Farbe Firma Pvt. Ltd. Job Posting for Sterile Injectable Roles in Ankleshwar

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Farbe Firma Pvt. Ltd. Job Posting for Sterile Injectable Roles

Join Farbe Firma Pvt. Ltd., a USFDA-approved and WHO-GMP certified leader in sterile injectable and parenteral formulations, as we expand our state-of-the-art facility in Ankleshwar, Gujarat. Established in 2012, Farbe Firma generates ₹25–50 Crore in revenue and employs 300+ professionals across 50+ countries, specializing in ampoules, vials, lyophilized products, and critical care injectables (e.g., Dexmedetomidine, Iron Sucrose).

Rated 4.1/5 for work-life balance and 4.2/5 for career growth on AmbitionBox (95+ reviews), salaries range from ₹3–10 Lakhs/year (Glassdoor). With a vision to “Splash Colour to Your Life,” we’re hiring for Production, Quality Control (QC), Quality Assurance (QA), Packing, Regulatory Affairs, PPIC/PPMC, Operators, and Engineering roles to support our growth in regulated markets (US, EU, Australia).

Job Posting Details

Notes:

  • Fraud Alert: Farbe Firma does not charge fees for recruitment. Verify via hr@farbefirma.com or official websites.

Why Farbe Firma?

Farbe Firma’s Ankleshwar facility, a brown-field project under the Vibrant Gujarat 2015 MOU, is equipped with cutting-edge technology for ampoules, vials, lyophilized products, liposomes, and biosimilars. As a CDMO/CMO, we serve national and multinational partners with contract manufacturing and formulation development.

Rated 4.1/5 overall (AmbitionBox), we offer robust training (3.8/5 for skill development, Indeed) but face criticism for inconsistent HR policies (3.5/5 for management). Benefits include health insurance, transport, and canteen. Our focus on US, EU, and emerging markets aligns with India’s $24.4 billion pharma export market (10% CAGR, Invest India). Farbe Firma’s 2024 expansion enhances our leadership in critical care injectables.

Job Positions

1. Production Injectable – Executive

  • Vacancies: 10
  • Qualification: B.Pharm, M.Pharm, B.Sc (Chemistry), B.Tech (Chemical)
  • Experience: 2+ years in sterile injectable production
  • Skills:
    • Operation of vial filling lines, lyophilizers, ampoule sealing, and high-speed injectable lines.
    • Knowledge of cGMP, BMR/BPR, aseptic processes, and USFDA/EMA audits.
  • Tasks: Manage production of ampoules/vials, ensure compliance, troubleshoot processes, support tech transfer.
  • Why Join?: Lead high-speed injectable production in a USFDA-approved facility.
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2. Quality Control (QC) – Executive/Officer (HPLC)

  • Vacancies: 8
  • Qualification: B.Sc, M.Sc (Chemistry), B.Pharm, M.Pharm
  • Experience: 2+ years in QC for injectables (HPLC focus)
  • Skills:
    • Expertise in HPLC, GC, UV spectroscopy, and method validation.
    • Familiarity with GLP, ICH Q2, OOS/OOT investigations, and audit readiness.
  • Tasks: Analyze samples, validate methods, maintain lab instruments, support USFDA/EMA audits.
  • Why Join?: Master analytical techniques for sterile injectables.

3. Quality Control (QC) – Microbiologist

  • Vacancies: 11
  • Qualification: B.Sc, M.Sc (Microbiology)
  • Experience: 2+ years in microbiology for injectables
  • Skills:
    • Proficiency in sterility testing, BET, microbial limit tests, and environmental monitoring.
    • Knowledge of cGMP, USP, and audit compliance.
  • Tasks: Conduct microbial testing, monitor cleanrooms, investigate deviations, prepare audit reports.
  • Why Join?: Ensure sterility in a high-compliance environment.

4. Quality Assurance (QA) – Executive/Officer

  • Vacancies: 5
  • Qualification: B.Pharm, M.Pharm, M.Sc (Chemistry)
  • Experience: 2+ years in QA for injectables
  • Skills:
    • Expertise in IPQA, QMS (CAPA, deviations), BMR review, and vendor qualification.
    • Familiarity with USFDA/EMA audits and SOP management.
  • Tasks: Perform in-process checks, manage QMS, review documentation, support audits.
  • Why Join?: Uphold quality standards for regulated markets.

5. Packing Department – Executive/Officer

  • Vacancies: 5
  • Qualification: B.Sc, B.Com, B.Pharm
  • Experience: 2+ years in injectable packing
  • Skills:
    • Knowledge of blister packing, cartonator, labeling, and Track & Trace.
    • Familiarity with cGMP and batch reconciliation.
  • Tasks: Oversee packing operations, ensure labeling compliance, manage batch records.
  • Why Join?: Streamline packing for global distribution.

