Ceph Lifesciences hiring FDA Officer
- Company Overview
- Job Role & Responsibilities
- FDA Officer – Documentation & Liaisoning
- Eligibility / Qualifications
- Educational Qualifications
- Experience Requirements
- Required Skills
- Location & Salary
- Application Process
- Why Join Ceph Lifesciences
- FAQs
- Who can apply for the FDA Officer position?
- Is FDA inspection experience mandatory?
- Are freshers eligible?
- Is there any application or recruitment fee?
- Summary Table
BPharm MPharm FDA Officer Jobs Baddi – Ceph Lifesciences
Ceph Lifesciences hiring FDA Officer in Baddi. BPharm, MPharm eligible. 1 vacancy. 2–5 yrs experience.
Ceph Lifesciences Pvt. Ltd. has announced an opening for an FDA Officer at its manufacturing unit in Baddi, Himachal Pradesh. This role is focused on FDA documentation, regulatory coordination, and liaison activities, making it a key position within the company’s regulatory and compliance framework. The opportunity is ideal for pharmacy professionals with hands-on exposure to regulatory documentation and inspections in a regulated pharmaceutical manufacturing environment.
With increasing regulatory scrutiny from global health authorities, FDA compliance roles have become mission-critical in the pharmaceutical industry. An FDA Officer plays a direct role in ensuring product quality, regulatory readiness, and uninterrupted supply of medicines to patients. This position at Ceph Lifesciences offers meaningful responsibility and long-term career growth in regulatory affairs and compliance.
Company Overview
Ceph Lifesciences Pvt. Ltd. is a growing pharmaceutical manufacturing organization operating in compliance with national and international regulatory standards. The company focuses on quality-driven manufacturing practices and maintains strong regulatory systems to meet expectations of authorities such as the USFDA and other global agencies.
Located in the Baddi pharmaceutical hub, Ceph Lifesciences benefits from a robust manufacturing ecosystem and skilled talent pool. The organization emphasizes documentation accuracy, audit preparedness, and regulatory discipline, making it a suitable workplace for professionals seeking specialization in FDA documentation and regulatory liaison roles.
Job Role & Responsibilities
FDA Officer – Documentation & Liaisoning
The FDA Officer will be responsible for managing regulatory documentation and acting as a liaison during audits and inspections.
Key Responsibilities:
- Preparation, review, and maintenance of FDA-related documentation
- Handling regulatory correspondence and liaison activities with authorities
- Supporting FDA and other regulatory inspections and audits
- Ensuring compliance with current GMP and regulatory guidelines
- Coordinating with QA, QC, and production teams for compliance matters
- Managing responses to regulatory queries and observations
- Maintaining inspection readiness and documentation control systems
This role aligns with high-demand FDA officer jobs in pharmaceutical companies and regulatory compliance careers.
Eligibility / Qualifications
Educational Qualifications
- B.Pharmacy
- M.Pharmacy
(Relevant courses: BPharm, MPharm – Regulatory Affairs, Quality Assurance)
Experience Requirements
- 2 to 5 years of experience in FDA documentation and regulatory liaisoning
Required Skills
- Strong understanding of FDA and GMP regulations
- Hands-on experience in regulatory documentation
- Audit and inspection handling exposure
- Attention to detail and compliance mindset
- Effective communication with internal and external stakeholders
These skills are closely associated with high-CPC regulatory affairs and FDA compliance job searches.
Location & Salary
Job Location: Baddi (Jharmajari), Himachal Pradesh
Salary: Salary will be competitive and in line with industry standards, based on qualification, experience, and interview performance. Ceph Lifesciences offers stable growth opportunities in regulatory and compliance functions.
Application Process
Interested and eligible candidates can apply by sharing their updated CV via email or contacting HR directly.
Apply via Email: hr.unit6@neclife.com
Contact Number: 9317911968
Candidates are advised to mention “FDA Officer – Baddi” in the subject line for faster shortlisting.
Why Join Ceph Lifesciences
- Specialized role in FDA documentation and regulatory liaisoning
- Exposure to regulatory inspections and audits
- Location advantage in Baddi pharma hub
- Long-term growth in regulatory affairs and compliance
- Direct contribution to safe and compliant medicine manufacturing
These openings are suitable for candidates searching for FDA officer jobs in Baddi, regulatory affairs jobs in pharma, pharmaceutical compliance roles, and GMP documentation careers.
FAQs
Who can apply for the FDA Officer position?
Candidates with B.Pharm or M.Pharm qualifications and 2–5 years of FDA documentation experience can apply.
Is FDA inspection experience mandatory?
Yes. Prior exposure to FDA documentation and liaisoning is expected.
Are freshers eligible?
No. This role requires prior regulatory experience.
Is there any application or recruitment fee?
No. Ceph Lifesciences does not charge any fees at any stage of recruitment.
Summary Table
| Company | Ceph Lifesciences Pvt. Ltd. |
|---|---|
| Vacancies | FDA Officer |
| Required Education | B.Pharm, M.Pharm |
| Experience | 2–5 years |

To apply for this job email your details to hr.unit6@neclife.com