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Associate Scientist / Scientist- HPLC , Dissolution , GMP
Pharmaceutical Product Development (PPD)
MA-Boston-FSP Boston MA
Submission for the position: Associate Scientist / Scientist- HPLC , Dissolution , GMP - (Job Number: 170668)We ARE HIRING!
In labs and health care facilities worldwide- HERE WE ARE
PPD is a leading global contract research organization. At PPD we are passionate, deliberate, and driven by our purpose - to improve health.
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.
As an Associate Scientist / Scientist, you will use state-of-the-art technologies to performtraditional and innovative analytical techniques and apply Quality-by-Design principles to develop and validate the analytical tools used to ensure the safety, efficacy and quality of the client pharmaceutical productswhile working onsite at a large pharmaceutical customer site. You will support the drug development programs at the client site through laboratory techniquescommonly used in the analysis of pharmaceuticals such as HPLC and dissolution.
Additional key responsibilities for the role on site at a major pharmaceutical company:
Develops, troubleshoots and conducts dissolution experiments and HPLC in support of drug product process development
Performs dissolution stability testing on drug products
Maintains accurate records of experiments and results in an electronic laboratory notebook and authors reports as assigned
Designs, executes, and interprets experiments with a high degree of reliability and independence
Performs statistical analysis of experimental data
Implements dissolution modeling to further understand dissolution mechanisms
Maintains general lab equipment, including HPLCs and dissolution systems.
Demonstrates knowledge of scientific principles and basic understanding of applicable drug development regulations
Performs other duties as assigned
At PPD we hire the best, develop ourselves and each other, and recognize the power of being one team. It's not just talk, our award-winning training programs speak for themselves.
Join PPD in our relentless pursuit of excellence - apply now!
What To Expect Next
We look forward to receiving your application. A member of our talent acquisition department will review your qualifications and if interested, you will be contacted for an interview.
We ARE HIRING!
In labs and health care facilities worldwide- HERE WE ARE
PPD is a leading global contract research organization. At PPD we are passionate, deliberate, and driven by our purpose - to improve health.
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.
As an Associate Scientist / Scientist, you will use state-of-the-art technologies to performtraditional and innovative analytical techniques and apply Quality-by-Design principles to develop and validate the analytical tools used to ensure the safety, efficacy and quality of the client pharmaceutical productswhile working onsite at a large pharmaceutical customer site. You will support the drug development programs at the client site through laboratory techniquescommonly used in the analysis of pharmaceuticals such as HPLC and dissolution.
Additional key responsibilities for the role on site at a major pharmaceutical company:
Develops, troubleshoots and conducts dissolution experiments and HPLC in support of drug product process development
Performs dissolution stability testing on drug products
Maintains accurate records of experiments and results in an electronic laboratory notebook and authors reports as assigned
Designs, executes, and interprets experiments with a high degree of reliability and independence
Performs statistical analysis of experimental data
Implements dissolution modeling to further understand dissolution mechanisms
Maintains general lab equipment, including HPLCs and dissolution systems.
Demonstrates knowledge of scientific principles and basic understanding of applicable drug development regulations
Performs other duties as assigned
At PPD we hire the best, develop ourselves and each other, and recognize the power of being one team. It's not just talk, our award-winning training programs speak for themselves.
Join PPD in our relentless pursuit of excellence - apply now!
What To Expect Next
We look forward to receiving your application. A member of our talent acquisition department will review your qualifications and if interested, you will be contacted for an interview.
Qualifications
Education and Experience:Bachelor's degree in Chemistry, Analytical Chemistry, Pharmaceutical Chemistry or equivalent and relevant formal academic/vocational qualificationPrevious experience that provides the knowledge, skills, and abilities to perform the job (comparable 0-2 years) or equivalent combination of education, training, and experience with preference to those with 1 years of industry experience
Knowledge, Skills and Abilities:HPLC and Dissolution Testing experience is desiredEmpower 3 experience is desired
Excellent experimental documentation is requiredcGMP experience is strongly preferred
The ability to work successfully in both a team/matrix environment as well as independentlyThe ability to work in a fast pace environment, manage priorities, and maintain timelines for multiple projects
Manual dexterity.Communicate effectively and follow detailed written and verbal instruction.Cooperate with coworkers within an organized team environment or work alone with supervision.Manage time effectively to complete assignments in expected time frame.Maintain a laboratory notebook and complete all documentation with clear and accurate language and according to the SOP.Ability to plan, schedule and carry out work for successful project completion.Proficient in the operation of the computer and data acquisition programs.Positive attitude and ability to work well with others.Ability to write protocols and reports with minimum supervision
PPD values the health and well-being of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable mannerAble to work upright and stationary and/or standing for typical working hoursAble to lift and move objects up to 25 poundsAble to work in non-traditional work environmentsAble to use and learn standard office equipment and technology with proficiencyMay have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environmentsAble to perform successfully under pressure while prioritizing and handling multiple projects or activitiesPPDFSP
*LI-NW1
Qualifications
Education and Experience:Bachelor's degree in Chemistry, Analytical Chemistry, Pharmaceutical Chemistry or equivalent and relevant formal academic/vocational qualificationPrevious experience that provides the knowledge, skills, and abilities to perform the job (comparable 0-2 years) or equivalent combination of education, training, and experience with preference to those with 1 years of industry experience
Knowledge, Skills and Abilities:HPLC and Dissolution Testing experience is desiredEmpower 3 experience is desired
Excellent experimental documentation is requiredcGMP experience is strongly preferred
The ability to work successfully in both a team/matrix environment as well as independentlyThe ability to work in a fast pace environment, manage priorities, and maintain timelines for multiple projects
Manual dexterity.Communicate effectively and follow detailed written and verbal instruction.Cooperate with coworkers within an organized team environment or work alone with supervision.Manage time effectively to complete assignments in expected time frame.Maintain a laboratory notebook and complete all documentation with clear and accurate language and according to the SOP.Ability to plan, schedule and carry out work for successful project completion.Proficient in the operation of the computer and data acquisition programs.Positive attitude and ability to work well with others.Ability to write protocols and reports with minimum supervision
PPD values the health and well-being of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable mannerAble to work upright and stationary and/or standing for typical working hoursAble to lift and move objects up to 25 poundsAble to work in non-traditional work environmentsAble to use and learn standard office equipment and technology with proficiencyMay have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environmentsAble to perform successfully under pressure while prioritizing and handling multiple projects or activitiesPPDFSP
*LI-NW1Submission for the position: Associate Scientist / Scientist- HPLC , Dissolution , GMP - (Job Number: 170668)
Job posted: 2020-06-02