Abryl Laboratories Hiring Production & QC Managers
- Company Overview
- Job Role & Responsibilities
- Production — Manufacturing / Filling (Manager / Dy. Manager)
- Quality Control — FG / AMV / GLP / QMS (Manager / Dy. Manager)
- PPIC — Production Planning & Inventory Control (Officer to Executive)
- AM/DM — Administration / Management (Any Graduate)
- Eligibility / Qualifications
- Location & Salary
- Application Process
- FAQs
- Summary Table
B.Pharm/M.Pharm Production & QC Managers | Dera Bassi
Abryl Laboratories hiring B.Pharm/M.Pharm for Production, QC, PPIC and AM/DM roles at Dera Bassi. Injectable experience required.
Abryl Laboratories (USFDA approved) is expanding its injectable manufacturing site at Dera Bassi and hiring senior and mid-level professionals across Production, Quality Control, PPIC and Administration. This is a targeted hiring drive for candidates with injectable and regulated‑market exposure (USFDA, EU‑GMP, MHRA) who can lead manufacturing, ensure product quality, and strengthen compliance systems.
Company Overview
Abryl Laboratories Pvt. Ltd. operates a USFDA‑approved injectable facility focused on sterile injectables and high‑quality formulation manufacturing. The company emphasizes regulatory compliance, robust quality systems, and continuous improvement. Working at Abryl gives professionals exposure to injectable processing, regulatory inspections, and opportunities to drive manufacturing excellence in a growing plant.
Job Role & Responsibilities
Production — Manufacturing / Filling (Manager / Dy. Manager)
Qualification: B.Pharm / M.Pharm
Experience: 12–15 years
- Lead sterile injectable manufacturing and filling operations.
- Ensure batch execution, line qualification, and aseptic controls.
- Drive adherence to GMP, SOPs and contamination control.
- Manage shift teams, production planning, and equipment readiness.
- Coordinate with QA/QC/Engineering for tech transfers and CAPA implementation.
Quality Control — FG / AMV / GLP / QMS (Manager / Dy. Manager)
Qualification: B.Pharm / M.Pharm
Experience: 12–15 years
- Oversee finished‑goods release, analytical method verification (AMV) and GLP practices.
- Maintain QMS modules: deviations, OOS/OOT investigations, change control, CAPA.
- Lead audit readiness for USFDA/EU‑GMP/MHRA inspections.
- Ensure laboratory compliance, instrument qualification, and data integrity (ALCOA+).
PPIC — Production Planning & Inventory Control (Officer to Executive)
Qualification: M.Sc / B.Pharm
Experience: 2–6 years
- Manage production scheduling, material availability and inventory control.
- Coordinate with procurement, warehouse and production to avoid shortages.
- Maintain online production records and MRN/GRN documentation.
AM/DM — Administration / Management (Any Graduate)
Qualification: Any Graduate
Experience: 8–14 years
- Handle administrative and managerial responsibilities across plant functions.
- Support regulatory documentation, vendor management, and HR coordination.
Eligibility / Qualifications
- Mandatory: Experience in injectable manufacturing and regulatory exposure (USFDA, EU‑GMP, MHRA).
- Educational requirements as per role: B.Pharm, M.Pharm, M.Sc or relevant graduate degree.
- Proven track record in sterile production, quality systems, or planning for regulated markets.
Relevant courses: B.Pharm, M.Pharm (Pharmaceutics/QA), M.Sc (Pharmaceutical Chemistry / Life Sciences), Diploma in Industrial Pharmacy, Certification in Sterile Manufacturing, QMS & Regulatory Affairs courses.
Location & Salary
- Location: Dera Bassi (Chandigarh) – Abryl Laboratories Pvt. Ltd.
- Salary: Competitive; aligned to seniority and regulatory expertise. Specifics will be discussed during the hiring process.
Application Process
Send your updated CV and a brief cover note highlighting injectable and regulatory inspection exposure to:
- Email: hr.2@abryl.in
- Contact: 9882859675
When applying, mention:
- Role you are applying for
- Total experience and years in injectable operations
- Specific exposure to USFDA / EU‑GMP / MHRA inspections
FAQs
Q1. Are only candidates with USFDA exposure considered?
Candidates without regulatory exposure may be considered for some roles, but USFDA/EU‑GMP/MHRA experience is mandatory for senior Production and QC managerial positions.
Q2. What documents should I share?
Send an updated CV. During interviews, be ready to present experience certificates, inspection/audit involvement proof, and educational documents.
Q3. Is relocation support available?
Relocation and compensation details will be shared during the hiring process based on seniority.
Q4. What is the interview process?
Shortlisted candidates will be contacted for HR screening followed by technical and managerial rounds.
Q5. Can mid‑level candidates apply for managerial roles?
Managerial roles require demonstrated leadership in injectable manufacturing; mid‑level candidates may be considered for Dy. Manager / Executive positions.
Summary Table
| Category | Details |
|---|---|
| Company | Abryl Laboratories Pvt. Ltd. (USFDA approved) |
| Vacancies | Production (Manager/Dy.Manager), QC (Manager/Dy.Manager), PPIC (Officer/Executive), AM/DM (Admin/Manager) |
| Required Education | B.Pharm, M.Pharm, M.Sc, Any Graduate |
| Experience | 2–15 years depending on the role; 12–15 yrs for senior Production/QC |

To apply for this job email your details to hr.2@abryl.in