Quality Control Analysts

Samjan Group Inc

East Brunswick, NJFull-time$76–79K/yrSeen todaySeen in employer's feed today

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At a glance

Compensation

$76–79K/yr

Location

East Brunswick, NJ

Schedule

Full-time

Work Authorization

Not specified

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Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

Quality Control Analysts develop quality assurance plans and optimize quality control methods for drug substances, intermediates, and finished products. They plan and monitor pharmaceutical product development, analyze samples, validate and optimize analytical methods, investigate out-of-specification results, and conduct FDA quality audits and inspections. The role requires a bachelor’s degree in Chemistry or Pharmaceutical Science and two years of experience in the job offered.

Skills & qualifications

RequiredNice to have

Skills

TrackWise Quality SystemsChange ControlOTCHPLCUSDMFCAPAANDAAnalytical Method ValidationRegulatory and Compliance AnalysiscGMPSOPsFDA Quality Audits

Qualifications

2 Years Job ExperienceBachelor's in Chemistry or Pharmaceutical Science

Full job description

Experience Required

2 years experience in job offered

Minimum Education Required

Bachelor’s Degree in Chemistry or Pharmaceutical Science

License(s) Required

Training Required/Provided

Compensation

$76,128.00 - $79,000.00 / Yearly

Hours Per Week

Number Of Positions

Shift

First Shift (Day)

Job Description

Quality Control Analysts (East Brunswick, NJ) – Develop quality assurance plans and optimize quality control methods for drug substances, intermediates, and finished products using TrackWise Quality Systems, Change Control, OTC; Plan, implement and monitor the development of pharmaceutical products with desired quality using HPLC, USDMF; Perform impurity analysis using CAPA, ANDA; Analyze regular and stability samples for development batches to ensure quality; Conduct Analytical Method validation and optimization for quality control of pharmaceutical product development process; Perform OOS/OOT investigation to identify the root cause and provide corrective and preventive action for the deviation with Quality assurance; Perform FDA Quality Audits and inspections in compliance with cGMP, SOPs using Regulatory and Compliance Analysis. Must have a Bachelor’s Degree in Chemistry or Pharmaceutical Science plus 2 years experience in job offered. Require skills and knowledge in cGMP, SOPs, CAPA, FDA Quality Audits, ANDA, HPLC, Analytical Method Validation, Regulatory and Compliance Analysis. Standard company benefits with $76,128~$79k/year. This position is eligible for Employee Referral Program. Submit résumé with referencing code VAP005 to HR, Samjan Group, Inc., 40E Cotters Lane, Suite A, East Brunswick, NJ 08816.