QC Associate I-Raw Materials Lab

Fareva Richmond Inc; Richmond (VA); On-site; USD 52,000 - 70,000; Full time

Benefits offered by this job

Onsite cafeteria

Paid vacation

Career advancement opportunities

Job summary

Fareva in Richmond, VA is seeking a QC Associate for the Raw Materials Lab. You will perform chemical and physical assays on raw materials and production intermediates, compare results to specifications, and document findings under GMP guidelines.

Ideal candidates hold a BS or MS in Chemistry or Biochemistry with 0–1 year of QA experience, familiarity with LIMS, and the ability to follow SOPs. We offer competitive salaries and a comprehensive benefits package.

Qualifications

• BS degree in Chemistry or Biochemistry; 0–1 year of relevant QA experience.
• MS degree in Chemistry or Biochemistry; 0–1 year of relevant QA experience.
• Requires basic knowledge of fundamental quality concepts and cGMPs.
• Desirable: experience with LIMS and electronic documentation systems.

Responsibilities

• Perform chemical or physical assays of raw materials, production intermediates and bulk samples.
• Analyze results, record observations and ensure accuracy and validity of test results.
• Use LIMS and SOPs to manage data and resolve technical issues.
• Schedule daily lab assignments and maintain related records and site housekeeping.
• Follow SOPs and applicable regulations to ensure compliant testing and documentation.

Skills

HPLC

GC

TLC

UV/VIS

FTIR/ATR

LIMS

cGMP

Quality control

Problem solving

Teamwork

Education

BS in Chemistry/Biochemistry

MS in Chemistry/Biochemistry

Tools

LIMS software

Job description

QC Associate – Raw Materials LabFareva is currently seeking an experienced QC Associate – Raw Materials Lab to join our team in Richmond, VA.Who we are:Fareva is a leading contract manufacturer of pharmaceutical and personal care products. Located at intersection of Darbytown Road and Laburnum Avenue in Eastern Henrico County. Employs 200+ full time employees. Comfortable climate controlled facility covering over 745,000 square feet.About the role:Performs chemical or physical assays of raw materials, production intermediate and bulk samples. Assays are qualitative, quantitative and investigational in nature and are performed in compliance with USP, FDA and other regulatory body requirements, and Fareva standard operating procedures. Results are compared with specifications and documented. Incumbent has working knowledge of fundamental technical and quality concepts and receives minimal supervision on routine assignments.What you'll do:Conducts assaysPerforms chemical or physical assays of raw materials, production intermediate and bulk samples.Analyzes resultsAccountable for the accuracy and validity of test results. Performs mathematical calculations, interprets results, records observations, and performs peer review. Identifies basic technical issues, atypical or out-of-specification test results, instrument malfunctions and methodology problems and participates in the investigation to resolve and correct. Uses LIMS and other electronic documentation systems to collect and manage data. Uses SOPs and problem solving skills to complete assignments.Lab SupportSchedules daily assignments and ensures appropriate workflow for testing and peer review activities of their lab. Maintains all related records, prepares and records media, buffers, and reagents, etc., and maintains work area in a neat and orderly manner.SOPs and AdministrativeLearns to analyze and interpret project/study/investigation results and findings. Determines next steps under guidance of management in compliance with SOPs and applicable regulations, carries out technical and administrative duties as assigned.Our ideal candidate:Education and experienceBS degree in Chemistry, Biochemistry or relevant science discipline; 0-1 year of relevant Quality experience preferably in the bio/pharmaceutical industry.MS degree in Chemistry, Biochemistry or relevant science discipline; 0-1 year of relevant quality experience preferably in the bio/pharmaceutical industry.Skills and abilities:Requires basic knowledge of fundamental quality concepts. Learns and performs defined procedures.Working knowledge and practical application of relevant techniques and instrumentation such as: HPLC, GC, TLC, UV/VIS, FTIR/ATR, etc.Ability to interpret and document test results according to standard operating procedures and using cGMPs; background using LIMS is desirable.Learns to identify technical problems and solve these under the guidance of management.Receives minimal supervision on routine work, and specific direction on new work. Organizes daily activities, including technical aspects, to ensure timely completion of assignments.Ability to participate on teams comprised of immediate group members or to work cross functionally, if necessary.What we offer:Competitive salaries, comprehensive health/vision/dental insurance, company paid short term disability, company paid life and accidental death insurance, 401(k) plan match of 4.5% with immediate vesting, generous employee referral program, paid vacation annually, paid holidays annually, onsite cafeteria, job advancement opportunities. Manufacturing employees also receive company paid work shoes, uniforms and prescription safety eyeglasses.