Senior Scientist, Analytical Research & Development

Veranova; West Deptford Township (NJ); On-site; USD 100,000 - 125,000; Full time

Benefits offered by this job

Comprehensive health & wellness benefits

Competitive base salary and performance-based bonuses

Tuition Assistance for further education

Generous PTO and holiday pay

Job summary

Veranova, a leader in manufacturing complex active pharmaceutical ingredients, seeks a Senior Scientist to advance analytical test methods and support GMP production. The ideal candidate will have extensive experience in method development, involving skills in various analytical techniques. Join our team to contribute to innovative therapeutics that save patient lives.

Qualifications

• PhD with 8+ years in GMP environment, or MS with 10+ years, or BS with 12+ years.
• Minimum 5 years experience in analytical method development for APIs.
• Experience with LC, GC, spectroscopy, and mentoring staff.

Responsibilities

• Develop and validate analytical procedures for small molecules and APIs.
• Conduct investigations, troubleshoot analyses, and prepare scientific reports.
• Interface with clients and document all analyses as per SOPs.

Skills

Analytical techniques

Problem-solving

Documentation

Interdisciplinary collaboration

Education

PhD in Analytical Chemistry

MS in Analytical Chemistry

BS in Analytical Chemistry

Tools

HPLC

LC-MS

GC-MS

Job description

Who We Are:

At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented workforce in our industry. Our commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference.

Who We Are:

At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented workforce in our industry. Our commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference.

Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation.

Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients.

Role Overview:

The Sr. Scientist is responsible for the implementation, development, and validation of analytical test methods in support of process research, and cGMP production with emphasis on development of LC, GC, GC-MS and LC/MS, ELISA, SEC-MALS, CE-SDS, cIEF, etc) methods for small molecules, ADCs, Oligonucleotides and Peptides Major support functions include sample analysis by various analytical techniques including HPLC, GC, LC-MS/MS, GC-MS, ICP-MS, CE, SEC-MALS, CE-SDS, cIEF, NMR, KF, titrations, and instrumental and wet chemical techniques. Other duties may involve analytical method modification, development, and validation. The incumbent may function as the primary contact on one or more development projects. In- depth involvement with the project team concerning the chemistry of the project and analytical chemistry needs is expected

Core Responsibilities:

• Develop and validate new analytical procedures. Independently, detects and solves complex problems of high technical difficulty.
• Perform sample analysis using various analytical techniques (e.g., LC, GC, LC-MS, GC-MS, ICP-MS, ELISA, SEC-MALS, CE-SDS, cIEF, etc.), interpret results, and prepare high-quality documentation such as protocols, analytical reports, and summary reports.
• Document all analyses per SOPs.
• Prepare SOPs, test methods, and other GMP documentation.
• Independently, detect and solve complex problems of high technical difficulty.
• Apply knowledge and expertise from multiple disciplines (including QA, QC, Analytical and production) to achieve project goals.
• Conduct investigations independently.
• Troubleshoot analyses and instruments.
• Support qualification of reference materials.
• Develop new analytical procedures.
• Validate analytical methods.
• Prepare and review scientific reports.
• Interface with internal and external clients.
  
  
  

Qualifications:

• PhD in Analytical Chemistry or equivalent with more than 8 years’ experience in a GMP environment.
• MS in Analytical Chemistry or equivalent with more than 10 years’ experience in a GMP environment.
• BS in Analytical Chemistry or equivalent with more than 12 years’ experience in a GMP environment.
• Minimum of 5 years’ experience in method development and validation for small molecules Active Pharmaceutical Ingredients (APIs). Experience with Process Development of APIs.
• Experience with LC, GC, GC-MS, LC-MS, IC, spectroscopy, and wet chemistry.
• Experience mentoring staff members in an analytical department.
• Formal project management training.
• Experience with writing method validation protocols and reports desirable.
• Experience with Microsoft Office and other complex computer software (UPLC, Empower 3) desirable.
  
  
  

Our Commitment:

• Health & Wellness: Comprehensive health & Wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies.
• Financial Wellness: Comprehensive total compensation package that includes competitive base salary, Defined Contribution Pension program, eligibility for performance-based bonuses, and attractive 401(k) Plan with company match.
• Professional Development: Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship. Tuition Assistance for Undergraduate and Graduate degree programs.
• Inclusive Culture: At Veranova an inclusive culture is integral to our values. We are committed to ensuring that everyone can bring their full self to work and thrive in their career.
  
  
  

How to Apply:

At Veranova, we are on a misson to meet people that believe in our values and can contribute to the team in a variety of ways. Please visit www.veranova.com to view all open roles and join our Talent Community to stay connected and learn about opportunities as they arise.

We value a range of experiences and perspectives. If you want to be part of improving and saving the lives of patients, we encourage you to apply regardless of whether you meet every qualification listed.

If you are a veteran, first responder, or in the process of transitioning from service member to civilian life, we encourage you to apply. Your experience brings invaluable skills and insights that can contribute to our team.

For applicants who may require a reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email to [e-mail] in order to confirm your request for an accommodation. Please include the job number, title, and location of role. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Veranova employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Additional Information:

Applicants for this role must be authorized to work in the United States without further employer sponsorship.

Agency and Search Firm Representatives: Veranova does not accept unsolicited resumes from agencies and/or search firms for this job posting.

Important Notice Regarding Recruitment Scams: Veranova is committed to providing a professional and secure recruitment experience for all applicants. Unfortunately, fraudulent job postings and recruitment scams are becoming more prevalent. We want to ensure that all candidates are aware of potential scams. Please see our notice here.

• Legitimate communications from Veranova will only come from official email addresses using our domain: @veranova.com.
• Legitimate LinkedIn communications will only come from active Veranova employees.
• Veranova will never ask candidates for sensitive personal information during the application process (e.g., bank account details or social security number).
• Veranova will never ask candidates for payment (e.g., for equipment, training, or background checks).
  
  
  

If you have any doubts or concerns about the authenticity of a job posting, please reach out to our HR department: [e-mail] (US) or [e-mail] (UK).

All your information will be kept confidential according to EEO guidelines.

Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law.

All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice .

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  Pharmaceutical Manufacturing

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