Job Tag: Pharma Jobs in Bangalore

Apply for Regulatory Affairs Analyst role at Beckman Coulter in Bangalore. Openings for Life Science/Engineering graduates with 8–10 years’ experience.

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Do you want to accelerate your potential and make a meaningful difference in the life sciences and diagnostics industry? Beckman Coulter Life Sciences, part of the Danaher group of companies, is hiring a Regulatory Affairs Analyst in Bangalore. This role provides the opportunity to contribute to global product registrations, compliance, and innovation that ultimately improves patient outcomes worldwide.

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Company Overview

Beckman Coulter Life Sciences, established in 1935, is a pioneer in providing cutting-edge laboratory solutions that help scientists and clinicians deliver life-saving therapies faster. As part of Danaher’s 15+ operating companies, Beckman Coulter focuses on accelerating answers in healthcare by automating workflows, reducing errors, and driving efficiency in labs worldwide.

With more than 3,300 colleagues globally, many of whom are scientists, the company is deeply committed to advancing human health through technology, innovation, and regulatory excellence.

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Job Role & Responsibilities

As a Regulatory Affairs Analyst, you will be responsible for supporting global regulatory submissions and ensuring compliance across product lifecycles. Key responsibilities include:

• Preparing registration dossiers for life sciences products across multiple countries (excluding the USA).
• Gathering and maintaining technical documentation for new product development.
• Ensuring documentation complies with evolving global regulatory requirements.
• Supporting product lifecycle management including design changes, labeling updates, and compliance improvements.
• Assessing regulatory impact and creating detailed action plans for timely compliance.
• Supporting global pre-market regulatory submissions such as Q-Subs, 510(k), IVDR, China registrations, and other global filings.
• Maintaining compliance with international standards such as ISO 13485, ISO 9001, IVDD/IVDR, and other applicable regulations.
• Supporting regulatory activities related to Software as a Medical Device (SaMD) and software used as accessories to medical devices.

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Eligibility / Qualifications

Minimum Requirements:

• Bachelor’s degree in Life Sciences, Engineering, or related field.
• 8–10 years of regulatory affairs experience in a regulated medical device or diagnostics industry (less with advanced degrees).
• Experience with global regulatory submissions, including premarket filings.
• Familiarity with international quality systems (ISO 13485, ISO 9001).
• Experience with Software as a Medical Device (SaMD) preferred.

Preferred Skills & Certifications:

• Regulatory or quality certifications (e.g., CQM, CQE, CQA, RAC, CLIA, Six Sigma, Lean).
• Experience in instrument and software development within the medical device sector.
• Strong project management, adaptability, and communication skills.
• Ability to work flexible hours to support global business operations.

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Location & Salary

• Location: Bangalore, Karnataka, India
• Job Type: Full-time | On-site
• Salary: Competitive with eligibility for bonus/incentive pay
• Benefits: Comprehensive healthcare, paid time off, career development, and global exposure under Danaher’s continuous improvement system

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Application Process

Interested candidates can apply through the official Danaher careers portal. Don’t miss your chance to join a world leader in diagnostics and regulatory excellence.

👉 Click here to apply now

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FAQs

1. Who can apply for this role?
Life Sciences or Engineering graduates with 8–10 years of regulatory experience in diagnostics or medical devices.

2. What regulatory standards should candidates be familiar with?
Standards such as IVDR, IVDD, ISO 13485, ISO 9001, and other applicable global quality systems.

3. Is software regulatory experience required?
Yes, experience with SaMD or software as a medical device accessory is highly desirable.

4. What certifications are advantageous?
Certifications like RAC, Six Sigma, Lean, CQA, CQE add significant value.

5. How can I apply?
Apply directly through the official Danaher Careers Website.

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Call to Action

Join Beckman Coulter Life Sciences and be part of a global team that accelerates answers for critical healthcare needs. Apply today for the Regulatory Affairs Analyst position in Bangalore and take your career in regulatory affairs to the next level.

