Quality Control Chemist

Position: Quality Control Chemist I
## Quality Control Chemist IApplyremote type:
Onsite locations:
Riverviewtime type:
Full time posted on:
Posted Todayjob requisition :
R
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***** Division
* * Piramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing  organization (CDMO), offering end-to-end development and manufacturing  solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.

This enables us to offer a comprehensive range of services including Drug Discovery  Solutions, Process & Pharmaceutical Development services, Clinical Trial  Supplies, Commercial supply of APIs and Finished dosage forms. We also offer  specialized services like development and manufacture of Highly Potent APIs  and Antibody Drug Conjugation.  Our capability as an integrated service provider  & experience with various technologies enables us to serve Innovator and  Generic companies worldwide.  

For more details, please visit :(Use the "Apply for this Job" box below). Title Quality Control Chemist IJob Description Piramal Pharma Solutions’ HPAPI Research and Manufacturing facility (Ash Stevens, LLC), located in Riverview, Michigan, is seeking a qualified Quality Control Chemist I to join our Quality Control team. The Quality Control Chemist II is responsible for providing analytical chemistry support for the facility.
** KEY ROLES:
*** Support manufacturing operations through the testing of raw materials and starting materials as required to meet production timelines.
* Perform cleaning verifications on multi-use equipment using approved methods.
* Test reference standards and stability samples.
* Document sample preparation, equipment set-up, and test results in laboratory notebooks or other appropriate test record forms.  Verify data with second quality team member as required.  Maintain all records as required to maintain compliance.
* As required, test intermediates and final products to meet production timelines/client requirements.
* Assist in the revision of documentation as required.
* Participate in quality unit projects, including but not limited to supplier certification, methods development, methods validation and training of both quality unit members as appropriate.
* Provide support in the maintenance and calibration of laboratory analytical instrumentation.
* Assist in the maintenance of the QC laboratory through routine housekeeping, as well as keeping personal bench area and desk organized.
* As required, perform routine testing on the water system (DI, ice, potable, and QC water), and prepare reports as needed.
** EDUCATION/EXPERIENCE.
*** Bachelor’s degree in Chemistry or Biochemistry or equivalent.
* One (1) year of experience in pharmaceutical quality control or equivalent is preferred
* Familiarity with analytical testing and instrumentation.
** JOB COMPETENCIES.
*** Excellent organizational and planning skills.
* Strong written, verbal, and interpersonal communication skills.
* High attention to detail.
* Demonstrated strong analytical skills, and the ability to work independently against multiple deadlines
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