Quality Control Analyst

PSG Global Solutions; Summit (NJ); On-site; USD 60,000 - 85,000; Full time

Job summary

A leading talent management firm is seeking candidates for a laboratory role in Summit, New Jersey. The responsibilities include assisting with laboratory analysis for clinical release and routine stability testing, conducting analytical experiments and documenting lab work following compliance protocols. Ideal candidates should possess a BS/MS in Chemistry and have 2-4 years of cGMP/GLP experience, alongside skills in HPLC and teamwork. This position represents an excellent opportunity for career advancement in a dynamic environment.

Qualifications

• Minimum 2-4 years recent cGMP/GLP pharmaceutical laboratory experience.
• Experience with HPLC, dissolution, FT-IR, UV/Vis spectrophotometry, KF.
• Able to work well in a team environment to achieve results.

Responsibilities

• Assist with laboratory analysis for clinical release and routine stability testing.
• Conduct testing independently and assist other analysts in analytical testing.
• Document laboratory work in compliance with GLP/cGMP requirements.

Skills

HPLC

Dissolution

Scientific judgment

Team collaboration

Analytical testing

Education

BS/MS in Chemistry or relevant discipline

Tools

UV/Vis spectrophotometry

FT-IR

Karl Fischer

Job description

At Real we're always looking for new and ambitious people to help deliver exceptional service levels, change the lives of the candidates we represent and partner with some of the world's best pharmaceutical, biotechnology and medical companies.

As specialists in recognising talent we pride ourselves on not just finding the best people for our client partners but on our ability to spot the best and brightest talent to work for us. We are also renowned for providing training and long-term career opportunities to help our employees be the best they can be, so they can continue to deliver the expertise Real has become famous for.

Relationships are at the heart of everything we do and ensure that our clients and candidates continue to work with us again and again. This ethos is also what shapes how we work as a business. We encourage and reward knowledge sharing and have various support networks and international forums to enable our employees to keep up-to-date with changes happening across their industries and share local insight to deliver true global perspectives.

Job Description

• Responsible for assisting with laboratory analysis for clinical release and routine stability testing. May conduct routine release and stability analyses of developmental compounds, prototype formulations and finished products in support of clinical testing for IND and NDA submissions.
• Perform laboratory analysis under guidance of a supervisor or designee.
• Responsibilities will include, but are not limited to, the following:
• Able to conduct testing independently and may assist other analysts in analytical testing including HPLC, dissolution, Karl Fischer, UV/Vis and other analytical laboratory testing.
• Conducts routine analytical experiments using analytical methods and procedures.
• Draws basic conclusions from data and results and communicates with other analysts and management.
• Performs instrument/method troubleshooting within analytical method parameters and management guidance.
• Performs testing for development and commercial samples, release and stability samples in accordance with established methods, specifications and protocols with limited supervision.
• Good laboratory documentation skills.
• Documents/reviews laboratory work using laboratory notebooks/worksheets that is detailed, timely and in compliance with GLP/cGMP requirements.
• Other duties as assigned by management.

Qualifications

• BS/MS Chemistry or relevant discipline with equivalent experience.
• Minimum 2 - 4 years recent cGMP/GLP pharmaceutical laboratory experience.
• Experience with HPLC, dissolution, FT-IR, UV/Vis spectrophotometry, KF.
• Able to work well in team environment to achieve results.
• Exhibits sound scientific judgment based on reasonable assumptions and available information.

Additional Information

All your information will be kept confidential according to EEO guidelines.

IF THIS IS THE JOB OPPORTUNITY FOR YOU GIVE ME A CALL AT 646-618-8925 ASAP! I want to know more about your preferences.

If in case you know someone who might be interested for this, feel free to pass it along. I look forward to hearing from you!