88 Pharmaceutical Companies jobs in India

Job Title: Pharmaceutical Research Associate

Location: Bangalore (IISc Campus) / Darjeeling

Team: Scientific R&D | Shonku Labs, Alt Carbon

Experience: 2–6 years in pharmaceutical QA/QC, analytical R&D, or process chemistry

Type: Full-time

About Alt Carbon: Alt Carbon is India’s leading Carbon Removal (CDR) company. We blend science, technology & tradition to undertake climate action to turn the clock on historic emissions in the atmosphere. Our science and technology takes place in Bangalore; our operations are undertaken in Darjeeling’s heritage tea estates.

Alt Carbon was started by sibling tea planters Shrey and Sparsh Agarwal, in order to rescue their family’s tea estate from being at-risk of climate impact to becoming the frontier of climate action.

Read about our journey below:

Our Journey to Revive Darjeeling

To read more about our work, check out this news feature about us, go through this twitter thread , or have a look at our work in Darjeeling.

About the Role

We are hiring pharma scientists to bring their analytical precision into a new frontier — carbon removal science. If you've worked in GMP labs, run elemental impurity testing, or handled titrations and instrument calibrations in a regulated setup, your skills are exactly what climate science needs.

Alt Carbon is building India’s most advanced Earth Sciences lab — and we need people who know how to run tight protocols, think in SOPs, and obsess over clean data. You’ll work on analyzing rocks, soils, water, and biochar samples to measure elemental movement and quantify CO₂ removal.

Why Pharma Folks?

Pharmaceutical scientists understand discipline, process, and validation. You’ve been trained to care about precision, batch integrity, lab hygiene, and reproducibility — the exact culture we need to build scalable, verifiable carbon removal systems.

What You’ll Do

• Run elemental analysis using ICP-MS, ICP-OES, XRD, IRMS, CHNS analyzers , and other tools (training provided)
• Perform sample prep workflows such as acid digestion, filtration, titration, and dilution with high reproducibility
• Maintain SOPs, QA/QC protocols, calibration records, and chain-of-custody for all lab workflows
• Assist in method development for quantifying cation flux, tracer signatures, and carbon removal pathways
• Collaborate with geochemists and environmental scientists to adapt pharma-style protocols to Earth systems
• Work closely with field teams to process and analyze real-world samples from farms, rivers, and rock quarries

Qualifications

• BPharm / MPharm / MSc in Pharmaceutical Sciences / Analytical Chemistry / Industrial Chemistry
• 2–6 years in analytical R&D, QC/QA, or process labs (pharma manufacturing, CROs, or GLP setups)
• Hands-on experience with:

– Elemental analysis (e.g., ICP-MS/OES, AAS)

– Analytical techniques (e.g., titrations, spectroscopy, gravimetric methods)

– Documentation rigor (logbooks, validation protocols, deviation reports, LIMS)

• Bonus: Experience with ICH Q3D / USP <232>/<233> elemental impurity testing
• Bonus: Background in method validation, risk assessments, or ISO audits

Who You Are

• Detail-obsessed, process-driven, and proud of your lab discipline
• Curious about new domains — even if you’ve never worked with rocks or soils before
• Eager to contribute to planetary health using your pharma training
• Open to working across geochemistry, climate science, and AI-enabled analysis
• Comfortable with both lab work and field exposure (training provided)

Why This Matters

Most climate science labs are starved of real lab culture. You’ve spent years in labs that can’t afford sloppiness. Bring that same culture here — and help us build the world's most reliable carbon removal infrastructure.

What We Offer

• A high-ownership role in one of South Asia’s most advanced Earth Sciences labs
• Cross-disciplinary exposure: work with scientists, climate modelers, AI engineers
• A chance to publish, prototype, and ship science that goes from lab → field.
• The satisfaction of doing real, measurable good for the planet

Job Title: Pharmaceutical Research Associate

Location: Bangalore (IISc Campus) / Darjeeling

Team: Scientific R&D | Shonku Labs, Alt Carbon

Experience: 2–6 years in pharmaceutical QA/QC, analytical R&D, or process chemistry

Type: Full-time

About Alt Carbon: Alt Carbon is India’s leading Carbon Removal (CDR) company. We blend science, technology & tradition to undertake climate action to turn the clock on historic emissions in the atmosphere. Our science and technology takes place in Bangalore; our operations are undertaken in Darjeeling’s heritage tea estates.

