Alivus Life Sciences Recruitment 2026 presents an excellent career opportunity for experienced professionals looking to work in the pharmaceutical and API manufacturing industry. Alivus Life Sciences, formerly known as Glenmark Life Sciences, has announced multiple job openings at its Ankleshwar facility.
The company is inviting applications from qualified and experienced candidates for positions in Human Resources, Quality Assurance, and Engineering Stores – Warehouse departments. Candidates with relevant API industry experience, knowledge of cGMP, regulatory documentation, analytical compliance, payroll management, and warehouse operations are encouraged to apply.
Alivus Life Sciences Recruitment – Job Overview
Particulars Details
Company Name
Alivus Life Sciences
Formerly Known As
Glenmark Life Sciences
Job Location
Ankleshwar
Industry
Pharmaceutical / API Manufacturing
Departments
Human Resources, Quality Assurance, Engineering Stores – Warehouse
Qualification
MBA-HR, B.Sc./M.Sc. Chemistry, and relevant qualifications/experience for Engineering Stores
Experience Required
1 to 7 Years, depending on the position
Application Mode
Email
Resume Email ID
prajet.khule@alivus.com
About Alivus Life Sciences
Alivus Life Sciences is a pharmaceutical company operating in the Active Pharmaceutical Ingredient (API) industry. Formerly known as Glenmark Life Sciences, the organization focuses on pharmaceutical manufacturing operations and works within regulated environments requiring high standards of quality, documentation, safety, and cGMP compliance.
The company is seeking young, energetic, passionate, and driven professionals who are interested in contributing to a dynamic work environment.
Available Departments, Qualifications and Experience
1. Human Resources
Alivus Life Sciences is hiring experienced HR professionals for its Ankleshwar facility.
Qualification: MBA – HR
Experience: 2 to 5 years of relevant experience in the API industry.
Candidates should have practical exposure to:
Contract Labour Management
Apprenticeship Management
Payroll Management
Pharmaceutical/API industry HR operations
Regulatory documentation and cGMP requirements
Candidates with experience managing workforce compliance and employee administration in pharmaceutical manufacturing environments may be suitable for this opportunity.
2. Quality Assurance
The Quality Assurance department is looking for experienced candidates with a strong background in analytical compliance and pharmaceutical quality systems.
Qualification: B.Sc. / M.Sc. in Chemistry
Experience: 2 to 7 years of relevant experience in the API industry.
Candidates should possess knowledge and experience in:
Analytical Compliance
Specification Activity
Stability Studies
Analytical Method Validation
Regulatory Documentation
cGMP Requirements
Applicants should have a good understanding of pharmaceutical quality systems and documentation practices used in regulated API manufacturing facilities.
3. Engineering Stores – Warehouse
Alivus Life Sciences is also recruiting candidates for its Engineering Stores – Warehouse function.
Experience: 1 to 3 years of experience in Engineering Stores.
Candidates should have exposure to:
Material Receipt
Material Issue Procedures
Gate Pass Management
Engineering Stores Operations
Inventory Documentation
Regulatory Documentation and cGMP requirements
Candidates with experience working in engineering stores or warehouse functions within pharmaceutical or similar regulated manufacturing environments may apply.
General Requirements for All Positions
According to the recruitment notification, candidates applying for the above positions should have exposure to regulatory requirements related to documentation and cGMP (Current Good Manufacturing Practices).
Applicants should ensure that their resumes clearly mention their educational qualifications, relevant experience, current job responsibilities, API industry exposure, cGMP knowledge, and technical skills related to the position.
How to Apply for Alivus Life Sciences Recruitment
Interested and eligible candidates should prepare an updated resume highlighting their relevant qualifications and professional experience.
Candidates can send their resumes to:
Email ID: prajet.khule@alivus.com
When sending the application, candidates should use a clear email subject line, such as:
Application for [Department Name] Position – [Candidate Name]
Applicants should verify their eligibility and carefully review the official recruitment advertisement before submitting their resumes.
Why Consider a Career at Alivus Life Sciences?
Working in an established pharmaceutical and API manufacturing organization can provide professionals with valuable exposure to regulated manufacturing operations, quality systems, compliance requirements, workforce management, and pharmaceutical supply chain processes.
This recruitment drive offers opportunities for professionals with 1 to 7 years of experience, depending on the department.
Technical FAQs – Alivus Life Sciences Recruitment
1. What is cGMP, and why is it important in API manufacturing?
cGMP stands for Current Good Manufacturing Practices. It is a system of regulations and procedures designed to ensure that pharmaceutical products and APIs are consistently manufactured and controlled according to established quality standards. cGMP covers areas such as documentation, personnel training, equipment maintenance, manufacturing controls, deviations, change control, data integrity, and quality systems.
2. What is Analytical Method Validation in pharmaceutical Quality Assurance?
Analytical Method Validation is the documented process of demonstrating that an analytical procedure is suitable for its intended purpose. Typical validation parameters include accuracy, precision, specificity, linearity, range, robustness, detection limit, and quantitation limit, depending on the type of analytical procedure and applicable regulatory requirements.
3. What is the purpose of stability studies in the pharmaceutical industry?
Stability studies evaluate how the quality of an API or pharmaceutical product changes over time under the influence of environmental factors such as temperature and humidity. Stability data supports the establishment of retest periods, expiry dates, storage conditions, and appropriate packaging requirements.
4. What is Contract Labour Management in a pharmaceutical manufacturing facility?
Contract Labour Management involves managing outsourced workers in accordance with applicable legal requirements and company procedures. Responsibilities may include contractor coordination, attendance management, statutory compliance, safety training, documentation, wage and payroll coordination, and ensuring that contract workers follow site-specific procedures and GMP requirements.
5. What are the key responsibilities of an Engineering Stores professional?
An Engineering Stores professional is responsible for receiving, storing, issuing, and maintaining records of engineering materials and spare parts. Key responsibilities may include material receipt and inspection, inventory control, material issuance, gate-pass management, stock reconciliation, documentation, traceability, and compliance with applicable SOPs and cGMP requirements.
Conclusion
Alivus Life Sciences Recruitment 2026 is a valuable opportunity for professionals seeking pharmaceutical and API industry jobs in Human Resources, Quality Assurance, and Engineering Stores – Warehouse departments.
Eligible candidates with relevant experience ranging from 1 to 7 years can submit their updated resumes via email. Applicants should ensure that their resumes clearly demonstrate the required technical skills, industry experience, and knowledge of regulatory documentation and cGMP practices.


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