Pharma Jobs in Roorkee: Walter Bushnell Lifesciences Opens Hiring for New Manufacturing Facility

Walter Bushnell Lifesciences Launches Major Hiring Drive for New State-of-the-Art Plant in Roorkee

ROORKEE, India – In a significant move to bolster its manufacturing capabilities, Walter Bushnell Lifesciences Pvt. Ltd., a part of the renowned Walter Bushnell Group, has announced a large-scale recruitment drive for its new Greenfield pharmaceutical manufacturing plant in Roorkee. This strategic expansion underscores the company’s commitment to innovation and growth within the Indian pharmaceutical sector.

The establishment of this new facility is a landmark project for the group, designed to incorporate cutting-edge technology and adhere to global manufacturing standards. The company is now inviting seasoned professionals to join its team and play a pivotal role in building this plant from the ground up.

A Ground-Up Opportunity for Pharma Professionals

This Greenfield project offers a unique career opportunity for candidates to be involved in the foundational stages of a major manufacturing unit. Successful applicants will have the chance to shape operational processes, establish quality systems, and influence the plant’s culture from its inception.

The company has listed openings across six critical functional areas:

· Production

· Quality Assurance

· Quality Control

· Engineering

· Warehouse

· Research & Development (R&D)

Ideal Candidate Profile

Walter Bushnell Lifesciences is seeking highly motivated professionals with a strong academic foundation in pharmaceutical sciences. Eligible candidates should hold qualifications such as B.Pharm, B.Sc, M.Sc, or M.Pharm.

A key requirement for all roles is substantial, hands-on experience ranging from 5 to 15 years in the pharmaceutical industry. The company has specified that expertise in Greenfield project implementation is crucial. This includes proven skills in:

· Equipment Qualification

· Documentation and Compliance

· Project Execution

· Experience with Pharma OSD (Oral Solid Dosage) forms is mandatory.

How to Apply?

Interested and qualified candidates are encouraged to seize this opportunity to be part of a dynamic and growing organization. Applications can be submitted by sending a detailed Curriculum Vitae (CV) to anupriya.1@walterbushnell.com. For further inquiries, prospective applicants can contact via mobile at 9650111639.

FAQ:

1. What does “Greenfield pharmaceutical project” mean, and why is it significant for applicants?

A Greenfield project refers to the construction of a new manufacturing facility from scratch — including design, layout, equipment installation, validation, and regulatory setup. For professionals, it’s a rare opportunity to contribute to the complete establishment of manufacturing systems, ensuring alignment with global GMP, WHO, and USFDA standards right from the beginning.

2. What specific experience in Oral Solid Dosage (OSD) is required for candidates applying to the Production and QA/QC departments?

Candidates should have hands-on experience with OSD manufacturing operations, such as granulation, compression, coating, and encapsulation. Additionally, knowledge of in-process quality checks, documentation under cGMP, and familiarity with regulatory audit readiness (USFDA, MHRA, WHO-GMP) is essential.

3. What does “Equipment Qualification” involve in a pharmaceutical Greenfield setup?

Equipment Qualification (EQ) is a critical part of the Validation Master Plan (VMP). It involves ensuring that every installed machine performs as intended and meets regulatory standards. EQ typically includes Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ), ensuring equipment reliability, safety, and compliance.

4. Which engineering systems and utilities are expected to be part of the new Roorkee facility?

The new facility will likely feature HVAC systems (AHUs with HEPA filters), Water Purification Systems (RO, EDI, PW, and WFI), Clean Room Panels, and Compressed Air/Nitrogen systems. Knowledge of preventive maintenance, calibration, and validation of these utilities will be advantageous for Engineering department applicants.

5. What kind of documentation and compliance expertise is expected from QA/QC professionals?

Professionals must be proficient in GMP documentation, including SOPs, BMR/BPR preparation, Change Control, Deviation Management, CAPA, and Validation Protocols. Additionally, experience with 21 CFR Part 11-compliant electronic systems, stability studies, analytical method validation, and data integrity audits is highly desirable.