Completing all training in a timely and complete manner; working with an experienced analyst/mentor performing various tasks and analyses of Bio/pharmaceutical ingredients and products; reviewing or preparing standards and samples for analysis and running any equipment or instrumentation independently and/or with guidance; working efficiently; ensuring that the client receives quality data by reviewing laboratory data for accuracy clarity and adherence to GMP and/or GLP regulations.
Essential Duties and Responsibilities:
- Applies GMP/GLP in all areas of responsibility as appropriate
- Applies the highest quality standard in all areas of responsibility
- Demonstrates strong client service skills communicate effectively both orally and in writing
- Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration
- Regular attendance and punctuality
- Performs laboratory operations with good dexterity good laboratory technique and high degree of accuracy and precision
- Perform/Review preparations of reagents samples and standards according to procedures.
- Document testing observations deviations and results clearly and completely and in compliance with regulatory requirements - striving to minimize errors
- Read and understand analytical procedures (compendial and client supplied) and internal SOPs
- Use MS Windows applications such as Excel Word Outlook email
- Process data generate reports and evaluate data
- Perform laboratory maintenance and maintain clean workspace
- Commitment to occasional overtime as workload requires
Qualifications :
To perform this job successfully the individual must be able to perform each essential duty satisfactorily. The requirements below are representative of the knowledge skill or ability required.
Minimum Qualifications:
- Bachelors degree in microbiology biology or related degree concentration
- Ability to work in the US without immediate or future sponsorship
- Microscopes and biological safety cabinets
- Media preparation
- Pipetting
- Organism/culture preparation
- Serial dilution
- Aseptic technique
- Gram stains
Additional Information :
Working schedule will be Full-Time Second Shift 3pm-11pm Tuesday-Saturday. 25% travel may be required for this position. Candidates currently living within a commutable distance of Lancaster PA are encouraged to apply.
What we Offer:
- Excellent full time benefits including comprehensive medical coverage dental and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.
Remote Work :
No
Employment Type :
Full-time