Apply before the position closes to secure your opportunity!

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Job Summary Table

Company	Beckman Coulter Life Sciences (Danaher)
Vacancies	Regulatory Affairs Analyst
Required Education	Bachelor’s in Life Sciences, Engineering (Advanced degrees preferred)
Experience	8–10 years in Regulatory Affairs (Medical Devices/Diagnostics)
Location	Bangalore, Karnataka, India

PhD & Postdoc Openings in Peptide R&D at Aurigene Pharma

Apply for PhD/Postdoc roles in Peptide Chemistry, R&D, and Engineering at Aurigene Pharmaceutical Services. Join a leading pharma innovator. camilla araujo videos

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Aurigene Pharmaceutical Services Ltd. is inviting exceptional scientists to be part of its peptide drug development division, contributing to cutting-edge research in therapeutic peptides. This is a unique opportunity for PhD scholars and Postdoctoral researchers to work on pioneering projects that advance global healthcare.

Company Overview

Aurigene Pharmaceutical Services Ltd. is a leading contract research, development, and manufacturing services provider (CRDMO) with a strong global presence. The company specializes in novel peptide chemistry, small molecule development, analytical services, and large-scale GMP manufacturing. With world-class infrastructure and a commitment to innovation, Aurigene empowers researchers to develop transformative medicines.

Job Role & Responsibilities

1. Analytical R&D (PhD/Postdocs)

• Develop advanced analytical methodologies for peptide API characterization.
• Validate complex peptide structures and ensure quality compliance.
• Collaborate with cross-functional R&D teams to support regulatory submissions.

2. Process R&D – Peptide (PhD/Postdocs)

• Design and execute novel solid-phase and solution-phase synthesis strategies.
• Optimize yield, purity, and scalability of therapeutic peptides.
• Work on innovation-driven peptide discovery and development projects.

3. Process Engineering (PhD/Postdocs)

• Lead peptide process scale-up and technology transfer.
• Engineer robust GMP-compliant manufacturing processes.
• Support continuous process improvement and validation for commercial peptide production.

Eligibility / Qualifications

• Education: PhD in Organic Chemistry, Peptide Chemistry, Biochemistry, Process Engineering, or related fields. Postdoctoral research experience is strongly preferred.
• Skills Required:
  • Strong background in peptide synthesis (solid-phase/solution-phase).
  • Expertise in analytical methods for peptide APIs.
  • Hands-on experience with scale-up and GMP manufacturing.
• Experience: Fresh Postdocs and experienced PhDs with a research-driven mindset.

Location & Salary

• Location: Aurigene Pharmaceutical Services Ltd., India (specific details provided during selection process).
• Salary: Competitive package aligned with candidate’s expertise, experience, and industry standards.

Application Process

Qualified candidates may send their updated CVs to:
krishnafulsure@aurigeneservices.com

Applicants should clearly mention the role they are applying for in the subject line of the email.

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Why Join Aurigene?

• Work on innovative peptide drug discovery programs.
• Exposure to state-of-the-art peptide R&D and process engineering platforms.
• Collaborative and research-driven work environment.
• Opportunity to contribute to healthcare advancements on a global scale.

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FAQs

Q1: Who can apply for these roles?
PhD holders and Postdoctoral researchers with expertise in peptide chemistry, analytical sciences, or process engineering are eligible.

Q2: What type of experience is preferred?
Candidates with hands-on experience in peptide synthesis, scale-up, GMP manufacturing, and analytical validation will be preferred.

Q3: Where will the selected candidates work?
The positions are based in Aurigene Pharmaceutical Services’ advanced facilities in India.

Q4: Is this a research or industrial role?
These are industry-driven research roles with a focus on scaling innovative peptide technologies from lab to commercial production.

Q5: How should I apply?
Send your CV directly to krishnafulsure@aurigeneservices.com, with the role title in the subject line.

