Anthea Pharma Hiring 2026 – QC & Analytical Jobs in Hyderabad

Looking for Quality Control and analytical research jobs in Hyderabad?

Anthea Pharma Private Limited is hiring experienced professionals for multiple Quality Control and analytical functions at its facility in Pashamylaram, Patancheru Mandal, Sangareddy District, Telangana.

The current openings cover areas including analytical data review, method verification, method validation, analytical method transfer, HPLC, GC, dissolution, laboratory compliance and GLP.

The recruitment drive is suitable for professionals with approximately 2 to 10 years of relevant experience, depending on the position.

About Anthea Pharma

Anthea Pharma Private Limited is a global Contract Development and Manufacturing Organization (CDMO) specializing in complex injectable formulations.

Its product expertise includes areas such as:

• Vials
• Lyophilized vials
• Emulsions
• Prefilled syringes

The current vacancies are focused on Quality Control and analytical laboratory functions, making them relevant for professionals with pharmaceutical analytical testing, method validation and laboratory compliance experience.

Anthea Pharma Job Overview

Details	Information
Company	Anthea Pharma Private Limited
Department	Quality Control
Functions	Analytical Review, Method Validation, GLP & QC
Location	Pashamylaram, Telangana
Experience	2–10 Years, role dependent
Work Type	On-site
Interview Type	Walk-In
Interview Date	10 October 2026
Interview Time	9:00 AM – 12:00 PM
Email	recruitment@antheapharma.com

Anthea Pharma QC Job Openings

1. Reviewer / Senior Reviewer – Quality Control

Experience: 8–10 Years

Qualification:

• M.Pharm
• M.Sc

Key Skills & Responsibilities

Candidates should have experience in:

• Protocol preparation
• Report preparation
• Protocol review
• Analytical data review
• Analytical Method Validation (AMV) documentation
• QMS investigations
• Regulatory compliance

Knowledge of pharmaceutical regulatory guidelines including ICH, USP and EP is relevant for this position.

2. Officer / Analyst – Quality Control

Experience: 2–4 Years

Qualification: Not separately specified in the supplied recruitment information.

Key Skills & Requirements

Candidates should have hands-on experience with:

• HPLC
• GC
• GC-HS
• UV
• Wet analysis
• Assay testing
• Related substances
• Dissolution
• Residual solvents
• Analytical documentation

Experience or exposure in the following areas is also relevant:

• API method verification
• Finished-product method validation
• Analytical method transfer
• Injectable/sterile products
• Regulated-market products

3. Executive / Senior Executive – Quality Control

Experience: 5–10 Years

Qualification:

• B.Pharm
• M.Pharm
• M.Sc

Key Skills & Requirements

The role requires strong experience in:

• Method verification
• Analytical method validation
• Method transfer
• HPLC
• UPLC
• GC-HS
• Dissolution
• Analytical troubleshooting
• Protocol execution
• Protocol preparation
• Report preparation

Experience with injectable/sterile products and regulated-market products is relevant.

4. Executive / Senior Executive – GLP

Experience: 4–8 Years

Qualification:

• B.Pharm
• M.Pharm
• M.Sc

Key Skills & Responsibilities

This position focuses on Good Laboratory Practices and laboratory compliance.

Relevant experience includes:

• GLP compliance
• Laboratory compliance
• Sample management
• Reagent management
• Standard management
• Column management
• Instrument logbooks
• Documentation review
• Audit readiness
• Data integrity and ALCOA+
• GMP/GLP compliance
• Laboratory investigations
• SOP management
• Regulatory inspection support

Eligibility Criteria

The requirements vary according to the position.

QC Reviewer / Senior Reviewer

• M.Pharm / M.Sc
• 8–10 years of relevant experience

QC Officer / Analyst

• 2–4 years of relevant analytical/QC experience
• Qualification is not separately specified in the supplied information

QC Executive / Senior Executive

• B.Pharm / M.Pharm / M.Sc
• 5–10 years of experience

GLP Executive / Senior Executive

• B.Pharm / M.Pharm / M.Sc
• 4–8 years of experience

Candidates with experience in pharmaceutical analytical laboratories, injectable/sterile products and regulated markets may be particularly relevant for several of the positions.

