Quality Control Jobs in Hyderabad | Anthea Pharma Careers
Anthea Pharma Private Limited is hiring for Quality Control and analytical functions at its facility in Pashamylaram, Patancheru Mandal, Sangareddy District, Telangana.
The company is a global CDMO specializing in complex injectable formulations including vials, lyophilized vials, emulsions and prefilled syringes.
The advertised positions cover analytical review, method validation, HPLC, GC, laboratory compliance and GLP functions.
Anthea Pharma Hiring for below positions
Department: Quality ControlÂ
1) Designation: Reviewer / Sr. Reviewer
Experience: 8–10 Years
Qualification: M.Pharm / M.Sc
Key Skills / Job Description:
Experience in protocol/report preparation, protocol/report review, Analytical Data review (AMV), QMS investigations, and regulatory guideline compliance (ICH, USP, EP).
B)Â Designation: Officer / Analyst
Experience: 2–4 Years
Qualification: Not separately specified in the poster
Key Skills / Job Description:
Experience in HPLC, GC, GC-HS, UV and Wet Analysis.
Exposure to API Method Verification, FP Method Validation, and Analytical Method Transfer activities.
Hands-on experience in Assay, Related Substances, Dissolutions, Residual Solvents, and documentation.
Candidates with Injectable (Sterile) Product Experience and exposure to regulated market products.
C)Â Designation: Executive / Sr. Executive
Experience: 5–10 Years
Qualification: B.Pharm / M.Pharm / M.Sc
Key Skills / Job Description:
Expertise in execution of Method Verification, Validation, and Transfers.
Strong hands-on experience in HPLC, UPLC, GC-HS, Dissolution, troubleshooting, protocol execution, protocol and report preparation.
Candidates with Injectable (Sterile) Product Experience and exposure to regulated market products.
D)Â Designation: Executive / Sr. Executive (GLP)
Experience: 4–8 Years
Qualification: B.Pharm / M.Pharm / M.Sc
Key Skills / Job Description:
Strong knowledge of Good Laboratory Practices, laboratory compliance, sample management, reagent/standard/Column management, instrument logbooks, documentation review, audit readiness, data integrity (ALCOA+), GMP/GLP compliance, laboratory investigations, SOP management, and regulatory inspection support.
Walk-In Interview Details:Â
Date: 10th October 2026
Time: 9:00 AM to 12:00 PM
Work Location / Interview Address: Plot No. 290, Sy. No. 219 & 183, Pashamylaram (V), Patancheru Mandal, Sangareddy District, Telangana – 502307
Benefits: Subsidized Canteen & Transportation
Preference: Male candidates preferred.
Joining: Immediate joiners will be given preference.
Email: recruitment@antheapharma.com
FAQs
1. Which analytical techniques are mentioned for the Anthea Pharma positions?
The poster mentions HPLC, UPLC, GC, GC-HS, UV, Wet Analysis and Dissolution among the analytical areas.
2. Which positions are specifically connected with method validation and verification?
The Officer/Analyst and Executive/Sr. Executive positions mention method verification, method validation and analytical method transfer activities.
3. What type of product experience is preferred for some positions?
The poster specifically mentions Injectable (Sterile) Product Experience and exposure to regulated market products.
4. What regulatory standards are mentioned for the Reviewer/Sr. Reviewer role?
The position mentions regulatory guideline compliance including ICH, USP and EP.
5. What does the GLP position focus on?
The GLP role covers laboratory compliance, sample management, reagent/standard/column management, documentation review, audit readiness, ALCOA+, GMP/GLP compliance, laboratory investigations, SOP management and regulatory inspection support.
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| Anthea Pharma Quality Control Method Validation Walk-In Interview |
