Scientist II: Method Development and Validation

BryceTech; Lancaster (Lancaster County); On-site; USD 75,000 - 95,000; Full time

Job summary

BryceTech is seeking a Scientist II for Method Development and Validation. You will perform various testing using advanced analytical techniques and ensure compliance with GMP standards. The ideal candidate will possess a relevant Bachelor's degree, with at least three years of experience in a pharmaceutical setting and excellent organizational skills. This role offers great benefits and is ideal for those located near Lancaster, PA.

Benefits

Comprehensive medical coverage

Paid vacation and holidays

401(k) with company match

Qualifications

• 3 years of related pharmaceutical experience preferred.
• Experience with protein chromatography is a plus.

Responsibilities

• Perform testing using various chromatography methods.
• Document work for GMP compliance.
• Troubleshoot instrumentation problems.

Skills

Organizational skills

Attention to detail

Communication

Education

Bachelor's degree in chemistry, analytical chemistry, or biochemistry

Tools

Chromatographic systems

HPLC

IC

Job description

Scientist II: Method Development and Validation

Scientist II: Method Development and Validation

1 day ago Be among the first 25 applicants

• Perform various type of testing using chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, various wet chemistry analyses, HPLC, IC, IR, ICP, AA, TGP, DSC, PDA, auto-titrators, TLC, and dissolution apparatus
• Execute specialized analyses and method transfer and feasibility testing
• Document work as required for GMP compliance
• Perform tests accurately
• Troubleshoot method and instrumentation problems
• Use office and instrumentation specific computer software
• Develop and execute validation plans
• Carry out method transfers and feasibility studies
• Train technical staff
• Some travel to client sites for technical meetings could be required
  
  

Job Description

• Perform various type of testing using chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, various wet chemistry analyses, HPLC, IC, IR, ICP, AA, TGP, DSC, PDA, auto-titrators, TLC, and dissolution apparatus
• Execute specialized analyses and method transfer and feasibility testing
• Document work as required for GMP compliance
• Perform tests accurately
• Troubleshoot method and instrumentation problems
• Use office and instrumentation specific computer software
• Produce written reports (e.g., SOP, OMC, client reports)
• Develop and execute validation plans
• Carry out method transfers and feasibility studies
• Train technical staff
• Some travel to client sites for technical meetings could be required
  
  

Qualifications

_ **Minimum Qualifications:**_

• Bachelor's degree in chemistry, analytical chemistry, biochemistry, or other related degree concentration
• 3 years of related pharmaceutical experience in a cGMP environment
• Authorization to work in the United States indefinitely without restriction or sponsorship
  
  

The Ideal Candidate Would Possess

• Strong computer, scientific, and organizational skills
• Experience working with protein chromatography
• 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
• Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
  
  

Additional Information

Position is full-time position, Monday - Friday 8:00am - 4:00pm. Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply.

• 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
  
  

**To learn more about Eurofins, please explore our website[www.eurofinsus.com](http://www.eurofinsus.com/).**

**\ **

**Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.**

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

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