Looking for pharma jobs, walk-in interviews, QA jobs, QC jobs, production jobs, or rewarding pharmaceutical careers in India? Anthea Pharma Private Limited is conducting a walk-in interview for experienced Quality Assurance professionals at its USFDA-approved sterile injectables manufacturing facility in Hyderabad on 1st July 2026.
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About the Company
Anthea Pharma Private Limited is a globally recognized Contract Development and Manufacturing Organization (CDMO) specializing in complex sterile injectable formulations.
The company manufactures vials, lyophilized vials, emulsions, and prefilled syringes through six advanced manufacturing lines supported by integrated quality systems.
With a strong focus on innovation, regulatory compliance, and operational excellence, Anthea Pharma continues to establish itself as a trusted global pharmaceutical manufacturing partner.
Its USFDA-approved facility follows international quality standards, offering employees excellent opportunities to build successful careers in the pharmaceutical industry.
Job Details
- Company Name: Anthea Pharma Private Limited
- Department: Quality Assurance (QA)
- Experience: 2–6 Years (varies by role)
- Qualification: B.Pharm, M.Pharm, or M.Sc.
- Location: Pashamylaram, Patancheru Mandal, Sangareddy District, Hyderabad, Telangana
- Work Type: On-site
- Industry: Pharmaceutical Manufacturing – Sterile Injectables
- Facility: USFDA Approved Manufacturing Facility
Job Description
Anthea Pharma is hiring experienced Quality Assurance professionals for multiple roles within its sterile injectable manufacturing facility.
Candidates with expertise in regulatory compliance, validation, quality systems, and injectable manufacturing are encouraged to attend the walk-in interview.
Senior Officer / Executive – QA QMS
- Department: Quality Assurance – Quality Management System (QA-QMS)
- Market: Sterile Injectables
- Role: Senior Officer / Executive
- Experience: 3–6 Years
- Education/Qualification: B.Pharm, M.Pharm, or M.Sc.
Officer / Executive – QA Process & Cleaning Validation
- Department: Quality Assurance – Process & Cleaning Validation
- Market: Sterile Injectables
- Role: Officer / Executive
- Experience: 2–5 Years
- Education/Qualification: B.Pharm, M.Pharm, or M.Sc.
Junior Executive / Executive – QA Validation
- Department: Quality Assurance – Validation
- Market: Sterile Injectables
- Role: Junior Executive / Executive
- Experience: 2–5 Years
- Education/Qualification: B.Pharm, M.Pharm, or M.Sc.
Skills & Qualifications
- B.Pharm, M.Pharm, or M.Sc. qualification.
- Experience in sterile injectable manufacturing.
- Knowledge of Quality Management Systems.
- Experience handling deviations and CAPA.
- Expertise in change control management.
- Market complaint investigation experience.
- Technical writing proficiency.
- Regulatory inspection exposure.
- Knowledge of USFDA and MHRA regulations.
- Strong analytical and problem-solving skills.
- Good communication and teamwork abilities.
Key Responsibilities
- Manage deviations and CAPA activities.
- Handle change control documentation.
- Investigate market complaints.
- Prepare technical quality documents.
- Execute process validation protocols.
- Perform cleaning validation studies.
- Compile APQR reports.
- Conduct validation documentation.
- Prepare SOPs and protocols.
- Execute IQ, OQ, and PQ activities.
- Support regulatory inspections.
- Ensure GMP compliance.
Benefits & Perks
- Subsidized canteen facility.
- Transportation support.
- Opportunity to work at a USFDA-approved facility.
- Exposure to global regulatory standards.
- Professional learning opportunities.
- Stable pharmaceutical career growth.
- Collaborative work environment.
- Competitive industry exposure.
- Career advancement opportunities.
- Experience with advanced sterile manufacturing technologies.
How to Apply
Eligible candidates can attend the walk-in interview directly with an updated resume and relevant educational and experience documents.
Applicants may also share their profiles through the official recruitment email:
Email: recruitment@antheapharma.com
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Anthea career page.
For additional pharmaceutical job opportunities across India, visit https://pharmarecruiter.in to explore the latest openings and career resources.
Apply early and take the next step toward building a successful career with one of India’s leading sterile injectable pharmaceutical manufacturers.
Walk-in Interview Details
- Interview Date: 1st July 2026
- Time: 9:00 AM – 12:00 PM
- Venue: Anthea Pharma Private Limited, Plot No. 290, Sy. No. 219 & 183, Pashamylaram Village, Patancheru Mandal, Sangareddy District, Telangana – 502307
- Contact: 08455 696000
- Email: recruitment@antheapharma.com
Why You Should Join Anthea Pharma
Anthea Pharma offers professionals the opportunity to work in a globally compliant pharmaceutical environment focused on innovation, quality, and continuous improvement.
Employees gain valuable exposure to international regulatory standards while contributing to the manufacturing of advanced sterile injectable products.
The organization promotes professional development through challenging projects, modern manufacturing technologies, and a culture built around quality excellence.
Working at a USFDA-approved facility strengthens technical expertise and creates long-term career opportunities within the global pharmaceutical industry.
FAQs
Who can apply for these Quality Assurance jobs?
Candidates holding B.Pharm, M.Pharm, or M.Sc. qualifications with 2–6 years of relevant injectable manufacturing experience are eligible.
Is this a walk-in interview?
Yes. Interested candidates can attend the walk-in interview on 1st July 2026 between 9:00 AM and 12:00 PM.
Is prior experience in sterile injectables required?
Yes. Relevant experience in sterile injectable manufacturing and Quality Assurance is required for all available positions.
Does Anthea Pharma offer career growth opportunities?
Yes. Employees benefit from exposure to international regulatory standards, advanced manufacturing technologies, professional development, and long-term career progression within a globally focused pharmaceutical organization.
