India's DMPLOI - Jobs & Networking AppElysium Pharmaceutical Ltd. has announced new job openings for experienced pharmaceutical professionals at its Vadodara, Gujarat location. The company is inviting applications for multiple positions across IPQA, Quality Assurance, QA Microbiology, and Production departments.
Candidates with relevant experience in pharmaceutical formulation manufacturing, GMP documentation, microbiological testing, QMS activities, and production operations can explore these career opportunities.
Interested and eligible candidates should carefully review the eligibility criteria, departmental requirements, experience, and application process before submitting their updated resumes.
Elysium Pharmaceutical Recruitment– Job Overview
Particulars Details
Company Name
Elysium Pharmaceutical Ltd.
Industry
Pharmaceutical / Healthcare
Job Type
Full-Time
Positions
IPQA Officer, QA Officer, QA Microbiologist Officer, Production Officer
Departments
IPQA, Quality Assurance, Microbiology & Production
Experience Required
1–4 Years, depending on the position
Job Location
Vadodara, Gujarat
Application Mode
Email Application
About Elysium Pharmaceutical Ltd.
Elysium Pharmaceutical Ltd. operates in the pharmaceutical sector with a focus on healthcare, quality, innovation, and manufacturing excellence. The company is recruiting experienced professionals for its formulation manufacturing operations in Vadodara, Gujarat.
The current recruitment drive offers opportunities for candidates with experience in Quality Assurance, IPQA activities, microbiological testing, GMP documentation, and pharmaceutical production.
Open Positions and Eligibility Criteria
1. IPQA Officer
Experience Required: 2–4 Years
Departments/Manufacturing Areas:
Softgel, Parenteral, Tablet & Ointment
Job Requirements:
Candidates should have experience in IPQA activities within a pharmaceutical formulation manufacturing plant.
Applicants should understand in-process quality assurance practices, GMP compliance, manufacturing documentation, line clearance, process monitoring, and shop-floor quality systems.
2. QA Officer – Documentation & QMS
Experience Required: 1–3 Years
Department: Quality Assurance – Documentation & Quality Management System
Job Requirements:
Candidates should have hands-on experience in:
Preparation and control of GMP documents.
Standard Operating Procedures (SOPs).
Batch Manufacturing Records (BMR).
Batch Packing Records (BPR).
Quality Management System activities.
Change control management.
Deviation handling.
Corrective and Preventive Action (CAPA).
Issuance and control of GMP documents.
Other related Quality Assurance documentation activities.
3. QA Microbiologist Officer
Experience Required: 1–3 Years
Department: QA Microbiology
Job Requirements:
Candidates should have practical experience in microbiological testing and pharmaceutical microbiology activities.
Key responsibilities and skills include microbiological testing, environmental monitoring, water analysis, media preparation, and GMP documentation.
Knowledge of contamination control, microbial testing procedures, laboratory documentation, and GMP practices can be beneficial for this position.
4. Production Officer
Experience Required: 1–4 Years
Manufacturing Departments:
Parenteral, Softgel, Ointment & Tablet
Job Requirements:
Candidates should have experience in pharmaceutical formulation manufacturing operations.
Applicants should possess a sound understanding of current Good Manufacturing Practices (cGMP), production processes, manufacturing documentation, equipment operation, process compliance, and shop-floor activities.
Job Location
Vadodara, Gujarat
Candidates should consider their willingness to work or relocate to Vadodara before submitting their applications.
How to Apply for Elysium Pharmaceutical Recruitment
Interested and eligible candidates can apply by sending their updated resumes to the email address provided in the official recruitment advertisement.
Application Email: aman.kumar@elysiumpharma.com
Candidates should mention the position or department they are applying for in the email subject line.
Suggested Email Subject:
Application for [Position Name] – [Years of Experience]
Applicants should attach an updated resume highlighting relevant pharmaceutical industry experience, educational qualifications, technical skills, current location, and contact information.
Important Documents and Information to Keep Ready
Candidates should keep their updated resume, educational qualification details, experience certificates, current and previous employment details, current CTC, expected CTC, notice period, and other relevant professional information ready before applying.
Why Consider This Opportunity?
Elysium Pharmaceutical Recruitment 2026 provides career opportunities for pharmaceutical professionals experienced in formulation manufacturing and quality operations.
The available roles cover important pharmaceutical functions, including IPQA, Quality Management Systems, GMP documentation, microbiological quality operations, and manufacturing production.
Professionals looking to develop their careers in pharmaceutical manufacturing and quality systems can review their eligibility and apply for the appropriate position.
5 Technical FAQs for Elysium Pharmaceutical Recruitment
1. What is the role of an IPQA Officer in a pharmaceutical formulation manufacturing plant?
An IPQA Officer performs in-process quality assurance activities on the manufacturing floor. Typical responsibilities include line clearance verification, monitoring manufacturing operations, reviewing batch records, checking compliance with SOPs, ensuring adherence to cGMP requirements, reporting deviations, and preventing quality-related issues during production.
2. What is the difference between deviation, change control, and CAPA in pharmaceutical QMS?
A deviation is an unplanned departure from an approved procedure, specification, or established process. Change control is a documented system used to evaluate, approve, implement, and monitor planned changes. CAPA (Corrective and Preventive Action) involves identifying the root cause of quality problems, implementing corrective measures to address existing issues, and taking preventive measures to reduce the possibility of recurrence.
3. What are BMR and BPR, and why are they important?
BMR (Batch Manufacturing Record) documents the complete manufacturing history of a pharmaceutical batch, including materials, equipment, processing parameters, and manufacturing activities.
BPR (Batch Packing Record) contains information related to the packaging operations of a batch.
Both records are critical for batch traceability, GMP compliance, investigation of deviations, quality review, and regulatory inspections.
4. What technical activities are commonly performed by a pharmaceutical microbiologist?
A pharmaceutical microbiologist may perform microbial limit testing, environmental monitoring, water testing, media preparation, growth promotion testing, microbial identification, laboratory documentation, and other microbiological quality control activities. The microbiologist must follow approved SOPs, data integrity requirements, and GMP practices.
5. What cGMP knowledge is important for a Production Officer?
A Production Officer should understand line clearance, equipment cleaning and operation, status labeling, prevention of cross-contamination, adherence to SOPs and BMR instructions, process parameter monitoring, Good Documentation Practices (GDP), deviation reporting, data integrity principles, and workplace safety requirements.
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