AcuLIFE Healthcare Hiring Sterile Injectables ADL & F&D
- Company Overview
- Job Role & Responsibilities
- Analytical Development Laboratory (ADL) – Sterile Dosage Forms
- ADL Designations Open
- Formulation & Development (F&D) – Sterile and Specialized Dosage Forms
- F&D Designations Open
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Why Join AcuLIFE Healthcare?
- Frequently Asked Questions (FAQs)
- Are freshers eligible for these positions?
- What departments are hiring at AcuLIFE?
- What analytical skills are required for ADL roles?
- Is regulatory documentation experience mandatory?
- How should I apply for this opportunity?
- SEO Title Suggestions
- Eligible Education Courses
B.Pharm, M.Pharm, M.Sc Vacancies at AcuLIFE – Ahmedabad
AcuLIFE Healthcare hiring B.Pharm, M.Pharm, M.Sc candidates for Sterile Injectables ADL & F&D roles in Ahmedabad. Multiple vacancies.
AcuLIFE Healthcare Private Limited is inviting applications from passionate and skilled professionals for its Sterile / Injectable Dosage Form Division. The company is expanding its Analytical Development Laboratory (ADL) and Formulation & Development (F&D) teams at its Ahmedabad manufacturing and R&D facility. This opportunity is ideal for both freshers with strong fundamentals and experienced professionals who want to build a long-term career in sterile injectables, analytical development, and pharmaceutical formulation development within a regulated environment.
Company Overview
AcuLIFE Healthcare Private Limited, formerly known as Nirlife, is a growing Indian pharmaceutical company with a strong focus on sterile dosage forms and complex pharmaceutical products. Operating from its modern facility near the Sanand–Viramgam Highway in Ahmedabad district, AcuLIFE is committed to delivering high-quality, safe, and effective medicines that meet global regulatory standards.
The company’s operations span research, development, scale-up, and manufacturing of sterile injectables and related dosage forms. AcuLIFE follows stringent cGMP practices and aligns its development and quality systems with international regulatory expectations, including ICH and pharmacopeial guidelines. Working at AcuLIFE offers professionals hands-on exposure to advanced pharmaceutical technologies, regulatory documentation, and real-world healthcare impact.
Job Role & Responsibilities
Analytical Development Laboratory (ADL) – Sterile Dosage Forms
Professionals joining the ADL team will be involved in analytical development, validation, and support activities for sterile injectable products. Key responsibilities include:
• Performing analytical testing using HPLC, GC, UV, Dissolution, TOC, and sterility testing techniques
• Developing and validating analytical methods for drug products and intermediates
• Supporting stability studies and data generation for regulatory submissions
• Ensuring compliance with ICH guidelines, cGMP, and regulatory standards
• Maintaining accurate analytical documentation and laboratory records
• Supporting quality control and microbiology testing as required
• Assisting in investigation of analytical deviations and OOS results
ADL Designations Open
• Analytical Scientists – Sterile Dosage Forms
• Research Associates – Method Development & Validation
• Quality Control Analysts
• Stability Analysts
• Microbiology Analysts
• Documentation & Compliance Executives
Formulation & Development (F&D) – Sterile and Specialized Dosage Forms
The F&D team will focus on development, scale-up, and regulatory readiness of complex sterile products. Responsibilities include:
• Formulation development of sterile injectables, ophthalmic, inhalation, and nasal products
• Development of solutions, suspensions, emulsions, and iron complex formulations
• Scale-up activities for vials, bags, BFS, PFS, cartridges, and ophthalmic containers
• Understanding and application of different sterilization techniques
• Aseptic processing, filtration, and compatibility studies
• Conducting stability studies and data evaluation
• Process optimization and product design based on QbD and DOE principles
• Preparation of laboratory, technology transfer, and regulatory submission documents
• Ensuring compliance with cGMP, ICH, and regulatory guidelines
F&D Designations Open
• Formulation Scientists
• Research Associates – Development & Scale-Up
• Regulatory Submission Associates
Eligibility / Qualifications
Candidates must possess one of the following educational qualifications:
B.Pharm, M.Pharm (Pharmaceutics, Pharmaceutical Chemistry, Analytical Chemistry), M.Sc (Analytical Chemistry, Pharmaceutical Chemistry, or related disciplines)
Experience requirements:
• 0 to 8 years of relevant experience
• Freshers with strong academic fundamentals and interest in sterile dosage forms may apply
• Candidates with 2 to 8 years of experience are preferred for advanced development roles
Strong conceptual knowledge of sterile manufacturing, analytical techniques, and regulatory expectations is essential for all roles.
Location & Salary
Job Location:
• Village Sachana, Taluka Viramgam, District Ahmedabad – 382150
• Near Railway Crossing, Sanand–Viramgam Highway
Salary and compensation will be offered as per industry standards and will depend on the candidate’s qualifications, experience, and technical expertise. AcuLIFE follows a performance-driven and transparent compensation structure.
Application Process
Interested candidates are requested to submit their updated resumes via official company email IDs. Candidates should clearly mention their area of expertise (ADL or F&D) and relevant experience in the subject line.
Apply via Email:
• rajeshthakor@aculife.co.in
• recruitment@aculife.co.in
Only shortlisted candidates will be contacted for further discussion and interview processes.
Why Join AcuLIFE Healthcare?
• Specialized exposure to sterile and injectable dosage forms
• Opportunity to work on complex and high-value pharmaceutical products
• Strong learning environment for freshers and experienced professionals
• Direct involvement in formulation development and regulatory submissions
• Contribution to safe and effective healthcare solutions
Frequently Asked Questions (FAQs)
Are freshers eligible for these positions?
Yes. Freshers with strong academic fundamentals and interest in sterile dosage forms are encouraged to apply.
What departments are hiring at AcuLIFE?
Analytical Development Laboratory (ADL) and Formulation & Development (F&D) for sterile dosage forms.
What analytical skills are required for ADL roles?
Hands-on experience or strong knowledge of HPLC, GC, UV, dissolution, TOC, sterility testing, and method validation.
Is regulatory documentation experience mandatory?
It is preferred but not mandatory for entry-level roles. Experienced candidates should have exposure to regulatory documentation.
How should I apply for this opportunity?
Candidates should send their updated CVs to the official AcuLIFE email addresses mentioned above.
SEO Title Suggestions
AcuLIFE Healthcare Hiring ADL & F&D Scientists – Sterile Injectables
Eligible Education Courses
B.Pharm, M.Pharm Pharmaceutics, M.Pharm Pharmaceutical Chemistry, M.Pharm Analytical Chemistry, M.Sc Analytical Chemistry, M.Sc Pharmaceutical Chemistry
| Company | AcuLIFE Healthcare Private Limited |
|---|---|
| Vacancies | Analytical Scientist, Research Associate, QC Analyst, Microbiology Analyst, Formulation Scientist, Regulatory Associate |
| Required Education | B.Pharm, M.Pharm, M.Sc |
| Experience | 0–8 Years |

To apply for this job email your details to recruitment@aculife.co.in