Intellectt is hiring R&D Scientists, QC Analysts, and Manufacturing Technicians across the USA for long-term pharmaceutical contracts. Apply now for high-paying pharma jobs with HPLC, LCMS, GMP, cGMP expertise.
Intellectt Pharma Hiring R&D Scientists, QC Analysts & Manufacturing Technicians in USA – High Paying Jobs 2025
Are you seeking a high-paying, long-term career in the pharmaceutical industry in the United States? This is your opportunity to join Intellectt, one of the most dynamic staffing and consulting companies partnering with leading pharmaceutical, biotech, and life sciences companies across the USA.
Intellectt is actively hiring R&D Scientists, Quality Control (QC) Analysts, and Manufacturing Technicians for multiple long-term contract roles. These positions offer excellent career growth, exposure to regulated markets, and competitive compensation packages.
With expertise in HPLC, LCMS, method development, method validation, analytical chemistry, GMP compliance, manufacturing operations, and lab documentation, you can step into some of the most lucrative pharmaceutical roles available in 2025.
🔎 Open Positions at Intellectt
1️⃣ R&D Scientist – Analytical Method Development
- Location: Open to candidates across the USA
- Employment Type: Long-Term Contract
Key Responsibilities:
- Develop and optimize analytical methods for complex pharmaceutical formulations.
- Conduct HPLC (High-Performance Liquid Chromatography) and LCMS (Liquid Chromatography Mass Spectrometry) testing.
- Perform method development, validation, and transfer in compliance with cGMP and ICH guidelines.
- Document experiments, validation protocols, and technical reports with accuracy.
- Maintain laboratory records as per regulatory and internal Standard Operating Procedures (SOPs).
- Collaborate with cross-functional teams including R&D, Quality Assurance, and Manufacturing.
Required Skills & Expertise:
- Strong hands-on experience in HPLC, LCMS, Analytical Chemistry, and Method Development.
- In-depth understanding of FDA, ICH, and global regulatory compliance standards.
- Experience in handling analytical instrumentation, troubleshooting, and validation processes.
- Solid documentation skills with accuracy and attention to detail.
- Knowledge of cGMP (current Good Manufacturing Practices) and GLP (Good Laboratory Practices).
Core Focus Areas:
HPLC | LCMS | Analytical Method Development | Method Validation | Analytical Chemistry | Pharmaceutical R&D | ICH Guidelines | cGMP | Documentation | Validation Protocols | Data Integrity | FDA Compliance
2️⃣ Quality Control Analyst – Analytical Testing
- Location: Open to candidates across the USA
- Employment Type: Long-Term Contract
Key Responsibilities:
- Conduct comprehensive analytical testing of pharmaceutical products.
- Perform routine and non-routine testing using HPLC, UV Spectrophotometry, Chromatography, and Dissolution Testing.
- Maintain compliance with GMP standards, FDA regulations, and internal SOPs.
- Accurately document and report results per regulatory requirements.
- Support investigations related to Out-of-Specifications (OOS), deviations, CAPA, and lab troubleshooting.
- Collaborate closely with QA, R&D, and Manufacturing departments.
Required Skills & Expertise:
- Hands-on experience in pharma QC testing using HPLC, Chromatography, UV Spectrophotometry.
- Understanding of cGMP regulations, FDA guidelines, and ICH standards.
- Strong experience in laboratory troubleshooting and documentation accuracy.
- Prior experience supporting regulatory inspections and audits is a strong plus.
- Excellent interpersonal and communication skills to work within cross-functional teams.
Core Focus Areas:
HPLC | Chromatography | Dissolution Testing | UV Spectrophotometry | Quality Control | GMP Compliance | FDA Audit Support | Lab Documentation | Data Integrity | CAPA | Deviation Handling | Analytical Testing
3️⃣ Manufacturing Technician – Pharmaceutical Production
- Locations: Multiple locations across the USA
- Employment Type: Long-Term Contract
- Start Date: Immediate
Key Responsibilities:
- Execute assembly, troubleshooting, and maintenance of pharmaceutical equipment.
- Work with hand tools and follow SOPs for manufacturing processes.
- Perform routine production activities ensuring cGMP and safety compliance.
- Maintain documentation for equipment maintenance, production logs, and deviation reports.
- Support equipment qualification and preventive maintenance procedures.
- Collaborate with Engineering, Manufacturing, and Quality Assurance teams for smooth operations.
Required Skills & Expertise:
- Solid experience with core manufacturing processes, troubleshooting, and equipment assembly.
- Working knowledge of cGMP, FDA regulatory compliance, and cleanroom protocols.
- Ability to follow detailed work instructions and operate within highly regulated environments.
- Prior experience with pharmaceutical equipment such as tablet presses, blister packaging, filling lines is highly desirable.
- Excellent safety awareness, teamwork, and communication skills.
Core Focus Areas:
Manufacturing Technician | Assembly & Troubleshooting | GMP Compliance | Pharmaceutical Equipment | Preventive Maintenance | Manufacturing SOPs | FDA Regulatory Compliance | Process Documentation | Safety Standards
💼 Why Join Intellectt?
- Work with some of the top pharmaceutical, biotech, and life sciences companies in the regulated US market.
- Exposure to USFDA inspections, global regulatory audits, and compliance requirements.
- Excellent compensation with benefits tailored for long-term contract roles.
- Opportunity to develop advanced skills in HPLC, LCMS, analytical chemistry, GMP manufacturing, and regulatory compliance.
- Join a high-growth company that values career development and offers a collaborative work culture.
📩 How to Apply:
Address: 1105, Gachibowli Cir,
P Janardhan Reddy Nagar, Gachibowli,
Hyderabad, Telangana 500081
Ph. No. +91 7324-126-999
Interested candidates should send their updated resumes to:
Or directly message via DM for faster screening and interview scheduling.
📊 Pharma Contract Staffing Growth in USA
The demand for skilled professionals in pharmaceutical contract positions in the USA is rapidly increasing due to rising regulatory scrutiny, expansion of biologics and gene therapies, advanced drug delivery systems (MDI, DPI, injectables), and global regulatory harmonization under ICH and FDA standards. Intellectt provides an excellent platform for professionals to gain hands-on experience across these fast-evolving sectors while ensuring career growth and job security in the highly competitive pharmaceutical labor market.
📈 Industry Outlook for 2025
- The global pharmaceutical contract workforce is expected to grow by 11% CAGR through 2025.
- Specializations such as analytical method validation, HPLC LCMS troubleshooting, cGMP manufacturing, FDA documentation, and regulatory audit preparedness are highly in-demand.
- Entry-level and mid-level professionals with 2-5 years experience in pharma R&D, QC, or manufacturing can command 6-figure salaries in the US market.
- Remote and hybrid work opportunities are expanding in regulatory documentation, data integrity management, and QA/QC virtual audits.
🔔 Disclaimer:
This job posting is provided for informational purposes. Candidates are encouraged to apply directly through the official email provided. No fees are charged for applications.
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