US Pharmacopeia (USP) Recruitment Laboratory Scientist | Pharmacy or Analytical Chemistry – Hyderabad
- US Pharmacopeia (USP) Recruitment Laboratory Scientist | Pharmacy or Analytical Chemistry – Apply Now!
- Overview of USP Laboratory Scientist Job Opening
- Why Join US Pharmacopeia (USP)?
- Job Details
- Position: Scientist I – Verification Program
- Key Responsibilities
- Eligibility Criteria
- Preferred Skills & Competencies
- Benefits of Working at USP
- How to Apply?
- Final Thoughts
US Pharmacopeia (USP) Recruitment Laboratory Scientist | Pharmacy or Analytical Chemistry – Apply Now!
Overview of USP Laboratory Scientist Job Opening
The US Pharmacopeia (USP) is hiring a Laboratory Scientist for its Verification Program in Hyderabad, India. This is a full-time, non-supervisory role where the candidate will conduct analytical tests on dietary supplements and pharmaceutical ingredients. Professionals with M.Pharm or M.Sc. in Analytical Chemistry and 1-3 years of laboratory experience are encouraged to apply.
Why Join US Pharmacopeia (USP)?
USP is a globally recognized scientific organization committed to ensuring the quality of medicines and dietary supplements. This role offers an excellent opportunity to work with cutting-edge analytical techniques, contribute to global public health, and be part of a prestigious organization known for its scientific excellence and research integrity.
Job Details
Position: Scientist I – Verification Program
- Location: Hyderabad, India
- Job Type: Full-Time
- Department: Chemistry & Scientific Standards
- Experience: 1-3 years
- Education Required: M.Pharm / M.Sc. in Analytical Chemistry
- Industry: Pharmaceutical & Scientific Research
- Application Deadline: Ongoing
Key Responsibilities
- Perform analytical testing for dietary supplements and pharmaceutical ingredients.
- Conduct high-precision laboratory analysis using advanced instrumentation.
- Ensure compliance with USP, ICH, and FDA guidelines.
- Prepare comprehensive technical reports and respond to Quality Assurance (QA) observations.
- Operate and troubleshoot HPLC, GC, ICP-MS, ICP-OES, LC-MS, and other analytical instruments.
- Maintain laboratory Good Laboratory Practices (GLP) and ISO certifications.
- Assist in method validation and verification for analytical procedures.
- Participate in internal and external quality audits to ensure compliance.
- Work collaboratively with cross-functional teams for project execution.
Eligibility Criteria
Educational Qualification:
- Master’s degree in Pharmacy (M.Pharm) or Analytical Chemistry (M.Sc.).
Experience Required:
- 1 to 3 years of hands-on experience in a pharmaceutical QC laboratory or contract research organization (CRO).
- Proficiency in HPLC operation with Empower software and dissolution analysis.
- Hands-on experience with GC, ICP-OES, ICP-MS, and LC-MS preferred.
- Knowledge of ICH guidelines, FDA regulations, and compendial procedures (USP, BP, EP, JP, etc.) is a plus.
- Prior experience with Electronic Laboratory Notebooks (ELN) is an advantage.
Preferred Skills & Competencies
- Strong analytical and troubleshooting skills in instrumental analysis.
- Ability to work on high-priority projects and meet deadlines.
- Excellent documentation and reporting skills.
- Strong interpersonal skills to collaborate with cross-functional teams.
- Commitment to continuous learning and innovation in laboratory practices.
Benefits of Working at USP
USP offers competitive salary packages along with a comprehensive benefits program, including:
- Health & wellness benefits
- Paid time off
- Professional development programs
- Retirement savings plans
- Collaborative and growth-oriented work environment
How to Apply?
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