Alt Carbon was started by sibling tea planters Shrey and Sparsh Agarwal, in order to rescue their family’s tea estate from being at-risk of climate impact to becoming the frontier of climate action.

Read about our journey below:

Our Journey to Revive Darjeeling

To read more about our work, check out this news feature about us, go through this twitter thread, or have a look at our work in Darjeeling.

About the Role

We are hiring pharma scientists to bring their analytical precision into a new frontier — carbon removal science. If you've worked in GMP labs, run elemental impurity testing, or handled titrations and instrument calibrations in a regulated setup, your skills are exactly what climate science needs.

Alt Carbon is building India’s most advanced Earth Sciences lab — and we need people who know how to run tight protocols, think in SOPs, and obsess over clean data. You’ll work on analyzing rocks, soils, water, and biochar samples to measure elemental movement and quantify CO₂ removal.

Why Pharma Folks?

Pharmaceutical scientists understand discipline, process, and validation. You’ve been trained to care about precision, batch integrity, lab hygiene, and reproducibility — the exact culture we need to build scalable, verifiable carbon removal systems.

What You’ll Do

• Run elemental analysis using ICP-MS, ICP-OES, XRD, IRMS, CHNS analyzers , and other tools (training provided)
• Perform sample prep workflows such as acid digestion, filtration, titration, and dilution with high reproducibility
• Maintain SOPs, QA/QC protocols, calibration records, and chain-of-custody for all lab workflows
• Assist in method development for quantifying cation flux, tracer signatures, and carbon removal pathways
• Collaborate with geochemists and environmental scientists to adapt pharma-style protocols to Earth systems
• Work closely with field teams to process and analyze real-world samples from farms, rivers, and rock quarries

Qualifications

• BPharm / MPharm / MSc in Pharmaceutical Sciences / Analytical Chemistry / Industrial Chemistry
• 2–6 years in analytical R&D, QC/QA, or process labs (pharma manufacturing, CROs, or GLP setups)
• Hands-on experience with:

– Elemental analysis (e.g., ICP-MS/OES, AAS)

– Analytical techniques (e.g., titrations, spectroscopy, gravimetric methods)

– Documentation rigor (logbooks, validation protocols, deviation reports, LIMS)

• Bonus: Experience with ICH Q3D / USP <232>/<233> elemental impurity testing
• Bonus: Background in method validation, risk assessments, or ISO audits

Who You Are

• Detail-obsessed, process-driven, and proud of your lab discipline
• Curious about new domains — even if you’ve never worked with rocks or soils before
• Eager to contribute to planetary health using your pharma training
• Open to working across geochemistry, climate science, and AI-enabled analysis
• Comfortable with both lab work and field exposure (training provided)

Why This Matters

Most climate science labs are starved of real lab culture. You’ve spent years in labs that can’t afford sloppiness. Bring that same culture here — and help us build the world's most reliable carbon removal infrastructure.

What We Offer

• A high-ownership role in one of South Asia’s most advanced Earth Sciences labs
• Cross-disciplinary exposure: work with scientists, climate modelers, AI engineers
• A chance to publish, prototype, and ship science that goes from lab → field.
• The satisfaction of doing real, measurable good for the planet

Job Title: Pharmaceutical Research Associate

Location: Bangalore (IISc Campus) / Darjeeling

Team: Scientific R&D | Shonku Labs, Alt Carbon

Experience: 2–6 years in pharmaceutical QA/QC, analytical R&D, or process chemistry

Type: Full-time

About Alt Carbon: Alt Carbon is India’s leading Carbon Removal (CDR) company. We blend science, technology & tradition to undertake climate action to turn the clock on historic emissions in the atmosphere. Our science and technology takes place in Bangalore; our operations are undertaken in Darjeeling’s heritage tea estates.

Alt Carbon was started by sibling tea planters Shrey and Sparsh Agarwal, in order to rescue their family’s tea estate from being at-risk of climate impact to becoming the frontier of climate action.

Read about our journey below:

Our Journey to Revive Darjeeling

To read more about our work, check out this news feature about us, go through this twitter thread , or have a look at our work in Darjeeling.

About the Role

We are hiring pharma scientists to bring their analytical precision into a new frontier — carbon removal science. If you've worked in GMP labs, run elemental impurity testing, or handled titrations and instrument calibrations in a regulated setup, your skills are exactly what climate science needs.

Alt Carbon is building India’s most advanced Earth Sciences lab — and we need people who know how to run tight protocols, think in SOPs, and obsess over clean data. You’ll work on analyzing rocks, soils, water, and biochar samples to measure elemental movement and quantify CO₂ removal.

