Medreich Pharma Hiring – FR&D, AR&D, QC & Technology Transfer

Medreich Pharma Hiring – FR&D, AR&D, QC & Technology Transfer | OSD Formulations | Bengaluru

Medreich Pharma (a Meiji Group Company) is expanding its pharmaceutical formulation operations and inviting experienced professionals from core OSD (Oral Solid Dosage) backgrounds to join its growing team in Bengaluru. The company is currently hiring across multiple strategic departments including Formulation Research & Development (FR&D), Analytical Research & Development (AR&D), Quality Control (QC), and Technology Transfer. These opportunities are ideal for candidates with strong exposure to solid oral dosage development, analytical validation, dissolution studies, and regulatory-driven pharmaceutical manufacturing.

This recruitment drive is focused on experienced professionals with 5–7 years of hands-on experience in OSD formulation environments. Candidates based in Bengaluru or those who can join within 30 days will be given preference. If you are looking to grow your career in pharmaceutical R&D, analytical development, quality systems, or technology transfer within a globally connected organization, this could be the right move.

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Company Overview – Medreich (A Meiji Group Company)

Medreich is a well-established pharmaceutical company and part of the globally recognized Meiji Group. The organization operates with a strong focus on formulation development, regulatory compliance, and high-quality manufacturing standards aligned with international guidelines.

With a commitment to innovation in oral solid dosage formulations, Medreich serves regulated and semi-regulated markets. The company emphasizes data integrity, GMP compliance, analytical excellence, and process robustness to ensure safe and effective pharmaceutical products reach global patients.

Being part of the Meiji Group strengthens Medreich’s global footprint, regulatory credibility, and research-driven pharmaceutical development capabilities. Professionals working here gain exposure to structured quality systems, global compliance frameworks, and advanced pharmaceutical technologies.

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Open Positions – OSD Formulation Background Required

Medreich Pharma is hiring for the following roles:

1. Formulation Research & Development (FR&D) – Solid Orals

Experience Required: 5–7 Years
Location: Bengaluru
Background Required: Core OSD Formulation Experience

2. Analytical Research & Development (AR&D) – Solid Orals

Experience Required: 5–7 Years
Location: Bengaluru
Background Required: OSD Analytical Development Experience

3. Quality Control Officer / Executive – Formulation

Experience Required: Relevant experience in QC for OSD
Location: Bengaluru

4. Technology Transfer – Solid Orals

Experience Required: 5–7 Years
Location: Bengaluru
Background Required: OSD Manufacturing & Process Transfer Exposure

Only candidates with core pharmaceutical formulation experience in oral solid dosage forms will be considered.

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Job Role & Responsibilities

FR&D – Solid Orals

The FR&D professional will be responsible for development and optimization of oral solid dosage formulations. Key responsibilities include:

• Development of tablet and capsule formulations.
• Pre-formulation studies and excipient compatibility evaluation.
• Scale-up activities and support for exhibit batches.
• Documentation aligned with regulatory submissions.
• Collaboration with analytical and technology transfer teams.
• Ensuring compliance with cGMP and data integrity standards.

This role demands strong formulation troubleshooting skills and practical exposure to solid oral dosage product lifecycle management.

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Analytical Research & Development (AR&D) – Solid Orals

The AR&D role focuses on analytical method development and validation for OSD products. Key skills and responsibilities include:

• Analytical method validation and analytical method transfer.
• Working standard qualification and reference standard management.
• Conducting stability studies and dissolution profiling.
• Calibration of analytical instruments.
• Compendia evaluation and method equivalency studies.
• Experience in AD/ADL/QC validation for formulation in OSD.
• Handling HPLC, GC, and dissolution apparatus.
• Supporting regulatory documentation and audit readiness.

The ideal candidate must demonstrate expertise in chromatographic techniques, regulatory compliance, and analytical troubleshooting within a pharmaceutical R&D environment.

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Quality Control Officer / Executive – Formulation

The QC professional will manage routine and stability testing activities. Responsibilities include:

• Analysis of raw materials and finished formulations.
• Stability studies and dissolution testing.
• Operation and calibration of HPLC and GC systems.
• Documentation as per GMP and GLP requirements.
• Ensuring accuracy, completeness, and compliance of analytical records.

Strong exposure to dissolution testing, stability protocols, and pharmacopeial methods is essential.

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Technology Transfer – Solid Orals

The Technology Transfer professional will be responsible for smooth scale-up and manufacturing transfer processes. Responsibilities include:

• Transferring developed formulations from R&D to commercial manufacturing.
• Preparing technology transfer documents and protocols.
• Coordinating with production, QA, and QC teams.
• Ensuring regulatory compliance during scale-up activities.
• Supporting validation batches and process optimization.

This role requires hands-on exposure to OSD manufacturing processes and cross-functional coordination skills.

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Eligibility / Qualifications

Educational Qualification (Relevant Courses):
B.Pharm, M.Pharm, M.Sc. (Pharmaceutical Chemistry, Analytical Chemistry, Organic Chemistry, Biotechnology, Microbiology, Life Sciences), B.Tech / M.Tech (Pharmaceutical Technology or related field)

Experience Requirements:

• 5–7 years of core OSD formulation experience (FR&D, AR&D, Technology Transfer).
• Relevant QC experience for Officer/Executive role.
• Strong understanding of cGMP guidelines and regulatory requirements.
• Exposure to analytical instruments such as HPLC and GC.
• Experience in dissolution studies, stability testing, and method validation.

Candidates must possess strong documentation skills, regulatory awareness, and the ability to work in structured pharmaceutical environments.

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Location & Joining Preference

Work Location: Bengaluru
Preference: Candidates based in Bengaluru or those who can join within 30 days.

Application Process

Interested candidates can share their updated resume at:

📧 vineeta.k@medreich.com

Please include the following details in your email:

• Current CTC
• Notice Period

Ensure your CV clearly highlights your OSD formulation experience, analytical exposure, validation activities, and regulatory knowledge.

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Frequently Asked Questions (FAQs)

1. Is OSD experience mandatory?

Yes. Only candidates with core oral solid dosage formulation experience will be considered.

2. What is the required experience range?

FR&D, AR&D, and Technology Transfer roles require 5–7 years of experience. QC roles require relevant formulation QC experience.

3. Which analytical instruments should candidates be familiar with?

Hands-on experience with HPLC, GC, dissolution systems, and calibration procedures is required.

4. Is this role open to freshers?

No. These openings are for experienced professionals only.

5. Where is the job location?

All roles are based in Bengaluru.

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Vertical Summary Table

Company	Medreich Pharma (A Meiji Group Company)
Vacancies	FR&D – Solid Orals, AR&D – Solid Orals, Quality Control Officer/Executive, Technology Transfer – Solid Orals
Required Education	B.Pharm, M.Pharm, M.Sc. (Pharmaceutical Chemistry, Analytical Chemistry, Life Sciences), B.Tech/M.Tech (Pharma)
Experience	5–7 Years (FR&D, AR&D, Tech Transfer); Relevant QC Experience Required

Tagged as: Pharma Jobs in Bangalore