Quality Specialist, Product Release (Day Shift)

Endo Pharmaceuticals

Rochester,MI  

2019-10-26 2019-11-25
quality administration pharma

Endo International plc is a global specialty pharmaceutical company focused on improving patients' lives while creating value. Endo develops, manufactures, markets and distributes quality branded pharmaceutical and generic pharmaceutical products as well as over-the-counter medications through its operating companies.

Endo has global headquarters in Dublin, Ireland and U.S. headquarters in Malvern, PA. We believe in making a difference, and the dedication and experience of our employees guide that aspiration. Both our company and the growth of our individuals are driven by a common purpose – to deliver therapies that make a significant, positive impact on patients' lives.









Quality Specialist, Product Release, Quality Assurance / Operations, Michigan – Rochester







About Endo International plc



Endo International plc (NASDAQ: ENDP) is a highly focused generics and specialty branded pharmaceutical company delivering quality medicines to patients in need through excellence in development, manufacturing and commercialization. Endo has global headquarters in Dublin, Ireland, and U.S. headquarters in Malvern, PA, employing approximately 3,000 people worldwide. For 2018 Endo, reported revenue of $2.947B and adjusted diluted EPS of $2.89. Learn more at www.endo.com.







POSITION SUMMARY:



The Quality Specialist, Product Release reviews all pertinent records, including Batch Production Records and laboratory Certificates of Analysis to confirm accuracy and, with guidance, makes the determination of acceptability for product release. In addition, confirms that all related Quality events such as CAPAs, Change Controls, etc. are closed prior to releasing the product. Partners with other departments to ensure that errors are addressed and corrected. Identifies errors that have potential product impact, escalates to supervision, and takes action to place lots on Quality Hold as needed. Ensures release meets internal requirements and is performed in a timely and accurate manner. May participate in “on the floor” activities during product manufacturing.







ROLE AND RESPONSIBILITIES:



Quality Product Release





+ Reviews, under minimal supervision, all pertinent records, including Batch Production Records and laboratory Certificates of Analysis to confirm accuracy and, with guidance, makes the determination of acceptability for product release



+ Identifies errors that have potential product impact, escalates to supervision, and takes action to place lots on Quality Hold as needed. Makes recommendations for corrective action to management



+ Confirms that all Quality events (Change Controls, CAPAs, investigations and any other documentation related to the lot to be released) are complete and closed prior to product release



+ Prioritizes reviews based on production and shipment schedules



+ With guidance, reviews and may approve laboratory Certificates of Analysis for accuracy, communicates with the laboratory on COA discrepancies



+ Performs MAPICS transactions to release product



+ Collaborates with Quality and Manufacturing personnel to correct errors and address Non-Conformances in a timely manner



+ Coordinates with production/ warehouse personnel to place material on Quality Hold as needed



+ May participate in “on the floor” Quality activities during product manufacturing.





Metrics Data





+ Provides data for metrics to measure business compliance to goals





Compliance





+ Follows internal processes related to controlled substances



+ Follows procedures to ensure compliance to regulatory requirements





Safety





+ Follows all procedures to ensure a safe and compliant work environment









REQUIRED QUALIFICATIONS:



Education & Experience









+ BA/BS degree in a related discipline with 3+ years’ relevant experience, including 1 year in Quality Operations





Knowledge





+ Strong understanding and ability to read and interpret SOPs and function within the scope of procedures



+ Knowledge and ability to work with and navigate computer systems such as MAPICs and LIMS





Skills & Abilities





+ Ability to handle and integrate multiple pieces of data to assure correctness



+ Ability to work with cross-functional teams



+ Able to recognize and identify complex errors such as calculation conversions



+ Able to reconcile batch record entries with other documentation



+ Proof-reading skills and ability to identify errors



+ Customer/stakeholder focused, understands impact of daily work to compliance and business



+ Communication skills



+ Strong basic math skills



+ Ability to follow complex processes



+ Attention to detail



+ Strong documentation skills









PHYSICAL REQUIREMENTS:





+ Lift 15 lbs.



+ Walk across plant/warehouse



+ Wear appropriate gowning/PPE as required



+ Ability to read for extended periods of time









ADDITIONAL INFORMATION:





+ Afternoon shift premium is 10% (non-union positions only)



+ Midnight shift premium is 15% (non-union positions only)













Endo recognizes the advantages of a diverse workforce achieved through a commitment to equal employment opportunities.







Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled







*LI-ENDP









Apply Now View all Endo Pharmaceuticals jobs Similar jobs Jobs near Rochester, MI