Why Endo?

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.

At Endo, we are building a diverse, equitable and inclusive workplace, and we are looking for talented individuals to join our team.

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 and 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

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.

Key Accountabilities -

Analysis & Testing

Develops, designs, and validates analytical methods for Finished Product and Raw Material release and stability testingEvaluates, troubleshoots/improves existing analytical methods when necessaryPrepares method validation protocols, reports, analytical test methods, and analytical sections for regulatory submissions, as requiredDevelops and validates experiments designed to provide support for process and formulation activities (e.g. excipient compatibility, solubility, dissolution studies, stability/impurity assessment)Independently performs scheduling and coordination of activities of assigned projectsPresents analytical data to project team for review and discussionReviews 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, in support of regulatory filings and commercial product maintenanceReviews and evaluates drug substance supplier’s technical documents and provides recommendations of API vendor selectionIs alert to and detects abnormalities during performances of tests and reviews

65%

Lab Equipment

Evaluates new technologies to improve efficiencies and to reduce cost of testingProvides general laboratory support such as routine instrument cleaning/preventative maintenance/calibration, sample receiving, chemical inventory, document filing and housekeepingCleans lab working surfaces and dispose of any excess chemicals, solutions, solvents, etc. in the special waste containers for each class of waste chemicalsTroubleshoots instrumentation and performs subsequent analyses

20%

Investigations

Elevates questionable sample results, OOS, and aberrant results immediately to supervisor and recommends a course of action related to LTS activitiesLeads the effort in root cause identification of complex laboratory investigationsWrites, edits, and reviews SOPs and laboratory investigations

10%

Training

Coaches and provides technical guidance to more junior Scientists in method development and validation as well as troubleshooting of methods and analytical techniquesContinuously updates knowledge with respect to the latest technologies related to analytical scienceMaintains assigned training records current and in-complianceActively assumes/demonstrates responsibility in training others in good documentation practice, practical lab skills, and chemical theories, methodologies and procedures

5%

Compliance

Identifies need for SOPs and writes or revises, as appropriatePerforms work in a timely and safe manner conforming to regulatory, company and compendiaI requirements within pharmaceutical manufacturing setting.  Work in compliance with cGMP/cGLP regulationsDocuments accurately data generated in notebooks/worksheets/LIMS in compliance with SOPsTakes active role in auditing laboratory records to ensure complianceFollows internal processes related to controlled substances

continuous

Safety

Follows EH&S procedures to ensure a safe work environmentFollows all applicable safety and standards guidelines, such as SOPs, cGMP, DEA regulations good documentation practice and/or MSDS

continuous

Total

100%

Qualifications

Education & 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 8 years’ relevant analytical laboratory experience ORMaster’s Degree in above disciplines with 6 years’ relevant analytical lab experience ORPhD in above disciplines with a minimum 2 years’ relevant pharmaceutical lab experience

Knowledge

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 reportsFull 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 MSDSHas demonstrated competence in conducting chemical analysesStrong knowledge of wet chemistry techniquesCompetency in Microsoft Office Suite

Skills

&

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, analyze data, interpret information, and draw conclusions from relevant or missing informationAbility to display and analyze data in a logical mannerStrong verbal and written communication skills as well as good computer skillsStrong attention to details and accurate record keepingEstablish and maintain cooperative working relationships with othersSolid organizational skillsAbility to coach less senior staff and develop laboratory skills and abilityAbility to take initiative, set priorities and follow through on assignments

Physical 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, climbing/balancing, kneeling/crouching/crawling, looking at monitor for extended periods, moderate noise levels and potential business travel.  Work is in an FDA and DEA-regulated pharma lab environment with risk of exposure to various chemicalsMust occasionally lift and/or move up to 15-25 lbs.Ability to wear personal protective equipment, including respirators, gloves, etc.Specific visions abilities are required by this job include close vision and color visionAbility to occasionally tolerate significant differences in temperature and/or humidity for short periods

Disclaimer:  The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications.  Management reserves the right to change or modify such duties as required.

Commitment to Diversity, Equity, and Inclusion:  

At Endo, our diversity unites and empowers us as One Team, and we are committed to cultivating, and valuing, each person’s unique perspective. We actively promote a culture of inclusion that draws strength from our broad spectrums of diversity, including race, ethnicity, religion, gender identity or expression, national origin, color, sexual orientation, disability status, age, and all our other unique characteristics, qualifications, demonstrated skills, achievements, and contributions, backgrounds, experiences, cultures, styles, and talents.

EEO Statement:

At Endo, we firmly believe in the principles of equal employment opportunity and strive to create an atmosphere where all employees, regardless of their race, color, creed, religion, sex, gender identity or expression, sexual orientation, national origin, genetics, disability (including pregnancy), age, or military or veteran status, feel valued, respected, and empowered. Our commitment to EEO extends to every aspect of employment, including recruitment, hiring, training, promotions, compensation, benefits, transfers, terminations, and all other employment practices. We are dedicated to ensuring that all employment decisions are based on qualifications, skills, and merit.