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Bal Pharma Limited – Hiring for roles in Maintenance, Quality Control, FR&D, AR&D, and Auto Cartonator Operations!

Bal Pharma Limited, a leading pharmaceutical company with a legacy of quality excellence, is hiring talented professionals for our Formulation Unit-1 in Bommasandra Industrial Area, Bangalore.

With over 25 years of expertise in manufacturing APIs, intermediates, and finished dosage forms, we are committed to delivering innovative healthcare solutions across 70+ countries. Join our dynamic team to contribute to our mission of quality and innovation in pharmaceuticals.

Apply now for roles in Maintenance, Quality Control (QC), Formulation R&D (FR&D), Analytical R&D (AR&D), and Auto Cartonator Operations!

Why Join Bal Pharma Limited?

Bal Pharma is a WHO-GMP and ISO 9001:2015 certified organization, recognized for its robust R&D and high-quality manufacturing. Our Bommasandra facility is equipped with advanced technology, fostering a collaborative and growth-oriented environment.

With a global presence and clients like Pfizer and GlaxoSmithKline, we offer opportunities to work on cutting-edge projects, ensuring professional development and impactful contributions to healthcare.

Open Positions at Bal Pharma Limited (Unit-1)

We are seeking skilled professionals for various roles at our Formulation Unit-1 in Bangalore. Candidates must have relevant experience in the pharmaceutical industry and a passion for quality excellence.

Deputy Manager – Maintenance

Lead maintenance operations to ensure seamless functioning of the formulation facility.

Responsibilities:

  • Oversee preventive and corrective maintenance of equipment like tablet presses and blenders.
  • Ensure compliance with cGMP and safety standards.
  • Manage breakdown maintenance and spare parts inventory.
  • Supervise documentation and train maintenance staff.

Qualifications:

  • BE/B.Tech in Mechanical or Electrical Engineering.
  • 10-14 years of experience in pharmaceutical plant maintenance.
  • Expertise in handling HVAC, utilities, and GMP compliance.

Assistant Manager – Quality Control (Stability In-Charge)

Oversee stability testing and quality control for finished dosage forms.

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Responsibilities:

  • Manage stability studies for tablets, capsules, and syrups per ICH guidelines.
  • Conduct testing using HPLC, GC, and UV-Vis spectroscopy.
  • Handle deviations, OOS, and CAPA processes.
  • Ensure cGMP and GLP compliance in documentation.

Qualifications:

  • B.Pharm, M.Pharm, or M.Sc. in Chemistry.
  • 8-10 years of experience in QC, with expertise in stability testing.
  • Proficiency in HPLC, GC, and analytical method validation.

Executive – Formulation R&D (FR&D)

Contribute to the development of innovative pharmaceutical formulations.

Responsibilities:

  • Develop and optimize formulations for tablets, capsules, and oral liquids.
  • Conduct pre-formulation and compatibility studies.
  • Support scale-up and technology transfer activities.
  • Maintain documentation as per cGMP standards.

Qualifications:

  • B.Pharm or M.Pharm.
  • 3-5 years of experience in formulation development.
  • Knowledge of cGMP and formulation processes.

Senior Executive – Analytical R&D (AR&D)

Support analytical method development and validation for new formulations.

Responsibilities:

  • Develop and validate analytical methods using HPLC, GC, and FTIR.
  • Perform impurity profiling and stability testing.
  • Prepare analytical reports for regulatory submissions.
  • Ensure compliance with cGMP and GLP standards.

Qualifications:

  • B.Sc., M.Sc., or M.Pharm in Chemistry or related field.
  • 5-7 years of experience in analytical R&D.
  • Expertise in analytical method development and validation.

Technician – Auto Cartonator

Operate and maintain auto cartonator equipment for packaging operations.

Responsibilities:

  • Operate auto cartonator machines for secondary packaging.
  • Perform in-process checks and ensure packaging quality.
  • Maintain equipment and follow cGMP-compliant SOPs.
  • Document packaging activities for audit readiness.

Qualifications:

  • Diploma or ITI in Mechanical or Electrical Engineering.
  • 2-5 years of experience in pharmaceutical packaging.
  • Familiarity with auto cartonator operations.

Skills Required for All Roles

To succeed at Bal Pharma, candidates must demonstrate expertise in the following areas:

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SkillDescription
cGMP ComplianceAdherence to Good Manufacturing Practices and SOPs
Analytical TestingProficiency in HPLC, GC, FTIR, and UV-Vis techniques
Equipment OperationKnowledge of production and packaging equipment
DocumentationAccurate record-keeping for audits and compliance
Regulatory KnowledgeFamiliarity with ICH, USFDA, and WHO-GMP standards
Team CollaborationStrong interpersonal and communication skills

Why Work with Bal Pharma Limited?

Bal Pharma is a trusted name in pharmaceuticals, with four manufacturing units and a strong R&D focus. Our Bommasandra Unit-1 is a state-of-the-art facility producing tablets, capsules, and syrups, adhering to stringent USFDA and WHO-GMP standards.

We offer competitive salaries, skill development opportunities (rated highly by employees), and a collaborative work culture. Join us to make a meaningful impact in global healthcare.

How to Apply

Interested candidates can email their resumes to unit1hr@balpharma.com, placement@balpharma.com, or headhr@balpharma.com. Please include your updated resume, academic certificates, and CTC proof. Immediate joiners are preferred. For more details about our company and mission, visit www.balpharma.com.

Bal Pharma Limited - Hiring for roles in Maintenance, Quality Control, FR&D, AR&D, and Auto Cartonator Operations!

Location and Contact Information

Join Our Mission of Quality Excellence

Bal Pharma Limited is dedicated to delivering innovative and high-quality pharmaceutical products to improve lives worldwide. Whether you’re a Maintenance Deputy Manager, QC Assistant Manager, FR&D Executive, AR&D Senior Executive, or Auto Cartonator Technician, your expertise will drive our success.

Apply today to join a team committed to quality excellence and innovation in pharmaceuticals!

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