Looking for career growth in sterile pharmaceutical manufacturing? Immacule Lifesciences is actively hiring for multiple roles in Sterile Production, Engineering, Quality Assurance (QA), and Quality Control (QC) at its advanced facility in Nalagarh, Himachal Pradesh.
This is a great opportunity for professionals with 2–14 years of experience seeking exposure to global regulatory environments and sterile injectables manufacturing.
About Immacule Lifesciences
Founded in 2012, Immacule Lifesciences is a rapidly growing pharmaceutical company specializing in liquid and lyophilized sterile injectables. The company operates as a Contract Development and Manufacturing Organization (CDMO), supplying high-quality products to global markets.
Key highlights:
- State-of-the-art facility in Nalagarh
- Compliance with USFDA, UK-MHRA, and ANVISA standards
- Expertise in ophthalmic, injectable, and lyophilized products
- Strong focus on quality, innovation, and affordability
Job Overview
- Company: Immacule Lifesciences
- Experience: 2–14 Years
- Qualification: B.Pharm, M.Sc, B.Tech, Diploma (Mechanical/Electrical)
- Location: Nalagarh, Himachal Pradesh
- Job Type: On-site
Open Positions
💉 Production – Sterile
- Roles: Officer / Sr. Officer / Operator
- Sections: Vial Filling, Ophthalmic, Lyophilization
- Experience: 2–5 Years
- Qualification: B.Pharm / Diploma
Engineering – Sterile
- Roles: AM / Executive / Officer / Technician
- Sections: Electrical & Mechanical Maintenance
- Experience: 5–12 Years
- Qualification: B.Tech / Diploma
Quality Assurance – Sterile
- Roles: DM / AM / Executive / Officer
- Focus: IPQA, Validation & Qualification
- Experience: 4–14 Years
- Qualification: B.Pharm
Quality Control – Chemical
- Roles: DM / AM / Executive / Officer
- Experience: 4–14 Years
- Qualification: M.Sc
Required Skills
- Strong knowledge of cGMP and regulatory compliance
- Experience in sterile manufacturing processes
- Hands-on expertise in vial filling, lyo, or ophthalmic production
- Skills in validation, qualification, and IPQA
- Experience in chemical analysis and QC testing
- Good teamwork, documentation, and problem-solving abilities
Key Responsibilities
- Operate and monitor sterile production lines
- Perform maintenance of plant equipment (Electrical/Mechanical)
- Conduct validation and qualification activities
- Execute QC testing and chemical analysis
- Ensure compliance with global regulatory standards
- Maintain documentation and support audits
Benefits & Perks
- Career growth in a rapidly expanding sterile pharma company
- Exposure to international regulatory standards 🌍
- Competitive salary packages 💰
- Learning and skill development opportunities
- Professional and innovation-driven work culture
How to Apply
Interested candidates can apply via:
- 📞 WhatsApp/Call: 8580412182
- 📧 Email: recruitment@immacule.in
👉 Send your updated CV with relevant experience details.
Why Join Immacule Lifesciences?
Joining Immacule Lifesciences offers a unique opportunity to work in a high-growth CDMO environment with global exposure.
Top reasons:
- Work in USFDA & international compliant facility
- Gain expertise in sterile injectables & lyophilization
- Strong career progression opportunities
- Exposure to global pharmaceutical markets
FAQs
Q1: What experience is required for Immacule Lifesciences jobs?
Experience ranges from 2–14 years depending on the role.
Q2: What qualifications are required?
B.Pharm, M.Sc, B.Tech, or Diploma in Mechanical/Electrical with regulatory exposure.
Q3: How can I apply?
Send your CV via WhatsApp (8580412182) or email recruitment@immacule.in.
Q4: Are these roles suitable for sterile pharma professionals?
Yes, these roles are specifically focused on sterile manufacturing and QA/QC functions.