Top 9 Hplc Jobs in Manassas, Va

Scientist I, AR&D
Granules Pharmaceuticals —Chantilly, VA
- $65,000 - $75,000 a year
- Full-time
- Microsoft Word
- Master's degree
- Bachelor's degree
Quick Apply
Scientist III, Analytical R&D
Granules Pharmaceuticals —Chantilly, VA
- $85,000 - $95,000 a year
- Full-time
- Writing skills
- 3 years
- Master's degree
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Research Scientist
Smoore Labs —Manassas, VA
- $85,000 - $100,000 a year
- Full-time
- English
- Analysis skills
- Doctor of Philosophy
- Health insurance
- Dental insurance
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4d
Biochemist I/II (QC Analyst)
Granules Pharmaceuticals —Chantilly, VA
- $55,000 - $80,000 a year
- Multiple hires
- Bachelor of Science
- Mid-level
- Bachelor's degree
Quick Apply
Formulation Scientist (Solid Orals)
Granules Pharmaceuticals —Chantilly, VA
- $100,000 - $110,000 a year
- Full-time
- Data analysis skills
- Master's degree
- Doctor of Philosophy
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Senior Chemist
Joint Research and Development, LLC —Indian Head, MD
- $120,000 - $140,000 a year
- Full-time
- Microsoft Excel
- Bachelor of Science
- Writing skills
- AD&D insurance
- Disability insurance
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Senior Staff, Clinical Chemistry
Guidehouse —Bethesda, MD
- $149,000 - $248,000 a year
- Full-time
- Medicine
- Management
- 8 years
- Commuter assistance
- Health savings account
Analytical Chemist
Guidehouse —Bethesda, MD
- $98,000 - $163,000 a year
- Full-time
- Bachelor of Science
- Bachelor's degree
- Continuous improvement
- Commuter assistance
- Health savings account

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Scientist I, AR&D

Granules Pharmaceuticals -
Chantilly, VA

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Job Details

Full-time
$65,000 - $75,000 a year

Qualifications

Microsoft Word
Computer operation
Personal protective equipment (PPE) use
Spreadsheets
Good documentation practices (GDP)
Pharmaceutical company experience
Pharmaceutical analysis
Compliance documentation
GMP for research safety and compliance
Chemical testing
Test validation method
Validation design
Respirator

Full Job Description

Description:

Granules Pharmaceuticals Inc., (GPI) is a subsidiary of Granules India LTD. Over the past 34 years, we have worked towards strengthening our core and we are currently the 10th fastest growing generic pharma company in the US!

With our sites in Chantilly and Manassas, Virginia, we have R&D through manufacturing and packaging of our medicines including pulsatile drug release in tablet and capsule dosage form, orally disintegrating modified release tablets (XR, MR, ER), modified release suspension and controlled substances capabilities in an abuse deterrent technology platform.

We are dedicated to excellence in manufacturing, quality, and commercialization of generic drugs to give customers reliable and affordable options.

**US Based CANDIDATES ONLY**

Job Summary:

As a Scientist I on our Analytical R&D team, you would be responsible for testing the product development samples and supporting R&D team on timely manner with analytical sample testing. This includes performing the Assay Dissolution, analytical method development, and method validation including preparing analytical method validation and verification protocols . Additionally, you would be responsible for the testing and release of in-process, finished product, and Stability samples including process evaluation samples.

Following SOPs to complete tasks, while ensuring safe and efficient execution of job duties is crucial in this role.

Job Duties and responsibilities include but not limited to:

Proficient in operating the laboratory instrumentation/equipment, including but not limited to: FTIR, HPLC, UPLC, Dissolution apparatus, ICP-MS, GC, UV-Vis, Karl fisher (KF), Ion chromatography (IC), Malvern Master sizer, etc.
Support the R&D team by testing the process development sample for content uniformity, blend uniformity, Assay, particle size distribution, density, water determination by KF, viscosity, and other tests as required.
Conduct analytical method development, method optimization, method validation, method verification and method transfer for finish products.
Draft test methods, method validation protocols and reports as per the Company SOPs and regulatory guidelines
Perform additional analytical testing (multimedia dissolution, photo stability, Dose dumping etc.) for ANDA submission
Timely execution and completion of assigned tasks
Document experiments accurately and complete all associated documents (Instrument, Standard and Column usage logbooks) in compliance with internal SOPs and FDA guidelines
Maintain work area and laboratory with good housekeeping practices and in compliant with cGMP.
Identify and communicate continuous improvement opportunities to the Analytical Manager and Director
Monitor and ensure availability of chemicals, columns, standards, and other consumable for sample testing.
Other duties assigned by management based on requirements

Management responsibilities include:

Assign daily work schedule in timely manner
Provide guidance in method Development and validation.
Interpret and review generated results
Provide assistance in professional development.

Requirements:

Minimum Education & Experience:

Bachelor's degree in Pharmaceutical Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or related area with 5+ years of directly related experience in pharmaceutical industry OR
Master's degree in Pharmaceutical Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or related area with 2+ years of directly related experience in pharmaceutical industry
Knowledge of Good Manufacturing Practices (cGMP)
Experience with software and information systems (e.g. Empower, Microsoft word and Excel)

Required Knowledge, Skills, & Abilities

Proven Knowledge of the major analytical techniques and operation of instruments such as HPLC, GC, dissolution, FT-IR, UV-VIS Spectrophotometer, Particle size analysis (Malvern Mastersizer, Sonic sifting and Sieve shaker), Karl Fisher Instrument, Potentiometric Titration, Density meter, pH meter, Melting point apparatus, Analytical Balances, Viscometer
Experience with HPLC Method development & validation
Proficient in documentation as per Good Documentation Practice
Computer skills including Microsoft and Excel
Excellent verbal and written communication and skills

Physical Requirements/Working Environment:

Must be able to stand for long periods of time (up to 12-hour shifts), maneuver at least 40 pounds, wear a respirator and pass associated respirator tests and/or requirements, and be able to wear all required PPE.
Vision - ability to see details at close range (within a few feet of the observer).

Disclaimer

The above information on this description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job.

We believe in fair and transparent pay practices. Actual compensation is determined based on relevant experience, qualifications, skills, and internal equity.

Quick Apply

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hplc jobs in manassas, va

Scientist I, AR&D

Scientist III, Analytical R&D

Research Scientist

Biochemist I/II (QC Analyst)

Formulation Scientist (Solid Orals)

Senior Chemist

Senior Staff, Clinical Chemistry

Analytical Chemist

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