Entry-Level Analytical Scientist - GMP Lab

Eurofins US Network; Lancaster (Lancaster County); On-site; USD 42,000 - 72,000; Full time

Benefits offered by this job

Medical, dental, vision

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins USA BioPharma Services in Lancaster, PA is seeking an entry-level Analyst to perform physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished products.

You will run chromatographic systems, prepare samples, set up and validate processes, and document work for GMP compliance. Monday–Friday 8:00 AM–5:00 PM with potential overtime; commutable distance encouraged.

Qualifications

• Strong computer, scientific, and organizational skills.
• Excellent communication (oral and written) and attention to detail.
• Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude.

Responsibilities

• Perform physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished pharmaceutical products (tablets, capsules, parenterals, devices, aerosols, liquids, creams, and gels).
• Run the instrumentation independently including, but not limited to, various chromatographic systems.
• Prepare samples for analysis and run some instrumentation with minimum supervision.
• Set up and validate new analytical or related processes used by the department.
• Prepare standards and samples for analysis.
• Execute method transfer protocols.
• Document work as required for GMP compliance.
• Perform monthly maintenance of laboratory equipment.

Skills

Communication

Attention to detail

Teamwork

Adaptability

Education

Bachelor's degree in chemistry

Job description

Eurofins USA BioPharma Services in Lancaster, PA is seeking an entry-level Analyst to perform physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished products.

You will run chromatographic systems, prepare samples, set up and validate processes, and document work for GMP compliance. Monday–Friday 8:00 AM–5:00 PM with potential overtime; commutable distance encouraged.