Job Description

EMPLOYEE RESPONSIBILITIES:

This position will be responsible for supervising a group of scientists as well as perform the functions as an individual scientist relating to laboratory activities that include compatibility studies, method transfer, method remediation and method development). This individual will also prepare and review technical documents, including validation protocols/ reports and test procedures. Additionally, he/she will also independently perform all technical assignments, and is able to troubleshoot analytical instrumentation.

Qualifications

THE IDEAL CANDIDATE WOULD POSSESS:

• Prior experience in supervision
• Strong leadership, initiative, and team-building skills
• Foster morale and teamwork
• Excellent communication and interpersonal skills, both written and verbal are required.
• Proficiency in HPLC/UPLC testing, method development and validation
• Support developmental batch testing, as well as other studies to support regulatory submissions.
• Support the development of HPLC/UPLC methods and validation
• When required perform experiments in accordance with cGMP regulations, established business processes and protocols, and applicable SOPs.
• Document laboratory work that is detailed, timely and in compliance with GSP/GMP requirements
• Conduct technical data reviews, and present data interpretation and conclusions to customers for making informed decisions.
• Prepares and reviews technical documents, including validation protocols and reports, analytical test procedures, investigation reports, and change controls.

MINIMUM QUALIFICATIONS:

• The applicant must have a BS in chemistry, analytical chemistry or related field with 5 – 10 years of pharmaceutical industry experience, MS in chemistry/analytical chemistry or related field and 2 – 5 years of pharmaceutical industry experience or PhD degree in chemistry/analytical chemistry or related field is preferred.
• Experience with HPLC/UPLC testing and method development.
• Excellent written and oral communication skills are required.
• Independent, accountable, attention to detail, ability to effectively balance multiple projects, and strong interpersonal/communication skills are required.
• Must be highly motivated and self-directed
• Demonstrates good interpersonal skills and works well with personnel at all levels.
• Authorization to work in the United States indefinitely without restriction or sponsorship

Additional Information

 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 IS A M/F, DISABLED, AND VETERAN EQUAL EMPLOYMENT OPPORTUNITY AND AFFIRMATIVE ACTION EMPLOYER.