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Associate Scientist / Scientist - GMP - HPLC ( Entry Level )

Pharmaceutical Product Development (PPD)

MA-Boston-FSP Boston MA

Submission for the position: Associate Scientist / Scientist - GMP - HPLC ( Entry Level ) - (Job Number: 173002)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 support early to late phase pharmaceutical development programs through analytical method validation, clinical supply release and stability sample analysis for both drug substance and drug product material in a GMP environment at the client lab facility.

Additional responsibilities for the role on site at a major pharmaceutical company: Perform cGMP analysis and data interpretation for various techniques such as HPLC, GC, KF, TOC, IR and dissolution on small molecules.Compile and summarize analytical raw data in various physical and electronic report formats.Maintains accurate records of experiments and results in a laboratory notebook and authors reports as assigned.Demonstrates knowledge of scientific principles and basic understanding of applicable drug development regulations.Data entry and various administrative functions for laboratory data systems.Maintain cGMP training compliance.May participate in regulatory agency audits and inspections.May perform peer review of analytical data and resultsAt 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!

Shift: Monday-Friday: 8am-5pm EST

What To Expect Next

We look forward to receiving your application. A member of our talent acquisition team will review your qualifications and if interested, you will be contacted for an interview.

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 support early to late phase pharmaceutical development programs through analytical method validation, clinical supply release and stability sample analysis for both drug substance and drug product material in a GMP environment at the client lab facility.

Additional responsibilities for the role on site at a major pharmaceutical company: Perform cGMP analysis and data interpretation for various techniques such as HPLC, GC, KF, TOC, IR and dissolution on small molecules.Compile and summarize analytical raw data in various physical and electronic report formats.Maintains accurate records of experiments and results in a laboratory notebook and authors reports as assigned.Demonstrates knowledge of scientific principles and basic understanding of applicable drug development regulations.Data entry and various administrative functions for laboratory data systems.Maintain cGMP training compliance.May participate in regulatory agency audits and inspections.May perform peer review of analytical data and resultsAt 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!

Shift: Monday-Friday: 8am-5pm EST

What To Expect Next

We look forward to receiving your application. A member of our talent acquisition team 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 qualification Previous 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 experienceWaters Empower, SLIM data management, or IDBS Electronic Lab Notebook (ELN) and/or Trackwise experience preferred

Knowledge, Skills and Abilities:Knowledge of applicable regulatory authority, compendia and ICH guidelinesAbility to understand and independently apply GMPs and /or GLPs to everyday work with regard to documentation and instrument useAbility to utilize Microsoft Excel and Word to perform tasksAbility to independently execute analytical methodsGood written and oral communication skillsTime management and project management skillsProblem solving and troubleshooting abilitiesAbility to work in a collaborative work environment with a team

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 activitiesPPD Defining Principles:

We have a strong will to win - We earn our customer’s trust - We are gamechangers - We do the right thing - We are one PPD -

If you resonate with our five principles above, and ultimately wish to accelerate the delivery of safe and effective therapeutics for some of the world’s most urgent health needs, then please submit your application – we’d love to hear from you.

key words: "analytical chemistry" , "research associate" , "chemistry" , "HPLC" , "analytical chemist" , "GMP"

*LI-NW

Qualifications

Education and Experience:Bachelor's degree in Chemistry, Analytical Chemistry, Pharmaceutical Chemistry or equivalent and relevant formal academic / vocational qualification Previous 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 experienceWaters Empower, SLIM data management, or IDBS Electronic Lab Notebook (ELN) and/or Trackwise experience preferred

Knowledge, Skills and Abilities:Knowledge of applicable regulatory authority, compendia and ICH guidelinesAbility to understand and independently apply GMPs and /or GLPs to everyday work with regard to documentation and instrument useAbility to utilize Microsoft Excel and Word to perform tasksAbility to independently execute analytical methodsGood written and oral communication skillsTime management and project management skillsProblem solving and troubleshooting abilitiesAbility to work in a collaborative work environment with a team

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 activitiesPPD Defining Principles:

We have a strong will to win - We earn our customer’s trust - We are gamechangers - We do the right thing - We are one PPD -

If you resonate with our five principles above, and ultimately wish to accelerate the delivery of safe and effective therapeutics for some of the world’s most urgent health needs, then please submit your application – we’d love to hear from you.

key words: "analytical chemistry" , "research associate" , "chemistry" , "HPLC" , "analytical chemist" , "GMP"

*LI-NW

Submission for the position: Associate Scientist / Scientist - GMP - HPLC ( Entry Level ) - (Job Number: 173002)

Job posted: 2020-07-30

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