Are you looking for an exciting opportunity, a rewarding, enriching, and fulfilling career, and the opportunity to grow to greater levels of success with a company that values you? Then look no further! Join Eurofins PSS: a world class company that is growing by leaps and bounds while making a difference to humanity.
At Eurofins PSS, you will gain experience working in state-of-the-art laboratories, and be a part of a team that is dedicated to testing, development, and advancement of life-saving drug products to make the world a healthier and happier place to live in. Our people are our chemistry and we need talented people like you now more than ever.
Job Description
The purpose of this role is to author technical documents to change current processes for drug development.
Collectdetails from cross-functional departments to author change controls for components and raw materials
Enterchange controls into electronic system (QTS) and routing to departments for assessments
Trackand project manage the assessment completion
Routechange control for approval, trackand manage approvals
Tracktask completion associated with approved change control and workwith owners to ensure tasks are completed by assigned due dates
Enternew enrollment tasks into electronic system (QTS) and assigntask owners
Extendenrollment due dates when needed
Adhere to site SOPs and cGMPs for production activities in the manufacturing facilities
Adhere to site safety standards, participate in routine safety training events, and enforce safety and biosafety requirements as they relate to the Clinical Manufacturing department
Qualifications
Bachelor's degree in a scientific or engineering discipline or similar, with aminimum of 1 yearGMP experience
Lab experience is beneficial, but not required.
Experience with changing lab processes, SOP's, procedures, etc.
Knowledge of pharmaceutical supply chain or QA experience preferred
Strong computer skills; specificallyExcelandSAP
Able to work both independently and as a member of a cross-functionalteam in a fast-paced environment
Authorization to work in the United States indefinitely without restriction or sponsorship
Valid driver's license and personal transportation
Additional Information
This is anon-lab based-role- all duties will take place in an office environment.
Position is full-time, Monday - Friday 8:00am - 5:00pm. Candidates currently living within a commutable distance ofSanford, NCare 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 holiday
Eurofins is aM/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
