Scientist

Posted 4 Days Ago
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Rochester, MI
Senior level
Healthtech • Pharmaceutical • Telehealth
The Role
The Senior Scientist is responsible for analytical method development, validation, commercial testing, and mentoring within a regulated laboratory environment.
Summary Generated by Built In

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.

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

POSITION SUMMARY:

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 Chemists.   

ROLE AND RESPONSIBILITIES:

Analysis & 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 reviews

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 analyses

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 investigations

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 procedures

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 substances

Safety

  • 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 MSDS

REQUIRED QUALIFICATIONS:

Education & Experience

  • 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 preferred

Knowledge

  • 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 Suite

Skills & Abilities

  • 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 assignments

PHYSICAL REQUIREMENTS:

  • 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 chemicals
  • Must 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 vision
  • Ability to occasionally tolerate significant differences in temperature and/or humidity for short periods

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

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.

Top Skills

Agilent Chemstation
Ft-Ir
Gc
Hplc
Microsoft Office Suite
Sotax Winsotax
Uv-Vis
Waters Empower
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The Company
Montreal, Quebec
1,722 Employees
On-site Workplace
Year Founded: 1997

What We Do

At Endo, our far-reaching vision is simple: to help everyone we serve live their best life. As a specialty pharmaceutical company, we’re motivated by a strong sense of purpose to find better ways to meet unique medical needs.

Our global team of passionate employees understands the importance of their work. We’re dedicated to supporting one another as we connect with communities and foster partnerships that elevate quality-of-life and bring the best treatments forward.

Our uncompromising commitment results in the delivery of life-enhancing therapies. From intelligent product selection to commercialization, we strive to make a meaningful, tangible impact to help everyone live their best life.

Endo has global headquarters in Malvern, Pennsylvania.

Community Guidelines:
1. Be respectful. Everyone who visits our page should feel comfortable and respected.
2. If we see a comment that violates anything in the following list, it may be removed.
• Comments that use profanity; personally attack or bully another individual; or are off-topic, misleading, factually inaccurate, political, spam, defamatory, discriminatory or promotional.
• Comments that are excessively repetitive and/or disruptive to the community.
• Comments that promote illegal activity, use copyrights or trademarks or are related to an ongoing legal matter.
• Comments that appear to be medical advice.
We reserve the right to remove a reply for any reason at any time.
3. Adverse Event Reporting: If we see a post about an adverse event, an Endo representative will need to contact you to find out more information to comply with regulatory guidelines. If you experience a side effect while using an Endo product, please consult your physician or pharmacist immediately. You may also report to the FDA at fda.gov/medwatch or 800-FDA-1088.

Replies from other users do not necessarily reflect the views of Endo. We do not endorse content added by other users.

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