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Manager Hplc Analyst Jobs in Virginia (NOW HIRING)

Scientist I, AR&D

Chantilly, VA · On-site

$65K - $75K/yr

FTIR, HPLC, UPLC, Dissolution apparatus, ICP-MS, GC, UV-Vis, Karl fisher (KF), Ion chromatography ... Identify and communicate continuous improvement opportunities to the Analytical Manager and ...

Scientist I, AR&D

Chantilly, VA · On-site

$65K - $75K/yr

FTIR, HPLC, UPLC, Dissolution apparatus, ICP-MS, GC, UV-Vis, Karl fisher (KF), Ion chromatography ... Identify and communicate continuous improvement opportunities to the Analytical Manager and ...

Manager, Analytical R&D

Chantilly, VA · On-site

$100K - $130K/yr

Manage day to day laboratory operations and supervise group's daily activities. * Plan and execute ... Hands-on experience with drug substance and drug product analytical techniques such as HPLC, GC, KF ...

PET Chemist

Salem, VA · On-site

$60K - $75K/yr

Support analytical methods for HPLC, GC and TLC. Quality Control testing of final product. 2.  ... Superior teamwork, multi-tasking and time/project management skills. Excellent communication ...

Review and approve batch records, analytical data, SOPs, and other quality documentation. * Lead ... Strong knowledge of HPLC, GC, FTIR, and wet chemistry techniques. * Deep understanding of data ...

New

Manager, Quality Control

Petersburg, VA · On-site

$100K - $140K/yr

Review and approve batch records, analytical data, SOPs, and other quality documentation. * Lead ... Strong knowledge of HPLC, GC, FTIR, and wet chemistry techniques. * Deep understanding of data ...

New

Manager, Quality Control

Petersburg, VA · On-site

$100K - $140K/yr

Review and approve batch records, analytical data, SOPs, and other quality documentation. * Lead ... Strong knowledge of HPLC, GC, FTIR, and wet chemistry techniques. * Deep understanding of data ...

New

PET Chemist

Salem, VA · On-site

$60K - $75K/yr

Support analytical methods for HPLC, GC and TLC. Quality Control testing of final product. 2.  ... Superior teamwork, multi-tasking and time/project management skills. Excellent communication ...

PET Chemist

Salem, VA · On-site

$60K - $75K/yr

Support analytical methods for HPLC, GC and TLC. Quality Control testing of final product. 2.  ... Superior teamwork, multi-tasking and time/project management skills. Excellent communication ...

Manages the AR&D function in the laboratory to ensure cGMP compliance. * Other duties related to ... Hands-on experience with drug substance and drug product analytical techniques such as HPLC, GC, KF ...

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Manager Hplc Analyst information

What is a Manager HPLC Analyst?

A Manager HPLC Analyst is a professional responsible for overseeing laboratory operations related to High Performance Liquid Chromatography (HPLC) analysis. They manage a team of analysts, ensure proper method development and validation, review data for quality and accuracy, and maintain compliance with regulatory standards. This role often involves troubleshooting instruments, training staff, and collaborating with other departments to support research and product development. Strong technical expertise in HPLC techniques and leadership skills are essential for this position.

What are the main challenges a Manager HPLC Analyst faces in leading a laboratory team?

A Manager HPLC Analyst often navigates challenges such as ensuring data integrity, maintaining compliance with regulatory standards, and troubleshooting complex analytical issues. Balancing managerial duties with hands-on technical work can be demanding, as you’ll oversee method development, validation processes, and team training while also handling client communications and project timelines. Building a cohesive team and fostering a culture of continuous improvement are essential for maintaining high productivity and quality results in the laboratory.

What key skills and qualifications are needed to thrive as a Manager HPLC Analyst, and why are they important?

To thrive as a Manager HPLC Analyst, you need deep expertise in analytical chemistry, particularly in high-performance liquid chromatography (HPLC), along with a relevant scientific degree such as chemistry, biochemistry, or pharmaceutical sciences. Familiarity with HPLC instrumentation, chromatography data systems (like Empower or ChemStation), and regulatory standards such as GLP or GMP is crucial, and certifications in laboratory management or analytical techniques are advantageous. Strong leadership, problem-solving abilities, and excellent communication skills enable effective team management and cross-functional collaboration. These competencies ensure accurate data generation, regulatory compliance, and efficient workflow in analytical laboratories.

What is the difference between Manager Hplc Analyst vs Hplc Analyst?

AspectManager Hplc AnalystHplc Analyst
CredentialsBachelor's degree, often with supervisory or management experienceBachelor's degree in chemistry, biochemistry, or related field
Work EnvironmentSupervisory role overseeing testing teams, quality control, and reportingPerforming HPLC testing, data analysis, and method development
Industry UsageUsed in pharmaceutical, biotech, and research industries for leadership rolesCommonly employed in laboratories for analytical testing

The main difference between a Manager Hplc Analyst and an Hplc Analyst is the level of responsibility. The Manager Hplc Analyst oversees testing teams, manages projects, and ensures quality standards, while the Hplc Analyst focuses on performing tests and analyzing data. Both roles require similar technical skills, but the manager position involves leadership and coordination duties.

What cities in Virginia are hiring for Manager Hplc Analyst jobs?

Cities in Virginia with the most Manager Hplc Analyst job openings:

$65K - $75K/yr

Full-time

Re-posted 3 days ago


Job description

Job Type
Full-time
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.
Salary Description
$65,000 - $75,000 per year