Paladin Labs Inc.
Scientist, Lab Tech Services - Microbiology
Paladin Labs Inc., Rochester, Michigan, us, 48308
We want the best and brightest people at Endo to help us achieve our mission to develop and deliver life-enhancing products through focused execution. Our nearly 3,000 global team members understand the important role we play in delivering healthcare and are dedicated to supporting each other as we work to bring the best treatments forward. Our shared values of Integrity & Quality, Innovation, Drive, Collaboration and Empathy guide our team and enable us to deliver upon our vision of helping everyone we serve live their best life.**Job Description Summary**The Senior Scientist, Laboratory Technical Services is primarily responsible for supporting the analytical testing requirements of commercial/pre-commercial materials and products, including method development, validation and transfer, pre-commercial/commercial testing of materials and samples in a regulated laboratory environment. Has expert proficiency and takes lead role in conducting all types of physical & chemical analyses (including the most complex analyses) using all equipment. This position will have a significant role supporting pending ANDA submissions, product launches, complex product investigations, product development, and method lifecycle activities to achieve company goals and initiatives, and is considered an SME for these areas. Write and review SOPs, test methods, validation protocols and validation reports. The Senior Scientist also provides mentoring to Scientists and Chemists.**Job Description**The Scientist, Laboratory Technical Services is primarily responsible for supporting the analytical testing requirements of commercial/pre-commercial materials and products, including method development, validation and transfer, pre-commercial/commercial testing of materials and samples in a regulated laboratory environment.
Has expert proficiency in conducting all types of physical and chemical analyses (including the most complex analyses) using all equipment.
This position will have a significant role supporting pending ANDA submissions, product launches, and method lifecycle activities to achieve company goals and initiatives.
Write and review SOPs, test methods, validation protocols and reports.
The Scientist also provides mentoring to Microbiologists.Scope of Authority *- span of control* *(work unit, site, department, division, etc.), monetary value of budget/spend authority* *( capital, operating, etc.), P&L responsibility, etc.*Typically supports one Par business, at a single siteKey Accountabilities *- key outcomes/deliverables, the major responsibilities, and % of time*AccountabilityResponsibilities% of TimeAnalysis & Testing* Validates analytical methods for Finished Product and Raw Material release and stability testing* Evaluates, troubleshoots/improves existing analytical methods when necessary* Prepares method validation protocols, reports, and analytical test methods* Performs testing to support process and formulation development (e.g. excipient compatibility, solubility, dissolution studies, stability/impurity assessment)* Performs work to support project as assigned with little oversight* Presents analytical data to project team for review and discussion* Reviews and approves laboratory test data and documentation (e.g. notebooks, raw data and technical documentation, test method, validation protocol, or validation report) for completeness and compliance when necessary* Reviews and evaluates drug substance supplier’s technical documents to ensure internal test requirements are adequate* Uses laboratory software for analyses* Is alert to and detects abnormalities during performances of tests and reviews65%Lab Equipment* Provides general laboratory support such as routine instrument cleaning/preventative maintenance/calibration, sample receiving, chemical inventory, document filing and housekeeping* Cleans lab working surfaces and dispose of any excess chemicals, solutions, solvents, etc. in the special waste containers for each class of waste chemicals* Troubleshoots instrumentation and performs subsequent analyses20%Investigations* Elevates questionable sample results, OOS, and aberrant results immediately to Supervisor and recommends a course of action related to LTS activities* Participates in root cause identification of complex laboratory investigations* Writes, edits, and reviews SOPs and laboratory investigations10%Training* Trains junior Scientists/Chemists on analytical techniques* Continuously updates knowledge with respect to the latest technologies related to analytical science* Maintains assigned training records current and in-compliance* Actively assumes/demonstrates responsibility in training others in good documentation practice, practical lab skills, and chemical theories, methodologies and procedures5%Compliance* Identifies need for SOPs and writes or revises, as appropriate* Performs work in a timely and safe manner conforming to regulatory, company and compendiaI requirements within pharmaceutical manufacturing setting.