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Summary Table

Company	Aurigene Pharmaceutical Services Ltd.
Vacancies	Analytical R&D, Process R&D, Process Engineering
Required Education	PhD in Chemistry, Biochemistry, Peptide Chemistry, Process Engineering
Experience	Postdoctoral research or relevant industrial R&D experience

<img class="size-full wp-image-123119" src="https://bpharmacyjobs.com/wp-content/uploads/2025/08/Aurigene-Pharmaceutical-Services-Hiring-Analytical-RD-Process-RD-Process-Engineering-1.webp" alt="Aurigene Pharmaceutical Services Hiring Analytical R&D, Process R&D, Process Engineering” width=”1536″ height=”1536″ /> Aurigene Pharmaceutical Services Hiring Analytical R&D, Process R&D, Process Engineering

B.Pharm/M.Pharm FR&D Vacancies at Medreich | Bangalore

Medreich is hiring FR&D professionals (Solid Orals) with 2–5 years’ experience in Bangalore. Apply now for career growth in formulation research.

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Medreich Limited, a part of the globally renowned Meiji Group, is inviting skilled professionals to join its Research & Development (R&D) team. This opportunity is ideal for experienced formulation scientists who are passionate about advancing solid oral dosage forms and contributing to cutting-edge pharmaceutical innovation.

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Company Overview

Medreich Limited, headquartered in Bangalore, is a leading pharmaceutical organization under the Meiji Group (Japan). With decades of expertise in research, development, and manufacturing, Medreich has built a strong global footprint, serving patients across multiple therapeutic areas. Its R&D division focuses on innovation in solid orals, injectables, and advanced formulations, ensuring high-quality, affordable medicines worldwide.

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Job Role & Responsibilities

The Formulation Research & Development (FR&D) Scientist will work on solid oral dosage forms. Responsibilities include:

• Designing and developing robust formulations for solid orals.

• Conducting pre-formulation and formulation trials, optimization, and scale-up.

• Preparing technical documents, development reports, and regulatory submissions.

• Collaborating with analytical, regulatory, and production teams for project execution.

• Ensuring compliance with cGMP, ICH, and regulatory standards.

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Eligibility / Qualifications

• Education: B.Pharm, M.Pharm (Pharmaceutics, Pharmaceutical Technology, or related fields).

• Experience: 2 to 5 years of hands-on experience in FR&D (Solid Orals).

• Note: Freshers are not eligible for this opening.

Preferred Skills:

• Strong knowledge of formulation techniques for solid orals.

• Experience with scale-up and technology transfer.

• Excellent documentation and communication skills.

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Location & Salary

• Job Location: Bangalore, Karnataka.

• Salary: Competitive, based on experience and qualifications (industry standards).

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Application Process

Interested candidates may send their updated CVs to:

vineeta.k@medreich.com

Apply as soon as possible to secure your chance to be part of Medreich’s prestigious R&D team.

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FAQs

Q1: Who can apply for this FR&D opening?
Candidates with 2–5 years of experience in FR&D (Solid Orals) and a degree in B.Pharm or M.Pharm can apply. Freshers are not eligible.

Q2: What skills are preferred?
Hands-on formulation expertise, knowledge of scale-up and tech transfer, and regulatory documentation skills are preferred.

Q3: Where is the job located?
The position is based at Medreich’s R&D facility in Bangalore, Karnataka.

Q4: What is the company background?
Medreich is a Meiji Group company with a strong global presence in pharmaceuticals, especially in R&D, manufacturing, and export.

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Summary Table

Company	Medreich Limited (Meiji Group)
Vacancies	FR&D – Solid Orals
Required Education	B.Pharm, M.Pharm (Pharmaceutics, Pharmaceutical Technology)
Experience	2–5 Years (Freshers not eligible)
Location	Bangalore, Karnataka

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Aragen Hiring Research Associates | Chemistry Synthesis | Bangalore

Meta Description: Apply for Research Associate & Sr. Research Associate roles in Chemistry Synthesis at Aragen, Bangalore. M.Sc Organic/Medicinal Chemistry, 2–6 yrs exp.

