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PharmaLex is a highly successful and growing consulting company for the Healthcare industry around the world.
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.
Location - Juncos, PR Requirements : Doctorate degree and 2 years of Scientific experience OR Master's degree and 6 years of Scientific experience OR Bachelor's degree and 8 years of directly related experience • Proficient in Automatic Visual Inspection Machines.
• Able to work under pressure.
• Good organization skills and team worker.
• Proficient in the preparation of technical reports and business/scientific presentations.
• Knowledge in raw materials, in-process controls, packaging material, labeling, and finished product variables.
• Fully Bilingual.
• Provide group technical guidance.
• Participate in global cross-functional teams, working effectively in a highly matrixed team environment to advance programs.
• Acts as an advisor to staff members to meet schedules.
• Able to develop solutions to routine technical problems of limited scope.
• Experience in Technology Transfer, pharmaceutical, medical devices, and biotechnology in manufacturing, inspection, and packaging processes.
• Meticulous, Committed, Skilled, Proactive, Risk-Taking, Structured, Excellent Interpersonal Skill, Energetic, Solution Oriented.
• Provides analytical skills and ability to understand the big picture in complex environment.
• Working cross functionally and building collaborative working relationships.
• Ability to manage, development, implementation, and adherence to processes.
• Strong verbal and written communication skills, emotional intelligence, and decision maker.
• Knowledge of GXP for Pharmaceuticals, Biotechnology, and Medical Operations.
• Knowledge in Pharmaceutical and Biotechnology equipment.
• Interface with Upper and Middle Management.
• Determines and pursues courses of action necessary to obtain desired functional results.
• Knowledge in pharmaceutical product commercialization and lifecycle management.
SUMMARY To independently conceive, design, implement and advance scientific experiments, which contribute to the successful completion of goals and/or projects.
Interprets experimental strategies or leads these activities.
Provides input to new processes to generate robust and reliable data.
Functions as a lead scientific / technical resource or as a project leader.
FUNCTIONS 1.
Independently monitors or conducts experiments, studies, or a series of experiments/studies to advance projects or technologies 2.
Provides advanced data analysis and interpretation, and assesses impact of data on the project and makes recommendations 3.
Expands knowledge-seeking beyond core area of expertise 4.
Identifies relevant external competitive knowledge 5.
Independently prepares new and novel protocols/experimental design 6.
Key contributor to an independent research/project team 7.
Initiates productive collaborations outside of the department or company 8.
Introduces new or advanced technologies and/or concepts 9.
May contribute to scientific journal articles or complex technical documents as lead author 10.
Leads department-wide support efforts such as safety, recruiting and committees 11.
Develops supervisory and mentoring skills 12.
Makes proactive decisions that contribute to the achievement of milestones 13.
Plans detailed procedures for defined projects, including timelines, milestones, methodological approaches, expected results and necessary resources 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.
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