Why Pharma Folks?

Pharmaceutical scientists understand discipline, process, and validation. You’ve been trained to care about precision, batch integrity, lab hygiene, and reproducibility — the exact culture we need to build scalable, verifiable carbon removal systems.

What You’ll Do

• Run elemental analysis using ICP-MS, ICP-OES, XRD, IRMS, CHNS analyzers , and other tools (training provided)
• Perform sample prep workflows such as acid digestion, filtration, titration, and dilution with high reproducibility
• Maintain SOPs, QA/QC protocols, calibration records, and chain-of-custody for all lab workflows
• Assist in method development for quantifying cation flux, tracer signatures, and carbon removal pathways
• Collaborate with geochemists and environmental scientists to adapt pharma-style protocols to Earth systems
• Work closely with field teams to process and analyze real-world samples from farms, rivers, and rock quarries

Qualifications

• BPharm / MPharm / MSc in Pharmaceutical Sciences / Analytical Chemistry / Industrial Chemistry
• 2–6 years in analytical R&D, QC/QA, or process labs (pharma manufacturing, CROs, or GLP setups)
• Hands-on experience with:

– Elemental analysis (e.g., ICP-MS/OES, AAS)

– Analytical techniques (e.g., titrations, spectroscopy, gravimetric methods)

– Documentation rigor (logbooks, validation protocols, deviation reports, LIMS)

• Bonus: Experience with ICH Q3D / USP <232>/<233> elemental impurity testing
• Bonus: Background in method validation, risk assessments, or ISO audits

Who You Are

• Detail-obsessed, process-driven, and proud of your lab discipline
• Curious about new domains — even if you’ve never worked with rocks or soils before
• Eager to contribute to planetary health using your pharma training
• Open to working across geochemistry, climate science, and AI-enabled analysis
• Comfortable with both lab work and field exposure (training provided)

Why This Matters

Most climate science labs are starved of real lab culture. You’ve spent years in labs that can’t afford sloppiness. Bring that same culture here — and help us build the world's most reliable carbon removal infrastructure.

What We Offer

• A high-ownership role in one of South Asia’s most advanced Earth Sciences labs
• Cross-disciplinary exposure: work with scientists, climate modelers, AI engineers
• A chance to publish, prototype, and ship science that goes from lab → field.
• The satisfaction of doing real, measurable good for the planet

JOB DETAILS

Pharmaceutical Industry

We are seeking expressions of interest from the Pharmaceutical Industry to fulfil the following vacancies

• Quality Assurance Manager
• Senior Packaging Technologist
• Packaging Technologist
• Senior Line Setters
• Senior Formulators

If you are interested in this exciting opportunity and want to join a company that will support your development call Kristine Tuazon on 0407 300 881 or click the Apply button below.

Thank you for your interest and we look forward to reviewing your application.

This position has been filled, but openings for this type of position come up very frequently. We highly recommend to Register Your Interest below so that you will be the first to know when the next position opens up.

IMPORTANT: It is a requirement of all our jobs that you have a PR or AU/NZ Citizenship. A work visa is not sufficient as all our jobs are permanent. Please do not apply if you do not meet these requirements.

Register Interest

Microbiologist - Pharmaceutical Industry

The company:

A well established Australian owned Pharmaceutical contract manufacturer located in Mulgrave. This large facility contains an R&D Department, large state of the art manufacturing plant, warehousing and logistic solutions, workforce of 250+ people to ensure clients requirements are met on-time and to their strict requirement guidelines.

Due to the contract manufacturing nature of this business there is plenty of variety and experience that can be gained as well as a career path for the tenacious and team focussed individual.

Responsibilities of the role:

The role is responsible for timely testing of food and pharmaceutical products in accordance to the TGA and NATA approved methodology. The role also involves reporting of results, client liaison, new method development and validation.

Testing includes:

• Sterility testing and validation
• Endotoxin testing and validation
• Pharmaceutical testing
• Laboratory maintenance reagent preparation

To be successful in this role you must possess:

• 2+ years of laboratory experience in a similar role within the food, beverage or pharmaceutical manufacturing industry
• Degree with a Microbiology Major and/or equivalent
• Good aseptic technique in laboratory practice
• High level of analysis and skills in laboratory methods and operations
• Diligence in documentation of data and attention to detail
• A solid understanding of microbiological outcomes and results
• Proven ability to work as part of a team where duties/tasks are on roster
• Sound knowledge of general laboratory safety

It is advantageous if you possess some of the below:

• Understand the principles of Good Manufacturing Practices (GMP) and Good Laboratory -Practices (GLP)
• Have knowledge of Microsoft Office software

This position has been filled, but openings for this type of position come up very frequently. We highly recommend to Register Your Interest below so that you will be the first to know when the next position opens up.