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Aragen, a Great Place to Work Certified CRO, is hiring Research Associates and Senior Research Associates for its Chemistry Synthesis Department in Bangalore. This opportunity is open exclusively to candidates from CRO backgrounds with expertise in Organic and Medicinal Chemistry. Professionals with 2–6 years of experience are encouraged to apply, with quick joiners (within 30 days) preferred.

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Company Overview

Aragen is a leading Contract Research Organization (CRO) with a global reputation for delivering high-quality research solutions in pharmaceuticals, biotechnology, and life sciences. The company is known for its innovative chemistry synthesis, drug discovery, and development services. With world-class facilities and a commitment to employee well-being, Aragen fosters professional growth and provides a collaborative work culture.

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Job Role & Responsibilities

Research Associate / Senior Research Associate – Chemistry Synthesis

• Experience: 2–6 Years
• Qualification: M.Sc (Organic Chemistry, Medicinal Chemistry)
• Responsibilities:
  • Execute chemical reactions to synthesize molecules/compounds as per client requirements.
  • Design and implement efficient synthetic routes using advanced techniques.
  • Ensure compliance with Good Laboratory Practices (GLP) and safety protocols.
  • Maintain proper documentation, ensure data integrity, and follow IP specifications.
  • Collaborate with cross-functional teams for project delivery.

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Eligibility / Qualifications

• Required Education: M.Sc in Organic Chemistry or Medicinal Chemistry.
• Experience Range: 2–6 years (CRO background mandatory).
• Other Requirements:
  • Candidates must have hands-on experience in synthetic organic chemistry.
  • Must be willing to work in a fast-paced CRO environment.
  • Quick joiners with ≤30 days notice period preferred.

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Location & Salary

• Job Location: Aragen, Bangalore, India.
• Salary: Competitive salary as per industry standards, with additional benefits and career advancement opportunities.

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Application Process

Interested candidates can share their updated resumes with the recruitment team:

Email Contacts:

• rajashree.hegde@aragen.com
• rajkumar.selvaraj@aragen.com

Apply early to secure your opportunity at a leading CRO. Quick joiners will be given preference.

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FAQs

1. Who can apply for these roles?
Candidates with an M.Sc in Organic or Medicinal Chemistry and 2–6 years of experience in a CRO environment.

2. Is CRO experience mandatory?
Yes, only candidates from Contract Research Organizations (CROs) are eligible.

3. What skills are required?
Strong expertise in synthetic chemistry, laboratory safety practices, and compliance with GLP/IP standards.

4. What is the preferred notice period?
Quick joiners with a notice period of 30 days or less are preferred.

5. Where is the role based?
At Aragen’s Bangalore facility, India.

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Summary Table

Category	Details
Company	Aragen Pvt. Ltd.
Vacancies	Research Associate, Senior Research Associate – Chemistry Synthesis
Required Education	M.Sc Organic Chemistry, M.Sc Medicinal Chemistry
Experience	2–6 Years (CRO background required)

M.Pharm/M.Sc Openings – Analytical R&D Vacancies in Bengaluru | Medreich

Apply for Analytical R&D vacancies at Medreich, Bengaluru. Openings for M.Pharm/M.Sc candidates with 5–7 years experience. Immediate opportunity!

Medreich, a leading global pharmaceutical company and part of the Meiji Group, is hiring experienced professionals for its Analytical Research & Development (R&D) division in Bengaluru. This is an excellent opportunity for qualified candidates with expertise in pharmaceutical analysis and analytical chemistry to advance their careers with a trusted name in the industry.

Company Overview

Medreich is a Meiji Group company with a strong presence in the global pharmaceutical sector, known for its innovation in research, manufacturing, and development of high-quality medicines. With a legacy of excellence and compliance with international regulatory standards, Medreich continues to provide career growth opportunities for skilled pharma professionals.

