R&D/Mfg Scientist II

NCBioImpact; Greenville (NC); On-site; USD 85,000 - 110,000; Full time

Job summary

NCBioImpact is seeking an R&D Scientist II to perform routine analyses in chemistry/biochemistry, supporting process development and manufacturing operations. The role includes method development, validation, and data reporting for HPLC, GC, and related techniques.

Responsibilities emphasize rigorous data review, adherence to regulatory guidelines, and collaboration with project teams to ensure timely delivery and quality.

Qualifications

• Bachelor’s degree in chemistry/biochemistry/molecular biology or related field with 3+ years of experience, or
• Master’s degree with 1+ year pharmaceutical experience preferred.
• Experience with HPLC.
• Experience with HPLC, GC, Dissolution, FT-IR, UV, Karl Fischer Titration, IEF, ELISA, CGE, Dot-Blot preferred.
• Experience with method development and validation, analytical techniques, and chromatographic/spectroscopic methods preferred.
• EMPOWER experience preferred.
• Strong knowledge of chemistry and analytical instrument technologies.
• Awareness of quality and regulatory requirements in pharmaceutical industry.
• Fluent in English.

Responsibilities

• Lead/execute development, evaluation, validation and transfer of test methods for pharmaceutical materials and products.
• Perform testing for strength, impurities, identity, potency, and dissolution by multiple analytical techniques.
• Identify out-of-spec results and communicate issues.
• Review data against specifications and standard procedures.
• Maintain compliance with cGMP, GLP, USP/EP, and data integrity requirements.
• Assist in trainings as SME and participate in client teleconferences.

Skills

Communication skills

Reading procedures

Organizational skills

Attention to detail

Written reports

Education

Bachelor’s degree in Chemistry/Biochemistry/Molecular Biology or related

Master’s degree in related field

Tools

HPLC

GC

Dissolution

FT-IR

UV

Karl Fischer Titration

IEF

ELISA

CGE

Dot-Blot

EMPOWER

Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

POSITION SUMMARY

The R&D Scientist II provides routine analyses in a chemistry and biochemistry environment within defined procedures and practices. Performs analytical methods for moderately sophisticated testing on samples, stability, and production intermediates to support process development and/or manufacturing operations. May research and implement new methods and technologies to improve operations. Makes detailed observations and reviews, documents, and communicates test results.

Key Responsibilities

• Lead/Execute the development, evaluation, validation and transfers of test methods for pharmaceutical raw materials and finished products for strength, impurities, identity, potency, and dissolution by HPLC, GC, IEF, CGE and compendial testing
• Execute testing for pharmaceutical raw materials and finished products for strength, impurities, identity, potency, and dissolution by HPLC, GC, IEF, CGE and compendial testing
• Recognize and report out-of-specification or unexpected results and non-routine analytical and product problems
• Determine if reported data meets specification or expected standards
• Demonstrate advanced knowledge and experience in Empower
• Demonstrate knowledge in methodvalidation/transfer/evaluation/development
• Perform daily instrument calibrations/verifications as required
• Perform cGMP analytical data review for various techniques to ensure adherence to established procedures, analytical standards, GVLs and SOP
• Ensure that all laboratory testing and activities are carried out in compliance with regulations, ICH guidelines, and USP/EP Pharmacopeia, GMP and data integrity requirements
• Might Author and/or review: OOS investigations, Deviations and Change Controls, technical reports, Protocols and validation summaries , SOPs, specification documents
• Ensure all job-related safety training and compliance requirements are met
• Might assist in trainings as an SME
• Communicate with Project Lead/Management concerning project status and/or concerns
• Strong attention to detail and organizational skills
• Must be able to set project priorities and time management in order to maximize productivity
• Actively participate in ongoing trainings and seek out opportunities to increase contributions for development of skills and responsibilities
• Might run projects at the broad task level under supervision, ensuring deliverables are met and next steps are clearly identified
• Participate in meetings/teleconferences with clients
• Performs all duties in compliance with Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices, and Safety guidelines. Maintains the compliance status required by company and facility standards

Qualifications

• Bachelor Degree in Chemistry, Biochemistry, Molecular Biology, or related physical/biological science field minimally required with 3+ years related experience, or
• Master’s degree, 1+ year related pharmaceutical industry experience strongly preferred.
• Experience with HPLC.
• Experience with HPLC, GC, Dissolution, FT-IR, UV, Karl Fischer Titration, IEF, ELISA, CGE, Dot-Blot preferred
• Experience performing method development and validation, chemical tests with chromatographic, spectroscopic, or other analytical techniques preferred
• Experience with EMPOWER preferred.
• Equivalent combinations of education, training, and meaningful work experience will be considered.
• Good knowledge and understanding of chemistry and analytical instrumental technologies.
• Good knowledge of qualitative and quantitative chemical or microbiological analysis.
• Awareness of quality and regulatory requirements in the pharmaceutical industry
• Strong interpersonal and communications skills, written and oral
• Ability to read, analyze, and interpret technical procedures and governmental regulations.
• Excellent organization and planning skills.
• Strong attention to detail and ability to implement to standard procedures.
• Ability to design and complete tasks and studies based on the deliverables.
• Ability to accurately detail work and write reports.
• Fluent in English

Physical Requirements

Position requires ordinary ambulatory skills and physical coordination sufficient to move about office locations. Ability to stand, walk, stoop, kneel, crouch periodically for prolonged periods of time Manipulation (lift, carry, move) of light to medium weights of 10-35 pound pounds. Arm, hand and finger dexterity, including ability to grasp and type for prolonged periods of time. Visual acuity to use a keyboard, computer monitor, operate equipment, and read materials for prolonged periods of time. Ability to sit, reach with hands and arms, talk, and hear for prolonged periods of time. Safety glasses, safety shoes, lab coat, nitrile or similar gloves, safety apron, organic respirator occasionally.