Eugia Hiring Production Executives (multiple vacancies)
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities
- Eligibility / Qualifications
- Required Education
- Experience
- Skills & Competencies
- Location & Salary
- Application Process
- Why this role matters (EEAT alignment)
- SEO & High‑CPC Keywords Used Naturally
- FAQs
- What is FML and why is it important?
- Is experience with international regulators mandatory?
- What documents should I send?
- Will this role involve shift work?
- How soon will I hear back after applying?
- Summary Table
MSc BPharm Production Executive (FML) — Bhiwadi
Eugia hiring MSc/BSc/B.Pharm Production Executives (multiple vacancies) for FML manufacturing in Bhiwadi, Rajasthan. USFDA/MHRA experience preferred.
Eugia is recruiting Production Executives for its FML manufacturing line in Bhiwadi. The role is ideal for life‑science professionals who want hands‑on exposure to regulated pharmaceutical manufacturing, quality management systems, and global compliance standards. Candidates with USFDA, MHRA, TGA or ANVISA experience will have an edge.
Company Overview
Eugia Pharma operates focused manufacturing units producing finished medical liquids (FML) and other regulated formulations. The company prioritizes cGMP compliance, robust quality systems, and continual improvement. Working at Eugia exposes candidates to international regulatory standards and structured manufacturing practices — valuable for advancing a career in pharmaceutical production and quality systems.
Job Role & Responsibilities
The Production Executive will work on the FML line and support manufacturing, quality, and compliance activities essential for safe and effective product delivery.
Key Responsibilities
- Execute daily production runs on FML (Finished Medical Liquids) lines per SOPs and batch records.
- Monitor process parameters and ensure adherence to GMP, safety, and cleanliness standards.
- Perform in‑process checks, material handling, and line clearance activities.
- Maintain accurate production documentation, logbooks, and batch manufacturing records (BMR/BPR).
- Support Quality (QA/QC) for deviations, change controls, and corrective actions (CAPA).
- Participate in internal audits and support regulatory inspections (USFDA/MHRA/TGA/ANVISA readiness).
- Contribute to continuous improvement projects to enhance yield, reduce deviations, and improve throughput.
These duties require practical knowledge of pharmaceutical manufacturing operations, familiarity with QMS, and strong documentation discipline.
Eligibility / Qualifications
Required Education
- M.Sc, B.Sc, B.Pharm, M.Pharm
Relevant courses: Pharmaceutical Science, Pharmaceutics, Industrial Chemistry, Analytical Chemistry, Quality Assurance, Process Chemistry, Biotechnology, Microbiology, Sterile Processing.
Experience
- 3 to 5 years preferred (or as specified by HR). Candidates with prior exposure to regulated markets (USFDA, MHRA, TGA, ANVISA) are strongly preferred.
- Experience in FML/manufacturing operations, production planning, or QMS support is advantageous.
Skills & Competencies
- Strong working knowledge of cGMP and cleanroom practices.
- Familiarity with batch record management, deviation handling, and CAPA systems.
- Good communication and team coordination skills.
- Ability to work in shifts and manage production timelines.
Location & Salary
Location: Bhiwadi, Rajasthan (Eugia Pharma manufacturing facility).
Salary: Competitive and commensurate with experience. Roles involving regulated manufacturing and USFDA/MHRA exposure typically command higher compensation due to specialized compliance requirements.
Application Process
Send your CV to: hreugia2@eugiapharma.com
Use the subject line: “Production Executive — FML | [Your Name] | Qualification” to speed processing. Shortlisted candidates will be contacted for further rounds.
Why this role matters (EEAT alignment)
As a Production Executive, you play a direct role in ensuring the safety and reliability of finished medical liquids distributed to patients. Strong manufacturing controls and accurate documentation reduce risk, support regulatory compliance, and protect public health — aligning this job with Eugia’s commitment to quality and industry authority.
SEO & High‑CPC Keywords Used Naturally
pharmaceutical manufacturing jobs, FML production, USFDA compliance, MHRA inspection readiness, GMP compliance, quality management system, finished product release, regulated manufacturing careers.
FAQs
What is FML and why is it important?
FML stands for Finished Medical Liquids — sterile and non‑sterile liquid formulations intended for therapeutic use. They require strict process controls and compliant manufacturing to ensure safety.
Is experience with international regulators mandatory?
Not strictly mandatory, but candidates with USFDA, MHRA, TGA, or ANVISA exposure are preferred given the global markets Eugia serves.
What documents should I send?
Updated CV, copies of degree/diploma, experience certificates, and any regulatory audit or training certificates that demonstrate USFDA/MHRA/TGA/ANVISA exposure.
Will this role involve shift work?
Production roles typically require shift coverage; confirm specifics during the interview.
How soon will I hear back after applying?
Shortlisted candidates will be contacted within 1–2 weeks, depending on application volume.
Summary Table
| Category | Details |
|---|---|
| Company | Eugia Pharma |
| Vacancies | Production Executive — FML (multiple vacancies) |
| Required Education | M.Sc, B.Sc, B.Pharm, M.Pharm |
| Experience | 3–5 years preferred; USFDA/MHRA/TGA/ANVISA exposure preferred |

To apply for this job email your details to hreugia2@eugiapharma.com