Job Role & Responsibilities

Selected candidates will join the Analytical Research & Development (R&D) team, where responsibilities include:

• Performing analysis related to assay, dissolution profiles, related substances, GC, IC, and physical parameters.
• Conducting dissolution/assay/related substance method development with AMD reports.
• Calibration and maintenance of analytical instruments.
• Analysis related to API qualification and DMF review.
• Preparing method development strategy reports for assay/related substances.
• Drafting impurity nature reports and conducting drug–excipient studies, forced degradation studies, and literature reviews.
• Ensuring compliance with GLP and GDP practices, including online documentation and reporting.
• Preparing and revising SOPs as per project requirements.
• Managing incidents, deviations, DCRFs, and change controls.
• Ensuring audit readiness for customer and regulatory inspections.
• Coordinating procurement of project-related chemicals, columns, and impurities.
• Collaborating with service engineers for instrument maintenance and calibration.

Eligibility / Qualifications

• Education: M.Pharm (Pharmaceutical Analysis), M.Sc. in General Chemistry or Applied Chemistry.
• Experience: 5 to 7 years in analytical research & development, pharmaceutical analysis, or related areas.
• Skills Required:
  • Strong knowledge of assay, dissolution, GC, IC, and impurity profiling.
  • Hands-on experience in calibration and analytical method development.
  • Familiarity with GLP, GDP, and regulatory documentation.
  • Ability to handle audits and regulatory compliance requirements.

Note: Freshers are not eligible for this position.

Location & Salary

• Work Location: Medreich, Bommasandra, Bengaluru, Karnataka.
• Salary: Competitive, based on experience and industry standards.

Application Process

Interested candidates can apply by sending their updated resume to vineeta.k@medreich.com. Applicants should clearly mention the department and role in the subject line.

Apply before 23rd August 2025 to secure your interview opportunity.

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FAQs

Q1. Who can apply for Medreich Analytical R&D jobs?
Candidates with an M.Pharm in Pharmaceutical Analysis or M.Sc. in Chemistry/Applied Chemistry with 5–7 years of experience are eligible.

Q2. Can freshers apply for this role?
No, this position is strictly for experienced professionals.

Q3. Where is the job located?
The position is based in Bommasandra, Bengaluru, Karnataka.

Q4. What skills are required for this role?
Candidates must have expertise in assay, dissolution, impurity profiling, method development, and regulatory compliance.

Q5. How can I apply for this job?
Send your updated CV to vineeta.k@medreich.com with the subject line mentioning your applied role.

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Summary Table

Company	Medreich – A Meiji Group Company
Vacancies	Analytical R&D (Pharmaceutical Analysis)
Required Education	M.Pharm (Pharmaceutical Analysis), M.Sc. (Chemistry, Applied Chemistry)
Experience	5–7 years (No freshers allowed)
Location	Bengaluru (Bommasandra), Karnataka

Apotex Walk-in Drive for B.Pharm/M.Pharm Vacancies | Bangalore

Attend Apotex danielle bregoli onlyfans leakedwalk-in drive in Bangalore on 24th Aug 2025. Openings for Production, QC, QA, and Engineering. B.Pharm/M.Pharm/M.Sc graduates apply now.

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Apotex, a Canadian-based global healthcare company and one of the world’s leading generic pharmaceutical manufacturers, is conducting a Walk-in Drive on 24th August 2025 (Sunday) at its Bangalore office. The company is seeking skilled professionals for roles in Production, Quality Control, Quality Assurance, and Engineering & Maintenance. Candidates with backgrounds in OSD (Oral Solid Dosage) formulations are highly preferred.

This recruitment drive provides a valuable opportunity for pharma professionals to join a multinational organization known for its commitment to innovation, patient care, and regulatory compliance.

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Company Overview

Apotex Research Private Limited is a subsidiary of Apotex Inc., Canada’s largest pharmaceutical company. With over four decades of expertise, Apotex operates globally, serving millions of patients with high-quality, affordable medicines across more than 100 countries.

The Bangalore facility is a hub for research, development, and manufacturing, specializing in Oral Solid Dosage forms. With strong regulatory approvals including USFDA, EMA, and Health Canada, Apotex is a trusted name in the global pharmaceutical landscape.

