JOIN OUR TEAM! PharmaLex is a highly successful and growing consulting company for the Healthcare industry worldwide. PharmaLex offers professional development, plus a stimulating and collaborative work environment. We are committed to providing exciting career opportunities in an atmosphere that values trust, respect, teamwork, creative talent, enthusiasm, and diligence. What we offer: Competitive salaries Ability to earn additional income based on hours worked (Biweekly basis) Free High-Quality webinars provided by experts from around the world Committed to keeping our consultants in project continuity Referral Program Wellness Program Recognition Program (for employees only) Service Award Program (for employees only) Discount Program (for employees only) An administrative team that is oriented to providing excellent service that pursues satisfying the needs of our consultants. For our projects in the US, we cover travel/lodging/transportation expenses (employees only) General Description: PharmaLex Puerto Rico is currently in search of a candidate who specializes in the field of Process Validation and can provide support participating in validation projects relating to biopharmaceutical and pharmaceutical manufacturing equipment, critical computer systems, manufacturing processes, and laboratory documentation for a Biotechnology located in Norwood, Massachusetts for a 6-month contract. FUNCTIONS Conceive, design, implement, and execute specific scientific experiments, which contribute to the successful completion of goals and/or projects under the general guidance of a supervisor. Conceives and designs executes evaluates, and interprets experimental strategies. Provides input to new processes to generate robust and reliable data. I would like to assure you that studies comply with the respective protocol and applicable guidelines and regulations. Designs, monitors, or conducts experimental strategies with general guidance from the supervisor. Provides data analysis and interpretation, and assesses the impact of the data on the project. Keeps current in the field of scientific expertise and areas relevant to their function. Monitors field of expertise, including literature and technology development, and communicates relevant observations. QUALIFICATIONS / REQUIREMENTS NEEDED Experience with Inspection Development process. Process development Execution and Creation of Protocols and Validations Basic Knowledge of statistics using Minitab or other statistical software Project Management Skills Knowledge of development documentation protocols and reports Excellent Communication and Teamwork skills EDUCATION: Doctorate or Master's degree and 5 years of Scientific experience or Bachelor's degree and 6 years of Scientific experience PharmaLex is an Equal Opportunity Employer. We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, creed, national origin, ancestry, sex, age, handicap or disability, marital status, sexual orientation, gender identity or expression, pregnancy or pregnancy-related condition, genetic information, veteran status, immigration or citizenship status, military obligations, status as a domestic violence victim or a victim of sexual assault or stalking, participation in discrimination complaint-related activities, or any other status protected under applicable federal, state or local law. Powered by JazzHR