Works in compliance with cGMP/cGLP regulations* Documents data generated in notebooks/worksheets/LIMS in compliance with SOPs* Takes active role in auditing laboratory logbooks/documentation to ensure compliance* Follows internal processes related to controlled substancescontinuousSafety* Follows EH&S procedures to ensure a safe work environment* Follows all applicable safety and standards guidelines, such as SOPs, cGMP, DEA regulations good documentation practice and/or MSDScontinuousTotal100%QualificationsEducation & Experience*Minimal acceptable level of education, work experience and
certifications required for the job** Bachelor of Science Degree in chemistry, chemical engineering or related field with 6 years’ relevant analytical laboratory experience OR* Master’s Degree in above disciplines with 4 years’ relevant analytical lab experience OR* PhD in above disciplines with some relevant analytical laboratory experience preferredKnowledge*Proficiency in a body of information required for the job**e.g. knowledge of FDA regulations, GMP/GLP/GCP, Lean Manufacturing, Six-Sigma, etc.** Has strong knowledge of laboratory software and has expanded knowledge of chromatographic software (e.g. Waters Empower, Agilent ChemStation and Sotax WinSotax), using custom fields, custom calculations and custom reports* Full proficiency with various laboratory techniques/instruments: HPLC, UV-Vis, FT-IR, GC and dissolution tester, melting point apparatus, viscometer, Karl Fischer titrator, pH meter, analytical balance, etc.* Thorough knowledge of applicable safety and standards guidelines, such as FDA, ICH, SOP, cGMP, GLP, DEA regulations and/or MSDS* Has demonstrated competence in conducting chemical analyses* Strong knowledge of wet chemistry techniques* Competency in Microsoft Office SuiteSkills&Abilities*Often referred to as “competencies”, leadership attributes, skills, abilities or behaviors that may be enterprise, functional or job specific
e.g. coaching, negotiation, calibration, technical writing* *etc.** Ability to critically review and analyze data, interpret information, and draw conclusions from relevant or missing information* Ability to display and analyze data in a logical manner* Strong verbal and written communication skills as well as good computer skills* Strong attention to details and accurate record keeping* Establish and maintain cooperative working relationships with others* Solid organizational skills* Ability to coach less senior staff and develop laboratory skills and ability* Ability to take initiative, set priorities and follow through on assignmentsPhysical Requirements*Physical & mental requirements e.g. lift 40 pounds, walk across plant/warehouse, business travel (% of time), driving as part of work responsibilities, etc.** Extended periods of sitting, standing, walking, reaching, #J-18808-Ljbffr
Has expert proficiency in conducting all types of physical and chemical analyses (including the most complex analyses) using all equipment.
This position will have a significant role supporting pending ANDA submissions, product launches, and method lifecycle activities to achieve company goals and initiatives.
Write and review SOPs, test methods, validation protocols and reports.