IMPORTANT: It is a requirement of all our jobs that you have a PR or AU/NZ Citizenship. A work visa is not sufficient as all our jobs are permanent. Please do not apply if you do not meet these requirements.

Register Interest

Job Title: Director of Regulatory Research & Intelligence

Location: Hybrid (Hyderabad)

Industry: Life Sciences / Healthcare Technology

Experience Level: 10+ years

Employment Type: Full-time

About the Role

Kamet Consulting Group is seeking a high-impact Director to lead our Global Regulatory Research & Intelligence function while driving strategic business development and market penetration. This dual-role leader will oversee a high-performing research intelligence team and own commercial growth initiatives, leveraging regulatory expertise to win new business, deepen client relationships, and expand our footprint in priority geographies.

The ideal candidate brings proven quota achievement over their tenure, deep knowledge of global regulatory frameworks, and the ability to translate regulatory insight into competitive advantage and revenue growth.

Core Responsibilities

· Regulatory Leadership & Intelligence Oversight

• Lead, mentor, and grow a multidisciplinary Regulatory Research & Intelligence team; set clear performance, quality, and delivery metrics.
• Define and evolve research agendas aligned to emerging regulatory trends (FDA, EMA, CDSCO, TGA, WHO, ICH, etc.) and client priorities.
• Oversee execution of complex regulatory intelligence projects—ensuring on-time, on-budget, and in-scope delivery.
• Serve as senior authority on regulatory intelligence, ensuring compliance with global quality standards and minimizing client risk.
• Present complex regulatory implications and recommendations to senior executives in clear, commercially relevant language.

Business Development & Market Penetration

• Develop and execute a go-to-market strategy to penetrate new regions and sectors within life sciences and healthcare technology.
• Leverage regulatory expertise to identify and secure high-value consulting, advisory, and outsourced service engagements.
• Own revenue targets and consistently achieve or exceed sales quotas through proactive pipeline building, solution selling, and account expansion.
• Partner with Leadership to position Kamet as a thought leader in global regulatory affairs.
• Negotiate and close complex, multi-year contracts with C-suite and senior decision-makers.

Cross-Functional Collaboration

• Collaborate closely with consultants, SMEs, and leadership across clinical, quality, supply chain, labeling, and M&A advisory services.
• Align business development activities with operational delivery to ensure client satisfaction and repeat engagements.

Required Qualifications

·      Education: Advanced degree in Pharmacy, Life Sciences, Regulatory Affairs, or related field; PhD or MBA preferred. RAC or equivalent certification a plus.

·   Experience:

- 10+ years in regulatory affairs, regulatory intelligence, or compliance within pharma/medical devices.

- 5+ years in consulting with direct client-facing and team leadership responsibilities.

- Proven track record of meeting or exceeding business development quotas and delivering measurable revenue growth.

·   Regulatory Expertise: Mastery of global and Indian regulatory frameworks (FDA, EMA, CDSCO, WHO, ICH, GMP, GCP, QMS).

·   Commercial Acumen: Skilled at identifying market opportunities, shaping client solutions, and closing strategic deals.

·   Leadership: Demonstrated success in managing high-performance, multicultural teams.

·   Communication: Exceptional English written and verbal skills with the ability to distill technical concepts for executive audiences.

Desired Traits

·      Entrepreneurial, growth-oriented mindset with a balance of technical and commercial skills.

·   Ability to operate seamlessly between strategic planning, operational oversight, and hands-on business development.

·   High ethical standards and commitment to excellence in client delivery.

About Kamet Consulting Group

Kamet Consulting Group is a Life Sciences Management Consulting firm providing Strategic Advisory, Implementation, Capability Building, and Outsourced Services to Pharmaceuticals, Medical Devices, Digital Health, and Consumer Health companies across their value chain. We are an equal opportunity employer. All qualified applicants are encouraged to apply.

Why Join Us

• Contribute to meaningful technology in the life sciences domain.
• Work with a collaborative, forward-thinking team committed to innovation.
• Competitive compensation and benefits package.
• Flexible working arrangements and growth opportunities.