Astrix
Direct message the job poster from Astrix
Scientific workforce solutions expert connecting industry leaders with top talent We are seeking an Analytical Scientist to join a reputable pharmaceutical manufacturing company to conduct routine and non-routine analyses of in-process materials, raw materials, environmental samples, finished goods, or stability samples.
No Relocation, No C2C Candidates
Pay:
Up to $50/hour.
RESPONSIBILITIES
Conduct and document chemical analyses for raw materials, in-process goods, and finished products.
Design, validate, and resolve issues with analytical methods, including HPLC for cleaning verification.
Collect and analyze equipment cleaning validation samples.
Prepare Certificates of Analysis, analytical reports, and maintain lab documentation.
Peer‑review records and support OOS or OOT investigations as per SOPs.
Ensure compliance with SOPs, cGMPs, and regulatory requirements.
Assist with environmental monitoring and other tasks as assigned.
QUALIFICATIONS
2 years hands‑on method development experience (HPLC)
Knowledge of cGMPs, pharmacopeia (USP, EP), and regulatory standards (21 CFR Part 210/211/820, ISO)
Bachelor’s in Chemistry‑related discipline with 2+ years of analytical lab experience.
This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!
Seniority level
Associate
Employment type
Contract
Job function
Science
Industries
Pharmaceutical Manufacturing
#J-18808-Ljbffr
Scientific workforce solutions expert connecting industry leaders with top talent We are seeking an Analytical Scientist to join a reputable pharmaceutical manufacturing company to conduct routine and non-routine analyses of in-process materials, raw materials, environmental samples, finished goods, or stability samples.
No Relocation, No C2C Candidates
Pay:
Up to $50/hour.
RESPONSIBILITIES
Conduct and document chemical analyses for raw materials, in-process goods, and finished products.
Design, validate, and resolve issues with analytical methods, including HPLC for cleaning verification.
Collect and analyze equipment cleaning validation samples.
Prepare Certificates of Analysis, analytical reports, and maintain lab documentation.
Peer‑review records and support OOS or OOT investigations as per SOPs.
Ensure compliance with SOPs, cGMPs, and regulatory requirements.
Assist with environmental monitoring and other tasks as assigned.
QUALIFICATIONS
2 years hands‑on method development experience (HPLC)
Knowledge of cGMPs, pharmacopeia (USP, EP), and regulatory standards (21 CFR Part 210/211/820, ISO)
Bachelor’s in Chemistry‑related discipline with 2+ years of analytical lab experience.
This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!
Seniority level
Associate
Employment type
Contract
Job function
Science
Industries
Pharmaceutical Manufacturing
#J-18808-Ljbffr