Analytical Skills Required

Depending on the position, candidates should have experience in:

• HPLC
• UPLC
• GC
• GC-HS
• UV spectroscopy
• Wet analysis
• Dissolution testing
• Assay
• Related substances
• Residual solvents
• Analytical method verification
• Analytical method validation
• Analytical method transfer
• Analytical data review
• Protocol and report preparation

Quality & Compliance Skills

The recruitment information also highlights experience in:

• GMP
• GLP
• QMS
• Data integrity
• ALCOA+
• Laboratory investigations
• SOP management
• Audit readiness
• Regulatory inspection support
• ICH guidelines
• USP requirements
• EP requirements

These skills are particularly relevant for senior QC review and GLP-focused positions.

Injectable & Regulated-Market Experience

Some of the positions specifically mention injectable/sterile product experience and exposure to regulated-market products.

Professionals who have worked with sterile pharmaceutical products and regulated-market requirements may therefore find these roles particularly relevant.

Anthea Pharma Walk-In Interview Details

🗓️ Date

10 October 2026

⏰ Time

9:00 AM to 12:00 PM

📍 Interview & Work Location

Anthea Pharma Private Limited
Plot No. 290, Sy. No. 219 & 183
Pashamylaram (V), Patancheru Mandal
Sangareddy District, Telangana – 502307

Benefits & Preferences

The recruitment information mentions:

• Subsidized canteen
• Transportation facility
• Immediate joiners preferred
• Male candidates preferred

Candidates should confirm the applicable employment terms and benefits with the recruitment team.

Documents to Carry

Candidates attending the walk-in should carry:

• Updated Resume/CV
• Educational certificates
• Relevant experience documents
• Government-issued ID proof
• Other documents requested by the recruitment team

Experienced candidates should be prepared to discuss their hands-on experience with analytical instruments, method validation/transfer, QC review or GLP activities, depending on the position.

How to Apply

Eligible candidates can attend the walk-in interview directly at the Pashamylaram facility.

Candidates can also contact the recruitment team through:

Email: recruitment@antheapharma.com

Before travelling, candidates are advised to confirm the latest vacancy status, position availability and interview arrangements.

Why Consider Anthea Pharma QC Careers?

These positions can be relevant for professionals looking to strengthen their careers in:

• Pharmaceutical Quality Control
• Analytical Method Validation
• Method Transfer
• Analytical Data Review
• Injectable/sterile product testing
• GLP and laboratory compliance
• Quality systems
• Regulatory inspection readiness

The range of positions also provides opportunities across different experience levels, from 2–4 years to 8–10 years.

Frequently Asked Questions

1. When is the Anthea Pharma walk-in interview?

The walk-in interview is scheduled for 10 October 2026, from 9:00 AM to 12:00 PM.

2. Where is the interview being conducted?

The interview will be held at Anthea Pharma Private Limited, Pashamylaram, Patancheru Mandal, Sangareddy District, Telangana – 502307.

3. What qualifications are required?

The listed senior QC and GLP positions accept B.Pharm, M.Pharm or M.Sc candidates. The qualification for the Officer/Analyst role is not separately specified in the supplied information.

4. What experience is required?

Experience requirements range from 2 to 10 years, depending on the position.

5. Which analytical instruments are mentioned?

The recruitment details mention HPLC, UPLC, GC, GC-HS and UV, along with wet analysis and dissolution testing.

6. Which positions involve method validation?

The Officer/Analyst and Executive/Senior Executive QC positions mention method verification, method validation and analytical method transfer.

7. Is injectable experience preferred?

Yes. Injectable/sterile product experience is specifically mentioned for some of the QC positions.

8. What does the GLP position involve?

The GLP role covers laboratory compliance, sample and reagent management, instrument logbooks, documentation review, audit readiness, ALCOA+, investigations, SOP management and regulatory inspection support.

9. Are immediate joiners preferred?

Yes. Immediate joiners are given preference according to the supplied recruitment information.

10. How can I apply?

Attend the walk-in interview or contact the recruitment team at recruitment@antheapharma.com.