RI: QC Senior Scientist II

Pharmaron

$75K — $95K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • BS or MS degree in chemistry or related field
  • 2+ years of pharmaceutical industry experience
  • Ability to perform routine QC work independently
  • Proven skills in analytical method verification and validation of small molecules
  • Experience with HPLC, GC, FTIR, UV and wet chemistry
  • Working knowledge of cGMP and applicable FDA, EMA and ICH guidance
  • Excellent communication skills, both verbal and written

Responsibilities

  • Sample raw materials and conduct QC testing according to established procedures
  • Document and report experimental results in a timely manner
  • Participate in method transfer or validation activities and report preparation
  • Review experimental data and qualification protocols
  • Write, revise, and evaluate SOPs
  • Maintain good laboratory practices and GMP compliance
  • Train team members on instrument and testing methods

Benefits

  • Insurance including Medical, Dental & Vision with significant employer contributions
  • Employer-funded Health Reimbursement Account
  • Healthcare & Dependent Care Flexible Spending Accounts
  • 100% Employer-paid Employee Life and AD&D Insurance
  • Short- and Long-Term Disability Insurance
  • 401k plan with generous employer match
  • Access to an Employee Assistance Program
Full Job Description
Position: QC Scientist II, Analytical Chemistry

Salary Range: $75,000-$95,000

Location: Coventry, RI

Job Overview:

This position will support manufacturing and process chemistry activities through analytical method validation, transfer, sample testing and ensuring QC lab in compliance with all applicable guidelines.

Key Responsibilities
  • Sample raw materials and conduct QC testing of raw materials, intermediates, API, IPC and cleaning verification samples following established procedures.
  • Document and report results of all experiments in a timely-manner consistent with department practices and governing procedures, as applicable.
  • Participate in method transfer or validation activities, including executing the protocols and preparing the reports.
  • Review experimental data, notebooks, and instrument qualification protocols / reports.
  • Write, revise, develop, and evaluate SOPs.
  • Maintain good laboratory practices and GMP in compliance with safety and environmental requirements.
  • Ability to work successfully in both a team/matrix environment as well as independently.
  • Report lab event or deviation and participate in the investigation.
  • Ensure high quality in QC and analytical work and accurately document all necessary and relevant information in a clear concise manner as per cGMPs.
  • Provide training to other team members on instrument and testing method.
  • Participate, support and facilitate site audits as directed and required.
  • Perform other related assignments and duties as required and assigned.

What We're Looking For
  • BS or MS degree in chemistry or related field
  • 2+ Years of pharmaceutical industry experience
  • Ability to perform routine QC work independently with minimal guidance
  • Proven skills in analytical method verification and validation of small molecules
  • Effective in managing multiple competing activities and delivering to timelines
  • Ability to work in a cross-function environment
  • Experience in HPLC, GC, FTIR, UV and wet chemistry
  • Working knowledge of cGMP and applicable FDA, EMA and ICH guidance
  • Excellent communication skills, both verbal and written

Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:
  • Insurance including Medical, Dental & Vision with significant employer contributions
  • Employer-funded Health Reimbursement Account
  • Healthcare & Dependent Care Flexible Spending Accounts
  • 100% Employer-paid Employee Life and AD&D Insurance, Short- and Long-Term Disability Insurance
  • 401k plan with generous employer match
  • Access to an Employee Assistance Program

How to Apply:

Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!

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