PPD Laboratories offers the most comprehensive set of laboratory services available in the industry and continues to deliver innovative solutions to our clients through our collaborative approach, including PPD Laboratories FSP. PPD Laboratories FSP is a unique partnership that allows our clients to leverage the experience of our PPD staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits/advantages of being a part of PPD.
Post : Associate Project Manager - LC-MS - GMP
Job Description
• Liaise with the PPD's operational divisions, affiliates and sponsors. Coordinate (in collaboration with Project Managers) the study setup, maintenance and closure activities for identified protocols and/or study programs. Consult on project management issues, and support overall function of the Project Management group.
• Position is responsible for supporting the successful delivery and conduct of projects resulting in revenues of USD 300k in average (range $25k to $5M) driving repeat business and acquisition of new business.
Candidate Profile
Bachelor’s degree in the Physical or Life Sciences with 3 years of formal laboratory training in a regulated environment post degree or non-laboratory training equivalent in general project management or project coordination with a non-Physical or Life Sciences degree.
Knowledge, Skills and Abilities
• Good organizational skills with the ability to adapt and adjust to changing priorities and to manage multiple assignments with challenging/conflicting deadlines
• Good computer skills
• Strong attention to detail and problem solving skills
• Good written and verbal communication skills
• Effectively conduct oral presentations
• Demonstrated experience in identification and resolution of technical problems in a professional environment
• Ability to maintain a high degree of confidentiality with clinical teams
• Ability to attain, maintain and apply a working knowledge of applicable Procedural Documents
• Demonstrated positive attitude, enthusiasm toward work, and the ability to work well with others
Working Conditions:
• Work is performed in a laboratory and/or a clinical environment with exposure to electrical office equipment.
• Occasional drives to site locations, occasional domestic travel.
• Exposure to biological fluids with potential exposure to infectious organisms.
• Rare exposure to skin and lung irritants, radiation, toxic materials and hazardous waste.
• Personal protective equipment required such as protective eyewear, garments and gloves.
• Exposure to fluctuating and/or extreme temperatures on rare occasions.
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Physical Demands:
• Ability to work in an upright and /or stationary position for 6-8 hours per day.
• Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.
• Occasional mobility needed.
• Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
• Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
• Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
• Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.
• Frequently interacts with others to obtain or relate information to diverse groups.
• Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Requires multiple periods of intense concentration.
Additional Information
Experience : 3 year
Qualification : Bachelor's degree in Life Sciences
Location : Middleton, USA
Industry Type: Pharma/ Healthcare/ Clinical research
Functional Area : LC-MS - GMP
End Date : 30th April, 2018
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