)
Experience: 2–4 Years

Key Responsibilities:

• Perform analytical method validation, verification, and transfer activities.
• Operate instruments like HPLC, GC, UV, and Dissolution testers.
• Prepare, review, and maintain test protocols, results, and analytical reports.
• Ensure data integrity and compliance with SOPs, GLP, and cGMP.
• Participate in laboratory investigations and OOS/OOT assessments.

Preferred Skills:

• Hands-on experience with method validation techniques.
• Knowledge of ICH guidelines, analytical documentation, and LIMS systems.

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3. Production (Autoclave / Washing / Filling)

Department: Production
Designation: Officer / Operator
Qualification: B.Pharm / ITI
Experience: 2–4 Years

Key Responsibilities:

• Operate and maintain production equipment such as autoclaves, vial washing machines, and filling systems.
• Monitor sterile manufacturing operations as per batch manufacturing records.
• Follow aseptic techniques and ensure compliance with cGMP requirements.
• Perform line clearance, cleaning validation, and equipment maintenance.
• Maintain documentation and ensure process accuracy during production.

Preferred Skills:

• Knowledge of sterile filling and washing processes.
• Experience in handling injectable production lines.

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Eligibility / Qualifications

Educational Requirements:

• B.Pharm / M.Sc (Chemistry) / ITI (Mechanical, Electrical, or Production)

Experience:

• 2–6 years of relevant experience in sterile injectable manufacturing, QA, or QC.

Preferred Industry:

• Injectable / Sterile Manufacturing Facilities approved by USFDA, EU-GMP, or WHO.

Relevant Courses (comma-separated):
B.Pharm, M.Pharm, M.Sc Chemistry, ITI (Mechanical/Electrical), PG Diploma in Pharmaceutical Quality Assurance, Certificate in GMP Compliance, Certificate in Analytical Method Validation, Diploma in Sterile Production Operations

Key Attributes:

• Strong knowledge of cGMP documentation and regulatory compliance.
• Willingness to work in a dynamic, fast-paced manufacturing setup.
• Excellent teamwork and problem-solving skills.

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Location & Salary

Work Location: Dera Bassi, Punjab
Employment Type: Full-time
Compensation: Competitive salary based on experience and qualification.
Work Environment: Regulated injectable facility with advanced technology and safety compliance.

Abryl Laboratories offers attractive benefits, employee development programs, and opportunities for career advancement within a growing organization.

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Application Process

How to Apply:
Interested candidates can apply via email or WhatsApp:

• Email: hr.2@abryl.in
• WhatsApp: 98828 59675

Application Format:

• Subject Line: Application for [Department/Section]
• Attach: Updated resume, academic credentials, and experience certificates.

Note: Only candidates with prior experience in Injectable Manufacturing Plants will be considered.

Selection Process:

1. Resume screening based on qualifications and experience.
2. Technical interview with department leads.
3. Final HR round and offer negotiation.

Apply early — shortlisted candidates will be contacted on a rolling basis.

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Why Join Abryl Laboratories

• Opportunity to work in a USFDA-approved injectable facility.
• Exposure to global regulatory environments and compliance standards.
• Continuous skill development and training programs.
• Collaborative culture with emphasis on innovation and safety.
• Competitive pay, benefits, and long-term career prospects.

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FAQs

Q1. What departments are open for recruitment at Abryl Laboratories?
A1. Openings are available in Quality Assurance, Quality Control, and Production departments.

Q2. What qualifications are required?
A2. B.Pharm, M.Sc (Chemistry), or ITI in relevant fields.

Q3. Is injectable experience mandatory?
A3. Yes, prior experience in sterile injectable manufacturing is required.

Q4. What is the work location?
A4. The positions are based at Abryl Laboratories’ facility in Dera Bassi, Punjab.

Q5. Can candidates apply via WhatsApp?
A5. Yes, candidates can apply directly by sending their CV via WhatsApp to 98828 59675.

Q6. Is this opportunity open to freshers?
A6. No, this is for professionals with 2–6 years of experience in the pharma injectable domain.

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Company	Abryl Laboratories Pvt. Ltd.
Vacancies	QA (QMS), QC (Method Validation), Production (Autoclave/Washing/Filling)
Required Education	B.Pharm, M.Sc (Chemistry), ITI
Experience	2–6 Years
Work Location	Dera Bassi, Punjab