The Scientist also provides mentoring to Microbiologists.Scope of Authority *- span of control* *(work unit, site, department, division, etc.), monetary value of budget/spend authority* *( capital, operating, etc.), P&L responsibility, etc.*Typically supports one Par business, at a single siteKey Accountabilities *- key outcomes/deliverables, the major responsibilities, and % of time*AccountabilityResponsibilities% of TimeAnalysis & Testing* Validates analytical methods for Finished Product and Raw Material release and stability testing* Evaluates, troubleshoots/improves existing analytical methods when necessary* Prepares method validation protocols, reports, and analytical test methods* Performs testing to support process and formulation development (e.g. excipient compatibility, solubility, dissolution studies, stability/impurity assessment)* Performs work to support project as assigned with little oversight* Presents analytical data to project team for review and discussion* Reviews and approves laboratory test data and documentation (e.g. notebooks, raw data and technical documentation, test method, validation protocol, or validation report) for completeness and compliance when necessary* Reviews and evaluates drug substance supplier’s technical documents to ensure internal test requirements are adequate* Uses laboratory software for analyses* Is alert to and detects abnormalities during performances of tests and reviews65%Lab Equipment* Provides general laboratory support such as routine instrument cleaning/preventative maintenance/calibration, sample receiving, chemical inventory, document filing and housekeeping* Cleans lab working surfaces and dispose of any excess chemicals, solutions, solvents, etc. in the special waste containers for each class of waste chemicals* Troubleshoots instrumentation and performs subsequent analyses20%Investigations* Elevates questionable sample results, OOS, and aberrant results immediately to Supervisor and recommends a course of action related to LTS activities* Participates in root cause identification of complex laboratory investigations* Writes, edits, and reviews SOPs and laboratory investigations10%Training* Trains junior Scientists/Chemists on analytical techniques* Continuously updates knowledge with respect to the latest technologies related to analytical science* Maintains assigned training records current and in-compliance* Actively assumes/demonstrates responsibility in training others in good documentation practice, practical lab skills, and chemical theories, methodologies and procedures5%Compliance* Identifies need for SOPs and writes or revises, as appropriate* Performs work in a timely and safe manner conforming to regulatory, company and compendiaI requirements within pharmaceutical manufacturing setting.
Works in compliance with cGMP/cGLP regulations* Documents data generated in notebooks/worksheets/LIMS in compliance with SOPs* Takes active role in auditing laboratory logbooks/documentation to ensure compliance* Follows internal processes related to controlled substancescontinuousSafety* Follows EH&S procedures to ensure a safe work environment* Follows all applicable safety and standards guidelines, such as SOPs, cGMP, DEA regulations good documentation practice and/or MSDScontinuousTotal100%QualificationsEducation & Experience*Minimal acceptable level of education, work experience and
certifications required for the job** Bachelor of Science Degree in chemistry, chemical engineering or related field with 6 years’ relevant analytical laboratory experience OR* Master’s Degree in above disciplines with 4 years’ relevant analytical lab experience OR* PhD in above disciplines with some relevant analytical laboratory experience preferredKnowledge*Proficiency in a body of information required for the job**e.g. knowledge of FDA regulations, GMP/GLP/GCP, Lean Manufacturing, Six-Sigma, etc.** Has strong knowledge of laboratory software and has expanded knowledge of chromatographic software (e.g. Waters Empower, Agilent ChemStation and Sotax WinSotax), using custom fields, custom calculations and custom reports* Full proficiency with various laboratory techniques/instruments: HPLC, UV-Vis, FT-IR, GC and dissolution tester, melting point apparatus, viscometer, Karl Fischer titrator, pH meter, analytical balance, etc.* Thorough knowledge of applicable safety and standards guidelines, such as FDA, ICH, SOP, cGMP, GLP, DEA regulations and/or MSDS* Has demonstrated competence in conducting chemical analyses* Strong knowledge of wet chemistry techniques* Competency in Microsoft Office SuiteSkills&Abilities*Often referred to as “competencies”, leadership attributes, skills, abilities or behaviors that may be enterprise, functional or job specific
e.g. coaching, negotiation, calibration, technical writing* *etc.** Ability to critically review and analyze data, interpret information, and draw conclusions from relevant or missing information* Ability to display and analyze data in a logical manner* Strong verbal and written communication skills as well as good computer skills* Strong attention to details and accurate record keeping* Establish and maintain cooperative working relationships with others* Solid organizational skills* Ability to coach less senior staff and develop laboratory skills and ability* Ability to take initiative, set priorities and follow through on assignmentsPhysical Requirements*Physical & mental requirements e.g. lift 40 pounds, walk across plant/warehouse, business travel (% of time), driving as part of work responsibilities, etc.** Extended periods of sitting, standing, walking, reaching, #J-18808-Ljbffr