India's DMPLOI - Jobs & Networking AppRavian Life Science Pvt. Ltd. has announced a recruitment drive for experienced pharmaceutical professionals at its manufacturing facility in SIDCUL, Haridwar, Uttarakhand. The company is inviting applications for Quality Control (QC), DRA, and Engineering departments. Candidates with relevant pharmaceutical experience are encouraged to apply by sending their updated CV via email.
If you are looking for senior-level pharma jobs in Regulatory Affairs, Quality Control, or Engineering, this is an excellent opportunity to join a growing pharmaceutical organization.
Job Highlights
Company Name: Ravian Life Science Pvt. Ltd.
Job Location: Plot No. 34, Sector-8A, IIE, SIDCUL, Haridwar, Uttarakhand
Job Type: Full-Time
Industry: Pharmaceutical Manufacturing
Application Mode: Email
Available Positions
Department
Designation
Experience
Quality Control (QC)
Assistant Manager / Deputy Manager
10–15 Years
DRA (Drug Regulatory Affairs)
Assistant Manager / Deputy Manager
10–12 Years
Engineering
Manager / Senior Manager
17–20 Years
Qualification
B.Pharm / M.Pharm
B.Sc / M.Sc (Relevant Discipline)
B.E. / B.Tech (Engineering)
Other relevant qualifications as per the position requirements.
Key Responsibilities
Quality Control (QC)
Review analytical testing and laboratory documentation.
Ensure compliance with GMP, GLP, and regulatory guidelines.
Handle OOS, OOT, deviations, CAPA, and stability studies.
Drug Regulatory Affairs (DRA)
Prepare and review CTD/eCTD dossiers.
Coordinate regulatory submissions and product registrations.
Ensure compliance with domestic and international regulations.
Engineering
Manage preventive and breakdown maintenance.
Handle HVAC, utilities, water systems, and equipment qualification.
Ensure engineering compliance with GMP standards.
Required Skills
Good Manufacturing Practices (GMP)
Regulatory Compliance
Documentation & Audit Readiness
Team Management
Analytical Problem Solving
Strong Communication Skills
How to Apply
Interested candidates should send their updated CV to:
Email: hr2@ravianlifescience.com
Use a professional subject line such as:
Application for QC Assistant Manager – Ravian Life Science
Why Join Ravian Life Science?
Opportunity to work with an established pharmaceutical company.
Leadership roles with excellent career growth.
Exposure to regulatory compliance and quality systems.
Professional work environment and learning opportunities.
Technical FAQs
1. What GMP knowledge is expected for the QC position?
Candidates should have experience with cGMP, GLP, data integrity (ALCOA+), laboratory investigations, OOS/OOT handling, stability studies, and audit compliance.
2. What are the responsibilities of a DRA Assistant Manager?
The role includes preparing CTD/eCTD dossiers, lifecycle management, regulatory submissions, product registration, variation filings, and ensuring compliance with national and international regulatory authorities.
3. What engineering systems should candidates be familiar with?
Candidates should have expertise in HVAC systems, purified water systems, compressed air, steam systems, preventive maintenance, equipment qualification (IQ/OQ/PQ), and utility management.
4. What pharmaceutical audits should experienced candidates be able to support?
Candidates should be capable of handling WHO-GMP, USFDA, MHRA, EU-GMP, and customer audits, including documentation review, CAPA implementation, and compliance activities.
5. What documents should applicants send while applying?
Applicants should send an updated resume highlighting educational qualifications, total experience, current CTC, expected CTC, notice period, and relevant pharmaceutical experience to the official HR email.
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