Analytical Chemist

Germer International - Pharmaceutical Recruiting

Hillsdale (NJ)

On-site

USD 60,000 - 85,000

Full time

14 days+
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Job summary

A recruiting firm in Hillsdale, NJ, is looking for a chemist to join a pharmaceutical client. The role involves conducting release and stability testing, maintaining compliance with laboratory practices, and ensuring data integrity. The ideal candidate holds a Bachelor’s degree in chemistry with at least two years of industry experience. This is a full-time position with a competitive salary range of $60,000 to $85,000 per year.

Qualifications

  • Minimum 2 years of experience in the pharmaceutical industry.
  • Hands-on experience with HPLC, GC, and dissolution testing.
  • Strong analytical and problem-solving skills.

Responsibilities

  • Conduct release and stability testing for pharmaceutical products.
  • Prepare solid dosage samples for analysis.
  • Maintain accurate records of experiments and results.

Skills

HPLC
GC
Dissolution Testing
Empower Software
Analytical Skills

Education

Bachelor’s degree in chemistry

Job description

Base pay range

$60,000.00/yr - $85,000.00/yr

Our pharmaceutical client is looking for a chemist to join their growing organization. If you are someone who wants to be part of a highly technical team, this may be the role for you.

Responsibilities
  • Conduct release and stability testing for pharmaceutical products with a focus on LC and GC chromatographic analyses as well as dissolution testing.
  • Prepare solid dosage samples for analysis by accurately weighing, blending, and homogenizing materials to ensure representative samples for testing.
  • Conduct dissolution testing of solid oral drug products using USP Apparatus I and Apparatus II.
  • Perform HPLC assays for the quantitative analysis of pharmaceutical components, including potency, purity, and samples from dissolution testing.
  • Ensure analytical instrumentation is properly maintained.
  • Ensure that all laboratory work complies with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP), following established Standard Operating Procedures (SOPs).
  • Maintain accurate and detailed records of experiments, results, and procedures in laboratory notebooks and electronic systems, ensuring data integrity.
  • Adhere to safety protocols and participate in laboratory safety initiatives, ensuring a safe and compliant work environment.
Minimum Qualifications
  • Bachelor’s degree in chemistry with at least two (2) years of experience in the pharmaceutical industry.
  • Hands-on experience with HPLC, GC, Dissolution, and use of Empower software.
  • Strong analytical and problem-solving skills.
  • Excellent communication and teamwork skills.
  • Attention to detail and commitment to maintaining data integrity.
Seniority level
  • Mid-Senior level
Employment type
  • Full-time
Job function
  • Research
Industries
  • Pharmaceutical Manufacturing

Conditions and notices: Referrals may increase your chances of interviewing. This description reflects the role as provided by the employer; details may be subject to change.

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