6. Operator – Ampoule and Vial Line

  • Vacancies: 10
  • Qualification: ITI, Diploma (Mechanical, Electrical)
  • Experience: 2+ years in ampoule/vial line operations
  • Skills:
    • Operation of Groninger vial fillers, ampoule sealing machines, and CIP/SIP systems.
    • Knowledge of cGMP and equipment maintenance.
  • Tasks: Operate and maintain vial/ampoule lines, perform CIP/SIP, ensure production efficiency.
  • Why Join?: Gain hands-on expertise in sterile production.
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7. Regulatory Affairs – Senior Executive

  • Vacancies: 5
  • Qualification: B.Pharm, M.Pharm, M.Sc (Chemistry)
  • Experience: 2+ years in regulatory affairs for injectables
  • Skills:
    • Expertise in dossier preparation (eCTD), post-approval filings, and USFDA/EMA submissions.
    • Knowledge of CDSCO, ICH, and query responses.
  • Tasks: Prepare/submit dossiers, manage regulatory queries, ensure compliance, support audits.
  • Why Join?: Shape regulatory strategies for global markets.

8. PPIC/PPMC (Production Planning & Inventory Control/Material Control)

  • Vacancies: 2
  • Qualification: B.Com, M.Com, B.Sc, PGD in SCM
  • Experience: 2+ years in PPIC/PPMC for injectables
  • Skills:
    • Proficiency in production planning, inventory management, and ERP systems.
    • Knowledge of cGMP-compliant supply chains.
  • Tasks: Plan production, manage raw material inventory, coordinate with vendors, ensure timely supply.
  • Why Join?: Optimize supply chains for sterile manufacturing.

9. Operator – Labelling Machine

  • Vacancies: 5
  • Qualification: ITI, Diploma
  • Experience: 2+ years in labeling machine operations
  • Skills:
    • Operation of labeling machines (e.g., Bosch, Uhlmann) and Track & Trace systems.
    • Knowledge of cGMP and batch documentation.
  • Tasks: Operate/maintain labeling machines, ensure accurate labeling, support packing operations.
  • Why Join?: Enhance packing efficiency in a USFDA setup.

10. Engineering – Executive/Officer

  • Vacancies: 5
  • Qualification: B.Tech, Diploma (Mechanical, Electrical)
  • Experience: 2+ years in engineering for injectables
  • Skills:
    • Maintenance of HVAC, autoclaves, vial fillers, and water systems (RO, DM).
    • Knowledge of cGMP and equipment qualification.
  • Tasks: Perform preventive maintenance, troubleshoot equipment, ensure uptime, support audits.
  • Why Join?: Maintain cutting-edge injectable infrastructure.

Who Can Apply?

  • Qualifications: B.Pharm, M.Pharm, B.Sc, M.Sc (Chemistry, Microbiology), B.Tech, B.Com, M.Com, Diploma, ITI, PGD (SCM).
  • Experience: Minimum 2 years in sterile injectables (ampoules, vials, lyophilized products).
  • Key Skills:
    • Production/Operators: Vial/ampoule lines, CIP/SIP, cGMP, high-speed production.
    • QC/QA: HPLC, sterility testing, IPQA, QMS, USFDA/EMA compliance.
    • Packing: Labeling, Track & Trace, batch reconciliation.
    • Regulatory: eCTD, dossier preparation, query responses.
    • PPIC/Engineering: ERP, inventory, HVAC, equipment maintenance.
  • Preferred: USFDA/EMA audit exposure, experience with Groninger/Pharmalab equipment, local candidates.
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How to Apply

  1. Submit Resume: Email to hr@farbefirma.com, hr2@farbefirma.com, and info@farbefirma.com, subject: “[Position] – Ankleshwar.” Highlight sterile injectable experience.
  2. Prepare Documents: If shortlisted, bring CV, mark sheets, degree certificate, experience letters, last 3 months’ payslips, CTC breakup, Aadhaar/PAN copies, 2 photos.
  3. Study Up:
    • Production/Operators: Review vial/ampoule line operations, cGMP, CIP/SIP. Prepare examples (e.g., “How did you optimize a filling line?”).
    • QC/QA: Study HPLC, sterility testing, IPQA, QMS. Share examples (e.g., “How did you handle an OOS?”).
    • Packing: Review labeling machines, Track & Trace. Discuss efficiency (e.g., “How did you reduce labeling errors?”).
    • Regulatory: Study eCTD, USFDA/EMA guidelines. Prepare examples (e.g., “How did you manage a dossier query?”).
    • PPIC/Engineering: Review ERP, HVAC maintenance. Share examples (e.g., “How did you resolve an autoclave issue?”).
    • Visit www.farbefirma.com for portfolio (e.g., Adrenaline, Amphonex).
    • Address policy concerns diplomatically (24% rate management ≤3/5, AmbitionBox).
  4. Interview: Expect technical (70%) and behavioral (30%) questions. Emphasize sterile injectable experience and regulatory knowledge. Process takes ~1–2 weeks (Indeed).

Why Ankleshwar, Gujarat?

Farbe Firma’s GIDC facility, 10 km from Bharuch via NH-48, is part of Gujarat’s $7 billion pharma sector (12% CAGR, Invest India). Ankleshwar offers 400+ pharma jobs (Naukri) and affordable living (₹8,000/month for 1BHK, AmbitionBox). Company transport from Bharuch ensures connectivity. Ideal for careers in USFDA-regulated sterile injectables.

Contact Information

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Farbe Firma Pvt. Ltd. Job Posting for Sterile Injectable Roles in Ankleshwar

Apply Now to join Farbe Firma’s sterile injectable expansion in Ankleshwar and contribute to high-quality global healthcare solutions!

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