Farbe Firma Hiring Production, QA, QC, Regulatory & Engineering

Sterile Injectable Executive & QA Roles – B.Pharm/M.Pharm – Ankleshwar

Farbe Firma hiring for Sterile Injectable Production, QA, QC, Regulatory & Engineering roles. Minimum 2 yrs experience required – Ankleshwar.

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Join Farbe Firma Pvt. Ltd, a leading pharmaceutical company, as we expand into a state-of-the-art sterile injectable facility in Ankleshwar. We are looking for skilled professionals with experience in ampoules, vials, lyophilized products, and high-speed injectable production lines to be part of our growing team.

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Company Overview

Farbe Firma Pvt. Ltd is a reputable name in the pharmaceutical manufacturing sector, dedicated to delivering high-quality sterile injectables. Our facility in GIDC Ankleshwar is equipped with advanced machinery and cleanroom infrastructure, ensuring the production of safe and effective products for patients worldwide.

The company emphasizes quality assurance, regulatory compliance, and innovation, providing a professional environment for career growth in the pharmaceutical and biotech industry.

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Job Roles & Responsibilities

We are currently hiring across multiple departments for our new sterile injectable facility. Key roles and responsibilities include:

Production Injectable – Executive

• Operate high-speed ampoule, vial, and lyophilized production lines.

• Ensure compliance with cGMP, SOPs, and cleanroom protocols.

• Monitor production parameters and maintain documentation for batch records.

Quality Control (QC) – Executive/Officer HPLC

• Perform analytical testing using HPLC, UV, GC, and other instruments.

• Conduct microbiological testing and environmental monitoring.

• Ensure accuracy and compliance in QC documentation and reporting.

QC – Microbiologist

• Conduct microbiological testing of raw materials, intermediates, and finished products.

• Monitor and maintain sterile environment and cleanroom protocols.

• Execute environmental monitoring programs and maintain compliance with regulatory guidelines.

Quality Assurance (QA) – Executive/Officer

• Review and approve Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), and SOPs.

• Support regulatory audits and internal inspections.

• Ensure adherence to cGMP standards and compliance throughout manufacturing operations.

Packing Department – Executive/Officer

• Supervise and operate packing lines for vials, ampoules, and lyophilized products.

• Maintain accuracy and efficiency in packaging operations.

• Ensure compliance with documentation and labeling requirements.

Operator – Ampoule & Vial Line

• Execute daily operations on ampoule and vial filling lines.

• Maintain cleanroom discipline and GMP compliance.

• Monitor equipment and report any deviations.

Regulatory Affairs – Senior Executive

• Prepare and submit regulatory documentation for sterile injectables.

• Liaise with regulatory authorities for approvals and compliance.

• Support lifecycle management and post-approval changes.

PPIC / PPMC

• Plan and monitor production schedules.

• Ensure material availability and production targets are met.

Operator – Labelling Machine

• Operate high-speed labeling machines for injectables.

• Ensure accuracy in labeling and documentation compliance.

Engineering – Executive/Officer

• Maintain and troubleshoot manufacturing and packaging equipment.

• Ensure compliance with facility maintenance and safety protocols.

Minimum Experience Required: 2 years in the relevant department.

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Eligibility / Qualifications

• Educational Qualification: B.Pharm, M.Pharm, B.Sc., M.Sc., Diploma in Pharmacy, or related fields.

• Experience: Minimum 2 years in sterile injectable manufacturing, QA/QC, regulatory affairs, or engineering operations.

• Skills:

  • Knowledge of cGMP, cleanroom protocols, and aseptic techniques.

  • Hands-on experience in ampoules, vials, lyophilized products, HPLC, GC, LC-MS, and regulatory submissions.

  • Strong teamwork, communication, and documentation skills.

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Location & Salary

• Work Location: Plot No. 1508, GIDC Ankleshwar, Gujarat – 393002

• Salary: Best in the industry (competitive and based on experience)

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Application Process

Interested candidates can submit their updated CV/resume to:

• Emails: hr@farbefirma.com | hr2@farbefirma.com | info@farbefirma.com

Tip: Highlight your experience in sterile injectable production, QA/QC operations, regulatory compliance, and cleanroom techniques to improve your chances.

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Why Join Farbe Firma?

• State-of-the-Art Facility: Work in a modern sterile injectable plant with advanced production and quality systems.

• Career Growth: Opportunities across Production, QA/QC, Regulatory, Engineering, and PPIC departments.

• Innovation in Healthcare: Contribute to life-saving sterile injectable products for patients.

• Professional Development: Work in a structured, compliant environment that encourages continuous learning and advancement.

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FAQs

Q1. What is the minimum experience required?

• 2 years in relevant pharmaceutical departments like sterile injectables, QA, QC, or engineering.

Q2. What are the key qualifications?

• B.Pharm, M.Pharm, B.Sc., M.Sc., or Diploma in Pharmacy.

Q3. Which roles are available?

• Production, QA, QC, Regulatory Affairs, Packing, PPIC, and Engineering roles.

Q4. What skills are preferred?

• Knowledge of cGMP, cleanroom protocols, HPLC, GC, LC-MS, aseptic techniques, and regulatory compliance.

Q5. How to apply?

• Send your CV to hr@farbefirma.com, hr2@farbefirma.com, or info@farbefirma.com.

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