Farbëfirma Hiring Production, QA, QC, RA, Engineering and more
- Company Overview
- Job Role & Responsibilities
- Production
- Packing
- Quality Assurance (QA)
- Quality Control (QC)
- Regulatory Affairs (RA)
- Engineering
- Store / Inventory
- Pharmacovigilance
- Human Resources (HR)
- Purchase
- Accounts
- Eligibility / Qualifications
- Experience Requirements
- Location & Salary
- Application Process
- FAQs
- Who can apply for these openings?
- Are freshers eligible?
- Which departments are hiring?
- What is the job location?
- How should I apply?
- Summary Table
Injectable Pharma Openings for Experienced Candidates | Ankleshwar
Multiple injectable manufacturing vacancies in Production, QA, QC, RA, Engineering and more at Ankleshwar. Apply now.
Farbefirma is inviting applications from experienced professionals across key departments supporting sterile and injectable manufacturing. These openings are suited for candidates with strong technical backgrounds, GMP expertise, and hands-on experience in aseptic operations. The company offers a structured environment, compliance-driven systems, and career opportunities across core pharmaceutical functions.
Company Overview
Farbefirma is an established injectable manufacturing organization with operations built around strict GMP compliance and sterile production systems. The company follows validated processes, modern utilities, and rigorous quality control to support domestic and regulated-market requirements. Its facilities are managed by trained professionals who ensure high-quality injectable products, safe manufacturing practices, and seamless execution across production, quality, and engineering functions.
Job Role & Responsibilities
Production
- Operate and monitor sterile manufacturing activities.
- Support aseptic filling, batch processing, and document compliance.
- Maintain production records, equipment readiness, and sterile protocols.
Packing
- Manage sterile injectable packing operations.
- Ensure adherence to labeling, sealing, and visual inspection requirements.
- Maintain packing documentation and batch traceability.
Quality Assurance (QA)
- Oversee batch record review and GMP compliance.
- Support line clearance, in-process checks, and deviation handling.
- Participate in internal audits and regulatory inspections.
Quality Control (QC)
- Perform analysis of injectable products, raw materials, and stability samples.
- Operate analytical instruments and follow validated test procedures.
- Document results in compliance with GDP requirements.
Regulatory Affairs (RA)
- Support dossier preparation and regulatory submissions.
- Coordinate with QA, QC, and Production for documentation.
- Assist in responding to regulatory queries.
Engineering
- Maintain utilities and sterile manufacturing equipment.
- Handle HVAC, AHU, purified water systems, and calibration activities.
- Ensure preventive maintenance and equipment qualification.
Store / Inventory
- Manage raw material and component inventory for sterile operations.
- Maintain GRN, material dispensing records, and GMP traceability.
Pharmacovigilance
- Support safety reporting, complaint tracking, and risk assessment.
- Maintain documentation for regulatory and global PV requirements.
Human Resources (HR)
- Manage recruitment, onboarding, compliance records, and employee relations.
- Support training programs and manpower planning.
Purchase
- Handle vendor interactions, procurement of materials, and cost optimization.
- Maintain purchase documentation and ensure timely supply.
Accounts
- Manage financial documentation, billing, and cost tracking.
- Support audits and internal financial compliance.
Eligibility / Qualifications
Preferred qualifications include:
- B.Pharm, M.Pharm, B.Sc, M.Sc, Diploma, B.Tech, MBA, M.Com (role-specific)
- Related courses: Pharmaceutical Technology, Industrial Pharmacy, Sterile Manufacturing, Instrumentation, HVAC Systems, Regulatory Compliance, Quality Management.
Experience Requirements
- Prior experience in injectables manufacturing is mandatory.
- Strong understanding of sterile guidelines, GMP compliance, and documentation accuracy.
- Ability to work in cross-functional teams with high attention to detail.
Location & Salary
- Location: Ankleshwar, Gujarat.
- Salary will match experience level and internal grading across departments.
Application Process
Eligible candidates can share their CVs to the following email addresses:
Mention the department and position you are applying for in the subject line.
FAQs
Who can apply for these openings?
Candidates with prior injectable manufacturing or sterile operations experience.
Are freshers eligible?
No. Only experienced candidates are eligible.
Which departments are hiring?
Production, Packing, QA, QC, RA, Engineering, PV, HR, Purchase, and Accounts.
What is the job location?
The positions are based in Ankleshwar.
How should I apply?
Email your resume to the given HR contacts.
Summary Table
+----------------------+--------------------------------------------------+
| Company | Farbëfirma |
+----------------------+--------------------------------------------------+
| Vacancies | Multiple departments for injectable operations |
+----------------------+--------------------------------------------------+
| Required Education | B.Pharm, M.Pharm, B.Sc, M.Sc, Diploma, B.Tech |
+----------------------+--------------------------------------------------+
| Experience | Experienced in injectables only |
+----------------------+--------------------------------------------------+

To apply for this job email your details to office2@farbefirma.com