- 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 NAME (Coulometric and Volumetric) UV/Spec various wet chemistry analyses HPLC IC IR ICP AA TGP DSC PDA auto-titrators TLC and dissolution apparatus
- 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
- Develop and optimize analytical methods for the quantification of pharmaceutical compounds and their impurities
- Collaborate with cross-functional teams to support drug development projects and ensure analytical method suitability
- Troubleshoot and resolve analytical issues related to method development and validation
- Participate in the writing and reviewing of Standard Operating Procedures (SOPs) and analytical reports
- Assist in the training of junior scientists on analytical techniques and instrument operation
- Stay current with relevant scientific literature and regulatory guidelines in the field of pharmaceutical analysis
- Contribute to continuous improvement initiatives within the laboratory to enhance efficiency and data quality
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
- Ability to learn new techniques perform multiple tasks simultaneously keep accurate records follow instructions and comply with company policies
Minimum Qualifications:
- Bachelors degree in chemistry or other related degree concentration or equivalent directly-related experience
- Authorization to work in the United States indefinitely without restriction or sponsorship
Additional Information :
Position is full-time Monday-Friday 8 a.m.-5 p.m. with additional hours as needed as workloads demand. Candidates currently living in a commutable distance to 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
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.
Remote Work :
No
Employment Type :
Full-time
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 NAM...
- 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 NAME (Coulometric and Volumetric) UV/Spec various wet chemistry analyses HPLC IC IR ICP AA TGP DSC PDA auto-titrators TLC and dissolution apparatus
- 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
- Develop and optimize analytical methods for the quantification of pharmaceutical compounds and their impurities
- Collaborate with cross-functional teams to support drug development projects and ensure analytical method suitability
- Troubleshoot and resolve analytical issues related to method development and validation
- Participate in the writing and reviewing of Standard Operating Procedures (SOPs) and analytical reports
- Assist in the training of junior scientists on analytical techniques and instrument operation
- Stay current with relevant scientific literature and regulatory guidelines in the field of pharmaceutical analysis
- Contribute to continuous improvement initiatives within the laboratory to enhance efficiency and data quality
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
- Ability to learn new techniques perform multiple tasks simultaneously keep accurate records follow instructions and comply with company policies
Minimum Qualifications:
- Bachelors degree in chemistry or other related degree concentration or equivalent directly-related experience
- Authorization to work in the United States indefinitely without restriction or sponsorship
Additional Information :
Position is full-time Monday-Friday 8 a.m.-5 p.m. with additional hours as needed as workloads demand. Candidates currently living in a commutable distance to 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
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.
Remote Work :
No
Employment Type :
Full-time
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