QC Technician - STAT testing , raw material , GMP ( 3rd Shift )

Submission for the position: QC Technician - STAT testing , raw material , GMP ( 3rd Shift ) - (Job Number: 182389)

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 join the Quality Control Department to perform laboratory STAT testing within a fast-paced GMP environment in support of manufacturing. You will perform testing in one or more of the following areas: in-process product, final Bulk product, stability, and/or validation activities while working onsite at a major pharmaceutical customer site.

Additional key responsibilities for the role on site at a major pharmaceutical company:Analyze data and evaluate resultsPerforms lab support activities as required to maintain calibration/maintenance requirements and provide support for departmentPerforms test methods and routine testing as written to support product/material releaseUnderstands and maintains a safe work environment for themselves and others in accordance with procedural requirementsUnderstands, implements and maintains GMP with respect to laboratory records, procedures and systems in accordance with procedural requirementsWill train and perform laboratory techniques such as pH, osmolality, and densitometry testing to support STAT testing for productionPerform lab support activities as necessary and provide support for departmentAccepts responsibility to complete assigned tasks as committed. Works with others to maintain a positive atmosphere to accomplish business objectivesSupport investigations***Shift: Monday-Friday 11:00pm EST (flexible 3rd shift start time)

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.

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 join the Quality Control Department to perform laboratory STAT testing within a fast-paced GMP environment in support of manufacturing. You will perform testing in one or more of the following areas: in-process product, final Bulk product, stability, and/or validation activities while working onsite at a major pharmaceutical customer site.

Additional key responsibilities for the role on site at a major pharmaceutical company:Analyze data and evaluate resultsPerforms lab support activities as required to maintain calibration/maintenance requirements and provide support for departmentPerforms test methods and routine testing as written to support product/material releaseUnderstands and maintains a safe work environment for themselves and others in accordance with procedural requirementsUnderstands, implements and maintains GMP with respect to laboratory records, procedures and systems in accordance with procedural requirementsWill train and perform laboratory techniques such as pH, osmolality, and densitometry testing to support STAT testing for productionPerform lab support activities as necessary and provide support for departmentAccepts responsibility to complete assigned tasks as committed. Works with others to maintain a positive atmosphere to accomplish business objectivesSupport investigations***Shift: Monday-Friday 11:00pm EST (flexible 3rd shift start time)

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.

Education and Experience:Bachelor's degree in Chemistry, Biochemistry, Medical Technology, Biology 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 experiencePrevious GMP experience strongly desired

Scientist level: Bachelor's degree and 2 years of experienceKnowledge, 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 tasksEmpower software a plus

Ability to independently optimize 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 teamStrong organization, attention to detail, and multi-tasking skills

Working Environment:

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 activities"raw material" , "compendial testing" , "compendia testing" , GMP , "QC Technician"

PPDFSP

*LI-NW1

Education and Experience:Bachelor's degree in Chemistry, Biochemistry, Medical Technology, Biology 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 experiencePrevious GMP experience strongly desired

Scientist level: Bachelor's degree and 2 years of experienceKnowledge, 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 tasksEmpower software a plus

Ability to independently optimize 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 teamStrong organization, attention to detail, and multi-tasking skills

Working Environment:

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 activities"raw material" , "compendial testing" , "compendia testing" , GMP , "QC Technician"

PPDFSP

*LI-NW1

Submission for the position: QC Technician - STAT testing , raw material , GMP ( 3rd Shift ) - (Job Number: 182389)