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Job Roles & Responsibilities

Production – Executive

• Supervise and manage manufacturing processes including compounding, dosing, and packaging.
• Ensure adherence to cGMP, SOPs, and regulatory standards.
• Coordinate with cross-functional teams to ensure timely batch completion.

Quality Control – Sr. Officer / Executive

• Conduct in-process, finished product, and stability testing of laboratory and commercial batches.
• Perform cleaning validation, HPLC operations, and LIMS-based analysis.
• Document and report testing outcomes in compliance with regulatory guidelines.

Quality Assurance – Sr. Officer / Executive

• Oversee process validation and cleaning validation execution.
• Perform AQL inspections, sampling, trending, and hold time studies.
• Ensure compliance with regulatory standards through documentation and audit readiness.

Engineering & Maintenance – Executive / Sr. Executive

• Manage mechanical maintenance of OSD formulation production equipment.
• Perform instrumentation troubleshooting, SCADA and PLC programming.
• Support equipment qualification, validation, and regulatory audit requirements.
• Lead projects involving facility upgrades and new equipment installations.

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Eligibility / Qualifications

• Production Executive: B.Pharm / M.Pharm with 4–5 years of experience.
• Quality Control (Sr. Officer/Executive): B.Pharm / M.Pharm / M.Sc with 3–5 years of experience.
• Quality Assurance (Sr. Officer/Executive): B.Pharm / M.Pharm / M.Sc with 3–5 years of experience.
• Engineering & Maintenance (Executive/Sr. Executive): Bachelor’s Degree in Instrumentation, Electronics, or Mechanical Engineering with 4–8 years of experience.

Preferred candidates should have prior experience in OSD background and regulatory audits.

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Location & Interview Details

• Walk-in Date: 24th August 2025 (Sunday)
• Time: 09:30 AM – 05:00 PM
• Venue: Apotex Research Private Limited, Gate 3, Plot No. 1 & 2, Jigani Link Road, 4th Phase, Bommasandra Industrial Area, Bengaluru, Karnataka – 560099

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Application Process

Interested candidates are encouraged to attend the walk-in interview at the given venue with an updated CV, passport-size photographs, and relevant certificates.

If unable to attend in person, candidates may share their resumes at ppawar4@apotex.co.in and fill the interest form via QR code provided in the official notice.

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Why Join Apotex?

• Be part of a Canadian-based global pharmaceutical leader.
• Work in a USFDA and EMA-approved OSD facility.
• Contribute to international regulatory-driven pharma operations.
• Attractive career growth opportunities in Production, QA, QC, and Engineering.

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FAQs

1. Who can apply for Apotex’s walk-in drive?
Professionals with degrees in B.Pharm, M.Pharm, M.Sc, or Engineering and relevant experience in OSD formulations.

2. Can freshers apply?
No, these roles require 3–8 years of relevant experience.

3. What documents are required for the walk-in?
Updated resume, educational certificates, ID proof, and passport-size photographs.

4. Is OSD experience mandatory?
Yes, preference will be given to candidates with OSD background.

5. Where should resumes be sent if unable to attend?
Resumes can be sent to ppawar4@apotex.co.in.

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Summary Table

Company	Apotex Research Private Limited
Vacancies	Production Executive, QC Sr. Officer/Executive, QA Sr. Officer/Executive, Engineering & Maintenance Executive/Sr. Executive
Required Education	B.Pharm, M.Pharm, M.Sc, Engineering (Instrumentation, Electronics, Mechanical)
Experience	3–8 years depending on role

<img class="size-full wp-image-122843" src="https://bpharmacyjobs.com/wp-content/uploads/2025/08/Apotex-Walk-in-Production-QC-QA-and-Engineering-1.webp” alt=”Apotex Walk-in Production, QC, QA, and Engineering” width=”1080″ height=”1920″ /> Apotex Walk-in Production, QC, QA, and Engineering