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.
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:
Skill | Description |
---|---|
cGMP Compliance | Adherence to Good Manufacturing Practices and SOPs |
Analytical Testing | Proficiency in HPLC, GC, FTIR, and UV-Vis techniques |
Equipment Operation | Knowledge of production and packaging equipment |
Documentation | Accurate record-keeping for audits and compliance |
Regulatory Knowledge | Familiarity with ICH, USFDA, and WHO-GMP standards |
Team Collaboration | Strong 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.

Location and Contact Information
- Work Location: Bal Pharma Limited, Formulation Unit-1, No. 21 & 22, Bommasandra Industrial Area, Bangalore, Karnataka 560099
- Email: unit1hr@balpharma.com, placement@balpharma.com, headhr@balpharma.com
- Website: www.balpharma.com
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!