Junior Pharmaceutical Analyst – GMP Lab

SmartRecruiters, Inc.; Lancaster (Lancaster County); On-site; USD 60,000 - 80,000; Full time

Benefits offered by this job

Excellent full time benefits including

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins USA BioPharma Services in Lancaster, PA is seeking a qualified professional to perform physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished dosage forms, including tablets, capsules, parenterals, devices, aerosols, liquids, creams and gels.

You will run instrumentation independently, set up and validate new analytical methods, prepare standards and samples, execute transfer protocols, and document work to GMP standards.

Qualifications

• Bachelor's degree in chemistry or related field (or equivalent).
• Authorization to work in the United States indefinitely without sponsorship.

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 instrumentation independently including, but not limited to, various chromatographic systems.
• Preparing samples for analysis and running 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

Strong computer skills

Scientific skills

Organizational skills

Excellent communication

Teamwork

Independent work

Adaptability

Attention to detail

Education

Bachelors degree in chemistry

Job description

Eurofins USA BioPharma Services in Lancaster, PA is seeking a qualified professional to perform physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished dosage forms, including tablets, capsules, parenterals, devices, aerosols, liquids, creams and gels.

You will run instrumentation independently, set up and validate new analytical methods, prepare standards and samples, execute transfer protocols, and document work to GMP standards.