HPLC Development Specialist

• Contributes as part of a small team of scientists towards the development/optimization and qualification/verification of analytical methods to support synthetic molecules analytical development.
• Applies in-depth knowledge of concepts and applications to fit-for-purpose methods development.
• Provided analytical support for process and formulation development related works.
• Reviews and interprets data then communicates results to relevant members.
• Identifies troubleshoots and implements resolutions to technical problems/issues. 
• Conducts work in compliance with cGMP/GLP safety and regulatory requirements.
• Writing technical reports for functional area
• Independently plans and designs experiments and operations within expertise. 
• Able to clarify requests and provide suggestions and put data into context. 
• Works with departmental and/or other function members to execute on assignments under limited supervision.
• Learn new techniques perform multiple tasks simultaneously keep accurate records follow instructions and comply with company policies.
• Effectively communicates complex data/decisions within department.
• Contributes significantly to project related lab works within functional area.
• Coordinates work with members in the team

Qualifications :

• Working knowledge of analytical techniques with experience using multiple techniques (LC GC Dissolution Karl Fisher spectroscopic instruments etc.) for synthetic molecules.
• Basic understanding of industry practices and standards.
• Experiences on method development and validation for synthetic molecule products
• Strong computer scientific and organizational skills.
• Analytical and Problem-Solving Skills - Able to troubleshoot critical issues or problems and determine causes and possible solutions using appropriate information
• Ability to work well in a team environment 
• Communication and Organizational skills 
• Authorization to work in the United States indefinitely without restriction or sponsorship

Education and Experience

• Bachelors degree in chemistry biology pharmacy engineering or related pharmaceutical science with 4 years relevant industry experience  
• Masters degree in chemistry biology pharmacy engineering or related pharmaceutical science with 2 years relevant industry experience

Additional Information :

What to Expect in the Hiring Process: 

• 10-15 Minute Phone Interview with Region Recruiter
• 45-60 Minute Virtual Interview with Manager and/or Group Leader
• 45-60 Minute In-Person Meeting to Meet the Team and Discuss the Role 

Additional Details: 

This is a full-time onsite position based on a first-shift schedule (Monday through Friday 8:00am to 5:00pm) with overtime required as needed. Candidates located within a commutable distance to Cambridge Massachusetts are strongly encouraged to apply. 

Excellent full-time benefits include:

• Comprehensive medical coverage dental and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays
• Hourly rate is between $39-$44 depending on education and experience 

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Remote Work :

No

Employment Type :

Full-time